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IMRT Plus Cisplatin Versus Conventional Radiotherapy Plus Cisplatin in Stage III-IV HNSCC

Primary Purpose

Oral Cancer, Oropharynx Cancer, Hypopharynx Cancer

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
IMRT 75 Gy
Conventional radiotherapy 70 Gy
concomitant cisplatin
Sponsored by
Groupe Oncologie Radiotherapie Tete et Cou
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Oral Cancer focused on measuring oral cancer, oropharynx cancer, hypopharynx cancer, IMRT

Eligibility Criteria

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

Inclusion Criteria: squamous cell carcinoma of oral cavity, oropharynx or hypopharynx Stage III - IV (T1-T4, N0-N2)(UICC 2002) Not resected Indication of radiotherapy to bilateral cervical nodes at dose>= 50 Gy Delineation of target volumes done before randomization Scintigraphy of parotid gland done before radiotherapy start Quality of life questionnaires (EORTC-C30 and EORTC-H&N35) filled in by the patient Informed consent signed Exclusion Criteria: N3 (UICC 2002) Distant metastasis Contra-indication to concomitant cisplatin History of cancer within the last 5 years History of head and neck radiotherapy Administration of drugs for treatment or prophylaxis of xerostomia (pilocarpine, ethyol)

Sites / Locations

  • Centre Alexis Vautrin
  • Institut Gustave Roussy

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

1

2

Arm Description

Conventional RT 70Gy + concomitant cisplatin

IMRT 75Gy + concomitant cisplatin

Outcomes

Primary Outcome Measures

Loco regional control

Secondary Outcome Measures

Survival
Xerostomia at 2 years (evaluated by parotid gland scintigraphy)
Quality of life (EORTC-QLQ-H&N35)

Full Information

First Posted
September 9, 2005
Last Updated
April 14, 2020
Sponsor
Groupe Oncologie Radiotherapie Tete et Cou
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1. Study Identification

Unique Protocol Identification Number
NCT00158678
Brief Title
IMRT Plus Cisplatin Versus Conventional Radiotherapy Plus Cisplatin in Stage III-IV HNSCC
Official Title
Phase III Trial of Intensity-modulated Radiotherapy Plus Cisplatin Versus Conventional Radiotherapy Plus Cisplatin in Patients With Stage III-IV Head and Neck Squamous Cell Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
September 27, 2005 (Actual)
Primary Completion Date
March 22, 2020 (Actual)
Study Completion Date
March 22, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Groupe Oncologie Radiotherapie Tete et Cou

4. Oversight

5. Study Description

Brief Summary
This is a multicentric randomized phase III trial comparing intensity-modulated radiotherapy (75 Gy) plus cisplatin versus conventional radiotherapy (70 Gy) plus cisplatin in patients with stage III-IV squamous cell carcinoma of oral cavity, oropharynx or hypopharynx. The main end points are the rate of locoregional control and the rate of xerostomia at 2 years.
Detailed Description
This is a multicentric randomized phase III trial comparing intensity-modulated radiotherapy plus concomitant cisplatin versus conventional radiotherapy plus concomitant cisplatin in patients with stage III-IV squamous cell carcinoma of oral cavity, oropharynx or hypopharynx. The main end points are the rate of locoregional control and the rate of xerostomia at 2 years. The IMRT total dose is 75 Gy (50 Gy to PTV1 and T0 + 25 Gy (10 fractions) to PTV2). The conventional radiotherapy total dose is 70 Gy (50 Gy to PTV1 + 20 Gy (10 fractions) to PTV2). In both arms, the cervical nodes will receive 50 Gy (65 Gy in case of Np) by conventional radiotherapy (IMRT is allowed in the IRMT arm). In the two arms, patients will receive concomitant cisplatin (100 mg/m² D1, D21, D42).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Oral Cancer, Oropharynx Cancer, Hypopharynx Cancer
Keywords
oral cancer, oropharynx cancer, hypopharynx cancer, IMRT

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
310 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Conventional RT 70Gy + concomitant cisplatin
Arm Title
2
Arm Type
Experimental
Arm Description
IMRT 75Gy + concomitant cisplatin
Intervention Type
Procedure
Intervention Name(s)
IMRT 75 Gy
Intervention Description
50 Gy in PTV1 and 25 Gy in 10 fractions in PTV2
Intervention Type
Procedure
Intervention Name(s)
Conventional radiotherapy 70 Gy
Intervention Description
50 Gy in PTV1 and 20 Gy in PTV2
Intervention Type
Drug
Intervention Name(s)
concomitant cisplatin
Intervention Description
100 mg/m2 D1, D22, D43
Primary Outcome Measure Information:
Title
Loco regional control
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Survival
Time Frame
2 years
Title
Xerostomia at 2 years (evaluated by parotid gland scintigraphy)
Time Frame
2 years
Title
Quality of life (EORTC-QLQ-H&N35)
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: squamous cell carcinoma of oral cavity, oropharynx or hypopharynx Stage III - IV (T1-T4, N0-N2)(UICC 2002) Not resected Indication of radiotherapy to bilateral cervical nodes at dose>= 50 Gy Delineation of target volumes done before randomization Scintigraphy of parotid gland done before radiotherapy start Quality of life questionnaires (EORTC-C30 and EORTC-H&N35) filled in by the patient Informed consent signed Exclusion Criteria: N3 (UICC 2002) Distant metastasis Contra-indication to concomitant cisplatin History of cancer within the last 5 years History of head and neck radiotherapy Administration of drugs for treatment or prophylaxis of xerostomia (pilocarpine, ethyol)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean Bourhis, PhD
Organizational Affiliation
Gustave Roussy, Cancer Campus, Grand Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michel Lapeyre, MD
Organizational Affiliation
Centre Alexis Vautrin
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Alexis Vautrin
City
Vandoeuvre les Nancy
ZIP/Postal Code
54511
Country
France
Facility Name
Institut Gustave Roussy
City
Villejuif
ZIP/Postal Code
94800
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
32417348
Citation
Tao Y, Auperin A, Blanchard P, Alfonsi M, Sun XS, Rives M, Pointreau Y, Castelli J, Graff P, Wong Hee Kam S, Thariat J, Veresezan O, Heymann S, Renard-Oldrini S, Lafond C, Cornely A, Casiraghi O, Boisselier P, Lapeyre M, Biau J, Bourhis J. Concurrent cisplatin and dose escalation with intensity-modulated radiotherapy (IMRT) versus conventional radiotherapy for locally advanced head and neck squamous cell carcinomas (HNSCC): GORTEC 2004-01 randomized phase III trial. Radiother Oncol. 2020 Sep;150:18-25. doi: 10.1016/j.radonc.2020.05.021. Epub 2020 May 15.
Results Reference
derived

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IMRT Plus Cisplatin Versus Conventional Radiotherapy Plus Cisplatin in Stage III-IV HNSCC

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