Publication:
Optimal cumulative dose of cisplatin for concurrent chemoradiotherapy among patients with non-metastatic nasopharyngeal carcinoma: A multicenter analysis in Thailand

dc.contributor.authorNuttapong Ngamphaiboonen_US
dc.contributor.authorArunee Dechaphunkulen_US
dc.contributor.authorJiraporn Setakornnukulen_US
dc.contributor.authorTanadech Dechaphunkulen_US
dc.contributor.authorRungarun Jiratrachuen_US
dc.contributor.authorBhoom Suktitipaten_US
dc.contributor.authorChuleeporn Jiarpinitnunen_US
dc.contributor.authorPoompis Pattaranutapornen_US
dc.contributor.authorPongwut Danchaivijitren_US
dc.contributor.otherFaculty of Medicine, Ramathibodi Hospital, Mahidol Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.contributor.otherPrince of Songkla Universityen_US
dc.date.accessioned2020-08-25T09:04:41Z
dc.date.available2020-08-25T09:04:41Z
dc.date.issued2020-06-03en_US
dc.description.abstract© 2020 The Author(s). Background: Chemoradiotherapy (CRT) with high cumulative doses (CDs) of cisplatin has been considered the standard of care for non-metastatic nasopharyngeal carcinoma (NPC). However, given most patients' inability to tolerate high CDs due to cisplatin-related toxicities, the optimal CD of cisplatin during CRT remains undetermined. Methods: Patients with non-metastatic NPC who received CRT with cisplatin between 2007 and 2017 were identified through the Thai head and neck cancer multicenter database and then categorized according to cisplatin CD (mg/m2) received. All complications and cisplatin-related toxicities during CRT were recorded. Results: We identified 779 non-metastatic NPC patients receiving low (≤150; n = 97), intermediate (151-250; n = 411), and high (> 250; n = 271) CDs of cisplatin. Low CD patients had significantly lower mean actual radiation dose (p < 0.001) and more radiotherapy delay (p = 0.010), while intermediate CD patients had the least hospitalization (p < 0.001). Overall, 39.3% of the patients experienced cisplatin-related toxicity, which was associated with poor overall survival (OS) (p = 0.001). Acute kidney injury was observed in 7% in all patients, which was highest among low CD patients (15.5%; p = 0.002). Intermediate CD patients had significantly longer median OS than the low and high groups (64 vs. 49.8 vs. 53.2, respectively; p = 0.015). Univariate, but not multivariate, analysis showed that CD of cisplatin was significantly associated with OS. Conclusion: CD of cisplatin during CRT was not an independent prognostic factor for OS. An intermediate CD induced minimal toxicity without compromising survival and should be considered the optimal CD. Nonetheless, a randomized phase 3 study evaluating the optimal CD of cisplatin is warranted.en_US
dc.identifier.citationBMC Cancer. Vol.20, No.1 (2020)en_US
dc.identifier.doi10.1186/s12885-020-07024-8en_US
dc.identifier.issn14712407en_US
dc.identifier.other2-s2.0-85085968956en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/57717
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85085968956&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleOptimal cumulative dose of cisplatin for concurrent chemoradiotherapy among patients with non-metastatic nasopharyngeal carcinoma: A multicenter analysis in Thailanden_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85085968956&origin=inwarden_US

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