Navigating resistance to ALK inhibitors in the lorlatinib era: a comprehensive perspective on NSCLC

被引:3
作者
Gemelli, Maria [1 ]
Albini, Adriana [2 ]
Catalano, Gianpiero [3 ]
Incarbone, Matteo [4 ]
Cannone, Maria [5 ]
Balladore, Emanuela [5 ]
Ricotta, Riccardo [1 ]
Pelosi, Giuseppe [5 ,6 ,7 ]
机构
[1] Ist Ricovero & Cura Carattere Sci IRCCS Multimed, Med Oncol Unit, Milan, Italy
[2] Ist Ricovero & Cura Carattere Sci IRCCS, Dept Sci Directorate, European Inst Oncol IEO, Milan, Italy
[3] Ist Ricovero & Cura Carattere Sci IRCCS Multimed, Radiat Oncol Ctr, Milan, Italy
[4] Ist Ricovero & Cura Carattere Sci IRCCS Multimed, Dept Surg, Milan, Italy
[5] Ist Ricovero & Cura Carattere Sci IRCCS Multimed, Interhosp Div Pathol, Milan, Italy
[6] Univ Milan, Dept Oncol & Hemato Oncol, Milan, Italy
[7] Ist Ricovero & Cura Carattere Sci IRCCS Multimed, Interhosp Div Pathol, Via Milanese 300, I-20099 Milan, Italy
关键词
Non-small cell lung cancer (NSCLC); ALK inhibitors; target therapy; resistance mechanisms; lung cancer; CELL LUNG-CANCER; ANAPLASTIC LYMPHOMA KINASE; CIRCULATING TUMOR DNA; PREFERRED 1ST-LINE OPTION; ACQUIRED-RESISTANCE; OPEN-LABEL; CRIZOTINIB RESISTANCE; REARRANGED ADENOCARCINOMA; TREATMENT-NAIVE; POSITIVE NSCLC;
D O I
10.1080/14737140.2024.2344648
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
IntroductionThe emergence of anaplastic lymphoma kinase (ALK) rearrangements in non-small cell lung cancer (NSCLC) has revolutionized targeted therapy. This dynamic landscape, featuring novel ALK inhibitors and combination therapies, necessitates a profound understanding of resistance mechanisms for effective treatment strategies. Recognizing two primary categories - on-target and off-target resistance - underscores the need for comprehensive assessment.Areas coveredThis review delves into the intricacies of resistance to ALK inhibitors, exploring complexities in identification and management. Molecular testing, pivotal for early detection and accurate diagnosis, forms the foundation for patient stratification and resistance management. The literature search methodology involved comprehensive exploration of Pubmed and Embase. The multifaceted perspective encompasses new therapeutic horizons, ongoing clinical trials, and their clinical implications post the recent approval of lorlatinib.Expert opinionOur expert opinion encapsulates the critical importance of understanding resistance mechanisms in the context of ALK inhibitors for shaping successful treatment approaches. With a focus on molecular testing and comprehensive assessment, this review contributes valuable insights to the evolving landscape of NSCLC therapy.
引用
收藏
页码:347 / 361
页数:15
相关论文
共 111 条
[11]   Lorlatinib Should Not be Considered as the Preferred First-Line Option in Patients With Advanced ALK Rearranged NSCLC [J].
Camidge, David Ross .
JOURNAL OF THORACIC ONCOLOGY, 2021, 16 (04) :528-531
[12]   Integration of Stereotactic Body Radiation Therapy With Tyrosine Kinase Inhibitors in Stage IV Oncogene-Driven Lung Cancer [J].
Campo, Meghan ;
Al-Halabi, Hani ;
Khandekar, Melin ;
Shaw, Alice T. ;
Sequist, Lecia V. ;
Willers, Henning .
ONCOLOGIST, 2016, 21 (08) :964-973
[13]   Treatment Efficacy and Resistance Mechanisms Using the Second-Generation ALK Inhibitor AP26113 in Human NPM-ALK-Positive Anaplastic Large Cell Lymphoma [J].
Ceccon, M. ;
Mologni, L. ;
Giudici, G. ;
Piazza, R. ;
Pirola, A. ;
Fontana, D. ;
Gambacorti-Passerini, C. .
MOLECULAR CANCER RESEARCH, 2015, 13 (04) :775-783
[14]   Crizotinib-Resistant NPM-ALK Mutants Confer Differential Sensitivity to Unrelated Alk Inhibitors [J].
Ceccon, Monica ;
Mologni, Luca ;
Bisson, William ;
Scapozza, Leonardo ;
Gambacorti-Passerini, Carlo .
MOLECULAR CANCER RESEARCH, 2013, 11 (02) :122-132
[15]   EML4-ALK Mutations in Lung Cancer That Confer Resistance to ALK Inhibitors [J].
Choi, Young Lim ;
Soda, Manabu ;
Yamashita, Yoshihiro ;
Ueno, Toshihide ;
Takashima, Junpei ;
Nakajima, Takahiro ;
Yatabe, Yasushi ;
Takeuchi, Kengo ;
Hamada, Toru ;
Haruta, Hidenori ;
Ishikawa, Yuichi ;
Kimura, Hideki ;
Mitsudomi, Tetsuya ;
Tanio, Yoshiro ;
Mano, Hiroyuki .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (18) :1734-1739
[16]   Transformation to neuroendocrine carcinoma as a resistance mechanism to lorlatinib [J].
Coleman, Niamh ;
Wotherspoon, Andrew ;
Yousaf, Nadia ;
Popat, Sanjay .
LUNG CANCER, 2019, 134 :117-120
[17]   Patient-derived models of acquired resistance can identify effective drug combinations for cancer [J].
Crystal, Adam S. ;
Shaw, Alice T. ;
Sequist, Lecia V. ;
Friboulet, Luc ;
Niederst, Matthew J. ;
Lockerman, Elizabeth L. ;
Frias, Rosa L. ;
Gainor, Justin F. ;
Amzallag, Arnaud ;
Greninger, Patricia ;
Lee, Dana ;
Kalsy, Anuj ;
Gomez-Caraballo, Maria ;
Elamine, Leila ;
Howe, Emily ;
Hur, Wooyoung ;
Lifshits, Eugene ;
Robinson, Hayley E. ;
Katayama, Ryohei ;
Faber, Anthony C. ;
Awad, Mark M. ;
Ramaswamy, Sridhar ;
Mino-Kenudson, Mari ;
Iafrate, A. John ;
Benes, Cyril H. ;
Engelman, Jeffrey A. .
SCIENCE, 2014, 346 (6216) :1480-1486
[18]   Phase II Study of Lorlatinib in Patients With Anaplastic Lymphoma Kinase-Positive Lung Cancer and CNS-Specific Relapse [J].
Dagogo-Jack, Ibiayi ;
Oxnard, Geoffrey R. ;
Evangelist, Makenzi ;
Digumarthy, Subba R. ;
Lin, Jessica J. ;
Gainor, Justin F. ;
Murphy, John F. ;
Rabin, Michael S. ;
Heist, Rebecca S. ;
Muzikansky, Alona ;
Shaw, Alice T. .
JCO PRECISION ONCOLOGY, 2022, 6
[19]   MET Alterations Are a Recurring and Actionable Resistance Mechanism in ALK-Positive Lung Cancer [J].
Dagogo-Jack, Ibiayi ;
Yoda, Satoshi ;
Lennerz, Jochen K. ;
Langenbucher, Adam ;
Lin, Jessica J. ;
Rooney, Marguerite M. ;
Prutisto-Chang, Kylie ;
Oh, Audris ;
Adams, Nathaniel A. ;
Yeap, Beow Y. ;
Chin, Emily ;
Do, Andrew ;
Marble, Hetal D. ;
Stevens, Sara E. ;
Digumarthy, Subba R. ;
Saxena, Ashish ;
Nagy, Rebecca J. ;
Benes, Cyril H. ;
Azzoli, Christopher G. ;
Lawrence, Michael S. ;
Gainor, Justin F. ;
Shaw, Alice T. ;
Hata, Aaron N. .
CLINICAL CANCER RESEARCH, 2020, 26 (11) :2535-2545
[20]   Strategies to overcome resistance to ALK inhibitors in non-small cell lung cancer: a narrative review [J].
Desai, Aakash ;
Lovly, Christine M. .
TRANSLATIONAL LUNG CANCER RESEARCH, 2023, 12 (03) :615-628