Cisplatin-docetaxel induction chemotherapy for patients with nasopharyngeal carcinoma in a non-endemic cohort

J Chemother. 2024 Apr;36(2):133-142. doi: 10.1080/1120009X.2023.2215090. Epub 2023 May 21.

Abstract

This is the report on our clinic's 15 years of experience (2004-2018) on nasopharyngeal carcinoma (NPC), treated with induction chemotherapy (IC) and subsequent concomitant chemoradiotherapy (CCRT), comprising population characteristics and treatment outcomes of 203 patients with non-metastatic NPC. IC comprised docetaxel (75 mg/m2) and cisplatin (75 mg/m2) combination (TP). Concurrent cisplatin (P) was applied either weekly (40 mg/m2, 32 cases) or every-3-week (100 mg/m2, 171 cases). The median follow-up duration was 85 months (range, 5-204 months). Overall and distant failure rates were observed in 27.1% (n = 55) and 13.8% (n = 28) patients, respectively. The 5-year locoregional recurrence-free survival (LRRFS), distant metastasis-free survival (DMFS), disease-free survival (DFS), and overall survival (OS) rates were 84.1%, 86.4%, 75%, and 78.7% respectively. The overall stage was an independent prognostic factor for the LRRFS, DMFS, DFS, and OS. The WHO histological type was a prognostic factor for the LRRFS, DFS, and OS. Age was a prognostic factor for the DMFS, DFS, and OS. Concurrent P schedule was independent prognostic only the LRRFS.

Keywords: Nasopharyngeal carcinoma; cisplatin; concomitant chemoradiotherapy; docetaxel; induction chemotherapy.

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Chemoradiotherapy
  • Cisplatin*
  • Docetaxel / therapeutic use
  • Humans
  • Induction Chemotherapy
  • Kaplan-Meier Estimate
  • Nasopharyngeal Carcinoma / drug therapy
  • Nasopharyngeal Carcinoma / etiology
  • Nasopharyngeal Neoplasms* / drug therapy
  • Nasopharyngeal Neoplasms* / pathology
  • Retrospective Studies

Substances

  • Cisplatin
  • Docetaxel