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Radiation Therapy, Mitomycin, and Either Fluorouracil or Cisplatin in Treating Patients With Locally Advanced Anal Cancer

Primary Purpose

Anal Cancer

Status
Terminated
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
cisplatin
fluorouracil
mitomycin C
radiation therapy
Sponsored by
European Organisation for Research and Treatment of Cancer - EORTC
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anal Cancer focused on measuring squamous cell carcinoma of the anus, stage II anal cancer, stage IIIA anal cancer, stage IIIB anal cancer

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

DISEASE CHARACTERISTICS: Histologically confirmed squamous cell anal carcinoma Keratinizing or non-keratinizing The following stages are eligible: T2, N0, M0 with maximum tumor diameter at least 4 cm T3-T4, N0, M0 Any T, N1-N3, M0 Tumor located in the anal canal OR in the anal margin and infiltrating the anal canal No primary adenocarcinoma of the anus Measurable disease PATIENT CHARACTERISTICS: Age 18 to 75 Performance status WHO 0-1 Life expectancy Not specified Hematopoietic Granulocyte count greater than 2,000/mm^3 Platelet count greater than 100,000/mm^3 Hepatic Not specified Renal Creatinine less than 1.4 mg/dL Cardiovascular No grade I angina pectoris with clinical symptoms within the past 3 months No grade II-IV angina pectoris within the past 3 months No stage II or greater distal arteritis Other Not pregnant or nursing Fertile patients must use effective contraception No other prior malignancy except adequately treated basal cell skin cancer or carcinoma in situ of the cervix No psychological, familial, sociological, or geographical condition that would preclude study compliance and follow-up PRIOR CONCURRENT THERAPY: Biologic therapy Not specified Chemotherapy No other concurrent chemotherapy Endocrine therapy Not specified Radiotherapy No other concurrent radiotherapy Surgery No prior colostomy Other No prior treatment for anal cancer

Sites / Locations

  • Ziekenhuis Netwerk Antwerpen Middelheim
  • Institut Jules Bordet
  • Centre Hospitalier Lyon Sud
  • Cliniques Universitaires Saint-Luc
  • Universitair Ziekenhuis Antwerpen
  • Cazk Groeninghe - Campus Maria's Voorzienigheid
  • U.Z. Gasthuisberg
  • Algemeen Ziekenhuis Sint-Augustinus
  • National Cancer Institute of Egypt
  • Institut Sainte Catherine
  • Centre Hospitalier Regional de Besancon - Hopital Jean Minjoz
  • Centre de Lutte Contre le Cancer Georges-Francois Leclerc
  • Urologische Klinik - Universitaetsklinikum Aachen
  • Charite - Campus Charite Mitte
  • Robert Roessle Comprehensive Cancer Center - Charite Campus Buch
  • Universitaetsklinikum Essen
  • Universitaetsklinikum Halle
  • Onkologische Schwerpunktpraxis - Leer
  • Universitaetsklinikum Tuebingen
  • Ospedale Sant Anna
  • Ospedale Busonera - Divisione Oncologia Medica
  • Arnhems Radiotherapeutisch Instituut
  • Dr. Bernard Verbeeten Instituut
  • Institute of Oncology and Radiology of Serbia

Outcomes

Primary Outcome Measures

Response as measured by RECIST at 8 weeks after completion of study treatment (Phase II)
Event-free survival as measured by Logrank at 12 and 26 weeks, then every 6 months thereafter (Phase III)

Secondary Outcome Measures

Acute toxicity and compliance to treatment as measured by CTC v 2.0 at completion of study treatment (Phase II)
Colostomy-free survival as measured by Logrank at 12 and 26 weeks, then every 6 months thereafter (Phase III)
Overall survival as measured by Logrank at 12 and 26 weeks, then every 6 months thereafter
Disease-free survival as measured by Logrank at 12 and 26 weeks, then every 6 months thereafter
Local control as measured by Gray at 12 and 26 weeks, then every 6 months thereafter
Late toxicity as measured by RTOG and EROTC every 6 months after week 26
Quality of life as measured by EORTC Quality of Life Questionnaire-C30 and ASCT at 12 and 26 weeks, then every 6 months for 2 years after entry

Full Information

First Posted
September 10, 2003
Last Updated
September 20, 2012
Sponsor
European Organisation for Research and Treatment of Cancer - EORTC
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1. Study Identification

Unique Protocol Identification Number
NCT00068744
Brief Title
Radiation Therapy, Mitomycin, and Either Fluorouracil or Cisplatin in Treating Patients With Locally Advanced Anal Cancer
Official Title
Continuous Fluorouracil Plus Mitomycin C Versus Mitomycin C Plus Cisplatin As Chemotherapy Combination In Combined Radiochemotherapy For Locally Advanced Anal Cancer. A Phase II-III Study
Study Type
Interventional

2. Study Status

Record Verification Date
September 2012
Overall Recruitment Status
Terminated
Why Stopped
low accrual
Study Start Date
July 2003 (undefined)
Primary Completion Date
November 2007 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
European Organisation for Research and Treatment of Cancer - EORTC

4. Oversight

5. Study Description

Brief Summary
RATIONALE: Drugs used in chemotherapy, such as mitomycin, fluorouracil, and cisplatin, use different ways to stop tumor cells from dividing so they stop growing or die. Combining radiation therapy with chemotherapy may kill more tumor cells. It is not yet known whether radiation therapy and mitomycin are more effective when combined with fluorouracil or with cisplatin in treating anal cancer . PURPOSE: This randomized phase II/III trial is studying how well giving radiation therapy and mitomycin together with fluorouracil works compared to radiation therapy, mitomycin, and cisplatin in treating patients with locally advanced anal cancer.
Detailed Description
OBJECTIVES: Phase II Primary Compare the early clinical response (tumor response at 8 weeks) of patients with locally advanced anal cancer treated with radiotherapy with mitomycin and cisplatin vs mitomycin and fluorouracil. Secondary Compare the feasibility of these regimens in these patients. Compare the acute toxicity of these regimens in these patients. Compare patient compliance to these regimens. Phase III Primary Compare the event-free survival of patients treated with these regimens. Secondary Compare colostomy-free, disease-free, and overall survival of patients treated with these regimens. Compare locoregional control in patients treated with these regimens. Compare the late toxicity of these regimens in these patients. Compare quality of life of patients treated with these regimens. OUTLINE: This is a randomized, multicenter study. Patients are stratified according to participating center, T stage (T2 vs T3 vs T4), and nodal status (N0 vs N+). Patients are randomized to 1 of 2 treatment arms. Arm I: Patients undergo radiotherapy once daily 5 days a week on weeks 1-4, 7-8, and 3 days of week 9 (total of 33 fractions). Patients concurrently receive fluorouracil IV continuously on days 1-26 and 43-59 and mitomycin IV over 15 minutes on days 1 and 43. Arm II: Patients receive radiotherapy and mitomycin as in arm I and cisplatin IV over 1 hour on days 1, 8, 15, 22, 43, 50, and 57. In both arms, treatment continues in the absence of disease progression or unacceptable toxicity. Quality of life is assessed at baseline, at weeks 12 and 26, and then every 6 months for 2 years. Patients are followed every 2 weeks for 8 weeks, at week 26, and then every 6 months thereafter. PROJECTED ACCRUAL: A total of 678 patients (80 [40 per treatment arm] for phase II and 598 [299 per treatment arm] for phase III) will be accrued for this study within 2-5 years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anal Cancer
Keywords
squamous cell carcinoma of the anus, stage II anal cancer, stage IIIA anal cancer, stage IIIB anal cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Allocation
Randomized
Enrollment
88 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
cisplatin
Intervention Type
Drug
Intervention Name(s)
fluorouracil
Intervention Type
Drug
Intervention Name(s)
mitomycin C
Intervention Type
Radiation
Intervention Name(s)
radiation therapy
Primary Outcome Measure Information:
Title
Response as measured by RECIST at 8 weeks after completion of study treatment (Phase II)
Title
Event-free survival as measured by Logrank at 12 and 26 weeks, then every 6 months thereafter (Phase III)
Secondary Outcome Measure Information:
Title
Acute toxicity and compliance to treatment as measured by CTC v 2.0 at completion of study treatment (Phase II)
Title
Colostomy-free survival as measured by Logrank at 12 and 26 weeks, then every 6 months thereafter (Phase III)
Title
Overall survival as measured by Logrank at 12 and 26 weeks, then every 6 months thereafter
Title
Disease-free survival as measured by Logrank at 12 and 26 weeks, then every 6 months thereafter
Title
Local control as measured by Gray at 12 and 26 weeks, then every 6 months thereafter
Title
Late toxicity as measured by RTOG and EROTC every 6 months after week 26
Title
Quality of life as measured by EORTC Quality of Life Questionnaire-C30 and ASCT at 12 and 26 weeks, then every 6 months for 2 years after entry

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically confirmed squamous cell anal carcinoma Keratinizing or non-keratinizing The following stages are eligible: T2, N0, M0 with maximum tumor diameter at least 4 cm T3-T4, N0, M0 Any T, N1-N3, M0 Tumor located in the anal canal OR in the anal margin and infiltrating the anal canal No primary adenocarcinoma of the anus Measurable disease PATIENT CHARACTERISTICS: Age 18 to 75 Performance status WHO 0-1 Life expectancy Not specified Hematopoietic Granulocyte count greater than 2,000/mm^3 Platelet count greater than 100,000/mm^3 Hepatic Not specified Renal Creatinine less than 1.4 mg/dL Cardiovascular No grade I angina pectoris with clinical symptoms within the past 3 months No grade II-IV angina pectoris within the past 3 months No stage II or greater distal arteritis Other Not pregnant or nursing Fertile patients must use effective contraception No other prior malignancy except adequately treated basal cell skin cancer or carcinoma in situ of the cervix No psychological, familial, sociological, or geographical condition that would preclude study compliance and follow-up PRIOR CONCURRENT THERAPY: Biologic therapy Not specified Chemotherapy No other concurrent chemotherapy Endocrine therapy Not specified Radiotherapy No other concurrent radiotherapy Surgery No prior colostomy Other No prior treatment for anal cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Francois Bosset, MD
Organizational Affiliation
Hopital Jean Minjoz
Official's Role
Study Chair
Facility Information:
Facility Name
Ziekenhuis Netwerk Antwerpen Middelheim
City
Antwerpen
ZIP/Postal Code
B-2020
Country
Belgium
Facility Name
Institut Jules Bordet
City
Brussels
ZIP/Postal Code
1000
Country
Belgium
Facility Name
Centre Hospitalier Lyon Sud
City
Brussels
ZIP/Postal Code
1200
Country
Belgium
Facility Name
Cliniques Universitaires Saint-Luc
City
Brussels
ZIP/Postal Code
1200
Country
Belgium
Facility Name
Universitair Ziekenhuis Antwerpen
City
Edegem
ZIP/Postal Code
B-2650
Country
Belgium
Facility Name
Cazk Groeninghe - Campus Maria's Voorzienigheid
City
Kortrijk
ZIP/Postal Code
B-8500
Country
Belgium
Facility Name
U.Z. Gasthuisberg
City
Leuven
ZIP/Postal Code
B-3000
Country
Belgium
Facility Name
Algemeen Ziekenhuis Sint-Augustinus
City
Wilrijk
ZIP/Postal Code
2610
Country
Belgium
Facility Name
National Cancer Institute of Egypt
City
Cairo
Country
Egypt
Facility Name
Institut Sainte Catherine
City
Avignon
ZIP/Postal Code
84082
Country
France
Facility Name
Centre Hospitalier Regional de Besancon - Hopital Jean Minjoz
City
Besancon
ZIP/Postal Code
25030
Country
France
Facility Name
Centre de Lutte Contre le Cancer Georges-Francois Leclerc
City
Dijon
ZIP/Postal Code
21079
Country
France
Facility Name
Urologische Klinik - Universitaetsklinikum Aachen
City
Aachen
ZIP/Postal Code
D-52074
Country
Germany
Facility Name
Charite - Campus Charite Mitte
City
Berlin
ZIP/Postal Code
D-10117
Country
Germany
Facility Name
Robert Roessle Comprehensive Cancer Center - Charite Campus Buch
City
Berlin
ZIP/Postal Code
D-13122
Country
Germany
Facility Name
Universitaetsklinikum Essen
City
Essen
ZIP/Postal Code
D-45122
Country
Germany
Facility Name
Universitaetsklinikum Halle
City
Halle
ZIP/Postal Code
D-06097
Country
Germany
Facility Name
Onkologische Schwerpunktpraxis - Leer
City
Leer
ZIP/Postal Code
D-26789
Country
Germany
Facility Name
Universitaetsklinikum Tuebingen
City
Tuebingen
ZIP/Postal Code
D-72076
Country
Germany
Facility Name
Ospedale Sant Anna
City
Como
ZIP/Postal Code
22100
Country
Italy
Facility Name
Ospedale Busonera - Divisione Oncologia Medica
City
Padova
ZIP/Postal Code
35128
Country
Italy
Facility Name
Arnhems Radiotherapeutisch Instituut
City
Arnhem
ZIP/Postal Code
6815 AD
Country
Netherlands
Facility Name
Dr. Bernard Verbeeten Instituut
City
Tilburg
ZIP/Postal Code
5042 SB
Country
Netherlands
Facility Name
Institute of Oncology and Radiology of Serbia
City
Belgrade
ZIP/Postal Code
11000
Country
Serbia

12. IPD Sharing Statement

Citations:
PubMed Identifier
19643599
Citation
Matzinger O, Roelofsen F, Mineur L, Koswig S, Van Der Steen-Banasik EM, Van Houtte P, Haustermans K, Radosevic-Jelic L, Mueller RP, Maingon P, Collette L, Bosset JF; EORTC Radiation Oncology and Gastrointestinal Tract Cancer Groups. Mitomycin C with continuous fluorouracil or with cisplatin in combination with radiotherapy for locally advanced anal cancer (European Organisation for Research and Treatment of Cancer phase II study 22011-40014). Eur J Cancer. 2009 Nov;45(16):2782-91. doi: 10.1016/j.ejca.2009.06.020. Epub 2009 Jul 28.
Results Reference
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Radiation Therapy, Mitomycin, and Either Fluorouracil or Cisplatin in Treating Patients With Locally Advanced Anal Cancer

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