Long-term outcomes of definitive chemoradiotherapy with docetaxel, cisplatin, and 5-fluorouracil for postoperative locoregional recurrent esophageal cancer: a prospective phase II study - Summary - MDSpire

Long-term outcomes of definitive chemoradiotherapy with docetaxel, cisplatin, and 5-fluorouracil for postoperative locoregional recurrent esophageal cancer: a prospective phase II study

  • By

  • Keiichi Jingu

  • Rei Umezawa

  • Takaya Yamamoto

  • Noriyoshi Takahashi

  • Yu Suzuki

  • Keita Kishida

  • So Omata

  • Hinako Harada

  • Masanobu Takahashi

  • Takashi Kamei

  • Haruo Matsushita

  • July 9, 2026

  • 0 min

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Objective:

To evaluate the efficacy and safety of chemoradiotherapy combined with docetaxel, cisplatin, and 5-fluorouracil (DCF-RT) for postoperative locoregional recurrence of esophageal cancer.

Approach:
  • Study Design: Single-arm, prospective phase II trial involving 29 patients with postoperative locoregional recurrent esophageal cancer.
  • Treatment Protocol: Patients received 60 Gy radiotherapy in 30 fractions with concurrent DCF chemotherapy.
Key Findings:
  • Median progression-free survival (PFS) was 48.0 months, exceeding the historical control of 12 months.
  • 3-year and 5-year PFS rates were 55.2% and 49.7%, respectively.
  • 3-year and 5-year overall survival (OS) rates were 75.2% and 58.8%, respectively.
  • High treatment compliance with 89.7% completing the regimen without dose reduction.
  • Grade 4 hematologic toxicities occurred in 3 patients; one patient developed grade 3 heart failure.
Interpretation:

DCF-based chemoradiotherapy showed durable disease control and a favorable safety profile in patients with postoperative locoregional recurrent esophageal cancer.

Limitations:
  • Single-arm study design limits generalizability.
  • Small sample size may affect the robustness of findings.
Conclusion:

DCF-based chemoradiotherapy may represent a promising curative-intent salvage strategy for postoperative locoregional recurrent esophageal cancer, warranting further validation in randomized controlled trials.

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