Phase II Trial of Cetuximab in Patients With Refractory Colorectal Cancer That Expresses the Epidermal Growth Factor Receptor

Author:

Saltz Leonard B.1,Meropol Neal J.1,Loehrer Patrick J.1,Needle Michael N.1,Kopit Justin1,Mayer Robert J.1

Affiliation:

1. From the Gastrointestinal Oncology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY; Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, PA; Indiana University Cancer Center and the Walther Cancer Institute, Indianapolis, IN; Imclone Systems Inc, Somerville, NJ; Bristol Myers Squibb Inc, Wallingford, CT; and the Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA

Abstract

PurposeTo evaluate the antitumor activity and toxicity of single-agent cetuximab in patients with chemotherapy-refractory colorectal cancer whose tumors express the epidermal growth factor receptor.Patients and MethodsPhase II, open-label clinical trial. Patients were required to have EGFr expression demonstrated on formalin-fixed paraffin-embedded tumor tissue by immunohistochemical staining before study participation. Patients were required to have received irinotecan, either alone or in a combination regimen, and to have demonstrated clinical failure on this regimen before study entry. Cetuximab was administered weekly by intravenous infusion. The first dose of 400 mg/m2was given during the course of 2 hours. Subsequent weekly treatments were given at a dose of 250 mg/m2during the course of 1 hour.ResultsFifty-seven eligible patients were treated. All were assessable for toxicity and response. The most commonly encountered grade 3 to 4 adverse events, regardless of relationship to study drug, were an acne-like skin rash, predominantly on the face and upper torso (86% with any grade; 18% with grade 3), and a composite of asthenia, fatigue, malaise, or lethargy (56% with any grade, 9% with grade 3). Two patients (3.5%) experienced grade 3 allergic reactions requiring discontinuation of study treatment. A third patient experienced a grade 3 allergic reaction that resolved, and the patient continued on the study. Neither diarrhea nor neutropenia were dose limiting in any of the 57 patients treated. Five patients (9%; 95% CI, 3% to 19%) achieved a partial response. Twenty-one additional patients had stable disease or minor responses. The median survival in these previously treated patients with chemotherapy-refractory colorectal cancer is 6.4 months.ConclusionCetuximab on this once-weekly schedule has modest activity and is well-tolerated as a single agent in patients with chemotherapy-refractory colorectal cancer whose tumors express the epidermal growth factor receptor. Further studies of cetuximab will evaluate the use of cetuximab in conjunction with first-line and adjuvant treatments for this disease.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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