Crizotinib versus Chemotherapy in Advanced <i>ALK</i> -Positive Lung Cancer

Alice T. Shaw(Massachusetts General Hospital), Dong‐Wan Kim(Seoul National University Hospital), Kazuhiko Nakagawa(Kindai University), Takashi Seto(National Hospital Organization Kyushu Cancer Center), Lucio Crinò(Azienda Ospedaliera di Perugia), Myung‐Ju Ahn(Samsung Medical Center), Tommaso De Pas(Mylan (Switzerland)), Benjamin Besse(Institut Gustave Roussy), Benjamin Solomon(Peter MacCallum Cancer Centre), Fiona Blackhall(National Health Service), Yi‐Long Wu(Guangdong General Hospital), Michael Thomas, Kenneth J. O’Byrne(Cancer Trials Ireland), Denis Moro‐Sibilot(Centre Hospitalier Universitaire de Grenoble), D. Ross Camidge(University of Colorado Anschutz Medical Campus), Tony Mok(Chinese University of Hong Kong), Vera Hirsh, Gregory J. Riely(Memorial Sloan Kettering Cancer Center), Shrividya Iyer(Pfizer (United States)), Vanessa Tassell(Pfizer (United States)), Anna Polli(Pfizer (Italy)), Keith D. Wilner(Pfizer (United States)), Pasi A. Jänne(Dana-Farber Cancer Institute)
New England Journal of Medicine
June 1, 2013
Cited by 3,403Open Access
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Abstract

BACKGROUND: In single-group studies, chromosomal rearrangements of the anaplastic lymphoma kinase gene (ALK) have been associated with marked clinical responses to crizotinib, an oral tyrosine kinase inhibitor targeting ALK. Whether crizotinib is superior to standard chemotherapy with respect to efficacy is unknown. METHODS: We conducted a phase 3, open-label trial comparing crizotinib with chemotherapy in 347 patients with locally advanced or metastatic ALK-positive lung cancer who had received one prior platinum-based regimen. Patients were randomly assigned to receive oral treatment with crizotinib (250 mg) twice daily or intravenous chemotherapy with either pemetrexed (500 mg per square meter of body-surface area) or docetaxel (75 mg per square meter) every 3 weeks. Patients in the chemotherapy group who had disease progression were permitted to cross over to crizotinib as part of a separate study. The primary end point was progression-free survival. RESULTS: The median progression-free survival was 7.7 months in the crizotinib group and 3.0 months in the chemotherapy group (hazard ratio for progression or death with crizotinib, 0.49; 95% confidence interval [CI], 0.37 to 0.64; P<0.001). The response rates were 65% (95% CI, 58 to 72) with crizotinib, as compared with 20% (95% CI, 14 to 26) with chemotherapy (P<0.001). An interim analysis of overall survival showed no significant improvement with crizotinib as compared with chemotherapy (hazard ratio for death in the crizotinib group, 1.02; 95% CI, 0.68 to 1.54; P=0.54). Common adverse events associated with crizotinib were visual disorder, gastrointestinal side effects, and elevated liver aminotransferase levels, whereas common adverse events with chemotherapy were fatigue, alopecia, and dyspnea. Patients reported greater reductions in symptoms of lung cancer and greater improvement in global quality of life with crizotinib than with chemotherapy. CONCLUSIONS: Crizotinib is superior to standard chemotherapy in patients with previously treated, advanced non-small-cell lung cancer with ALK rearrangement. (Funded by Pfizer; ClinicalTrials.gov number, NCT00932893.).


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