Brigatinib in the first-line treatment of ALK plus metastatic NSCLC: safety and efficacy

被引:3
作者
Bronte, Giuseppe [1 ]
Cafaro, Alessandro [2 ]
Pasini, Luigi [3 ]
Priano, Ilaria [1 ]
Andrikou, Kalliopi [1 ]
Cravero, Paola [1 ]
Burgio, Marco Angelo [1 ]
Delmonte, Angelo [1 ]
Crino, Lucio [1 ]
机构
[1] IRCCS Ist Romagnolo Studio Tumori IRST Dino Amado, Dept Med Oncol, Via Piero Maroncelli, I-4047014 Meldola, FC, Italy
[2] IRCCS Ist Romagnolo Studio Tumori IRST Dino Amado, Oncol Pharm Unit, Meldola, Italy
[3] IRCCS Ist Romagnolo Studio Tumori IRST Dino Amado, Biosci Lab, Meldola, Italy
关键词
Non-small cell lung cancer; oncogene-addicted; ALK inhibitor; brigatinib; ALTA-1L; CELL LUNG-CANCER; ANAPLASTIC LYMPHOMA KINASE; OPEN-LABEL; CRIZOTINIB; CHEMOTHERAPY; POTENT; MECHANISMS; RESISTANCE; INHIBITOR; DISCOVERY;
D O I
10.1080/14737140.2021.1923485
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Among the oncogene-addicted non-small cell lung cancer patients, those bearing ALK rearrangement can be currently treated with next-generation ALK inhibitors. Brigatinib was first used to treat Crizotinib-resistant patients because it can target resistance mutations in ALK fusion protein. Recently, Brigatinib was also studied as upfront treatment of newly diagnosed ALK-positive patients. Areas covered: We outline the drug profile of Brigatinib as first-line treatment and compare it with other ALK inhibitors available. The context of ALK-rearranged non-small cell lung cancer and pharmacological aspects of Brigatinib are reviewed before the analysis of the results from the study ALTA-1 L in terms of efficacy and safety. Expert opinion: The superior efficacy of Brigatinib over Crizotinib as first-line treatment is undoubted. Consequently, Brigatinib is a new option in untreated ALK+ metastatic NSCLC patients, among the other drugs available for this indication, such as Ceritinib and Alectinib. Each of these ALK inhibitors has a specific tolerability profile, so that the choice may be also guided by patient preference according to potential side effects. In the future other factors could impact treatment choice, for instance the kind of resistance ALK mutations develop under treatment could influence the sequence of ALK inhibitors.
引用
收藏
页码:809 / 817
页数:9
相关论文
共 39 条
[21]   Brigatinib in Patients With Crizotinib-Refractory Anaplastic Lymphoma Kinase-Positive Non-Small-Cell Lung Cancer: A Randomized, Multicenter Phase II Trial [J].
Kim, Dong-Wan ;
Tiseo, Marcello ;
Ahn, Myung-Ju ;
Reckamp, Karen L. ;
Hansen, Karin Holmskov ;
Kim, Sang-We ;
Huber, Rudolf M. ;
West, Howard L. ;
Groen, Harry J. M. ;
Hochmair, Maximilian J. ;
Leighl, Natasha B. ;
Gettinger, Scott N. ;
Langer, Corey J. ;
Rodriguez, Luis G. Paz-Ares ;
Smit, Egbert F. ;
Kim, Edward S. ;
Reichmann, William ;
Haluska, Frank G. ;
Kerstein, David ;
Camidge, D. Ross .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35 (22) :2490-+
[22]   Updated overall survival and final progression-free survival data for patients with treatment-naive advanced ALK-positive non-small-cell lung cancer in the ALEX study [J].
Mok, T. ;
Camidge, D. R. ;
Gadgeel, S. M. ;
Rosell, R. ;
Dziadziuszko, R. ;
Kim, D-W ;
Perol, M. ;
Ou, S-H, I ;
Ahn, J. S. ;
Shaw, A. T. ;
Bordogna, W. ;
Smoljanovic, V ;
Hilton, M. ;
Ruf, T. ;
Noe, J. ;
Peters, S. .
ANNALS OF ONCOLOGY, 2020, 31 (08) :1056-1064
[23]   Metastatic non-small-cell lung cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up [J].
Novello, S. ;
Barlesi, F. ;
Califano, R. ;
Cufer, T. ;
Ekman, S. ;
Levra, M. Giaj ;
Kerr, K. ;
Popat, S. ;
Reck, M. ;
Senan, S. ;
Simo, G. V. ;
Vansteenkiste, J. ;
Peters, S. .
ANNALS OF ONCOLOGY, 2016, 27 :v1-v27
[24]   Anaplastic lymphoma kinase: signalling in development and disease [J].
Palmer, Ruth H. ;
Vernersson, Emma ;
Grabbe, Caroline ;
Hallberg, Bengt .
BIOCHEMICAL JOURNAL, 2009, 420 :345-361
[25]   Making the first move in EGFR-driven or ALK-driven NSCLC: first-generation or next-generation TKI? [J].
Recondo, Gonzalo ;
Facchinetti, Francesco ;
Olaussen, Ken A. ;
Besse, Benjamin ;
Friboulet, Luc .
NATURE REVIEWS CLINICAL ONCOLOGY, 2018, 15 (11) :694-708
[26]  
Rivera VM, 2010, CANCER RES, V70, P3623, DOI DOI 10.1158/1538-7445.AM10-3623
[27]   Understanding and targeting resistance mechanisms in NSCLC [J].
Rotow, Julia ;
Bivona, Trever G. .
NATURE REVIEWS CANCER, 2017, 17 (11) :637-658
[28]   Oncogenic Signaling Pathways in The Cancer Genome Atlas [J].
Sanchez-Vega, Francisco ;
Mina, Marco ;
Armenia, Joshua ;
Chatila, Walid K. ;
Luna, Augustin ;
La, Konnor C. ;
Dimitriadoy, Sofia ;
Liu, David L. ;
Kantheti, Havish S. ;
Saghafinia, Sadegh ;
Chakravarty, Debyani ;
Daian, Foysal ;
Gao, Qingsong ;
Bailey, Matthew H. ;
Liang, Wen-Wei ;
Foltz, Steven M. ;
Shmulevich, Ilya ;
Ding, Li ;
Heins, Zachary ;
Ochoa, Angelica ;
Gross, Benjamin ;
Gao, Jianjiong ;
Zhang, Hongxin ;
Kundra, Ritika ;
Kandoth, Cyriac ;
Bahceci, Istemi ;
Dervishi, Leonard ;
Dogrusoz, Ugur ;
Zhou, Wanding ;
Shen, Hui ;
Laird, Peter W. ;
Way, Gregory P. ;
Greene, Casey S. ;
Liang, Han ;
Xiao, Yonghong ;
Wang, Chen ;
Iavarone, Antonio ;
Berger, Alice H. ;
Bivona, Trever G. ;
Lazar, Alexander J. ;
Hammer, Gary D. ;
Giordano, Thomas ;
Kwong, Lawrence N. ;
McArthur, Grant ;
Huang, Chenfei ;
Tward, Aaron D. ;
Frederick, Mitchell J. ;
McCormick, Frank ;
Meyerson, Matthew ;
Van Allen, Eliezer M. .
CELL, 2018, 173 (02) :321-+
[29]   Future Options of Molecular-Targeted Therapy in Small Cell Lung Cancer [J].
Schulze, Arik Bernard ;
Evers, Georg ;
Kerkhoff, Andrea ;
Mohr, Michael ;
Schliemann, Christoph ;
Berdel, Wolfgang E. ;
Schmidt, Lars Henning .
CANCERS, 2019, 11 (05)
[30]  
Selvaggi G, 2020, J THORAC ONCOL, V15, pE41