Racial disparities in the immunotherapeutic outcomes of patients with non-small cell lung cancer (NSCLC): An in-depth systematic review and meta-analysis

dc.contributor.authorWannaphut C.
dc.contributor.authorSaowapa S.
dc.contributor.authorPolpichai N.
dc.contributor.authorWattanachayakul P.
dc.contributor.authorLalitnithi P.
dc.contributor.authorTanariyakul M.
dc.contributor.authorSiladech P.
dc.contributor.correspondenceWannaphut C.
dc.contributor.otherMahidol University
dc.date.accessioned2025-12-07T18:09:06Z
dc.date.available2025-12-07T18:09:06Z
dc.date.issued2024-01-01
dc.description.abstractBackground: The utilization of immunotherapy has become prevalent in the therapeutic approach to non-small cell lung cancer (NSCLC), owing to its association with enhanced survival outcomes. Nevertheless, a notable gap exists in the available information regarding potential variations in the survival benefits of immunotherapy based on the racial demographics of NSCLC patients. Methods: A systematic search for articles published until January 2023 was performed on PubMed, EMBASE, and Google Scholar databases. Articles that aligned with the research objective were included, while non-English articles, case reports, conference abstracts, studies combining immunotherapy with other cancer therapies, and studies on small-cell lung cancer were excluded. Data required for review and analysis was independently abstracted into separate Excel files by two reviewers. Furthermore, Statistical analyses were performed using the Review Manager software, and the methodological quality evaluation was done using the Newcastle Ottawa Scale. Results: Seven cohort studies were used for review and analysis. A subgroup analysis of data from these studies showed that Black/African American and Asian NSCLC patients receiving immunotherapy had improved overall survival (OS) than White patients (HR: 0.84; 95% CI: 0.75 – 0.95; p = 0.006 and HR: 0.53; 95% CI: 0.30 – 0.93; p = 0.03, respectively). However, the difference in OS is statistically insignificant when Hispanic patients are compared with white patients (HR: 0.68; 95% CI: 0.46 – 1.00; p = 0.05). On the other hand, the subgroup analyses did not demonstrate any significant difference in progression-free survival (PFS) when comparing Black/African American, Asian or Hispanic patients to White patients (HR: 0.93; 95% CI: 0.79 – 1.09; p = 0.35, HR: 0.89; 95% CI: 0.51 – 1.55; p = 0.69, and HR: 1.01; 95% CI: 0.82 – 1.23; p = 0.96, respectively). Conclusions: Among non-small cell lung cancer (NSCLC) patients undergoing immunotherapeutic interventions, it is discerned that Black/African American and Asian individuals exhibit superior overall survival (OS) outcomes compared to their White counterparts. However, it is noteworthy that the observed racial disparity does not appear to exert a discernible influence on the progression-free survival (PFS) of NSCLC patients subjected to immunotherapy. Research Sponsor: None.
dc.identifier.citationJournal of Clinical Oncology Vol.42 No.16 (2024)
dc.identifier.doi10.1200/JCO.2024.42.16_suppl.1579
dc.identifier.eissn15277755
dc.identifier.issn0732183X
dc.identifier.scopus2-s2.0-105023305357
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/113425
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.subjectMedicine
dc.titleRacial disparities in the immunotherapeutic outcomes of patients with non-small cell lung cancer (NSCLC): An in-depth systematic review and meta-analysis
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105023305357&origin=inward
oaire.citation.issue16
oaire.citation.titleJournal of Clinical Oncology
oaire.citation.volume42
oairecerif.author.affiliationUniversity of Hawaiʻi at Mānoa
oairecerif.author.affiliationJohn A. Burns School of Medicine
oairecerif.author.affiliationTexas Tech University Health Sciences Center at Lubbock
oairecerif.author.affiliationRamathibodi Hospital
oairecerif.author.affiliationCaritas St. Elizabeth's Medical Center
oairecerif.author.affiliationAlbert Einstein Healthcare Network
oairecerif.author.affiliationWeiss Memorial Hospital

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