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HEMI BODY IRRADIATION
&
TUMOR REGISTRY
Dr. Taruni Bhattacharya
D.N.B. Resident
Difference with TBI
• Field size needed is smaller.
• Less side effects
• Stem cell support not needed
• Different therapeutic goal.
AIM
• To give a sufficiently high dose to alleviate
effects of symptomatic diseases & at the same
time,maintaining a sufficiently low dose to
minimize complications.
• Delay progression of existing asymptomatic
mets & clinical development of new mets
CLINICAL INDICATION
1) Palliation of widely disseminated metastatic
disease
2) Adjuvant therapy for Ewing’s Sarcoma &
Brochogenic Ca
3) Lower Hemi Body Irradiation for ovarian
ablation in Metastatic Breast Cancer.
TECHNIQUE
• Bottom of L4 separates upper & lower HBI
• A/P parallel opposed fields used
• Patient positioned with vertical beam
allowing coverage of hemibody
• Shielding of previously irradiated areas to
reduce toxicity(salivary glands,lungs)
• Dose prescribed to mid-plane of the patient
at the central axis of the beam.
DOSE
• 6Gy:upper HBI
• 8Gy:lower HBI and Middle HBI
• For treating the other half of the body
wait for 6-8 weeks apert to allow a sufficient
recovery of blood cells & irradiated marrow.
• Planned sequential upper and lower HBI 6-8
wks apart,used to treat multiple
myeloma,malignant lymphoma.
COMPLICATIONS
• M/C S/E: nausea and vomiting(when abdomen is
included within fields)
Occur shortly after radiation admin & last a few
hours.
Rx:Premedication with steroids & antiemetics.
• Intestines:diarrohea occurs when significant volume
is irradiated.It’s severity can be limited by limiting
dose to 6Gy
• Hematological recovery:within 4-6 wks usually
• Lungs: HBI can cause interstitial pneumonitis,
with cough and breathlessness at around 6
weeks, although this may be delayed by up to
6 months
R/o pneumonitis is less with single fraction
dose 7Gy
For 8Gy Upper body TBI use lung blocks.
• Reversible alopecia, dry mouth, parotid
swelling, stomatitis and fatigue are other s/e
seen.
CANCER REGISTRY
• CANCER registration is the process of
systematically and continuously collecting
information on malignant neoplasm.
• Broadly, there are two types of cancer
registries:
1.Hospital
2.population based
National Cancer Registry Programme
Commenced by ICMR with a network of cancer
registries across the country in December 1981.
Started with three PBCR -Bangalore, Chennai and
Mumbai and three HBCR -Chandigarh, Dibrugarh
and Thiruvananthapuram
Now there are 28 PBCR and 7 HBCR sites in India
USES
• Resource of information for clinicians,
researchers, scientists, policy makers,and the
public
• Identifying High-Risk Groups
• Increasing Screening in underserved areas
• Investigating possible cancer causes
• Evaluating patterns of clinical care
Objectives of this programme
• To generate reliable data on magnitude and
patterns of cancer
• Undertake epidemiological studies based on results
of registry data
• Help in designing, planning, monitoring and
evaluation of cancer control activities under the
National Cancer Control Programme (NCCP)
• Develop training programmes in cancer registration
and epidemiology
Cancer registration in India is active and voluntary
– Active method: The workers from registry,
scan through the patient records in different
hospitals, clarify incomplete or contradictory
information, and abstract data with collection of data
from hospital record interviews of patients.
– Passive method: The hospitals in areas with
compulsory notification and the hospital
cancer registries, abstract the information
from the patient records on a specified
proforma and send it to the registry.
POPULATION BASED CANCER
REGISTRY
Data collection by-
1.Facilities
2.Clinicians and pathologists
3.Death certificates
Hospital Based Cancer Registries
• The primary purpose -to contribute to patient care by
providing readily accessible information on the patients
• Data - used for clinical research and for epidemiological
purposes
• Within the hospital: a registry is maintained which is an
integral part of the hospital ’s cancer programme or
health care delivery system
• HBCR have no denominator of population at risk .
Incidence rate cannot be derived from such data.
However, cancer extent,stages,therapy and
survival rate information are more reliable on such
data
THANK YOU

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Hemi body irradiation

  • 1. HEMI BODY IRRADIATION & TUMOR REGISTRY Dr. Taruni Bhattacharya D.N.B. Resident
  • 2. Difference with TBI • Field size needed is smaller. • Less side effects • Stem cell support not needed • Different therapeutic goal.
  • 3. AIM • To give a sufficiently high dose to alleviate effects of symptomatic diseases & at the same time,maintaining a sufficiently low dose to minimize complications. • Delay progression of existing asymptomatic mets & clinical development of new mets
  • 4. CLINICAL INDICATION 1) Palliation of widely disseminated metastatic disease 2) Adjuvant therapy for Ewing’s Sarcoma & Brochogenic Ca 3) Lower Hemi Body Irradiation for ovarian ablation in Metastatic Breast Cancer.
  • 5. TECHNIQUE • Bottom of L4 separates upper & lower HBI • A/P parallel opposed fields used • Patient positioned with vertical beam allowing coverage of hemibody • Shielding of previously irradiated areas to reduce toxicity(salivary glands,lungs) • Dose prescribed to mid-plane of the patient at the central axis of the beam.
  • 6.
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  • 8. DOSE • 6Gy:upper HBI • 8Gy:lower HBI and Middle HBI • For treating the other half of the body wait for 6-8 weeks apert to allow a sufficient recovery of blood cells & irradiated marrow. • Planned sequential upper and lower HBI 6-8 wks apart,used to treat multiple myeloma,malignant lymphoma.
  • 9. COMPLICATIONS • M/C S/E: nausea and vomiting(when abdomen is included within fields) Occur shortly after radiation admin & last a few hours. Rx:Premedication with steroids & antiemetics. • Intestines:diarrohea occurs when significant volume is irradiated.It’s severity can be limited by limiting dose to 6Gy • Hematological recovery:within 4-6 wks usually
  • 10. • Lungs: HBI can cause interstitial pneumonitis, with cough and breathlessness at around 6 weeks, although this may be delayed by up to 6 months R/o pneumonitis is less with single fraction dose 7Gy For 8Gy Upper body TBI use lung blocks. • Reversible alopecia, dry mouth, parotid swelling, stomatitis and fatigue are other s/e seen.
  • 11.
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  • 15. CANCER REGISTRY • CANCER registration is the process of systematically and continuously collecting information on malignant neoplasm. • Broadly, there are two types of cancer registries: 1.Hospital 2.population based
  • 16.
  • 17. National Cancer Registry Programme Commenced by ICMR with a network of cancer registries across the country in December 1981. Started with three PBCR -Bangalore, Chennai and Mumbai and three HBCR -Chandigarh, Dibrugarh and Thiruvananthapuram Now there are 28 PBCR and 7 HBCR sites in India
  • 18. USES • Resource of information for clinicians, researchers, scientists, policy makers,and the public • Identifying High-Risk Groups • Increasing Screening in underserved areas • Investigating possible cancer causes • Evaluating patterns of clinical care
  • 19.
  • 20. Objectives of this programme • To generate reliable data on magnitude and patterns of cancer • Undertake epidemiological studies based on results of registry data • Help in designing, planning, monitoring and evaluation of cancer control activities under the National Cancer Control Programme (NCCP) • Develop training programmes in cancer registration and epidemiology
  • 21. Cancer registration in India is active and voluntary – Active method: The workers from registry, scan through the patient records in different hospitals, clarify incomplete or contradictory information, and abstract data with collection of data from hospital record interviews of patients. – Passive method: The hospitals in areas with compulsory notification and the hospital cancer registries, abstract the information from the patient records on a specified proforma and send it to the registry.
  • 22. POPULATION BASED CANCER REGISTRY Data collection by- 1.Facilities 2.Clinicians and pathologists 3.Death certificates
  • 23. Hospital Based Cancer Registries • The primary purpose -to contribute to patient care by providing readily accessible information on the patients • Data - used for clinical research and for epidemiological purposes • Within the hospital: a registry is maintained which is an integral part of the hospital ’s cancer programme or health care delivery system • HBCR have no denominator of population at risk . Incidence rate cannot be derived from such data. However, cancer extent,stages,therapy and survival rate information are more reliable on such data