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https://hdl.handle.net/2445/214061
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DC Field | Value | Language |
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dc.contributor.author | Nadal, Ernest | - |
dc.contributor.author | Rifi, Nada | - |
dc.contributor.author | Kane, Sarah | - |
dc.contributor.author | Mbacke, Sokhna | - |
dc.contributor.author | Starkman, Lindsey | - |
dc.contributor.author | Suero, Beatrice | - |
dc.contributor.author | Le, Hannah | - |
dc.contributor.author | Samjoo, Imtiaz A. | - |
dc.date.accessioned | 2024-07-01T14:13:28Z | - |
dc.date.available | 2024-07-01T14:13:28Z | - |
dc.date.issued | 2024-06-01 | - |
dc.identifier.issn | 1872-8332 | - |
dc.identifier.uri | https://hdl.handle.net/2445/214061 | - |
dc.description.abstract | Background: Crizotinib was approved to treat patients with advanced non -small cell lung cancer (aNSCLC) with ROS proto-oncogene 1 (ROS1) gene fusion in 2016. We conducted a systematic literature review to identify realworld evidence (RWE) studies and estimated the efficacy and safety of crizotinib using meta-analyses (MA) for objective response rate (ORR), real -world progression -free survival (PFS), and overall survival (OS). Methods: We searched MEDLINE (R), Embase, and Cochrane CENTRAL from January 2016 to March 2023 using Ovid (R) for published single -arm or comparative RWE studies evaluating patients (N >= 20) receiving crizotinib monotherapy for aNSCLC with ROS1 gene fusion. Pooled estimates for ORR and grade 3/4 adverse events (AEs) were derived using the metafor package in R while pooled estimates for median real -world PFS (rwPFS) and OS were derived using reconstructed individual patient data from published Kaplan -Meier curves. The primary analysis included all studies regardless of crizotinib line of therapy; a subgroup analysis (SA) was conducted using studies evaluating patients receiving first -line crizotinib. Results: Fourteen studies met the eligibility criteria and were considered feasible for MA. For the primary analysis, the pooled ORR (N = 9 studies) was 70.6 % (95 % confidence interval [CI]: 57.0, 81.3), median rwPFS was 14.5 months (N = 11 studies), and OS was 40.2 months (N = 9 studies). In the SA, the pooled ORR (N = 4 studies) was 81.1 % (95 % CI: 76.1, 85.2) and the median rwPFS (N = 4 studies) and OS (N = 2 studies) were 18.1 and 60 months, respectively. All MAs were associated with significant heterogeneity (I2 > 25 %). Grade 3/4 AEs occurred in 18.7 % of patients (pooled estimate). Conclusion: The results from this study are consistent with clinical trial data and, taken collectively, supports crizotinib as a safe and effective treatment across different lines of therapy in patients with ROS1 aNSCLC in the real -world setting. | - |
dc.format.extent | 11 p. | - |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | Elsevier BV | - |
dc.relation.isformatof | Reproducció del document publicat a: https://doi.org/10.1016/j.lungcan.2024.107816 | - |
dc.relation.ispartof | Lung Cancer, 2024, vol. 192 | - |
dc.relation.uri | https://doi.org/10.1016/j.lungcan.2024.107816 | - |
dc.rights | cc by (c) Nadal, Ernest et al, 2024 | - |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.source | Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) | - |
dc.subject.classification | Càncer de pulmó | - |
dc.subject.classification | Genètica mèdica | - |
dc.subject.other | Lung cancer | - |
dc.subject.other | Medical genetics | - |
dc.title | Efficacy and safety of crizotinib in the treatment of advanced non-small cell Lung cancer with ROS1 gene fusion: A systematic literature review and Meta-Analysis of real-world evidence | - |
dc.type | info:eu-repo/semantics/article | - |
dc.type | info:eu-repo/semantics/publishedVersion | - |
dc.date.updated | 2024-07-01T13:30:03Z | - |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | - |
dc.identifier.pmid | 38749072 | - |
Appears in Collections: | Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) |
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PIIS0169500224003507.pdf | 1.73 MB | Adobe PDF | View/Open |
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