The document summarizes the pathogenesis and treatment of hypercalcemia of malignancy (HCM). It describes how HCM occurs via increased bone resorption from factors released by tumor cells like PTHrP, as well as the kidney's increased reabsorption of calcium. Signs and symptoms of HCM include fatigue, confusion and kidney problems. Treatment involves rehydration, bisphosphonates like zoledronic acid which strongly inhibits bone resorption, and calcitonin to reduce calcium levels. Zoledronic acid is the most potent bisphosphonate available and can reduce HCM within 24 hours.
Metastatic Bone Disease & Role of Zoledronic AcidMRINMOY ROY
Metastatic Bone Disease is Cancer that begins in an organ, such as the lungs, breast, or prostate, and then spreads to bone.
More than 1.2 million new cancer cases are diagnosed each year. Approximately 50% of these tumours can spread (metastasize) to the skeleton.
With improved medical treatment of many cancers — especially breast, lung, and prostate — patients are living longer. However, the primary cancers in more of these patients are spreading to bone. The tumours that result are called bone metastases.
Here the role of Zoledronic Acid have been fall in place in treatment.
Dr. Sehdev explains bone health as it relates to cancer, including bone metastases, treatment options, the impact of cancer treatment on bone health, and what you can do to keep your bones strong.
Metastatic Bone Disease & Role of Zoledronic AcidMRINMOY ROY
Metastatic Bone Disease is Cancer that begins in an organ, such as the lungs, breast, or prostate, and then spreads to bone.
More than 1.2 million new cancer cases are diagnosed each year. Approximately 50% of these tumours can spread (metastasize) to the skeleton.
With improved medical treatment of many cancers — especially breast, lung, and prostate — patients are living longer. However, the primary cancers in more of these patients are spreading to bone. The tumours that result are called bone metastases.
Here the role of Zoledronic Acid have been fall in place in treatment.
Dr. Sehdev explains bone health as it relates to cancer, including bone metastases, treatment options, the impact of cancer treatment on bone health, and what you can do to keep your bones strong.
How can immunotherapy be used to treat metastatic breast cancer? Ian Krop, MD, PhD, discusses the latest research and treatment options.
This presentation was originally given as part of the 2015 Metastatic Breast Cancer Forum, held on October 17 and hosted by the Susan F. Smith Center for Women's Cancers at Dana-Farber Cancer Institute in Boston, Mass.
For more information, visit www.susanfsmith.org
Ortho: to make straight or right. The use of biologic substances to prompt, stimulate or support a “healing event” within the body.The use of biologic substances to promote healing or reduce pain.The use of platelets and stem cells in treatment and management of musculoskeletal conditions
1º. Presentación: Este acto pertenece a una acción colectiva que se llama “La Gran lección” o “Lección para todos” dentro de la Semana de Acción Mundial por la Educación. Con él pretendemos batir un record.
2. Se pregunta al auditorio ¿Qué es un record? ¿Conocéis a algún recordman o a algunas recordwoman?. Se deja que contesten.
En la diapostiva tenemos a Usain Bolt, atleta jamaicano recorman de los 100 metros lisos con 9,58 y a la rusa Isinbayeva recordwoman de altura con 5,01.
3. Nosotros vamos a intentar batir otro record mundial: el de la lección con más audiencia jamás realizada.
Hoy, 20 de Abril, esta misma lección que vosotros seguís va a ser recibida simultáneamente por más de 30 millones de personas en 100 países del mundo.
Nuestra lección versa sobre la necesidad de alcanzar la escolarización plena para todos los niños y niñas en el 2015.
4. El mundo del fútbol, que celebra su campeonato mundial del 11 de Junio al 11 de Julio, ha ofrecido su apoyo a esta reivindicación.
5. Muchos futbolistas apoyan a través de la campaña “1 Gol por la educación” esta aspiración de escolarización universal. Además de los que veis en la diapositiva Casillas, Villa, Torres y otros futbolistas españoles también la apoya.
6. Futbolistas africanos como Desailly o Mokoena son muy conscientes de las necesidades educativas de su continente y por eso piden vuestro apoyo a la campaña.
Otros la apoyan por solidaridad, como el defensa francés del Arsenal, Silvestre que tiene su propia Organización para este fin: •Escuelas para la esperanza”.
[Se lee la parte de este futbolista]
7. Más de 75 millones de niños y niñas en el mundo no pueden ir al cole. Más del 60 por ciento de ellos son niñas. En África hay millones de casos como el de Molly.
8. Niñas como Arti Kumasi de India han de atender a sus hermanos y las tareas de la casa. Los padre de muchas de estas chicas ni siquiera entienden que tengan que ir a la escuela
[Leer sus palabras]
9. El trabajo infantil impide en muchos casos que los niños puedan materializar sus sueños.
[Se deja tiempo para que el auditorio pueda leer el texto]
10. La carencia de medios, de escuelas y de maestros es otra dificultad. El pequeño tanzano Dires tiene la escuela más cercana a 20 Kilómetros.
11. Hay casos emocionante de esfuerzo y lucha por la educación a pesar de todas las adversidades. Yherlin compatibiliza a duras penas trabajo y estudios.
12. La escasez de maestros y los bajos salarios que perciben muchos de ellos dificulta la continuidad del trabajo. En zonas rurales de Malawi la media es de 120 alumnos/as por docente.
13. Ya hemos dicho que hay cerca de 75 millones de niños que no van a la escuela pero ¿por qué? [Se pregunta en general al auditorio y se repiten alguna de las respuestas acertadas]
14. [Se repasan las respuestas que se han dicho y se aportan algunas más no dichas fijándonos en la diapositiva].
15. ¿Cuáles son las ventajas de la Educación? [Se permite que el auditorio de algunas respuestas]. La educación de las personas repercute en muchos ámbitos de su vida.
Las personas con estudios gozan de mejor salud porque tienen mayor acceso a la información sobre hábitos de vida saludables.
16. Si los padres están instruidos, los hijos se quedan más tiempo en la escuela y rinden más.
17. La ignorancia y los prejuicios favorecen la propagación del SODA. La educación es fundamental para frenarlo.
18. La educación salva vidas. Se ha demostrado la relación entre la prolongación de la vida y la cobertura educativa.
19. El umbral de la pobreza es un dólar al día (menos de un euro). La mayor parte de los hombres y mujeres que no han tenido educación pertenecen a este grupo.
20. La educación permite crear ciudadanos y ciudadanas conscientes de sus derechos y responsables en la solución de los problemas. La Democracia quiere una ciudadanía instruida.
21. Los países con mayor tasa de alfabetización tienen un mayor
How can immunotherapy be used to treat metastatic breast cancer? Ian Krop, MD, PhD, discusses the latest research and treatment options.
This presentation was originally given as part of the 2015 Metastatic Breast Cancer Forum, held on October 17 and hosted by the Susan F. Smith Center for Women's Cancers at Dana-Farber Cancer Institute in Boston, Mass.
For more information, visit www.susanfsmith.org
Ortho: to make straight or right. The use of biologic substances to prompt, stimulate or support a “healing event” within the body.The use of biologic substances to promote healing or reduce pain.The use of platelets and stem cells in treatment and management of musculoskeletal conditions
1º. Presentación: Este acto pertenece a una acción colectiva que se llama “La Gran lección” o “Lección para todos” dentro de la Semana de Acción Mundial por la Educación. Con él pretendemos batir un record.
2. Se pregunta al auditorio ¿Qué es un record? ¿Conocéis a algún recordman o a algunas recordwoman?. Se deja que contesten.
En la diapostiva tenemos a Usain Bolt, atleta jamaicano recorman de los 100 metros lisos con 9,58 y a la rusa Isinbayeva recordwoman de altura con 5,01.
3. Nosotros vamos a intentar batir otro record mundial: el de la lección con más audiencia jamás realizada.
Hoy, 20 de Abril, esta misma lección que vosotros seguís va a ser recibida simultáneamente por más de 30 millones de personas en 100 países del mundo.
Nuestra lección versa sobre la necesidad de alcanzar la escolarización plena para todos los niños y niñas en el 2015.
4. El mundo del fútbol, que celebra su campeonato mundial del 11 de Junio al 11 de Julio, ha ofrecido su apoyo a esta reivindicación.
5. Muchos futbolistas apoyan a través de la campaña “1 Gol por la educación” esta aspiración de escolarización universal. Además de los que veis en la diapositiva Casillas, Villa, Torres y otros futbolistas españoles también la apoya.
6. Futbolistas africanos como Desailly o Mokoena son muy conscientes de las necesidades educativas de su continente y por eso piden vuestro apoyo a la campaña.
Otros la apoyan por solidaridad, como el defensa francés del Arsenal, Silvestre que tiene su propia Organización para este fin: •Escuelas para la esperanza”.
[Se lee la parte de este futbolista]
7. Más de 75 millones de niños y niñas en el mundo no pueden ir al cole. Más del 60 por ciento de ellos son niñas. En África hay millones de casos como el de Molly.
8. Niñas como Arti Kumasi de India han de atender a sus hermanos y las tareas de la casa. Los padre de muchas de estas chicas ni siquiera entienden que tengan que ir a la escuela
[Leer sus palabras]
9. El trabajo infantil impide en muchos casos que los niños puedan materializar sus sueños.
[Se deja tiempo para que el auditorio pueda leer el texto]
10. La carencia de medios, de escuelas y de maestros es otra dificultad. El pequeño tanzano Dires tiene la escuela más cercana a 20 Kilómetros.
11. Hay casos emocionante de esfuerzo y lucha por la educación a pesar de todas las adversidades. Yherlin compatibiliza a duras penas trabajo y estudios.
12. La escasez de maestros y los bajos salarios que perciben muchos de ellos dificulta la continuidad del trabajo. En zonas rurales de Malawi la media es de 120 alumnos/as por docente.
13. Ya hemos dicho que hay cerca de 75 millones de niños que no van a la escuela pero ¿por qué? [Se pregunta en general al auditorio y se repiten alguna de las respuestas acertadas]
14. [Se repasan las respuestas que se han dicho y se aportan algunas más no dichas fijándonos en la diapositiva].
15. ¿Cuáles son las ventajas de la Educación? [Se permite que el auditorio de algunas respuestas]. La educación de las personas repercute en muchos ámbitos de su vida.
Las personas con estudios gozan de mejor salud porque tienen mayor acceso a la información sobre hábitos de vida saludables.
16. Si los padres están instruidos, los hijos se quedan más tiempo en la escuela y rinden más.
17. La ignorancia y los prejuicios favorecen la propagación del SODA. La educación es fundamental para frenarlo.
18. La educación salva vidas. Se ha demostrado la relación entre la prolongación de la vida y la cobertura educativa.
19. El umbral de la pobreza es un dólar al día (menos de un euro). La mayor parte de los hombres y mujeres que no han tenido educación pertenecen a este grupo.
20. La educación permite crear ciudadanos y ciudadanas conscientes de sus derechos y responsables en la solución de los problemas. La Democracia quiere una ciudadanía instruida.
21. Los países con mayor tasa de alfabetización tienen un mayor
Increase in Bone Mass Density and Overall Bone Health Following High-Impact o...CrimsonPublishers-SBB
Vitamin D3 and calcium are the main bone health supplements required for quality of life. The present study aimed to find out the role of Consciousness Energy Healing based vitamin D3 and DMEM medium on bone health parameters in vitro using MG-63 cells. The parameters of bone health tested are Alkaline Phosphatise Enzyme (ALP) activity, collagen levels, and bone mineralization. The Test Items (TI) i.e. vitamin D3 and DMEM medium were divided into two parts. The test samples received Consciousness Energy Healing Treatment by Krista Joanne Callas and samples were defined as the Bio-field Energy Treated (BT) samples, while the other parts of each sample were denoted as the untreated test items (UT). Cell viability using MTT assay exhibited increased cell viability range from 72% to 122% with safe and nontoxic profile among test samples on the MG-63 cell line. was significantly increased by 129.6%, 392%, and 255.7%in the UT-DMEM+BT-TI, BT-DMEM+UT-TI, and BT-DMEM+BT-TI groups, respectively at 100μg/mL as compared with the untreated group.
This is a power point presentation titled Hypercalcemia of malignancy. For medical power point, x-rays, CT scans, medical projects or other downloads, visit www.medicaldump.com
DISSERTATION on NEW DRUG DISCOVERY AND DEVELOPMENT STAGES OF DRUG DISCOVERYNEHA GUPTA
The process of drug discovery and development is a complex and multi-step endeavor aimed at bringing new pharmaceutical drugs to market. It begins with identifying and validating a biological target, such as a protein, gene, or RNA, that is associated with a disease. This step involves understanding the target's role in the disease and confirming that modulating it can have therapeutic effects. The next stage, hit identification, employs high-throughput screening (HTS) and other methods to find compounds that interact with the target. Computational techniques may also be used to identify potential hits from large compound libraries.
Following hit identification, the hits are optimized to improve their efficacy, selectivity, and pharmacokinetic properties, resulting in lead compounds. These leads undergo further refinement to enhance their potency, reduce toxicity, and improve drug-like characteristics, creating drug candidates suitable for preclinical testing. In the preclinical development phase, drug candidates are tested in vitro (in cell cultures) and in vivo (in animal models) to evaluate their safety, efficacy, pharmacokinetics, and pharmacodynamics. Toxicology studies are conducted to assess potential risks.
Before clinical trials can begin, an Investigational New Drug (IND) application must be submitted to regulatory authorities. This application includes data from preclinical studies and plans for clinical trials. Clinical development involves human trials in three phases: Phase I tests the drug's safety and dosage in a small group of healthy volunteers, Phase II assesses the drug's efficacy and side effects in a larger group of patients with the target disease, and Phase III confirms the drug's efficacy and monitors adverse reactions in a large population, often compared to existing treatments.
After successful clinical trials, a New Drug Application (NDA) is submitted to regulatory authorities for approval, including all data from preclinical and clinical studies, as well as proposed labeling and manufacturing information. Regulatory authorities then review the NDA to ensure the drug is safe, effective, and of high quality, potentially requiring additional studies. Finally, after a drug is approved and marketed, it undergoes post-marketing surveillance, which includes continuous monitoring for long-term safety and effectiveness, pharmacovigilance, and reporting of any adverse effects.
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
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ABDOMINAL TRAUMA in pediatrics part one.drhasanrajab
Abdominal trauma in pediatrics refers to injuries or damage to the abdominal organs in children. It can occur due to various causes such as falls, motor vehicle accidents, sports-related injuries, and physical abuse. Children are more vulnerable to abdominal trauma due to their unique anatomical and physiological characteristics. Signs and symptoms include abdominal pain, tenderness, distension, vomiting, and signs of shock. Diagnosis involves physical examination, imaging studies, and laboratory tests. Management depends on the severity and may involve conservative treatment or surgical intervention. Prevention is crucial in reducing the incidence of abdominal trauma in children.
How STIs Influence the Development of Pelvic Inflammatory Disease.pptx
Zometa Hcm Slide Kit
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2. Pathogenesis of HCM Types of HCM Signs and symptoms of HCM Diagnosis of HCM Overview of treatment of HCM ZOMETA™ (zoledronic acid for injection) Overview of hypercalcemia of malignancy (HCM)
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13. Signs and symptoms of HCM 1 1. Morton AR, Lipton A. Clin Oncol. 1995;527-542. 2. Barnett ML. Semin Oncol Nurs. 1999;190-201. CNS Altered levels of consciousness; lethargy; somnolence; stupor; coma; depression; psychosis; ataxia Neuromuscular Muscle weakness; proximal myopathy; hypertonia CV Hypertension; bradycardia; shortened QT interval Renal Kidney stones; decreased glomerular filtration; polyuria; acidosis; increase in corrected serum calcium GI Nausea; vomiting; constipation; anorexia Skeletal 2 Bone pain
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Editor's Notes
Overview of hypercalcemia of malignancy (HCM) HCM is excess calcium in the blood brought about when a tumor stimulates or releases substances whose activity causes bone resorption to exceed bone synthesis. HCM is a medical emergency associated with metastatic disease, and is one of the most common metabolic complications of malignancy. 1-4 HCM affects approximately 10% to 20% of all cancer patients at some point during the course of disease, and 20% to 40% of patients with advanced disease. 5-8 This segment of the presentation will review the pathogenesis, types, symptoms, and diagnosis of HCM. This will lay the foundation for a greater understanding of the importance of treating HCM—and the new, highly potent bisphosphonate therapy, ZOMETA™ (zoledronic acid for injection). 1. Coleman RE. Skeletal complications of malignancy. Cancer . 1997;80(suppl 8):1588-1594. 2. Rubens RD, Coleman RE. Bone metastases. In: Abeloff MD, Armitage JO, Lichter AS, et al, eds. Clinical Oncology. New York, NY: Churchill Livingstone; 1995;643-648. 3. Morton AR, Lipton A. Hypercalcemia. In: Abeloff MD, Armitage JO, Lichter AS, et al, eds. Clinical Oncology. New York, NY: Churchill Livingstone; 1995;527-542. 4. Ralston SH. In: Body JJ (ed). Tumor Bone Diseases and Osteoporosis in Cancer Patients. New York, NY: Marcel Dekker; 2000;393-407. 5. Mundy GR, Ibbotson KJ, D’Souza SM, et al. The hypercalcemia of cancer: clinical implications and pathogenic mechanisms. N Engl J Med. 1984;310:1718-1727. 6. Vassilopoulou-Sellin R, et al. Incidence of hypercalcemia in patients with malignancy referred to a comprehensive cancer center. Cancer. 1993;71:1309-1312. 7. Watters J, et al. The management of malignant hypercalcemia. Drugs. 1996;52:837-848. 8. CancerNet™. Hypercalcemia (PDQ ® ) Supportive Care-Health Professionals. 2000.
Overview of mechanisms of HCM There are four main mechanisms of HCM. While these mechanisms differ, they share an underlying osteoclast activation that triggers bone resorption and its consequent increase in serum calcium. The four main mechanisms involved are 1 : Increased bone destruction , either local or generalized, which brings about a release of calcium from the skeleton and consequently an increase in the flow of calcium through the extracellular space. This mechanism appears to be the main cause of HCM in patients with hematological disorders such as myeloma and in many patients with various metastases. Increased tubular reabsorption of calcium by the kidney , as a result of factors produced by tumor cells. The renal mechanism occurs with solid tumors such as squamous cell carcinoma of the lung and carcinomas of other organs. In many solid tumors with bone metastases, both the osseous and renal mechanisms coexist. Decreased urinary calcium excretion as a result of impaired glomerular filtration rate and dehydration may also contribute to HCM. Less frequent mechanisms include, as in myeloma, a decrease in bone formation, which can contribute to hypercalcemia through the diminished efflux of calcium from the extracellular space to bone. 1. Fleisch H. In: Bisphosphonates in Bone Disease. San Diego, California: Academic Press; 2000:90-92.
Factors involved in HCM 1,2 Metastatic tumor cells release factors that are associated with HCM. They are generally grouped into four categories 1,2 : Parathyroid hormone-related protein (PTHrP), which acts on the kidneys and bone Bone-resorbing cytokines, which appear to act directly on bone cells 1,25 (OH) 2 D, the active metabolite of vitamin D Prostaglandins, whose role in HCM remains unclear 1. Mundy GR. (ed). Bone Remodeling and Its Disorders. 2nd ed. London, England: Martin Dunitz Ltd; 1999;107-122. 2. Mundy GR. Bisphosphonates as cancer drugs. Hosp Pract. 1999;81-94.
Parathyroid hormone-related protein (PTHrP) PTHrP, one of the factors produced by solid tumors, is the most common mediator of enhanced bone resorption by tumors. 1 PTHrP is a protein that resembles parathyroid hormone (PTH) and stimulates diffuse osteoclastic bone resorption. 2 The subsequent release of transforming growth factor beta (TGF- ) into the local bone microenvironment further stimulates tumor production of PTHrP. 2 This perpetuates a vicious cycle of bone resorption and destruction that contributes to HCM. 1,2 PTHrP also increases renal tubular calcium reabsorption by stimulating renal production of cyclic adenosine monophosphate (cAMP). 1,3 cAMP increases tubular permeability to water, a factor in increasing reabsorption of water—and therefore of calcium. 3 Thus, the correlation between the production of PTHrP and development of HCM is high. 1. Goltzman D, Kremer R, Rabbani SA. Molecular basis of the spectrum of skeletal complications of malignancy. Abstract presented at the Second North American Symposium on Skeletal Complications of Malignancy. October 15–16, 1999; Montréal, Canada. 2. Guise TA. Molecular mechanisms of osteolytic metastases. Abstract presented at the Second North American Symposium on Skeletal Complications of Malignancy. October 15–16, 1999; Montréal, Canada. 3. Mundy GR (ed). Bone Remodeling and Its Disorders . London, England: Martin Dunitz Ltd; 1989;113-119.
Bone-resorbing cytokines Cytokines, protein substances normally released by the immune system, act as intercellular messengers and enhance the immune response. Certain cytokines associated with HCM are released by tumors; in addition, tumors may stimulate the release of cytokines by the immune system. These cytokines are thought to mediate elevated serum calcium by increasing bone resorption. Although research has identified many cytokines, four in particular appear to be associated with bone resorption: Transforming growth factors (TGF- and TGF- ) exhibit potent bone-resorbing activity 1 Tumor necrosis factors (TNF- and TNF- ) stimulate bone resorption and inhibit bone formation by decreasing collagen synthesis, reducing alkaline phosphatase, and increasing monocyte-macrophage colony stimulating factor (mCSF) 2,3 Colony-stimulating factors (CSFs) increase bone resorption by stimulating osteoclasts, increase development of osteoclast precursors, and stimulate production of interleukins 2 Interleukins increase bone resorption by stimulating osteoclasts 4 1. Todaro GJ, Fryling D, DeLarco JE. Transforming growth factors produced by certain human tumor cells: polypeptides that interact with epidermal growth factor receptors. Proc Natl Acad Sci USA. 1980;77:5258-5262. 2. Mundy GR (ed). Bone Remodeling and Its Disorders. London, England: Martin Dunitz Ltd; 1989;45-82; 113-119. 3. Mundy GR. Hypercalcemic factors other than parathyroid hormone-related protein. Endocrinol Metab Clin North Am. 1989;18:795-806. 4. Kelly PJ, Eisman JA. Hypercalcemia of malignancy. Cancer Metastasis Rev. 1989;8:23-52.
1,25 (OH) 2 D 1 Uncontrolled production of 1,25 (OH) 2 D, either by tumor cells directly or by the kidney under the influence of PTHrP, may contribute significantly to the development of HCM. 1,25 (OH) 2 D stimulates bone resorption by recruiting osteoclast precursors and by producing osteoclast stimulating factors from osteoblasts. This mechanism is probably only important in the development of HCM in certain leukemias and lymphomas. 1. Mundy GR (ed). Bone Remodeling and Its Disorders. London, England: Martin Dunitz Ltd; 1989;45-82; 113-119.
Prostaglandins Prostaglandins are naturally occurring fatty acids involved in a number of regulatory functions throughout the body. They are also associated with such disease processes as pain and inflammation. The role of prostaglandins in HCM is unclear. Prostaglandins may have a bidirectional effect on osteoclasts — an immediate transient effect to slow or inhibit bone resorption, but a more sustained long-lasting effect to increase osteoclastic bone resorption. 1 At least part of the effects of some of the cytokines on osteoclastic bone resorption in vivo as well as in vitro are mediated through prostaglandin synthesis. 1 It is possible that prostaglandins may exert more direct effects on osteoclastic bone resorption. They are produced by cultured tumor cells in vitro . Whether a similar phenomenon happens in vivo is unknown. One possibility is that prostaglandins, like cytokines such as TNF, could be produced by host immune cells in response to the tumor. 1 1. Mundy GR (ed). Bone Remodeling and Its Disorders. 2nd ed. London, England: Martin Dunitz Ltd; 1999;56-59, 118.
Types of hypercalcemia of malignancy (HCM) There are three types of hypercalcemia: humoral hypercalcemia of malignancy; local osteolytic hypercalcemia associated with bone metastases; and hypercalcemia associated with hematologic malignancies. Humoral hypercalcemia and local osteolytic hypercalcemia are the two main mechanisms that contribute to the occurrence of HCM. Humoral and local osteolytic mechanisms may act independently, but usually both mechanisms are involved in malignancy-related hypercalcemia—an increase in osteoclast activity that releases large amounts of calcium. 1 All three types of hypercalcemia have in common an underlying increase in osteoclast activity. 1. Barnett ML. Hypercalcemia. Semin Oncol Nurs . 1999;15(3):190-201.
Humoral hypercalcemia of malignancy (HHM) 1 Humoral hypercalcemia of malignancy is caused by the production of circulating humoral factors, such as PTHrP and cytokines, in patients who have solid tumors with or without bone metastases. These factors stimulate osteoclasts and bone resorption, while increasing renal tubular reabsorption of calcium. These actions ultimately raise serum calcium, resulting in HCM. HHM is most commonly associated with squamous cell carcinomas of the lung, head and neck, and is sometimes associated with renal cell carcinoma and genitourinary cancers . 1. Mundy GR. Malignancy and hypercalcemia—Humoral hypercalcemia of malignancy, hypercalcemia associated with osteolytic metastases. In: Mundy GR (ed). Calcium Homeostasis: Hypercalcemia and Hypocalcemia. London, England: Martin Dunitz Ltd; 1990;69-99.
Local osteolytic HCM associated with bone metastases 1-3 HCM results from a vicious cycle of tumor-induced osteolysis. 1-3 1. Metastatic tumor cells release factors—PTHrP, prostaglandin E, growth factors, and cytokines—that directly stimulate osteoclast activity 1,2 2. Osteoclastic activity releases growth factors (ie, TGF- ) that stimulate tumor-cell growth, perpetuating a vicious cycle of bone resorption 2 3. Bone resorption releases calcium from the skeleton, increasing the flow of calcium through the extracellular space, resulting in elevated serum calcium 1 1. Guise TA, Mundy GR. Cancer and bone. Endocr Rev. 1998;19:18-54. 2. Mundy GR (ed). Cellular mechanisms of bone resorption. In: Bone Remodeling and Its Disorders . 2nd ed. London, England: Martin Dunitz Ltd; 1999;23-25. 3. Mundy GR. Cancer. 1997;80 (suppl 8):1546-1556.
Hypercalcemia associated with hematologic malignancies Hypercalcemia associated with multiple myeloma is due to extensive destruction of bone adjacent to myeloma cells, in combination with impaired glomerular filtration and an inability of the kidney to excrete the excess calcium. The pathophysiology of this type of hypercalcemia is unique when compared with other types of HCM. Patients with other hematologic malignancies—such as malignant lymphomas and, occasionally, leukemia—also develop hypercalcemia. In these cases, tumor-produced factors may act independently or synergistically to directly increase bone resorption, resulting in worsening hypercalcemia.
Signs and symptoms of HCM 1 The clinical presentation of HCM can vary substantially. Symptoms of HCM appear mainly in the nervous, gastrointestinal, cardiovascular, and renal systems. HCM is considered a medical emergency, and since it can be life-threatening it must be dealt with immediately. 1 Clinical features of the hypercalcemic syndrome include: altered levels of consciousness; lethargy; somnolence; stupor; coma; depression; psychosis; ataxia; muscle weakness; proximal myopathy; hypertonia; hypertension; bradycardia; shortened QT interval; kidney stones; decreased glomerular filtration; polyuria; acidosis; nausea; vomiting; constipation; and anorexia. 1 However, symptoms of HCM can be relatively nonspecific and may be easily confused with those of the underlying cancer. 3 1. Morton AR, Lipton A. Clin Oncol. 1995;527-542. 2. Barnett ML. Semin Oncol Nurs . 1999; 190-201. 3. Ralston SH. Treatment of tumor-induced hypercalcemia. In: Body JJ (ed). Tumor Bone Diseases and Osteoporosis in Cancer Patients. New York, NY: Marcel Dekker; 2000;393-407.
Diagnosis (Dx) of HCM Because the symptoms of HCM can be confused easily with the symptoms of the underlying cancer, it is important to consider the possibility of hypercalcemia in any person with cancer who starts to experience symptomatic deterioration. 1 While symptoms generally increase in proportion to the degree of hypercalcemia, there is considerable variation between individuals, such that some patients experience severe symptoms with relatively mild hypercalcemia, and vice versa. 1 Hypercalcemia should be confirmed by measurement of total serum calcium levels, but it is important to emphasize that these must be adjusted for serum albumin concentrations. Since hypoalbuminemia is common in persons with cancer, unadjusted total calcium concentrations seriously underestimate the severity of HCM. 2 While no algorithm is 100% sensitive for the detection of all true cases of hypercalcemia, the equation shown has the merits of accuracy and simplicity. 3,4 CSC, mg/dL = Serum Ca, mg/dL + 0.8 (4.0 – serum albumin, g/dL) 1. Ralston SH. Treatment of tumor-induced hypercalcemia. In: Body JJ (ed). Tumor Bone Diseases and Osteoporosis in Cancer Patients. New York, NY: Marcel Dekker; 2000; 393-407. 2. Iqbal SJ, Giles M, Ledger S, Nanji N, Howl T. Need for albumin adjustments of urgent total serum calcium. Lancet . 1988;ii:1477-1478. 3. Payne RB, Little AJ, Williams RB, Milner JR. Interpretation of serum calcium in patients with abnormal serum proteins. BMJ . 1973;4:643. 4. Morton AR, Hercz G. Hypercalcemia in dialysis patients: comparison of diagnostic methods. Dialysis Transplant. 1991;20:661.
Principles of antihypercalcemic treatment HCM can be treated successfully in the majority of patients once it is recognized and confirmed by measuring corrected serum calcium. It must be emphasized that the only truly effective way of controlling HCM in the long term is to treat the underlying malignancy. However, in instances in which the hypercalcemia persists, treatment is based predominantly on symptoms and level of patient discomfort. For patients who have mild HCM, therapy should include basic measures, such as ambulation (weight-bearing activities) whenever possible, to decrease the rate of bone resorption—thus retaining calcium in the skeleton. Patients should avoid salt restrictions, which would actually promote volume contraction and renal calcium retention, leading to severe dehydration and worsening HCM. As a standard course of therapy, adequate hydration should be maintained in all patients with HCM. There is no need for restriction of dietary calcium intake, unless the patient has hypercalcemia associated with lymphoma, which is mediated by 1,25 (OH) 2 D. For patients who have moderate-to-severe HCM (corrected serum calcium levels of 12.8 to greater than 13.5 mg/dL), effective treatment consists of essentially two approaches: rehydration with intravenous fluid therapy to promote urinary excretion of calcium; and antiresorptive drug therapy to inhibit osteoclastic bone resorption.
Treatment of moderate-to-severe HCM by rehydration 1 Many patients who have HCM become so dehydrated that it may take as much as 2 to 4 liters of extracellular fluid to restore their volume status during the initial 24 hours. During the process of volume depletion, the proximal tubules increase their rate of reabsorption of calcium and sodium. Intravenously administered isotonic saline is recommended for rehydration, which will help promote sodium diuresis, thereby inducing calcium excretion as well. Once rehydration is initiated, the patient must be closely monitored for urinary output and cardiac status, as well as for serum calcium, creatinine and electrolyte concentrations. Rehydration will cause serum calcium levels to decrease and, in a few cases, to fall within the normal range. This decrease is only transient, however, and additional therapy directed at inhibiting active bone resorption must be instituted to maintain the lowered serum calcium levels. In rare cases, a patient who has myeloma may have renal failure and therefore is not a suitable candidate for rehydration. In this situation, hemodialysis or peritoneal dialysis may be used to lower serum calcium levels. Once the patient is rehydrated and volume expansion is achieved, a loop diuretic can be administered to further increase renal excretion of calcium. It is important that the patient be completely rehydrated before instituting this therapy, since loop diuretics may worsen the hypercalcemia by promoting additional depletion of extracellular fluid, which will again cause increased calcium reabsorption. 1. Barnett ML. Hypercalcemia. Semin Oncol Nurs . 1999;15(3):190-201.
Treatment of moderate-to-severe HCM by antiresorptive therapy Although rehydration and monitoring of renal function should be the initial therapy for moderate-to-severe HCM, treatment with antiresorptive agents is essential to decrease the rate of bone resorption and to prevent worsening or recurrence of the hypercalcemia. These therapies can often be initiated concurrently with volume expansion, since there is generally a 24-to-48-hour delay in the onset of action. A number of agents are available to reduce bone resorption. These include salmon calcitonin, gallium nitrate, and the IV bisphosphonates pamidronate and ZOMETA™ (zoledronic acid for injection).
Salmon calcitonin 1 Calcitonin is an antiresorptive agent that inhibits osteoclastic bone resorption by decreasing the formation of osteoclasts and contracting the cytoplasmic membrane of osteoclasts. It also decreases renal tubular calcium reabsorption. These mechanisms work in concert to produce a rapid lowering of serum calcium levels. Salmon calcitonin is administered intramuscularly or subcutaneously at dosages ranging from 4 to 8 IU/kg every 6 to 12 hours. Salmon calcitonin may cause nausea with or without vomiting, and allergic reactions such as skin rashes. The effects of calcitonin alone are transient and reversible, lasting only 24 to 72 hours. Therefore, its usefulness in long-term management of hypercalcemia is unclear. 1. Mundy GR, Martin TJ. The hypercalcemia of malignancy: pathogenesis and management. Metabolism. 1982;31(12):1247-1277.
Gallium nitrate 1 Gallium nitrate is a cytotoxic agent that was first noted to cause hypocalcemia in cancer patients, an observation that prompted investigation of its use in patients who have HCM. It is currently approved for the treatment of HCM. Its mechanism of action is not known, but one hypothesis is that it may stabilize bone crystals. The recommended dosage is 200 mg/m 2 body surface/day for 5 consecutive days, given as a continuous infusion. If serum calcium falls to within the normal range before 5 days, treatment may be discontinued early. Lower dosages of 100 mg/m 2 /day for 5 consecutive days may be effective in patients who have mild hypercalcemia. Gallium nitrate should not be given to patients who have renal insufficiency, because nephrotoxicity has been noted in some patients. To help avoid this toxicity, patients should be adequately hydrated before gallium nitrate is administered. The concurrent use of aminoglycoside antibiotics may increase the risk of nephrotoxicity; therefore their use should be avoided for 48 hours before or after treatment when gallium nitrate is initiated. Some patients have become hypophosphatemic after receiving gallium nitrate. 1. Warrel RP Jr. Gallium nitrate and bone metastases. In: Body JJ (ed). Tumor Bone Diseases and Osteoporosis in Cancer Patients. New York, NY: Marcel Dekker; 2000;483-492.
IV bisphosphonate for HCM An IV bisphosphonate, such as pamidronate and ZOMETA™ (zoledronic acid for injection), remains the treatment of choice for HCM. IV bisphosphonates are the most effective drugs available to inhibit osteoclastic activity. Since osteolysis is mainly due to excess osteoclast activity, reducing osteoclast activity can reduce bone destruction and resorption and associated complications such as hypercalcemia. In addition to being very effective in lowering serum calcium, IV bisphosphonates are comparatively nontoxic. Therefore, they can be administered to treat even mild HCM; they are not associated with adverse reactions that could complicate the treatment of underlying cancer or of HCM, or compromise the condition of the patient.
ZOMETA ™ (zoledronic acid for injection) ZOMETA belongs to a new class of highly potent bisphosphonates. ZOMETA is a heterocyclic, nitrogen-containing bisphosphonate that is composed of a core bisphosphonate moiety (similar in structure to pyrophosphate) and an imidazole-ring side chain. The imidazole group is a five-member ring containing 2 critically positioned nitrogen atoms. The unique structural features of ZOMETA distinguish it from other bisphosphonates, and in preclinical studies are associated with its increased potency and therapeutic ratio, relative to compounds without the imidazole ring. 1. Green J, Müller K, Jaeggi KA. Preclinical pharmacology of CGP 42’446, a new, potent, heterocyclic bisphosphonate compound. J Bone Miner Res. 1994;9(5):745-751. 2. Green J, Seltenmeyer Y, Jaeggi KA, Widler L. Renal tolerability profile of novel, potent bisphosphonates in two short-term rat models. Pharmacol Toxicol . 1997;80(5):225-230.
Evaluation of potency of bisphosphonates 1 In vivo studies were performed to measure the effects of different bisphosphonates on bone resorption. 1 The effect of bisphosphonates in the hypercalcemic rat model is shown here (ED 50 is the dose required to reduce hypercalcemia by 50%). ZOMETA™ (zoledronic acid for injection) is the most potent bisphosphonate, with up to 850 times more activity than conventional bisphosphonates. These data are supported by in vitro studies. The good correlation between the in vitro and in vivo assays confirms that the pharmacodynamic action of ZOMETA is due to direct inhibition of bone resorption in vivo . Thus, ZOMETA is a more potent inhibitor of osteoclasts than are conventional bisphosphonates, being 100 to 850 times more potent than pamidronate as an inhibitor of bone resorption. 1 1. Green J, Müller K, Jaeggi KA. Preclinical pharmacology of CGP 42’446, a new, potent, heterocyclic bisphosphonate compound. J Bone Miner Res. 1994;9(5):745-751.
ZOMETA™ (zoledronic acid for injection)—mechanisms of action The structural features of ZOMETA distinguish it from other bisphosphonates. ZOMETA has an imidazole-ring side chain in addition to its core bisphosphonate structure. Preclinical studies have associated its unique structure with its increased potency and therapeutic ratio, in contrast to compounds without the imidazole ring. 1 ZOMETA inhibits the activity of osteoclasts, which play a major role in the development of complications of bone metastases. 1 Proposed mechanisms of action include: Functional suppression of mature osteoclast 1 Inhibition of osteoclast maturation 2 Inhibition of osteoclast recruitment to the site 2 Reduction in the production of cytokines, eg, IL-1, IL-6 3 Inhibition of tumor-cell invasion and adhesion to bone matrix 4,5 Preclinical data suggest that ZOMETA also may have anti-tumor activity. 6 In vitro studies indicate that ZOMETA reduces human tumor-cell proliferation, 7 induces apoptosis 6 and inhibits angiogenesis. The anti-angiogenic effect has been confirmed by in vivo data. These anti-osteoclastic and anti-cancer activities are believed to be related to the unique structure of ZOMETA. Consequently, an important biosynthetic pathway (protein prenylation) is inhibited, disrupting cell function and altering cell survival. 8 1. Green J, Müller K, Jaeggi KA. Preclinical pharmacology of CGP 42’446, a new, potent, heterocyclic bisphosphonate compound. J Bone Miner Res. 1994;9(5):745-751. 2. Evans CE, Braidman IP. Effects of two novel bisphosphonates on bone cells in vitro . Bone Miner . 1994;26:95-107. 3. Derenne S, Amiot M, Barille S, et al. Zoledronate is a potent inhibitor of myeloma cell growth and secretion of IL-6 and MMP-1 by the tumoural environment. J Bone Miner Res. 1999;14:2048-2056. 4. Boissier S, Ferreras M, Peyruchaud O, et al. Bisphosphonates inhibit breast and prostate carcinoma cell invasion, an early event in the formation of bone metastases. Cancer Res. 2000;60:2949-2954. 5. Marion G, Serre CM, Trzeciak MC, et al. Bisphosphonates inhibit the platelet-aggregating activity of tumor cells, a process involved during hematogenous dissemination of metastatic cells (Abstract T330). Bone . 1998;23:S279. 6. Aparicio A, Gardner A, Tu Y, et al. In vitro cytoreductive effects on multiple myeloma cells induced by bisphosphonates. Leukemia. 1998;12:220-229. 7. Fromignè O, Siwek B, Body JJ. Bisphosphonates inhibit breast cancer cell proliferation. Acta Clinica. 1999. Abstract 54-2. 8. Fleisch H. Actions. In: Bisphosphonates in Bone Disease . San Diego, California: Academic Press; 2000;34-55.
ZOMETA™ (zoledronic acid for injection)—product summary Nitrogen-containing bisphosphonates are more potent inhibitors of bone resorption than bisphosphonates that do not contain nitrogen Nitrogen-containing bisphosphonates with a nitrogen atom in a heterocyclic ring structure yield further potency ZOMETA is a heterocyclic, nitrogen-containing bisphosphonate—with a core bisphosphonate moiety and an imidazole side-ring containing 2 critically positioned nitrogen atoms ZOMETA is the most potent bisphosphonate ever tested in humans to date: a 100 to 850 times more potent inhibitor of osteoclasts than pamidronate
ZOMETA ™ (zoledronic acid for injection) vs pamidronate disodium for injection in HCM These are currently the largest HCM trials ever conducted. The trials were conducted in Europe and North America. 287 patients were enrolled into two randomized, double-blind, double-dummy, parallel-group trials to compare the efficacy and tolerability of a single dose of ZOMETA (4 mg or 8 mg) as a 5-minute infusion vs a single 90-mg dose of pamidronate as a 2-hour infusion in the treatment of HCM. 1 Given the difference in infusion times for the two agents being studied, a double-dummy technique was used. This technique retains the blind when two treatments in a clinical trial cannot be made identical. In such cases, subjects then take two sets of treatment, one being the randomized drug and one being a placebo. In this study, patients were given both a 5-minute infusion and a 2-hour infusion regardless of the group to which they were randomized. A planned pooled analysis of the data was conducted. The primary end-point variable was complete response, defined as corrected serum calcium level <10.8 mg/dL (2.70 mmol/L) by Day 10. Secondary end points included time to relapse and duration of complete response. Patients were followed for 56 days or until their corrected serum calcium level was 11.6 mg/dL (2.90 mmol/L). Any patient who relapsed by Day 56 or was refractory to initial treatment with either ZOMETA or pamidronate was eligible for retreatment with a single dose of ZOMETA 8 mg in a second phase of the trial. 1. Major P, Lortholary A, Hon J, et al. Zoledronic acid is superior to pamidronate in the treatment of hypercalcemia of malignancy—A pooled analysis of two randomized, controlled clinical trials. J Clin Oncol. In press.
Patient demographics 1 275 patients with corrected serum calcium (CSC) > 12 mg/dL (3.00 mmol/L) and serum creatinine < 4.5 mg/dL (1.12 mmol/L) were evaluable as per protocol. 1 162 male, 113 female; Mean age 59 years (range 21–87) 144 with bone metastases, 131 without 186 PTHrP 2 pmol/L, 69 PTHrP >2 pmol/L Most common primary cancer sites included lung (22.9%) and breast (18.5%) Baseline corrected serum calcium levels were similar in all three groups; the mean for all patients was 13.86 mg/dL (3.47 mmol/L). 1. Major P, Lortholary A, Hon J, et al. Zoledronic acid is superior to pamidronate in the treatment of hypercalcemia of malignancy—A pooled analysis of two randomized, controlled clinical trials. J Clin Oncol. In press.
Patient demographics 1 (continued) Other demographic characteristics were generally similar in the three treatment groups, with a few exceptions. The majority of patients in both ZOMETA groups had bone metastases at baseline, whereas the majority of patients in the pamidronate group did not have bone metastases at baseline. However, the proportion of patients with baseline PTHrP 2 pmol/L or >2 pmol/L was similar in the group of patients with and without bone metastases. Few patients (<11%) in any treatment group had previously been treated with bisphosphonates in the year prior to enrollment in these trials. 1. Major P, Lortholary A, Hon J, et al. Zoledronic acid is superior to pamidronate in the treatment of hypercalcemia of malignancy—A pooled analysis of two randomized, controlled clinical trials. J Clin Oncol. In press.
Mean CSC by day Patients treated with ZOMETA had a signficantly faster normalization of corrected serum calcium (CSC) compared with the pamidronate group. 1 Mean CSC levels at Days 4, 7, and 10 were significantly lower ( P .05) in patients treated with 4 mg of ZOMETA versus pamidronate-treated patients. 1 Data not shown for ZOMETA 8 mg, as this is not the recommended dose in HCM. 1. Major P, Lortholary A, Hon J, et al. Zoledronic acid is superior to pamidronate in the treatment of hypercalcemia of malignancy—A pooled analysis of two randomized, controlled clinical trials. J Clin Oncol. In press.
Median duration of relapse of HCM ZOMETA had a significantly longer therapeutic effect than pamidronate. 1 A single dose of ZOMETA 4 mg normalized CSC for 30 days versus 17 days for the pamidronate 90-mg group ( P =.001). 1 Data not shown for ZOMETA 8 mg, as this is not the recommended dose in HCM. 1. Major P, Lortholary A, Hon J, et al. Zoledronic acid is superior to pamidronate in the treatment of hypercalcemia of malignancy—A pooled analysis of two randomized, controlled clinical trials. J Clin Oncol. In press.
Time to relapse 1 The pooled analysis of time to relapse demonstrated a statistically significant improvement in median time to relapse for the 4-mg ZOMETA group compared with pamidronate ( P =.001). 1 The median time to relapse was 30 days in the 4-mg ZOMETA group compared with only 17 days in the pamidronate group. 1 Data not shown for ZOMETA 8 mg, as this is not the recommended dose in HCM. 1. Major P, Lortholary A, Hon J, et al. Zoledronic acid is superior to pamidronate in the treatment of hypercalcemia of malignancy—A pooled analysis of two randomized, controlled clinical trials. J Clin Oncol. In press.
Complete response rate 1 Complete response rate was defined as the normalization of corrected serum calcium 10.8 mg/dL (2.7 mmol/L) by Day 10. 1 The complete response rate was significantly higher in both ZOMETA groups compared with pamidronate at Days 4, 7 and 10, with the majority of responding patients achieving normal levels of serum calcium within 4 to 7 days. On Day 10, 88% of patients in the 4-mg ZOMETA group had a complete response, compared with only 70% of patients in the pamidronate group ( P =.002). Data not shown for ZOMETA 8 mg, as this is not the recommended dose in HCM. 1. Major P, Lortholary A, Hon J, et al. Zoledronic acid is superior to pamidronate in the treatment of hypercalcemia of malignancy—A pooled analysis of two randomized, controlled clinical trials. J Clin Oncol. In press.
Results 1 ZOMETA is superior to pamidronate in the treatment of HCM 1 : Faster normalization of CSC: significantly lower mean CSC levels were reached at Days 4, 7, and 10 vs pamidronate ( P .05) Significantly longer therapeutic effect: a single dose of ZOMETA 4 mg normalized CSC for 30 days vs 17 days for pamidronate 90 mg ( P =.001) Significantly higher response rate: 82.6% achieved normalization of CSC with ZOMETA 4 mg by Day 7 vs 63.6% for pamidronate 90 mg ( P =.005); 88.4% vs 69.7% by Day 10 ( P =.002) ZOMETA is well tolerated at the 4-mg dose, with a safety profile similar to that of pamidronate ZOMETA is more convenient than pamidronate, offering a more rapid administration 1. Major P, Lortholary A, Hon J, et al. Zoledronic acid is superior to pamidronate in the treatment of hypercalcemia of malignancy—A pooled analysis of two randomized, controlled clinical trials. J Clin Oncol. In press.
Summary—ZOMETA™ ZOMETA in single intravenous doses of 4 mg, given as a rapid infusion, was highly effective in the treatment of HCM. ZOMETA 4 mg was more effective than pamidronate 90 mg. Thus, ZOMETA 4 mg is the recommended dose for treatment of HCM.
ZOMETA™ (zoledronic acid for injection)—Administration ZOMETA has more rapid administration than that of pamidronate — 15-minute infusion compared to 2-hour infusion for pamidronate. 1 Recommended dose in HCM is 4 mg given as a single 15-minute IV infusion. 1 As a standard course of therapy, adequate hydration should be maintained in all patients with HCM. 1. Data on file. Novartis Oncology.
ZOMETA™ (zoledronic acid for injection)—Safety and tolerability Adverse reactions to ZOMETA are usually mild and transient, and similar to those reported for pamidronate. 1 There were no clinically significant differences in the frequency of commonly reported adverse events between ZOMETA 4 mg and pamidronate 90 mg in clinical trials. The most common treatment-related adverse experiences in clinical trials of ZOMETA 4 mg (N = 86) vs pamidronate 90 mg (N = 99) were: fever, 7.0% vs 9.7%; hypocalcemia, 5.8% vs 1.9%; hypophosphatemia, 3.5% vs 1.0%; nausea, 1.2% vs 1.0%; and pruritus, 1.2% vs 0%. 1 In hypercalcemia of malignancy (HCM), ZOMETA has renal tolerability comparable with other bisphosphonates, including pamidronate. 1 In patients requiring repeated administration, serum creatinine must be evaluated prior to each dose; patients with evidence of deterioration of renal function should be appropriately evaluated, and consideration should be given as to whether the potential benefit outweighs the possible risks. 1 As with pamidronate, serum calcium, electrolytes, phosphate, magnesium, creatinine and CBC (differential and hematocrit/hemoglobin) must be closely monitored in patients treated with ZOMETA. 2 ZOMETA is contraindicated in patients with clinically significant hypersensitivity to zoledronic acid or other bisphosphonates, or any of the excipients in the formulation of ZOMETA. 1. Data on file. Novartis Oncology. 2. Major P, Lortholary A, Hon J, et al. J Clin Oncol . In press.
HCM: Current clinical perspectives summary Hypercalcemia of malignancy (HCM) is one of the most common metabolic complications of malignancy. The diagnosis of HCM can be difficult, especially since many of the signs and symptoms can be interpreted as related to the underlying cancer or to the therapy used to treat it. It is important to consider the possibility of hypercalcemia in any person with cancer who starts to experience symptomatic deterioration. The diagnosis should be confirmed by measuring corrected serum calcium. Treatment of HCM should be tailored to the degree of hypercalcemia present. IV bisphosphonates, such as ZOMETA™ (zoledronic acid for injection), are the treatment of choice for HCM. They are very effective in lowering serum calcium, and can be used to treat even mild HCM. Unlike other treatments for HCM, IV bisphosphonates are not associated with adverse reactions that could complicate the treatment of underlying cancer or compromise the condition of the patient.