» Articles » PMID: 29966800

Results of PROFILE 1029, a Phase III Comparison Of First-Line Crizotinib Versus Chemotherapy In East Asian Patients with ALK-Positive Advanced Non-Small Cell Lung Cancer

Overview
Journal J Thorac Oncol
Publisher Elsevier
Date 2018 Jul 4
PMID 29966800
Citations 100
Authors
Affiliations
Soon will be listed here.
Abstract

Introduction: The phase III randomized PROFILE 1014 study demonstrated superiority of crizotinib to first-line chemotherapy in prolonging progression-free survival (PFS) in previously untreated patients with ALK receptor tyrosine kinase gene (ALK)-positive advanced nonsquamous NSCLC. This result was consistent with that in the smaller subset of East Asian patients in PROFILE 1014. The subsequent study reported here prospectively evaluated crizotinib in a larger East Asian patient population.

Methods: In this open-label phase III study (PROFILE 1029), patients were randomized 1:1 to receive orally administered crizotinib 250 mg twice daily continuously (3-week cycles) or intravenously administered chemotherapy (pemetrexed 500 mg/m, plus cisplatin 75 mg/m, or carboplatin [at a dose to produce area under the concentration-time curve of 5-6 mg·min/mL]) every 3 weeks for a maximum of six cycles. PFS confirmed by independent radiology review was the primary end point.

Results: Crizotinib significantly prolonged PFS (hazard ratio, 0.402; 95% confidence interval [CI]: 0.286-0.565; p < 0.001). The median PFS was 11.1 months with crizotinib and 6.8 months with chemotherapy. The objective response rate was 87.5% (95% CI: 79.6-93.2%) with crizotinib versus 45.6% (95% CI: 35.8-55.7%) with chemotherapy (p < 0.001). The most common adverse events were increased transaminase levels, diarrhea, and vision disorders with crizotinib and leukopenia, neutropenia, and anemia with chemotherapy. Significantly greater improvements from baseline in patient-reported outcomes were seen in crizotinib-treated versus chemotherapy-treated patients.

Conclusions: First-line crizotinib significantly improved PFS, objective response rate, and patient-reported outcomes compared with standard platinum-based chemotherapy in East Asian patients with ALK-positive advanced NSCLC, which is similar to the results from PROFILE 1014. The safety profiles of crizotinib and chemotherapy were consistent with those previously published.

Citing Articles

Plasma-Based Comprehensive Genomic Profiling DNA Assays for Non-Small Cell Lung Cancer: A Health Technology Assessment.

Ont Health Technol Assess Ser. 2024; 24(8):1-306.

PMID: 39698418 PMC: 11650780.


Sex differences in patients with Non-Small Cell Lung Cancer harboring driver fusions treated with tyrosine kinase inhibitors: a systematic review.

Leporati R, Auclin E, Morchon D, Ferriol-Galmes M, Laguna J, Gorria T Ther Adv Med Oncol. 2024; 16:17588359241306940.

PMID: 39697619 PMC: 11653452. DOI: 10.1177/17588359241306940.


Time to deterioration of patient-reported outcome endpoints in cancer clinical trials: targeted literature review and best practice recommendations.

Cocks K, King-Kallimanis B, Sims J, Worthy G, Stein J, Ayala-Nunes L J Patient Rep Outcomes. 2024; 8(1):150.

PMID: 39694990 PMC: 11655910. DOI: 10.1186/s41687-024-00824-7.


The Use of Anaplastic Lymphoma Kinase Inhibitors in Non-Small-Cell Lung Cancer Treatment-Literature Review.

Gorzelak-Magiera A, Domagala-Haduch M, Kabut J, Gisterek-Grocholska I Biomedicines. 2024; 12(10).

PMID: 39457620 PMC: 11504905. DOI: 10.3390/biomedicines12102308.


Correlation between ALK+ non-small cell lung cancer targeted therapy and thrombosis: a systematic review and network meta-analysis.

Qi Y, Wang X, Guo T, You T, Wang P BMJ Open. 2024; 14(9):e078173.

PMID: 39349372 PMC: 11448140. DOI: 10.1136/bmjopen-2023-078173.