Concurrent Chemoradiotherapy With Weekly Cisplatin Versus Concurrent Chemoradiotherapy With Weekly Cisplatin and Paclitaxel in Locally Advanced Carcinoma Cervix
Primary Purpose
Carcinoma Cervix
Status
Unknown status
Phase
Phase 3
Locations
India
Study Type
Interventional
Intervention
Paclitaxel, Cisplatin
Cisplatin
Sponsored by

About this trial
This is an interventional treatment trial for Carcinoma Cervix
Eligibility Criteria
Inclusion Criteria:
- histologically proven carcinoma cervix
- age 18 years to 65 years
- stage IIA, IIB, IIIA & IIIB according to FIGO 2009
Exclusion Criteria:
- age > 65 years and < 18 years
- stage IA, IB, IVA & IVB
- Histology other than squamous cell, adenocarcinoma or adenosquamous carcinoma
- history of prior pelvic surgery for cancer, prior pelvic radiotherapy or prior chemotherapy.
- deranged renal function test and liver function test
- KPS >= 60
- distant metastasis
Sites / Locations
- Indira Gandhi Medical CollegeRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
cisplatin and paclitaxel with concurrent radiotherapy
cisplatin with concurrent radiotherapy
Arm Description
weekly cisplatin at 30mg/m2 and paclitaxel at 50mg/m2 are given with concurrent radiotherapy at 2Gy per fraction at 5 fractions per week for 5 weeks followed by either low dose rate (LDR) Intracavitary (I/C) Brachytherapy or supplement Chemoradiotherapy (CRT); if not fit for I/C Brachytherapy
weekly cisplatin @ 40mg/m2 is given along with concurrent radiotherapy at 2Gy per fraction with 5 fractions per week for 5 weeks followed by LDR I/C brachytherapy or supplement CRT; if not fit for I/C Brachytherapy
Outcomes
Primary Outcome Measures
clinical response of the disease
to compare clinically, the disease response and local control of combination chemotherapy with weekly cisplatin and paclitaxel with concurrent Radiotherapy Vs single agent cisplatin with concurrent Radiotherapy in locally advanced carcinoma cervix
Secondary Outcome Measures
number of patients with adverse events
to monitor number of treatment related adverse events in both the arms
Full Information
NCT ID
NCT01593306
First Posted
May 3, 2012
Last Updated
May 7, 2012
Sponsor
Indira Gandhi Medical College, Shimla
1. Study Identification
Unique Protocol Identification Number
NCT01593306
Brief Title
Concurrent Chemoradiotherapy With Weekly Cisplatin Versus Concurrent Chemoradiotherapy With Weekly Cisplatin and Paclitaxel in Locally Advanced Carcinoma Cervix
Study Type
Interventional
2. Study Status
Record Verification Date
May 2012
Overall Recruitment Status
Unknown status
Study Start Date
July 2011 (undefined)
Primary Completion Date
October 2012 (Anticipated)
Study Completion Date
February 2013 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indira Gandhi Medical College, Shimla
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to check whether addition of paclitaxel to cisplatin and radiation therapy will improve the outcome in locally advanced carcinoma cervix.
Detailed Description
Carcinoma cervix is the 2nd most common malignancy among females and about 86% of this burden occurs in developing countries. India accounts for 27% of world cervical cancer burden; and most of them are of locally advanced stage ie stage IIA to IVA.
Significant development in radiation techniques and addition of cisplatin based chemotherapy to radiation schedule has led to improved survival but still it is far from satisfactory with 20 to 25% patients failing locally while 10 to 20% patients fail at distant sites. Novel techniques are required to improve this dismal rate.
Thus investigators intended to use combination chemotherapy with paclitaxel and cisplatin, considering that paclitaxel is a taxane which has shown good efficacy in other solid tumors such as ovary, lung and breast; it has also shown radiosensitizing effect in cervical cancer cell lines and it has also been shown to be effective in phase III trials with cisplatin in metastatic and recurrent carcinoma cervix.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carcinoma Cervix
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
cisplatin and paclitaxel with concurrent radiotherapy
Arm Type
Experimental
Arm Description
weekly cisplatin at 30mg/m2 and paclitaxel at 50mg/m2 are given with concurrent radiotherapy at 2Gy per fraction at 5 fractions per week for 5 weeks followed by either low dose rate (LDR) Intracavitary (I/C) Brachytherapy or supplement Chemoradiotherapy (CRT); if not fit for I/C Brachytherapy
Arm Title
cisplatin with concurrent radiotherapy
Arm Type
Active Comparator
Arm Description
weekly cisplatin @ 40mg/m2 is given along with concurrent radiotherapy at 2Gy per fraction with 5 fractions per week for 5 weeks followed by LDR I/C brachytherapy or supplement CRT; if not fit for I/C Brachytherapy
Intervention Type
Drug
Intervention Name(s)
Paclitaxel, Cisplatin
Intervention Description
intravenous paclitaxel infusion at 50mg/m2/week and cisplatin at 30mg/m2/week for 5 weeks. if supplement Chemo Radiotherapy is required then similar dose per week for 2 more weeks.
Intervention Type
Drug
Intervention Name(s)
Cisplatin
Intervention Description
intravenous infusion of cisplatin 40mg/m2/week for 5 weeks. if I/C Brachytherapy is not feasible then supplement CRT given with similar dose of cisplatin for 2 more cycles.
Primary Outcome Measure Information:
Title
clinical response of the disease
Description
to compare clinically, the disease response and local control of combination chemotherapy with weekly cisplatin and paclitaxel with concurrent Radiotherapy Vs single agent cisplatin with concurrent Radiotherapy in locally advanced carcinoma cervix
Time Frame
up to 1 year
Secondary Outcome Measure Information:
Title
number of patients with adverse events
Description
to monitor number of treatment related adverse events in both the arms
Time Frame
during treatment, 14 weeks
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
histologically proven carcinoma cervix
age 18 years to 65 years
stage IIA, IIB, IIIA & IIIB according to FIGO 2009
Exclusion Criteria:
age > 65 years and < 18 years
stage IA, IB, IVA & IVB
Histology other than squamous cell, adenocarcinoma or adenosquamous carcinoma
history of prior pelvic surgery for cancer, prior pelvic radiotherapy or prior chemotherapy.
deranged renal function test and liver function test
KPS >= 60
distant metastasis
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pragyat Thakur, MBBS
Phone
919418029244
Email
pragyat28rpgmc@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pragyat Thakur, MBBS
Organizational Affiliation
Indira Gandhi Medical College, Shimla
Official's Role
Principal Investigator
Facility Information:
Facility Name
Indira Gandhi Medical College
City
Shimla
State/Province
Himachal Pradesh
ZIP/Postal Code
171001
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pragyat Thakur, MBBS
Phone
919418029244
Email
pragyat28rpgmc@gmail.com
First Name & Middle Initial & Last Name & Degree
Pragyat Thakur, MBBS
12. IPD Sharing Statement
Citations:
PubMed Identifier
26904570
Citation
Thakur P, Seam R, Gupta M, Gupta M. Prospective randomized study comparing concomitant chemoradiotherapy using weekly cisplatin & paclitaxel versus weekly cisplatin in locally advanced carcinoma cervix. Ann Transl Med. 2016 Feb;4(3):48. doi: 10.3978/j.issn.2305-5839.2015.11.19.
Results Reference
derived
Learn more about this trial
Concurrent Chemoradiotherapy With Weekly Cisplatin Versus Concurrent Chemoradiotherapy With Weekly Cisplatin and Paclitaxel in Locally Advanced Carcinoma Cervix
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