Gefitinib in Combination With Gemcitabine and Cisplatin in Advanced Non–Small-Cell Lung Cancer: A Phase III Trial—INTACT 1

Author:

Giaccone Giuseppe1,Herbst Roy S.1,Manegold Christian1,Scagliotti Giorgio1,Rosell Rafael1,Miller Vincent1,Natale Ronald B.1,Schiller Joan H.1,von Pawel Joachim1,Pluzanska Anna1,Gatzemeier Ulrich1,Grous John1,Ochs Judith S.1,Averbuch Steven D.1,Wolf Michael K.1,Rennie Pamela1,Fandi Abderrahim1,Johnson David H.1

Affiliation:

1. From the Free University Medical Center, Amsterdam, the Netherlands; Thoraxklinik, Heidelberg; Asklepios Fachkliniken, Munich-Gauting; Krankenhaus Grosshansdorf, Grosshansdorf, Germany; S. Luigi Gonzaga Hospital, Turin, Italy; Hospital Germans Trias i Pujol, Barcelona, Spain; Regional Center of Oncology, Lodz, Poland; AstraZeneca, Alderley Park, United Kingdom; University of Texas M.D. Anderson Cancer Center, Houston, TX; Memorial Sloan-Kettering Cancer Center, New York, NY; Cedars-Sinai Comprehensive...

Abstract

Purpose The purpose of this study was to determine whether the addition of the epidermal growth factor receptor tyrosine kinase inhibitor gefitinib (Iressa, ZD1839; AstraZeneca, Wilmington, DE) to standard first-line gemcitabine and cisplatin provides clinical benefit over gemcitabine and cisplatin alone in patients with advanced or metastatic non–small-cell lung cancer (NSCLC). Gefitinib has demonstrated encouraging efficacy in advanced NSCLC in phase II trials in pretreated patients, and a phase I trial of gefitinib in combination with gemcitabine and cisplatin showed favorable tolerability. Patients and Methods This was a phase III randomized, double-blind, placebo-controlled, multicenter trial in chemotherapy-naive patients with unresectable stage III or IV NSCLC. All patients received up to six cycles of chemotherapy (cisplatin 80 mg/m2 on day 1 and gemcitabine 1,250 mg/m2 on days 1 and 8 of the 3-week cycle) plus either gefitinib 500 mg/d, gefitinib 250 mg/d, or placebo. Daily gefitinib or placebo was continued until disease progression. End points included overall survival (primary), time to progression, response rates, and safety evaluation. Results A total of 1,093 patients were enrolled. There was no difference in efficacy end points between the treatment groups: for the gefitinib 500 mg/d, gefitinib 250 mg/d, and placebo groups, respectively, median survival times were 9.9, 9.9, and 10.9 months (global ordered log-rank [GOLrank] P = .4560), median times to progression were 5.5, 5.8, and 6.0 months (GOLrank; P = .7633), and response rates were 49.7%, 50.3%, and 44.8%. No significant unexpected adverse events were seen. Conclusion Gefitinib in combination with gemcitabine and cisplatin in chemotherapy-naive patients with advanced NSCLC did not have improved efficacy over gemcitabine and cisplatin alone. The reasons for this remain obscure and require further preclinical testing.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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