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A Phase II Trial With Radiotherapy Plus Cetuximab to Evaluate Specific Survival Free of Laryngectomy in Patients With Resectable and Locally Advanced Larynx Cancer, After Treatment With TPF

Phase 2
18 Years
70 Years
Open (Enrolling)
Head and Neck Cancer

Thank you

Trial Information

A Phase II Trial With Radiotherapy Plus Cetuximab to Evaluate Specific Survival Free of Laryngectomy in Patients With Resectable and Locally Advanced Larynx Cancer, After Treatment With TPF

This study is being sponsored by a cooperative medical group.

Inclusion Criteria:

1. Signed Informed Consent Form.

2. Men or women, age (18 and 70).

3. ECOG scale:0-1.

4. Life expectancy superior to 3 months.

5. Larynx squamous carcinoma histologically demonstrated.

6. Patients with larynx squamous carcinoma, stage III-IVA, with resectable disease whose
surgery will imply a total laryngectomy. The T should be a T3, T4A, or a T2 not
candidate for a partial laryngectomy. In case of T2 of any of both locations it will
be required a III or IVA stadium.

7. Patients to be able to receive treatment with TPF followed by normofractionated
radiotherapy with cetuximab.

8. Measurable disease (OMS criteria).

9. Neutrophils superior or equal to 1500/mm3, platelets superior or equal to
150.000/mm3, hemoglobin superior or equal to 10 g/dl.

10. Adequate renal function: creatinin lower or equal to 120 µmol/l (1,4mg/dl)

11. Adequate hepatic function: bilirubin lower or equal to 1 x UNL, AST and ALT lower or
equal to 2,5 UNL, alkaline phosphatase lower or equal to 5 UNL.

12. Seric calcium adjusted to albumine lower or equal to 1,25 UNL.

13. Adequate nutritional condition: loss of weight <20% with relation to the theoretical
weight and albumin superior or equal to 35 g/L.

14. Use of an effective contraceptive method.

Exclusion Criteria:

1. Metastatic disease

2. Surgical treatment, previous radiotherapy and/or chemotherapy for the study disease.

3. Other tumour locations in H&N that are not larynx.

4. Other stages that are not III or IVa without metastasis and resectable disease.

5. The following cases, which will be considered candidates for radical surgery, will
not be included in the study:

- Tumors of the subglottis.

- Tumors of glottis or supraglottis with subglottal extension

- Tumor that destroys the thyroid cartilage and/or cricoid and it extends to
thyroid gland or soft necks's tissues.

- Tumor of supraglottis with a superior extension to 1 cm towards the tongue base
(the extension will be measured since the vallecula).

6. Other previous and/or synchronic squamous carcinoma.

7. Diagnosis of another neoplasia in the last 5 years, excepting carcinoma in situ of
uterine neck and/or a cutaneous carcinoma basocellular properly treated.

8. Active infection(at needs endovenous antibiotics), including active tuberculosis and
diagnosed HIV.

9. Not controlled hypertension defined as arterial systolic tension superior or equal to
180 mm Hg and/or diastolic arterial tension superior or equal to 130 mm Hg baseline.

10. Pregnancy or breastfeeding.

11. Immunity systemic treatment, chronic and concomitant, or hormonal treatment of the

12. Other antineoplasic concomitant treatments.

13. Coronary clinically significant arteriopathy or precedents of myocardial infarction
in the last 12 months or high risk of not controlled arrhythmia or cardiac not
controlled insufficiency.

14. Pulmonary obstructive chronic disease that had needed 3 or more hospitalizations in
the last 12 months.

15. Active non controlled peptic ulcer.

16. Presence of a psychological or medical disease that could prevent to accomplish the
study by the patient or to grant his/her signature in the informed consent form.

17. Known drugs abuse (excepting excessive consumption of alcohol).

18. Known allergic reaction to some of the components of the treatment of the study.

19. Previous treatment with monoclonal antibodies or other transduction of the sign
inhibitors or treatment directed against the EGFR.

20. Any experimental treatment in 30 days before entry in the study.

Type of Study:


Study Design:

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Outcome Measure:

Specific survival

Outcome Time Frame:

Three years after the end of treatment with radiotherapy and cetuximab

Safety Issue:


Principal Investigator

Ricard Mesía Nin, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Hospital Durán i Reynals


Spain: Spanish Agency of Medicines

Study ID:




Start Date:

October 2008

Completion Date:

May 2014

Related Keywords:

  • Head and Neck Cancer
  • Head and Neck Cancer
  • Laryngeal Neoplasms
  • Head and Neck Neoplasms