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Concomitant Chemoradiation in Advanced Stage Carcinoma Cervix (CRACx)

Primary Purpose

Cancer of Cervix

Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
CT + RT
Sponsored by
Tata Memorial Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cancer of Cervix focused on measuring Carcinoma Cervix, FIGO Stage IIIB, Radiation therapy, Chemoradiation, Treatment related toxicities, Cervical Cancer, Cervix Cancer

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Histologically proven squamous carcinoma of cervix Performance index world health organization (WHO) grade 0 or 1 Patients below 65 years of age FIGO Stage IIIB Normal ECG and Cardiovascular system Normal hematological parameters Normal renal and liver function tests Exclusion Criteria: Co-morbid conditions like medical renal disease Medical or Psychological condition that would preclude treatment H/o Previous treatment / Pregnancy Patient unreliable for treatment completion and follow-up.

Sites / Locations

  • Tata Memorial Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Radiation (RT) Alone

CT + RT

Arm Description

Standard radical radiation therapy alone

Injection Cisplatin 40mg/m2 weekly for 5 weeks during the entire course of external radiation therapy

Outcomes

Primary Outcome Measures

To compare the disease free survivals.

Secondary Outcome Measures

To compare the overall survivals
To compare the distant metastasis rates
To compare the quality of life in both the groups
To compare the normal tissue toxicities (Acute & Late) of standard radiation therapy with concomitant chemo-radiation.

Full Information

First Posted
September 13, 2005
Last Updated
September 13, 2019
Sponsor
Tata Memorial Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00193791
Brief Title
Concomitant Chemoradiation in Advanced Stage Carcinoma Cervix
Acronym
CRACx
Official Title
Concomitant Chemo-radiation in Advanced Stage Carcinoma Cervix: A Phase III Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2019
Overall Recruitment Status
Completed
Study Start Date
July 7, 2003 (Actual)
Primary Completion Date
May 2017 (Actual)
Study Completion Date
December 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tata Memorial Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A study to evaluate the efficacy of concomitant chemoradiation as compared to radiotherapy alone. Concomitant chemoradiation is not a new treatment modality for carcinoma cervix. Studies have shown improvement in survivals with chemoradiation, but majority of the patients was in early stages. Since this treatment modality has not been tested adequately in advanced stages in our setting, the present study is being undertaken. The study arm of chemoradiation has the potential to improve the survivals by 10%, but is associated with additional 5% risk of toxicities, which are treatable. In the study arm, apart form the standard radiotherapy treatment, you will receive weekly chemotherapy injections (Cisplatin) during external radiation therapy. The study arm is associated with additional 5% acute hematological and gastrointestinal toxicities, which are treatable with medications, blood transfusions, modifications in the ongoing treatment etc.
Detailed Description
Carcinoma cervix is the commonest malignancy seen in Asian women and constitutes approximately 30% of all cancers (1). It is also the leading cause of cancer mortality in India. Nearly 50% of the patients present with advanced stages (FIGO Stage III/IV). The main stay of treatment has traditionally been radical radiation therapy and over decades the survival rates have achieved a plateau of 30 - 45% at 5 years. In developing countries the socioeconomic problems, illiteracy, late presentation and irregular follow-up have further compromised our survivals. Over the last decade there have been studies on the use of chemo-radiotherapy in carcinoma cervix. Over 19 randomized trials have been published addressing the issue of chemo-radiotherapy. However, heterogeneous data, poor randomization, inadequate number of patients, sub-optimal radiotherapy, non-uniform use of chemotherapeutic drugs, its sequencing and poor documentation have not yet provided the evidence to substantially alter the practice. Hence, meta-analysis of these trials was undertaken to further evaluate the role of chemo-radiotherapy in carcinoma cervix (2,3). The first meta-analysis published by Cochrane Collaborative Group of 4580 randomized patients (19 randomized trials) suggested that chemo-radiation did show an absolute survival benefit improvement both in progression free and overall survivals by 16% and 12% respectively (p<0.0001). The survivals were significantly better with Cisplatin based concomitant chemo-radiation (p<0.0001). Incidentally, the distant metastasis rates were also significantly lower in chemo-radiation (p<0.0001). However, all these benefits were seen only in early stages. In addition, acute grade 3/4 hematological and gastro-intestinal toxicities were higher with chemo-radiation (additional 8% and 5% respectively). The data was insufficient to report on late toxicity (2). The second meta-analysis of 9 randomized trials, recently published by the Canadian Group to evaluate only cisplatin based concomitant chemo-radiation confirms the improvement in overall survival (4year survival data) in advanced stages, bulky IB tumors (prior to surgery) and high risk early disease (post-surgery). Although acute grade 3/4 hematological and gastro-intestinal toxicities were higher in chemo-radiation, they were short-lived, with only 2 deaths and the remaining resolved with medical treatment. There was no significant increase in the late toxicity from the data available. Both the Cochrane and Canadian meta-analysis have to a large extent tried to address the role of concomitant chemo-radiation, but Carcinoma Cervix Stage III accounted for only 30-35% and moreover evaluation with optimal radiation schedules and comparison of late toxicities still remains unanswered. What is more important is that the cisplatin is relatively inexpensive and is available worldwide. This means that cisplatin-based chemo-radiation is affordable in the developing countries where carcinoma cervix still forms the major cancer. However, the role of chemo-radiation in Carcinoma Cervix Stage IIIB in a developing countries including India still remains unexplored. We propose this randomized study to evaluate the role and benefit of chemo-radiation in-patients with cervical cancer.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer of Cervix
Keywords
Carcinoma Cervix, FIGO Stage IIIB, Radiation therapy, Chemoradiation, Treatment related toxicities, Cervical Cancer, Cervix Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Concomitant chemo-radiation versus radiation alone
Masking
None (Open Label)
Allocation
Randomized
Enrollment
850 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Radiation (RT) Alone
Arm Type
No Intervention
Arm Description
Standard radical radiation therapy alone
Arm Title
CT + RT
Arm Type
Experimental
Arm Description
Injection Cisplatin 40mg/m2 weekly for 5 weeks during the entire course of external radiation therapy
Intervention Type
Other
Intervention Name(s)
CT + RT
Intervention Description
Injection Cisplatin 40mg/m2 weekly for 5 weeks during the entire course of external radiation therapy
Primary Outcome Measure Information:
Title
To compare the disease free survivals.
Time Frame
December 2009
Secondary Outcome Measure Information:
Title
To compare the overall survivals
Time Frame
December 2010
Title
To compare the distant metastasis rates
Time Frame
December 2010
Title
To compare the quality of life in both the groups
Time Frame
December 2010
Title
To compare the normal tissue toxicities (Acute & Late) of standard radiation therapy with concomitant chemo-radiation.
Time Frame
June 2017

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 squamous carcinoma of cervix Performance index world health organization (WHO) grade 0 or 1 Patients below 65 years of age FIGO Stage IIIB Normal ECG and Cardiovascular system Normal hematological parameters Normal renal and liver function tests Exclusion Criteria: Co-morbid conditions like medical renal disease Medical or Psychological condition that would preclude treatment H/o Previous treatment / Pregnancy Patient unreliable for treatment completion and follow-up.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shyamkishore J Shrivastava, MD,DNB(RT)
Organizational Affiliation
Professor & Head, Department of Radiation Oncology, Tata Memorial Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tata Memorial Hospital
City
Mumbai
State/Province
Maharastra
ZIP/Postal Code
400 012
Country
India

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual patient data (IPD) related to patient characteristics, treatment and outcome variables.
Citations:
PubMed Identifier
11564482
Citation
Green JA, Kirwan JM, Tierney JF, Symonds P, Fresco L, Collingwood M, Williams CJ. Survival and recurrence after concomitant chemotherapy and radiotherapy for cancer of the uterine cervix: a systematic review and meta-analysis. Lancet. 2001 Sep 8;358(9284):781-6. doi: 10.1016/S0140-6736(01)05965-7.
Results Reference
background
PubMed Identifier
12109823
Citation
Lukka H, Hirte H, Fyles A, Thomas G, Elit L, Johnston M, Fung MF, Browman G; Cancer Care Ontario Practice Guidelines Initiative Gynecology Disease Site Group. Concurrent cisplatin-based chemotherapy plus radiotherapy for cervical cancer--a meta-analysis. Clin Oncol (R Coll Radiol). 2002 Jun;14(3):203-12. doi: 10.1053/clon.2002.0076.
Results Reference
background
PubMed Identifier
29423520
Citation
Shrivastava S, Mahantshetty U, Engineer R, Chopra S, Hawaldar R, Hande V, Kerkar RA, Maheshwari A, Shylasree TS, Ghosh J, Bajpai J, Gurram L, Gulia S, Gupta S; Gynecologic Disease Management Group. Cisplatin Chemoradiotherapy vs Radiotherapy in FIGO Stage IIIB Squamous Cell Carcinoma of the Uterine Cervix: A Randomized Clinical Trial. JAMA Oncol. 2018 Apr 1;4(4):506-513. doi: 10.1001/jamaoncol.2017.5179.
Results Reference
derived

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Concomitant Chemoradiation in Advanced Stage Carcinoma Cervix

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