Adjuvant Cetuximab and Chemoradiation in Head and Neck Cancer (ACCRA-HN)

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.

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.

Study Overview

• Status: Completed
• Conditions: Head and Neck Cancer
• Intervention / Treatment: Drug: Cetuximab

Detailed 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.

• Study Type: Interventional
• Enrollment (Actual): 80
• Phase: Phase 2

Contacts and Locations

Study Locations

• Germany
  • Berlin, Germany, 13353
    • Charité University Medicine, Department of Radiotherapy and Radiological Oncology
  • BW
    • Freiburg, BW, Germany, 79106
      • Department of Radiotherapeutics of the University Hospital Freiburg
    • Heidelberg, BW, Germany, 69120
      • Department of Radiological Oncology University Hospital Heidelberg
    • Tuebingen, BW, Germany, 72076
      • Department of Radiotherapy and Radiological Oncology University Hospital Tuebingen
    • Ulm, BW, Germany, 89091
      • Department of Radiotherapy and Radiological Oncology University Hospital Ulm
  • Bavaria
    • Munich, Bavaria, Germany, 81377
      • Department of Radiotherapy and Radiological Oncology, University Hospital Munich
  • NW
    • Essen, NW, Germany, 45122
      • Department of Radiotherapy an Radiological Oncology University Hospital Essen
  • Rheinland-Pfalz
    • Mainz, Rheinland-Pfalz, Germany, 55131
      • Department of Radiotherapy and Radiological Oncology University Hospital Mainz
  • Schleswig Hostein
    • Lübeck, Schleswig Hostein, Germany, 23538
      • Department of Radiotherapy, University Hospital Schleswig Holstein, Campus Lübeck
  • Thueringen
    • Jena, Thueringen, Germany, 07743
      • Department of Radiotherapy and Radiological Oncology Universität Hospital Jena

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 70 years (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

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, γ-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 β-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 Plan

How is the study designed?

Design Details

• Primary Purpose: TREATMENT
• Allocation: NA
• Interventional Model: SINGLE_GROUP
• Masking: NONE

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
EXPERIMENTAL: Cetuximab; Cetuximab in combination with radiotherapy, cisplatin and 5-FU. After chemoradiotherapy all patients receive a cetuximab maintenance therapy.	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.; Other Names: Erbitux

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
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

Secondary Outcome Measures

Outcome Measure	Time Frame
Incidence of Loco-regional relapse	assessment after patient has completed follow-up
Disease-free survival	time from start of surgery to the first evidence of loco-regional or distant tumor relapse or death
Progression-free survival	from start of surgery to the first observation of disease progression or death
Overall survival	censored at the time of last documented efficacy
The rate of patients with secondary primary neoplasm	assessment after patient has completed follow-up
The incidence of late toxicity	beyond 90 days after start of radiation therapy

Collaborators and Investigators

• Sponsor: Heinrich-Heine University, Duesseldorf
• Investigators: Principal Investigator: Wilfried Budach, Prof. Dr., Department of Radiotherapy and Radiological Oncology

Publications and helpful links

General Publications

• Budach W, Bolke E, Homey B. Severe cutaneous reaction during radiation therapy with concurrent cetuximab. N Engl J Med. 2007 Aug 2;357(5):514-5. doi: 10.1056/NEJMc071075. No abstract available.

Study record dates

Study Major Dates

• Study Start: August 1, 2008
• Primary Completion (ACTUAL): April 1, 2013
• Study Completion (ACTUAL): September 1, 2013

Study Registration Dates

• First Submitted: November 13, 2008
• First Submitted That Met QC Criteria: November 13, 2008
• First Posted (ESTIMATE): November 14, 2008

Study Record Updates

• Last Update Posted (ESTIMATE): January 23, 2014
• Last Update Submitted That Met QC Criteria: January 22, 2014
• Last Verified: January 1, 2014

More Information

Terms related to this study

• Keywords: Head and Neck Cancer; Chemotherapy; Radiation therapy; Chemoradiotherapy; adjuvant cetuximab administration
• Additional Relevant MeSH Terms: Neoplasms; Neoplasms by Site; Head and Neck Neoplasms; Antineoplastic Agents; Antineoplastic Agents, Immunological; Cetuximab
• Other Study ID Numbers: ACCRA-HN