Evidence map›Paper›PMID 41473377›Full record

ArticleSouth Asian journal of cancer2025

Spectrum of Resistance Mechanisms to ALK TKIs in NSCLC: Largest Single-Center Experience from India.

Ullas Batra, Shrinidhi Nathany, Mansi Sharma, Amrith B P, Shriya Vaidya, Sakshi Mattoo, Dushyant Kumar, Anurag Mehta

Abstract read
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Article in South Asian journal of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Ullas BatraDepartment of Medical Oncology, Rajiv Gandhi Cancer Institute and Research Center, New Delhi, India.ORCID 0000-0003-3306-9824
Shrinidhi NathanyDepartment of Molecular Diagnostics, Rajiv Gandhi Cancer Institute and Research Center, New Delhi, India.
Mansi SharmaDepartment of Medical Oncology, Rajiv Gandhi Cancer Institute and Research Center, New Delhi, India.
Amrith B PDepartment of Medical Oncology, Rajiv Gandhi Cancer Institute and Research Center, New Delhi, India.ORCID 0000-0002-7066-0173
Shriya VaidyaDepartment of Medical Oncology, Rajiv Gandhi Cancer Institute and Research Center, New Delhi, India.
Sakshi MattooDepartment of Molecular Diagnostics, Rajiv Gandhi Cancer Institute and Research Center, New Delhi, India.
Dushyant KumarDepartment of Molecular Diagnostics, Rajiv Gandhi Cancer Institute and Research Center, New Delhi, India.
Anurag MehtaLaboratory Services, Rajiv Gandhi Cancer Institute and Research Center, New Delhi, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Anaplastic lymphoma kinase (ALK) rearranged non-small cell lung carcinoma (NSCLC) has emerged as a distinct entity with growing number of potent ALK tyrosine kinase inhibitors (TKIs). Despite showing durable responses and promising survival rates, resistance to these ensue. This is the largest series of repeat biopsies from patients of ALK-positive NSCLC progressing on ALK-directed therapy from this part of the world. Using a combinatorial approach of genomics and histology, we describe the spectrum of various resistance mechanisms encountered. Methods: This is a cross-sectional study recruiting ALK-positive NSCLC cases who have progressed on any line ALK TKI and have undergone repeated biopsies followed by genomic sequencing by next-generation sequencing (NGS). Results: Thirty-two ALK-positive NSCLC patients progressed on TKI were enrolled. Median age was 53 years (range: 36-75 years) with a male predilection (male:female 1.3:1). Twenty-seven (84.4%) cases harbored an additional resistance mechanism. Eighteen of these harbored an on-target ALK alteration, with L1196M gatekeeper mutation being the most common, in 11 cases, and G1202 alteration in 3 cases. In 9 cases an off-target alteration was detected, the most frequent being TP53 mutation in 8 cases, KRAS mutation in 4 cases and MET amplification in 3 cases. Four patients underwent sequential NGS testing and allele frequency changes in ALK fusion and resistance mechanisms were demonstrated. Sixteen patients have been offered lorlatinib therapy, the median progression-free survival of which has not yet been reached. Conclusion: This is the largest series depicting ALK resistance mechanisms from a single center to date. The SPACEWALK study which demonstrated ALK TKI resistance mechanisms using plasma-based genotyping was a multicentric study. The spectrum encountered in this study is distinct from the rest of the world, thus highlighting heterogeneity within ALK-rearranged tumors. Comprehensive clinical evaluation at disease progression coupled with NGS-based genotyping will pave the way for lucid understanding of disease biology, thus aiding in the institution of optimal therapy.

Indexed as

ALKliquid biopsyNGSresistance

Identifiers

PMID41473377
PMCPMC12747733

What Socratic holds

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.