Precision and Future Medicine (Mar 2019)

Results from the safety interim analysis of the adjuvant chemoradiotherapy in stomach tumors 2 trial: a multicenter, randomized phase III clinical trial

  • Se Hoon Park,
  • Jeeyun Lee,
  • Tae Sung Sohn,
  • Do Hoon Lim,
  • Kyoung-Mee Kim,
  • Ji Yeong An,
  • Min Gew Choi,
  • Jun Ho Lee,
  • Jae Moon Bae,
  • Sung Kim,
  • Su Jin Lee,
  • Seung Tae Kim,
  • Joon Oh Park,
  • Young Suk Park,
  • Ho Yeong Lim,
  • Won Ki Kang

DOI
https://doi.org/10.23838/pfm.2018.00177
Journal volume & issue
Vol. 3, no. 1
pp. 24 – 29

Abstract

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Purpose The Adjuvant chemoRadioTherapy In Stomach Tumors 2 (ARTIST 2) trial was conducted to compare the efficacy between adjuvant chemotherapy regimens and chemoradiotherapy in D2-resected, node-positive, stage 2 or 3 gastric cancer. Methods In this prospective, multicenter, phase IIItrial, we randomly assigned patients to three treatment arms: patients who receive adjuvant S-1 for 1 year, S-1 plus oxaliplatin (SOX) for 6 months, or SOX plus chemoradiotherapy (SOXRT). Herein, we report the safety outcomes of patients who received adjuvant chemotherapy or chemoradiotherapy. Results Among a total of 514 patients registered between February 2013 and December 2017, 499 patients who either completed or discontinued the assigned study treatments were included in the present analysis. Allthe three treatment arms were generally well-tolerated, with the overall treatment completion rate of 94% (96% in S-1, 93% in SOX, and 92% in SOXRT). The median delivered dose of radiotherapy in the SOXRT arm was 4,500 cGy (range, 0 to 4,500 cGy). The most frequently observed adverse events were fatigue (29%) in S-1 arm and peripheral neuropathy in the SOX and SOXRT arms (59% and 50%,respectively). Conclusion Our preliminary data confirm that there are no significant safety concerns in ARTIST 2 trial (ClinicalTrials.gov, NCT0176146). According to the Independent Data Monitoring Committee, patient accrual is underway.

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