Outcome of patients treated with chemotherapy and Radiation in Cervical Cancer.
Not Applicable
- Conditions
- Health Condition 1: null- Cancer of Cervix
- Registration Number
- CTRI/2014/06/004699
- Lead Sponsor
- A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
Histologically confirmed FIGO stage Ib2-IVa squamous, adeno or adenosquamous carcinoma of the cervix.
Received Neo-adjuvant chemotherapy (NACT) followed by Chemo-radiotherapy (CRT) or Radiotherapy (RT).
Minimum follow-up of 2 years after completion of Chemo-radiotherapy (CRT) / Radiotherapy (RT).
Exclusion Criteria
Incomplete definitive treatment.
Not received Chemo-radiotherapy (CRT) / Radiotherapy (RT).
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate Neoadjuvant chemortherapy(NACT)followed by radical chemoradiotherapy(CRT) or radiotherapy(RT) in locally advanced cervical cancer in terms of Response rates, Compliance of NACT followed by Radical Chemoradiotherapy/Radiotherapy & Disease free & overall survivals & factors affecting the outcome.Timepoint: 2 Years
- Secondary Outcome Measures
Name Time Method To evaluate Neoadjuvant chemortherapy(NACT)followed by radical chemoradiotherapy(CRT) or radiotherapy(RT) in locally advanced cervical cancer in terms of Response rates, Compliance of NACT followed by Radical Chemoradiotherapy/Radiotherapy & Disease free & overall survivals & factors affecting the outcome.Timepoint: 2 Years