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Phase III Trial Comparing Conventional RT With Concomitant CT Versus Accelerated RT With Concomitant CT Versus Very Accelerated RT Alone in Patients With Head and Neck Squamous Cell Carcinoma


Phase 3
20 Years
75 Years
Not Enrolling
Both
Oral Cancer, Oropharynx Cancer, Hypopharynx Cancer, Larynx Cancer

Thank you

Trial Information

Phase III Trial Comparing Conventional RT With Concomitant CT Versus Accelerated RT With Concomitant CT Versus Very Accelerated RT Alone in Patients With Head and Neck Squamous Cell Carcinoma


This is a multicentric randomized phase III trial comparing conventional radiotherapy with
concomitant chemotherapy (arm A) versus middle accelerated radiotherapy with concomitant
chemotherapy (arm B) versus very accelerated radiotherapy alone (arm C) in patients with
stage III-IV head and neck squamous cell carcinoma (HNSCC). The main end point is the event
free survival.

The treatments are

Bras A : Conventional radiotherapy given once daily, delivering 70 Gy in 7 weeks (5
fractions of 2 Gy per week) and chemotherapy: 5FU : 600 mg/m²/d, Paraplatin : 70 mg/m²/d,
D1-4 and D22-25 and D43-46

Bras B: middle accelerated radiotherapy delivering 70 Gy in 6 weeks and chemotherapy: 5FU :
600 mg/m²/d, Paraplatin : 70 mg/m²/d, D1-5 and D29-33

- first part : radiotherapy given once daily delivering 40 Gy in 4 weeks and 20 fractions
of 2 Gy

- second part : radiotherapy given twice daily with "concomitant boost" delivering 30 Gy
in 20 fractions in 2 weeks (1,5 Gy x 2 / day)

Bras C: very accelerated radiotherapy given twice daily delivering 64.8 Gy in 3.5 weeks in
36 fractions of 1.8 Gy


Inclusion Criteria:



- Squamous cell carcinoma of oral cavity, oropharynx, hypopharynx or larynx

- Stage III-IV (UICC 1997): T2, T3 or T4 with N0-N3 or T0 with N2-N3

- Not resectable

- Karnofsky PS >= 70

- Renal/liver/cardiac functions and blood counts compatible with the use of paraplatin
and 5-FU

- Informed consent signed

Exclusion Criteria:

- Distant metastasis

- Contra-indication to concomitant chemotherapy

- History of cancer

- History of head and neck radiotherapy

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Event free survival (event=progression, relapse, death from any cause)

Outcome Time Frame:

3 years

Safety Issue:

No

Principal Investigator

Jean Bourhis, PhD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Gustave Roussy, Cancer Campus, Grand Paris

Authority:

France: Ministry of Health

Study ID:

GORTEC 99-02

NCT ID:

NCT00158652

Start Date:

March 2000

Completion Date:

March 2011

Related Keywords:

  • Oral Cancer
  • Oropharynx Cancer
  • Hypopharynx Cancer
  • Larynx Cancer
  • Head and neck squamous cell carcinoma
  • Radiotherapy
  • Chemotherapy
  • Laryngeal Neoplasms
  • Carcinoma, Squamous Cell
  • Mouth Neoplasms
  • Oropharyngeal Neoplasms
  • Hypopharyngeal Neoplasms
  • Head and Neck Neoplasms

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