Clinical impact of sequential treatment with ALK-TKIs in patients with advanced ALK-positive non-small cell lung cancer: Results of a multicenter analysis

被引:38
|
作者
Chiari, Rita [1 ]
Metro, Giulio [1 ]
Iacono, Daniela [2 ]
Bellezza, Guido [3 ]
Rebonato, Alberto [4 ]
Dubini, Alessandra [5 ]
Sperduti, Isabella [6 ]
Bennati, Chiara [1 ]
Paglialunga, Luca [1 ]
Burgio, Marco Angelo [7 ]
Baglivo, Sara [1 ]
Giusti, Raffaele [2 ]
Minotti, Vincenzo [1 ]
Delmonte, Angelo [7 ]
Crino, Lucio [1 ]
机构
[1] Azienda Osped Perugia, Santa Maria della Misericordia Hosp, Med Oncol, Perugia, Italy
[2] Univ Roma La Sapienza, St Andrea Hosp, Med Oncol, I-00185 Rome, Italy
[3] Univ Perugia, Sch Med, Sect Anat Pathol & Histol, Dept Expt Med, I-06100 Perugia, Italy
[4] Univ Perugia, Sch Med, Dept Diagnost Imaging, I-06100 Perugia, Italy
[5] Morgagni Pierantoni Hosp, Pathol Unit, Forli, Italy
[6] Regina Elena Inst Canc Res, Biostat, Rome, Italy
[7] IRCCS, Ist Sci Cura & Studio Tumori IRST, Med Oncol, Meldola, FC, Italy
关键词
Alectinib; ALK; ALK-TKI; Ceritinib; Crizotinib; Non-small cell lung cancer; ANAPLASTIC LYMPHOMA KINASE; EML4-ALK FUSION GENE; ADULT PATIENTS PTS; SINGLE-ARM; OPEN-LABEL; NSCLC PATIENTS; PHASE-II; CRIZOTINIB; CHEMOTHERAPY; CERITINIB;
D O I
10.1016/j.lungcan.2015.09.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: Anaplastic lymphoma kinase (ALIC)-positive non-small cell lung cancer (NSCLC) is sensitive to treatment with an ALK-tyrosine kinase inhibitor (-TKI). However, the benefit of sequential treatment with a 2nd ALK-TKI in patients who fail a 1st ALK-TKI has been poorly addressed. Materials and methods: We collected the data of 69 advanced ALK-positive NSCLCs who were treated with one or more ALK-TKIs at three Italian institutions. The clinical outcome of treatment with an ALK-TKI and the patterns of treatment upon failing a 1st ALK-TKI were recorded. Results: Objective response rate (ORR) and median progression-free survival (PFS) on a 1st ALK-TKI (mostly crizotinib) were 60.9% and 12 months, respectively. Of the 50 patients who progressed on a 1st ALK-TKI, 22 were further treated with a 2nd ALK-TKI (either ceritinib or alectinib), for whom an ORR of 86.4% and median PFS of 7 months, respectively, were reported. Conversely, 13 patients underwent rapid clinical/radiographic disease progression leading to death shortly after discontinuation of the 1st ALK-TKI, 7 patients were managed with a 1st ALK-TKI beyond progression, and 8 patients transitioned to other systemic treatments (mostly chemotherapy). Post-progression survival (PPS) significantly favored the 22 patients who were sequentially treated with a 2nd ALK-TKI over those who transitioned to other systemic treatments (P = 0.03), but not versus those who were treated with a 1st ALK-TKI beyond progression (P = 0.89). Conclusion: Sequential treatment with a 2nd ALK-TKI is effective in patients who fail a 1st ALK-TKI. Continuous ALK-inhibition upon failing a 1st ALK-TKI may be associated with improved clinical outcome. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:255 / 260
页数:6
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