Publication:
Comparison of three different chemotherapy regimens for concomitant chemoradiotherapy in locally advanced non-small cell lung cancer

dc.contributor.authorYUMUK, PERRAN FULDEN
dc.contributor.authorsAkdeniz, Nadiye; Kucukoner, Mehmet; Kaplan, Muhammet Ali; Urakci, Zuhat; Karhan, Ogur; Sezgin, Yasin; Bilen, Erkan; Ebinc, Senar; Teke, Fatma; Lacin, Sahin; Alan, Ozkan; Ercelep, Ozlem; Isikdogan, Abdurrahman; Yumuk, Perran Fulden
dc.date.accessioned2022-03-12T22:42:58Z
dc.date.accessioned2026-01-11T13:37:19Z
dc.date.available2022-03-12T22:42:58Z
dc.date.issued2020
dc.description.abstractPurpose The optimal chemotherapy regimen for concurrent chemoradiation in locally advanced non-small cell lung cancer (NSCLC) remains unclear. Cisplatin-etoposide regimen related toxicity is high, weekly regimens have been investigating. We aimed to compare the efficacy and safety of different concurrent chemotherapy regimens in the context. Methods A total of 225 patients with locally advanced, unresectable stage III NSCLC were included. Patients who were treated with weekly docetaxel-platin (DP), paclitaxel-platin (PP) and standard dose etoposide-platin (EP) chemotherapy regimens were selected and divided into groups for the comparison of toxicity, response rate, progression free survival (PFS), and overall survival (OS) times. Results There was a statistically significant difference between overall response rate of each treatment groups (DP: 96.1%, PP: 94% and EP: 76.7%,p < 0.001). The median PFS time of patients who were treated with DP, PP and EP was 16, 15 and 13.3 months, respectively (p = 0.435). The median OS time of patients treated with DP, PP and EP was 19.2, 29.7 and 28.3 months, respectively (p < 0.001). The rates of adverse events such as nausea, vomiting, neuropathy and anaphylaxis was similar. Grade 1-2 mucositis or esophagitis, anemia, pneumonitis were significantly higher in PP group than other groups. However, hematologic toxicities were higher in the EP group than other groups. Conclusions Compared to the weekly chemotherapy regimens with the standard dose, our study demonstrated similar PFS, but a prolonged OS with the EP regimen. The clinical response rate of weekly regimens was better than the full-dose regimen. Adverse events and toxicity rates were different and depended on the type of chemotherapy regimen used.
dc.identifier.doi10.1007/s10147-020-01767-x
dc.identifier.eissn1437-7772
dc.identifier.issn1341-9625
dc.identifier.pubmed32797321
dc.identifier.urihttps://hdl.handle.net/11424/236278
dc.identifier.wosWOS:000559682600001
dc.language.isoeng
dc.publisherSPRINGER JAPAN KK
dc.relation.ispartofINTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectConcomitant chemoradiotherapy
dc.subjectNon-small cell lung cancer
dc.subjectLocally advanced
dc.subjectDocetaxel
dc.subjectPaclitaxel
dc.subjectEtoposide
dc.subjectRANDOMIZED PHASE-II
dc.subjectCONSOLIDATION CHEMOTHERAPY
dc.subjectCONCURRENT CHEMORADIATION
dc.subjectTHORACIC RADIOTHERAPY
dc.subjectCISPLATIN
dc.subjectPACLITAXEL
dc.subjectDOCETAXEL
dc.subjectTRIAL
dc.subjectCARBOPLATIN
dc.subjectETOPOSIDE
dc.titleComparison of three different chemotherapy regimens for concomitant chemoradiotherapy in locally advanced non-small cell lung cancer
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage2024
oaire.citation.issue12
oaire.citation.startPage2015
oaire.citation.titleINTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY
oaire.citation.volume25

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