The Impact of Comprehensive Genomic Profiling (CGP) on the Decision-Making Process in the Treatment of ALK-Rearranged Advanced Non-Small Cell Lung Cancer (aNSCLC) After Failure of 2nd/3rd-Generation ALK Tyrosine Kinase Inhibitors (TKIs)

被引:1
作者
Raphael, Ari [1 ,2 ]
Onn, Amir [2 ,3 ]
Holtzman, Liran [2 ]
Dudnik, Julia [4 ]
Urban, Damien [3 ]
Kian, Waleed [5 ]
Cohen, Aharon Y. [4 ]
Moskovitz, Mor [6 ]
Zer, Alona [6 ]
Bar, Jair [2 ,3 ]
Rabinovich, Natalie Maimon [7 ]
Grynberg, Shirly [3 ]
Oedegaard, Cecilie [3 ]
Agbarya, Abed [8 ]
Peled, Nir [5 ,9 ]
Shochat, Tzippy [10 ]
Dudnik, Elizabeth [9 ,11 ,12 ]
机构
[1] Tel Aviv Sourasky Med Ctr, Dept Oncol, Tel Aviv, Israel
[2] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[3] Sheba Med Ctr, Inst Oncol, Thorac Oncol Serv, Ramat Gan, Israel
[4] Soroka Univ Med Ctr, Inst Canc, Thorac Oncol Serv, Beer Sheva, Israel
[5] Shaare Zedek Med Ctr, Dept Oncol, Jerusalem, Israel
[6] Rambam Hlth Care Campus, Thorac Canc Serv, Haifa, Israel
[7] Meir Med Ctr, Thorac Canc Serv, Kefar Sava, Israel
[8] Bnai Zion Med Ctr, Dept Oncol, Haifa, Israel
[9] Ben Gurion Univ Negev, Fac Hlth Sci, Beer Sheva, Israel
[10] Rabin Med Ctr, Stat Consulting Unit, Petah Tiqwa, Israel
[11] Assuta Med Ctr, Thorac Oncol Serv, Tel Aviv, Israel
[12] Rabin Med Ctr, Thorac Oncol Serv, Petah Tiqwa, Israel
来源
FRONTIERS IN ONCOLOGY | 2022年 / 12卷
关键词
comprehensive genomic profiling; next-generation sequencing; ALK; failure of ALK TKI; acquired resistance; decision impact; ANAPLASTIC LYMPHOMA; CRIZOTINIB; RESISTANCE; ADENOCARCINOMA; TRANSFORMATION; CHEMOTHERAPY; CERITINIB; ALECTINIB;
D O I
10.3389/fonc.2022.874712
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundThe use of CGP in guiding treatment decisions in aNSCLC with acquired resistance to ALK TKIs is questionable. MethodsWe prospectively assessed the impact of CGP on the decision-making process in ALK-rearranged aNSCLC patients following progression on 2(nd)/3(rd)-generation ALK TKIs. Physician's choice of the most recommended next-line systemic treatment (NLST) was captured before and after receival of CGP results; the percentage of cases in which the NLST recommendation has changed was assessed along with the CGP turnaround time (TAT). Patients were divided into groups: patients in whom the NLST was initiated after (group 1) and before (group 2) receival of the CGP results. Time-to-treatment discontinuation (TTD) and overall survival (OS) with NLST were compared between the groups. ResultsIn 20 eligible patients (median [m]age 63 years [range, 40-89], females 75%, adenocarcinoma 100%, failure of alectinib 90%, FoundationOne Liquid CDx 80%), CGP has altered NLST recommendation in 30% of cases. CGP findings were as follows: ALK mutations 30% (l1171X 10%, G1202R, L1196M, G1269A, G1202R+l1171N+E1210K 5% each), CDKN2A/B mutation/loss 10%, c-met amplification 5%. CGP mTAT was 2.9 weeks [IQR, 2.4-4.4]. mTTD was 11.3 months (95% CI, 2.1-not reached [NR]) and 5.4 months (95% CI, 2.0-NR) in groups 1 and 2, respectively (p-0.34). mOS was 13.2 months (95% CI, 2.9-NR) and 13.0 months (95% CI, 6.0-NR) in groups 1 and 2, respectively (p-0.86). ConclusionCGP has a significant impact on the decision-making process in ALK-rearranged aNSCLC following progression on 2(nd)/3(rd)-generation ALK TKIs.
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页数:9
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