Health Condition 1: C539- Malignant neoplasm of cervix uteri, unspecified
Conditions
Interventions
Intervention1: Prophylactic EFRT with concurrent chemotherapy -: Prophylactic EFRT with concurrent chemotherapy (Inj. Cisplatin 40 mg/m2 IV weekly during radiation) , SIB plan(45-50Gy , 1.8-2 Gy per
Sponsors
Dr Pritanjali Singh
Eligibility
Inclusion criteria
Inclusion criteria: DIAGNOSED CASE OF CANCER CERVIX, IIIC1 STAGE (FIGO 2018) PATIENT WILLING TO TAKE PART IN STUDY
Exclusion criteria
Exclusion criteria: Medical contraindication for Chemo radiotherapy. Pregnancy Patient with prior chemotherapy history.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| overall survival (OS), disease free survival (DFS) para-aortic lymph node metastases (PAO-LNM) Timepoint: To assess the overall survival (OS), disease free survival (DFS) and para-aortic lymph node metastases (PAO-LNM) at the end of 1st, 2nd and 3rd year. | — |
Secondary
| Measure | Time frame |
|---|---|
| Percentage of cases of IIIC1 LACC who gets upstaged post PET CT scan. To categories the acute & late toxicity related to chemo radiation according to RTOG/EORTC morbidity scoring scheme. To correlate the toxicities with the doses to OARs. Timepoint: Yearly for 3 year post chemoradiation. | — |
Countries
India
Contacts
Public ContactDr Pritanjali Singh
AIIMS PATNA
Outcome results
None listed