Adjuvant Cetuximab and Chemoradiation in Head and Neck Cancer

Head and Neck Cancer Clinical Trial

— ACCRA-HN  

Official title:

Multicenter, Open-label Phase II Trial on Post-surgery Chemoradiation in Combination With Cetuximab in Squamous Cell Carcinoma of the Head and Neck With High Risk of Locoregional Recurrence.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00791141
• Other study ID #: ACCRA-HN
• Status: Completed
• Phase: Phase 2
• First received: November 13, 2008
• Last updated: January 22, 2014
• Start date: August 2008
• Est. completion date: September 2013

Study information

• Verified date: January 2014
• Source: Heinrich-Heine University, Duesseldorf
• Contact: n/a
• Is FDA regulated: No
• Health authority: Germany: Paul-Ehrlich-Institut
• Study type: Interventional

Clinical Trial Summary

This multicenter, open-label, uncontrolled phase II trial evaluates safety and efficacy of post-operative chemoradiation in combination with cetuximab in squamous cell carcinoma of the head and neck.

Description:

Advanced squamous cell carcinoma of the head and neck still has a poor prognosis and loco-regional recurrence frequently occurs. Efforts have been made to improve response rates and survival and different therapeutic regimens including concurrent chemo-radiotherapy or sequential chemo-radiotherapy have been developed.

To further increase the outcome of patients with locally advanced SCCHN effective new treatments with minimal toxicities are needed. Molecular targeted agents, which do not demonstrate overlapping toxicities with commonly used chemotherapy agents, have therefore been investigated. The EGFR is widely expressed at high levels in SSCHN and is associated with poor prognosis.

Cetuximab has already been investigated in combination with radiotherapy or chemotherapy in patients with head and neck cancer. The immunoradiotherapy was well tolerated with most of the side effects related to the high dose irradiation. The most common side effects are mucositis and dysphagia. Additionally, skin reactions appear sometimes more frequently in cetuximab administration. Grade 3 to 4 infusion reactions were observed in 3% of the patients treated with cetuximab. Based on the current promising results with RCT in patients with locally advanced head and neck cancer and clinical results with EGFR-antibodies plus RT, the present study was primarily designed to define the acute grade 3/4 toxicity.

We expect to show effective results in reducing the risk of distant metastasis, with administration of an additional six month adjuvant cetuximab treatment, in patient with recurrent SCCHN.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: September 2013
• Est. primary completion date: April 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Signed written informed consent;

• Males or females between 18 and 70 years of age;

• Surgically resected squamous cell carcinomas of the hypopharynx, oropharynx, larynx and oral cavity with high risk of locoregional recurrence not more than 6-9 weeks (maximum) ago;

• To be categorized as high risk patients have to fulfil at least one of the following criteria:

• R0 - resection <5 mm margin

• R1 - resection

• Extracapsular nodal extension;

• no previous chemotherapy, radiotherapy;

• Performance status ECOG: 0 - 1;

• Contraception in male and female patients if of childbearing potential, willingness to use effective contraceptive method for the study duration and 2 months post-dosing;

• Adequate renal, liver and hematological functions (within maximum 9 weeks until surgery):

• Adequate bone marrow function: neutrophils > 1.5 x 10^9/L, platelets > 100 x 10^9/L, hemoglobin > 10.0 g/dL

• Adequate liver function: Bilirubin < 2.0 mg/dL, AST, ALT, AP, ?-GT < 3 x ULN

• Adequate renal function: creatinine clearance > =60 ml/min

• No distant metastases;

Exclusion Criteria:

• Nasopharyngeal carcinoma;

• R2 resection;

• Invalid informed consent;

• Performance Status > 1;

• Previous chemotherapy or radiotherapy for carcinoma of the head and neck;

• Prior exposure to EGFR pathway targeting therapy;

• Other serious illness or medical conditions:

• Unstable cardiac disease despite treatment, congestive heart failure NYHA grade 3 and 4;

• Clinically significantly abnormal electrocardiogram (ECG) or left ventricular ejection fraction (LVEF) below the institutional range of the normal

• Significant neurologic or psychiatric disorders including dementia or seizures;

• Active uncontrolled infection;

• Active disseminated intravascular coagulation;

• Other serious underlying medical conditions which could impair the ability of the patient to participate in the study;

• Symptomatic peripheral neuropathy National Cancer Institute-Common Toxicity Criteria (NCI-CTC v3.0) grade 2 or ototoxicity grade 2, except if due to trauma or mechanical impairment due to tumor mass;

• Having participated in another therapeutic clinical trial or any investigational agent in the preceding 30 days;

• Known allergic/hypersensitivity reaction to any of the components of the treatment;

• Pregnancy (absence confirmed by serum/urine ß-HCG) or breast-feeding;

• Known drug abuse;

• Other previous malignancy within 5 years, with exception of a history of a previous basal cell carcinoma of the skin or pre-invasive carcinoma of the cervix;

• Legal incapacity or limited legal capacity;

• Sensitivity and incompatibility against 5-Fluorouracil

• Sensitivity and incompatibility against platinum-compounds

• Known incompatibilities >grade 3 towards cetuximab

• expected incompliance of patient (e.g. in case of severe alcohol addiction)

• Dental evaluation: Pre treatment dental care before start of radiochemotherapy (approximately 8 to 10 days lapse-time is needed for complete recovery before initiation of radiation therapy).

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Head and Neck Cancer
• Head and Neck Neoplasms

Intervention

Drug:
• Cetuximab
Loading dose prior to chemoradiotherapy 400 mg/m², followed by every week infusion of 250 mg/m² during chemoradiotherapy. After chemoradiotherapy every 2 week infusions of 500 mg/m² over 6 months.

Locations

Country	Name	City	State
Germany	Charité University Medicine, Department of Radiotherapy and Radiological Oncology	Berlin
Germany	Department of Radiotherapy an Radiological Oncology University Hospital Essen	Essen	NW
Germany	Department of Radiotherapeutics of the University Hospital Freiburg	Freiburg	BW
Germany	Department of Radiological Oncology University Hospital Heidelberg	Heidelberg	BW
Germany	Department of Radiotherapy and Radiological Oncology Universität Hospital Jena	Jena	Thueringen
Germany	Department of Radiotherapy, University Hospital Schleswig Holstein, Campus Lübeck	Lübeck	Schleswig Hostein
Germany	Department of Radiotherapy and Radiological Oncology University Hospital Mainz	Mainz	Rheinland-Pfalz
Germany	Department of Radiotherapy and Radiological Oncology, University Hospital Munich	Munich	Bavaria
Germany	Department of Radiotherapy and Radiological Oncology University Hospital Tuebingen	Tuebingen	BW
Germany	Department of Radiotherapy and Radiological Oncology University Hospital Ulm	Ulm	BW

Sponsors (1)

Lead Sponsor	Collaborator
Heinrich-Heine University, Duesseldorf

Country where clinical trial is conducted

Germany, 

References & Publications (1)

Budach W, Bölke E, Homey B. Severe cutaneous reaction during radiation therapy with concurrent cetuximab. N Engl J Med. 2007 Aug 2;357(5):514-5. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of patients experiencing grade 3/4 acute toxicities not considering grade 3/4 skin tox. outside the radiation portals combined with 2-years disease-free survival rate.		any toxicities occurring within 90 days post radiation start	Yes
Secondary	Incidence of Loco-regional relapse		assessment after patient has completed follow-up	No
Secondary	Disease-free survival		time from start of surgery to the first evidence of loco-regional or distant tumor relapse or death	No
Secondary	Progression-free survival		from start of surgery to the first observation of disease progression or death	No
Secondary	Overall survival		censored at the time of last documented efficacy	No
Secondary	The rate of patients with secondary primary neoplasm		assessment after patient has completed follow-up	Yes
Secondary	The incidence of late toxicity		beyond 90 days after start of radiation therapy	Yes