4.5 Article

Will the clinical development of 4th-generation double mutant active ALK TKIs (TPX-0131 and NVL-655) change the future treatment paradigm of ALK plus NSCLC?

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TRANSLATIONAL ONCOLOGY
卷 14, 期 11, 页码 -

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.tranon.2021.101191

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TPX-0131; NVL-655; Single mutant active; Double mutant active; ALK plus NSCLC; Anaplastic lymphoma kinase tyrosine kinase; inhibitors 4th-generation ALK TKI

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The current treatment paradigm for advanced ALK+ NSCLC classifies ALK TKIs into three generations, but there are now fourth generation double mutant active ALK TKIs. The success of 4G ALK TKIs will depend on specific properties and clinical trial designs tailored for their use, potentially ushering in a new treatment paradigm based on functional capabilities rather than generational classification.
Our current treatment paradigm of advanced anaplastic lymphoma kinase fusion (ALK+) non-small cell lung cancer (NSCLC) classifies the six currently approved ALK tyrosine kinase inhibitors (TKIs) into three generations. The 2nd-generation (2G) and 3rd-generation (3G) ALK TKIs are all single mutant active with varying potencies across a wide spectrum of acquired single ALK resistance mutations. There is a vigorous debate among clinicians which is the best upfront ALK TKI is for the first-line (1L) treatment of ALK+ NSCLC and the subsequent sequencing strategies whether it should be based on the presence of specific on-target ALK resistance mutations or not. Regardless, sequential use of single mutant active ALK TKIs will eventually lead to double ALK resistance mutations in cis. This has led to the creation of fourth generation (4G) double mutant active ALK TKIs such as TPX-0131 and NVL-655. We discuss the critical properties 4G ALK TKIs must possess to be clinically successful. We proposed conceptual first-line, second-line, and molecularly-based third-line registrational randomized clinical trials designed for these 4G ALK TKIs. How these 4G ALK TKIs would be used in the future will depend on which line of treatment the clinical trial design(s) is adopted provided the trial is positive. If approved, 4G ALK TKIs may usher in a new treatment paradigm for advanced ALK+ NSCLC that is based on classifying ALK TKIs based on the intrinsic functional capabilities (singe mutant active versus double mutant active) rather than the loosely-defined generational (first-, second-,third-,fourth-) classification and avoid the current clinical approaches of seemingly random sequential use of 2G and 3G ALK TKIs.

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