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Carcinoma Cervix- case
Rajiv Gandhi cancer Institute and
Research Centre
New Delhi
CASE
• 52yr old Female
• Normotensive, nondiabetic,
• Post Menopausal
• Obstetric History : P4L4
• LCB : 24yrs back
• Full term normal vaginal home deliveries
• No Relevant family History
Chief complaints ---
• Painless blood stained discharge P/V since
one month and a half
• Bleeding P/V- since one month
.
Clinical examination
• Average built, mild pallor.
• B/L Breasts, abdomen, Chest-- normal
• PS/PV/PR—
Foul smelling blood stained discharge seen
Large Growth occupying the entire Cervix,
growth involving the upper third of the vagina.
Right parametria involved, but not reaching
the pelvic side walls
Investigations done--
• CBC, KFT, LFT,
• Urine R/E
• Biopsy
• Chest X ray
• USG Abdomen
• Viral Markers
What Next?—
Work up Investigations?
EUA ?
Biopsy / PAP ?
For local imaging- CT ?
MRI?
PET Scan?
Any role of Cystoscopy? Sigmoidoscopy?
HPV ?
MRI PELVIS
• Diffuse infiltrative mass lesion, 5APx4.5TRx8.6CC cm involving
the entire thickness of the cervix, causing cervical stenosis and
distension of the upper endometrial cavity with fluid collection.
• Involving lower 2/3rd of the uterine corpus and upper 1/3rd of
vagina.
• Right parametrial fat stranding/extension not reaching up to the
pelvic side wall.
• Multiple enlarged necrotic lymphnodes along the bilateral
common iliac, internal and external iliac vessels, Largest-
3.2x2.5cm
Biopsy
• HPE: Sections shows poorly differentiated
carcinoma with high N:C ratio and
hyperchromatic nuclei suggestive of poorly
differentiated Ca.
• IHC S/O CK Positive, P40 Positive
Path Images
Questions-
• Any other investigations?
• Role of PET CT Scan?
Whole body PET-CT
• FDG avid heterogeneously enhancing infiltrating
soft tissue lesion involving lower 2/3rd of uterine
body cranially and upper 1/3rd of vagina caudally
5.6x6.5x7.7cm, SUV max 16.9
• Few FDG avid aortocaval, retrocaval, precaval,
paraaortic, bilateral common iliac and bilateral
external iliac lymphnodes, largest - 2.6x2.2cm,
SUV max 11.3.
PET CT
Plan Of Treatment?
• Surgery vs Radiochemotherapy?
• Role of Chemotherapy?
• How would RT be Planned—Dose?
Conventional? Conformal? Field?
Treatment Received
• IMRT on 6MV Linac, SIB To Nodes,
Extended field including Para-
aortic nodes
• Dose- PTV- 50Gy in 25
fractions ,
PTV NODE-- 55Gy in 25
fractions
Para Aortic LN--45Gy in 25
fractions
• Along with weekly cisplatin
based concurrent chemotherapy
Pre ICRT MRI
• Near complete regression.
She Underwent--3 Sessions of ICRT @ 7.5 Gy Per Fraction
How To Plan follow up?
• Follow-up:
- Clinical examination and SCC each three
months
- Abdominal US each six months
- Thorax- abdomen and pelvis CT scan
each year
After 2 years
Abdominal pelvic CT
scan: metastatic
paraortic nodes + liver
metastases
PET scan: pathological
aortic uptake + multiple
liver lesions
1. Radiotherapy
2. Chemotherapy ( paclitaxel/cisplatin)
3. Chemotherapy (Carboplatin/ Paclitaxel and bevacizumab)
4. Concurrent chemo-radiation
5. Surgery
6. Enrolment in a clinical trial
What is the best treatment?
6 cycles
 Paclitaxel 175 mg/m2 - Cisplatin 75 mg/m2- bevacizumab q3wks
 Negative CT scan (performed at the end of chemo)
GOG-169: Phase III study of cisplatin with or
without paclitaxel in stage IVB, recurrent, or
persistent squamous cell carcinoma of the
cervix
GOG 169: Results
GOG-204: Phase III trial of four cisplatin-
containing doublet combinations in stage IVB,
recurrent, or persistent cervical carcinoma
GOG-204:Results
Outcome in recurrent or advanced
cervical cancer
Ca Cervix: HPV Induced Neo-
angiogenesis
GOG 240:Bevacizumab for advanced
cervical cancer: 2017 Update
GOG 240:PFS&OS 7 yr follow up
Cis+ Pacli± Bev and Topo+ Pacli±
Bev
17·5 vs 15·0 months 16·2 vs 12·0 months
GOG 240:Summary
Patient selection for Bev+CT:
Moore’s Criteria
1) Race (African ancestry or not),
2) ECOG PS (1 or 0)
3) Measurable disease in the pelvis
(yes/ no)
4) Prior platinum as a radiation
sensitizer (yes/ no)
5) PFS(≤365 days or >365 days)
LOW RISK 0-1 INTERMEDIATE RISK 2-3
HIGH RISK 4-5
Successive improvement in median overall
survival among women with advanced cervical
cancer.
Krishnansu S. Tewari et al. Clin Cancer Res 2015;21:5480-5487
201
7
Bevacizumab is more effective in cervical cancer
than in ovarian cancer
Ca Ovary
• Only PFS Benefit
• genomic instability
• heterogeneous
disease
Ca Cervix
• OS & PFS benefit
• HPV oncogene driven
angiogenesis
• homogeneous tumour
cough
Thorax TC scan: bilateral lung metastases
Biopsy of lung lesion: metastasis of squamocellular tumour
After 5 months
1. Chemotherapy with bevacizumab
2. Radiotherapy
3. Supportive care
4. Topotecan
5. Weekly paclitaxel
6. Carboplatin
What is the next step?
The patient received 3 cycles of chemotherapy with topotecan
But … after three cycles, CT scan showed a progression of disease
(multiple lesions in the lung, lomboaortic nodes and in the pelvis)
After 4 months
Patient died after receiving supportive care
Any Further Questions???

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ca cervix-DR TALWAR.ppt

  • 1. Carcinoma Cervix- case Rajiv Gandhi cancer Institute and Research Centre New Delhi
  • 2. CASE • 52yr old Female • Normotensive, nondiabetic, • Post Menopausal • Obstetric History : P4L4 • LCB : 24yrs back • Full term normal vaginal home deliveries • No Relevant family History
  • 3. Chief complaints --- • Painless blood stained discharge P/V since one month and a half • Bleeding P/V- since one month .
  • 4. Clinical examination • Average built, mild pallor. • B/L Breasts, abdomen, Chest-- normal • PS/PV/PR— Foul smelling blood stained discharge seen Large Growth occupying the entire Cervix, growth involving the upper third of the vagina. Right parametria involved, but not reaching the pelvic side walls
  • 5. Investigations done-- • CBC, KFT, LFT, • Urine R/E • Biopsy • Chest X ray • USG Abdomen • Viral Markers
  • 6. What Next?— Work up Investigations? EUA ? Biopsy / PAP ? For local imaging- CT ? MRI? PET Scan? Any role of Cystoscopy? Sigmoidoscopy? HPV ?
  • 7. MRI PELVIS • Diffuse infiltrative mass lesion, 5APx4.5TRx8.6CC cm involving the entire thickness of the cervix, causing cervical stenosis and distension of the upper endometrial cavity with fluid collection. • Involving lower 2/3rd of the uterine corpus and upper 1/3rd of vagina. • Right parametrial fat stranding/extension not reaching up to the pelvic side wall. • Multiple enlarged necrotic lymphnodes along the bilateral common iliac, internal and external iliac vessels, Largest- 3.2x2.5cm
  • 8.
  • 9.
  • 10. Biopsy • HPE: Sections shows poorly differentiated carcinoma with high N:C ratio and hyperchromatic nuclei suggestive of poorly differentiated Ca. • IHC S/O CK Positive, P40 Positive
  • 12. Questions- • Any other investigations? • Role of PET CT Scan?
  • 13. Whole body PET-CT • FDG avid heterogeneously enhancing infiltrating soft tissue lesion involving lower 2/3rd of uterine body cranially and upper 1/3rd of vagina caudally 5.6x6.5x7.7cm, SUV max 16.9 • Few FDG avid aortocaval, retrocaval, precaval, paraaortic, bilateral common iliac and bilateral external iliac lymphnodes, largest - 2.6x2.2cm, SUV max 11.3.
  • 15. Plan Of Treatment? • Surgery vs Radiochemotherapy? • Role of Chemotherapy? • How would RT be Planned—Dose? Conventional? Conformal? Field?
  • 16. Treatment Received • IMRT on 6MV Linac, SIB To Nodes, Extended field including Para- aortic nodes • Dose- PTV- 50Gy in 25 fractions , PTV NODE-- 55Gy in 25 fractions Para Aortic LN--45Gy in 25 fractions • Along with weekly cisplatin based concurrent chemotherapy
  • 17. Pre ICRT MRI • Near complete regression. She Underwent--3 Sessions of ICRT @ 7.5 Gy Per Fraction
  • 18. How To Plan follow up? • Follow-up: - Clinical examination and SCC each three months - Abdominal US each six months - Thorax- abdomen and pelvis CT scan each year
  • 19. After 2 years Abdominal pelvic CT scan: metastatic paraortic nodes + liver metastases PET scan: pathological aortic uptake + multiple liver lesions
  • 20. 1. Radiotherapy 2. Chemotherapy ( paclitaxel/cisplatin) 3. Chemotherapy (Carboplatin/ Paclitaxel and bevacizumab) 4. Concurrent chemo-radiation 5. Surgery 6. Enrolment in a clinical trial What is the best treatment?
  • 21. 6 cycles  Paclitaxel 175 mg/m2 - Cisplatin 75 mg/m2- bevacizumab q3wks  Negative CT scan (performed at the end of chemo)
  • 22. GOG-169: Phase III study of cisplatin with or without paclitaxel in stage IVB, recurrent, or persistent squamous cell carcinoma of the cervix
  • 24. GOG-204: Phase III trial of four cisplatin- containing doublet combinations in stage IVB, recurrent, or persistent cervical carcinoma
  • 26. Outcome in recurrent or advanced cervical cancer
  • 27. Ca Cervix: HPV Induced Neo- angiogenesis
  • 28. GOG 240:Bevacizumab for advanced cervical cancer: 2017 Update
  • 29. GOG 240:PFS&OS 7 yr follow up
  • 30. Cis+ Pacli± Bev and Topo+ Pacli± Bev 17·5 vs 15·0 months 16·2 vs 12·0 months
  • 32. Patient selection for Bev+CT: Moore’s Criteria 1) Race (African ancestry or not), 2) ECOG PS (1 or 0) 3) Measurable disease in the pelvis (yes/ no) 4) Prior platinum as a radiation sensitizer (yes/ no) 5) PFS(≤365 days or >365 days) LOW RISK 0-1 INTERMEDIATE RISK 2-3 HIGH RISK 4-5
  • 33. Successive improvement in median overall survival among women with advanced cervical cancer. Krishnansu S. Tewari et al. Clin Cancer Res 2015;21:5480-5487 201 7
  • 34. Bevacizumab is more effective in cervical cancer than in ovarian cancer Ca Ovary • Only PFS Benefit • genomic instability • heterogeneous disease Ca Cervix • OS & PFS benefit • HPV oncogene driven angiogenesis • homogeneous tumour
  • 35. cough Thorax TC scan: bilateral lung metastases Biopsy of lung lesion: metastasis of squamocellular tumour After 5 months
  • 36. 1. Chemotherapy with bevacizumab 2. Radiotherapy 3. Supportive care 4. Topotecan 5. Weekly paclitaxel 6. Carboplatin What is the next step?
  • 37. The patient received 3 cycles of chemotherapy with topotecan But … after three cycles, CT scan showed a progression of disease (multiple lesions in the lung, lomboaortic nodes and in the pelvis) After 4 months Patient died after receiving supportive care