Value of chemotherapy post immunotherapy in stage IV non-small cell lung cancer (NSCLC)

dc.contributor.authorAssi, Hazem I.
dc.contributor.authorZerdan, Maroun Bou
dc.contributor.authorHodroj, Mohammad Hassan
dc.contributor.authorKhoury, Makram
dc.contributor.authorNaji, Nour Sabiha
dc.contributor.authorAmhaz, Ghid
dc.contributor.authorZeidane, Reine Abou
dc.contributor.authorEl-Karak, Fadi
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:44:58Z
dc.date.available2025-01-24T11:44:58Z
dc.date.issued2023
dc.description.abstractBackground: Lung cancer is the number one cause of mortality among all types of cancer worldwide. Its treatment landscape has shifted from the classic chemotherapy alone to newer regimens based on the discovery of new immunotherapy and targeted therapy drugs. However, chemotherapy is still an option for treatment of advanced non-small cell lung cancer (NSCLC) after progression on immunotherapy alone or in combination with first-line chemotherapy. Methods: This is a retrospective study based on chart review of patients diagnosed with advanced NSCLC cases who received Docetaxel as second or third line after being treated by immunotherapy and/or chemotherapy in previous lines. The data was collected from the medical records of physicians’ clinics in three different hospital centers in Lebanon over the period of 5 years from July 2015 until December 2020. February 2021 was data analysis cut off time. The main aim was to assess the role of Docetaxel post-chemoimmunotherapy for patients with diagnosed NSCLC. Results: A total of 21 patients were included in this study. The majority of our patients were males (81%). As for histologic type, most patients had non-squamous lung cancer (67%) as compared to 33% who had squamous lung cancer. Overall, our study reported a 24% response rate to Docetaxel including stable disease and partial response and a median progression free survival (PFS) of 3 months. The mean time interval elapsed from diagnosis to the initiation of Docetaxel was 11.5 months. Conclusion: New therapeutic options should be validated for the treatment of NSCLC in the second and subsequent lines of therapy considering the poor prognosis of this disease. The chemotherapy in second and third line may keep an important role in the treatment after progression on newer agents, but it needs more evidence in prospective studies including a larger number of patients. Copyright: © 2023 Assi et al.
dc.identifier.doihttps://doi.org/10.18632/oncotarget.28444
dc.identifier.eid2-s2.0-85160380037
dc.identifier.pmid37235814
dc.identifier.urihttp://hdl.handle.net/10938/30516
dc.language.isoen
dc.publisherImpact Journals LLC
dc.relation.ispartofOncotarget
dc.sourceScopus
dc.subjectAntineoplastic combined chemotherapy protocols
dc.subjectCarcinoma, non-small-cell lung
dc.subjectDocetaxel
dc.subjectFemale
dc.subjectHumans
dc.subjectImmunotherapy
dc.subjectLung neoplasms
dc.subjectMale
dc.subjectProspective studies
dc.subjectRetrospective studies
dc.subjectTaxoids
dc.subjectAtezolizumab
dc.subjectCarboplatin
dc.subjectCisplatin
dc.subjectDurvalumab
dc.subjectGemcitabine
dc.subjectNivolumab
dc.subjectPembrolizumab
dc.subjectPemetrexed
dc.subjectVinorelbine tartrate
dc.subjectAntineoplastic agent
dc.subjectTaxoid
dc.subjectAdvanced cancer
dc.subjectArticle
dc.subjectCancer chemotherapy
dc.subjectCancer immunotherapy
dc.subjectCancer staging
dc.subjectCancer survival
dc.subjectClinical article
dc.subjectCohort analysis
dc.subjectComputer assisted tomography
dc.subjectControlled study
dc.subjectHistology
dc.subjectHuman
dc.subjectHuman tissue
dc.subjectLine of treatment
dc.subjectMulticenter study
dc.subjectNon small cell lung cancer
dc.subjectRetrospective study
dc.subjectLung tumor
dc.subjectProspective study
dc.titleValue of chemotherapy post immunotherapy in stage IV non-small cell lung cancer (NSCLC)
dc.typeArticle

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