Evidence map›Paper›PMID 41706716›Full record

ArticlePloS one2026

Rapidly progressive arthropathy identified on imaging of patients treated with Crizotinib for ALK-rearranged/ROS1-positive non small cell lung cancer: A retrospective single-center study.

Yael Eshet, Liran Domachevsky, Noam Tau, Gregory Peters Founshtein, Michal Eifer, Jair Bar, Iris Eshed

Abstract read
In one paragraph

Article in PloS one, 2026. 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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1 · What the graph read from it

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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

7 authors.

Yael EshetDepartment of Nuclear Imaging, Sheba Medical Center, Ramat Gan, Israel.ORCID https://orcid.org/0000-0002-8339-5823
Liran DomachevskyDepartment of Nuclear Imaging, Sheba Medical Center, Ramat Gan, Israel.
Noam TauDepartment of Diagnostic Imaging, Sheba Medical Center, Ramat Gan, Israel.
Gregory Peters FounshteinDepartment of Nuclear Imaging, Sheba Medical Center, Ramat Gan, Israel.
Michal EiferDepartment of Nuclear Imaging, Sheba Medical Center, Ramat Gan, Israel.
Jair BarInstitute of Oncology, Sheba Medical Center, Ramat Gan, Israel.
Iris EshedDepartment of Diagnostic Imaging, Sheba Medical Center, Ramat Gan, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesProgressive arthropathy was anecdotally described in patients exposed to crizotinib, a receptor tyrosine kinases inhibitor (TKI) used to treat anaplastic lymphoma kinase (ALK) or ROS Proto-Oncogene 1 (ROS1) positive non-small cell lung cancer (NSCLC). We aimed to evaluate the incidence of this adverse effect.

methodsWe retrospectively evaluated imaging studies of all patients in our institution receiving TKI for ALK-rearranged or ROS1-positive NSCLC (crizotinib, alectinib, lorlatinib, brigatinib).

resultsBetween February 2012 and August 2023, out of a total number of 71 subjects (51% male, 36-88 years old) who received TKI's for ALK-rearranged/ ROS1 positive NSCLC, 34/71 (47%) were exposed at least once to crizotinib treatment, while the other 37/71 (53%) patients received other TKI's. Significantly higher incidence (p = 0.02) of irreversible, progressive arthropathy in one or more joints was detected in 18% (6/34, 95% CI: 0.1-0.26) of crizotinib-treated patients, up to 6 years after treatment initiation. Imaging findings included synovial proliferation and progressive arthropathy in hip and shoulder joints, and vertebral endplate destruction.

conclusionWe found progressive arthropathy, mostly painless, in one or more joints or intervertebral spaces of patients receiving crizotinib for NSCLC.

Indexed as

Anaplastic Lymphoma KinaseCarcinoma, Non-Small-Cell LungCrizotinibLung NeoplasmsProtein Kinase InhibitorsProtein-Tyrosine KinasesProto-Oncogene ProteinsAdultAgedAged, 80 and overAminopyridinesFemaleGene RearrangementHumansLactamsMaleALK protein, humanAminopyridinesAnaplastic Lymphoma KinaseCrizotinibLactamslorlatinibMAS1 protein, humanPiperidinesProtein Kinase InhibitorsProtein-Tyrosine KinasesProto-Oncogene MasProto-Oncogene ProteinsPyrazolesROS1 protein, human

Identifiers

PMID41706716
PMCPMC12915974

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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 OpenQuestion graph.