Evofosfamide sensitizes esophageal carcinomas to radiation without increasing normal tissue toxicity

Linda Spiegelberg, Stefan J. van Hoof, Rianne Biemans, Natasja G. Lieuwes, Damienne Marcus, Raymon Niemans, Jan Theys, Ala Yaromina, Philippe Lambin, Frank Verhaegen, Ludwig J. Dubois*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

15 Citations (Web of Science)

Abstract

Background and purpose: Esophageal cancer incidence is increasing and is rarely curable. Hypoxic tumor areas cause resistance to conventional therapies, making them susceptible for treatment with hypoxia-activated prodrugs (HAPs). We investigated in vivo whether the HAP evofosfamide (TH-302) could increase the therapeutic ratio by sensitizing esophageal carcinomas to radiotherapy without increasing normal tissue toxicity.

Materials and methods: To assess therapeutic efficacy, growth of xenografted esophageal squamous cell (OE21) or adeno (OE19) carcinomas was monitored after treatment with TH-302 (50 mg/kg, QD5) and irradiation (sham or 10 Gy). Short- and long-term toxicity was assessed in a gut mucosa and lung fibrosis irradiation model, sensitive to acute and late radiation injury respectively. Mice were injected with TH-302 (50 mg/kg, QD5) and the abdominal area (sham, 8 or 10 Gy) or the upper part of the right lung (sham, 20 Gy) was irradiated. Damage to normal tissues was assessed 84 hours later by histology and blood plasma citrulline levels (gut) and for up to 1 year by non-invasive micro CT imaging (lung).

Results: The combination treatment of TH-302 with radiotherapy resulted in significant tumor growth delay in OE19 (P = 0.02) and OE21 (P = 0.03) carcinomas, compared to radiotherapy only. Irradiation resulted in a dose-dependent decrease of crypt survival (P <0.001), mucosal surface area (P <0.01) and citrulline levels (P <0.001) in both tumor and non-tumor bearing animals. On the long-term, irradiation increased CT density in the lung, indicating fibrosis, over time. TH-302 did not influence the radiation-induced short-term and long-term toxicity, confirmed by histological evaluation.

Conclusion: The combination of TH-302 and radiotherapy might be a promising approach to improve the therapeutic index for esophageal cancer patients. (C) 2019 The Author(s). Published by Elsevier B.V.

Original languageEnglish
Pages (from-to)247-255
Number of pages9
JournalRadiotherapy and Oncology
Volume141
DOIs
Publication statusPublished - Dec 2019

Keywords

  • TH-302
  • Radiotherapy
  • Esophageal cancer
  • Short-term gut toxicity
  • Long-term lung fibrosis
  • Therapeutic index
  • HYPOXIA-ACTIVATED PRODRUG
  • TOTAL-BODY IRRADIATION
  • PRO-DRUG TH-302
  • TUMOR HYPOXIA
  • PHASE-I
  • CANCER
  • RADIOTHERAPY
  • COMBINATION
  • DOXORUBICIN
  • INJURY

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