Real-world treatment patterns and survival of patients with BRAF V600-mutated metastatic non-small cell lung cancer

被引:13
作者
Horn, Leora [1 ]
Bauml, Joshua [2 ]
Forde, Patrick M. [3 ]
Davis, Keith L. [4 ]
Myall, Nathaniel J. [5 ]
Sasane, Medha [6 ,10 ]
Dalal, Anand [6 ]
Culver, Ken [6 ]
Wozniak, Antoinette J. [7 ]
Baik, Christina S. [8 ]
Mutebi, Alex [6 ,11 ]
Zhang, Pingkuan [6 ]
Wakelee, Heather A. [5 ]
Johnson, Bruce E. [9 ]
机构
[1] Vanderbilt Ingram Canc Ctr, 1301 Med Ctr Dr, Nashville, TN 37232 USA
[2] Univ Penn, Perelman Sch Med, 3400 Civ Ctr Blvd, Philadelphia, PA 19104 USA
[3] Johns Hopkins Sidney Kimmel Comprehens Canc Ctr, 401 N Broadway, Baltimore, MD 21287 USA
[4] RTI Hlth Solut, 200 Pk Off Dr, Res Triangle Pk, NC 27709 USA
[5] Stanford Univ, Med Ctr, 291 Campus Dr, Stanford, CA 94305 USA
[6] Novartis Pharmaceut, One Hlth Plaza, E Hanover, NJ 07936 USA
[7] Karmanos Canc Inst, 4100 John R St, Detroit, MI 48201 USA
[8] Univ Washington, Fred Hutchinson Canc Res Ctr, 1100 Fairview Ave N, Seattle, WA 98109 USA
[9] Dana Farber Canc Inst, 450 Brookline Ave, Boston, MA 02215 USA
[10] Sanofi Pasteur Inc, Lyon, France
[11] Vertex Pharmaceut, Boston, MA USA
关键词
BRAF; Non-small cell lung cancer; Real-world evidence; Outcomes; CLINICAL CHARACTERISTICS; OPEN-LABEL; MUTATIONS; FEATURES; MULTICENTER; DABRAFENIB; OUTCOMES; GENE;
D O I
10.1016/j.lungcan.2018.12.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Clinical outcomes data on BRAF-mutated non-small cell lung cancer (NSCLC) patients treated in routine practice is limited. To address this gap, we described treatment patterns and survival in a cohort of these patients evaluated/treated at 7 US academic cancer centers during 2009-2016. Methods: This was a retrospective chart review. Patients with BRAF V600-mutated metastatic NSCLC were selected. Current/previous participants in BRAF-related trials were excluded. Onset of metastatic NSCLC defined a patient's index date, which had to occur >= 6 months before the chart review date. Analyses were descriptive, including Kaplan-Meier analyses for overall survival (OS). Results: The study included 72 patients. At index, median age (range) was 65 (44-90) years; 61.1% were female. Fifty-two patients received >= 1 line of systemic therapy for metastatic disease. Platinum-based doublet chemotherapy was the most common first-line (1L) regimen (76.9% of 1 I recipients); no patient received 1 I targeted therapy (TT) with a BRAF/MEK inhibitor. In total, 20 patients received TT in any treatment line (21 or later). At time of review, 38 patients were deceased. Median (95%CI) OS from index for all patients was 31.0 (14.5, 63.8) months. Median (95%CI) OS was 56.5 (13.4, 89.1) months from index for TT recipients and 27.2 (10.6, 64.6) months in patients not treated with TT. Conclusion: Survival time in BRAF V600-mutated metastatic NSCLC patients studied here was higher than expected based on indirect comparisons with historical NSCLC cohorts for whom no oncogenic driver (BRAF or otherwise) was present. TT recipients had a numerically longer OS from metastatic onset than patients receiving usual care, further highlighting the importance of TT in BRAF V600-mutant NSCLC.
引用
收藏
页码:74 / 90
页数:17
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