4.8 Article

Machine-learning model derived gene signature predictive of paclitaxel survival benefit in gastric cancer: results from the randomised phase III SAMIT trial

Journal

GUT
Volume 71, Issue 4, Pages 676-685

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/gutjnl-2021-324060

Keywords

gastric cancer; chemotherapy; adjuvant treatment

Funding

  1. Epidemiological & Clinical Research Information Network (ECRIN)
  2. Kanagawa Standard Anti-Cancer Therapy Support System (KSATSS)
  3. JSPS KAKENHI [842038, 26461984]
  4. Japan Agency for Medical Research and Development (AMED) [18lk0201061t0003, 20lk0201061t0005]
  5. National Medical Research Council (NMRC) Fellowship, Singapore [NMRC/Fellowship/0059/2018]
  6. Duke-NUS Medical School
  7. Genome Institute of Singapore, Agency for Science, Technology and Research
  8. Cancer Science Institute of Singapore, NUS, under the National Research Foundation Singapore
  9. Singapore Ministry of Education under its Research Centres of Excellence initiative
  10. Singapore Ministry of Health's National Medical Research Council under its Open Fund-Large Collaborative Grant (OF-LCG) [MOH-OFLCG18May-0003]
  11. National Medical Research Council [NR13NMR111OM, NMRC/STaR/0026/2015]
  12. Grants-in-Aid for Scientific Research [26461984] Funding Source: KAKEN

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In the SAMIT trial, a gene signature predicting survival benefit from paclitaxel chemotherapy in gastric cancer patients was identified using machine-learning techniques. Patients were divided into Pac-Sensitive and Pac-Resistant groups, with Pac-Sensitive patients showing significant improvement in disease-free survival. This gene signature was validated in an external cohort, providing the first predictive biomarker for paclitaxel benefit in gastric cancer patients.
Objective To date, there are no predictive biomarkers to guide selection of patients with gastric cancer (GC) who benefit from paclitaxel. Stomach cancer Adjuvant Multi-Institutional group Trial (SAMIT) was a 2x2 factorial randomised phase III study in which patients with GC were randomised to Pac-S-1 (paclitaxel +S-1), Pac-UFT (paclitaxel +UFT), S-1 alone or UFT alone after curative surgery. Design The primary objective of this study was to identify a gene signature that predicts survival benefit from paclitaxel chemotherapy in GC patients. SAMIT GC samples were profiled using a customised 476 gene NanoString panel. A random forest machine-learning model was applied on the NanoString profiles to develop a gene signature. An independent cohort of metastatic patients with GC treated with paclitaxel and ramucirumab (Pac-Ram) served as an external validation cohort. Results From the SAMIT trial 499 samples were analysed in this study. From the Pac-S-1 training cohort, the random forest model generated a 19-gene signature assigning patients to two groups: Pac-Sensitive and Pac-Resistant. In the Pac-UFT validation cohort, Pac-Sensitive patients exhibited a significant improvement in disease free survival (DFS): 3-year DFS 66% vs 40% (HR 0.44, p=0.0029). There was no survival difference between Pac-Sensitive and Pac-Resistant in the UFT or S-1 alone arms, test of interaction p<0.001. In the external Pac-Ram validation cohort, the signature predicted benefit for Pac-Sensitive (median PFS 147 days vs 112 days, HR 0.48, p=0.022). Conclusion Using machine-learning techniques on one of the largest GC trials (SAMIT), we identify a gene signature representing the first predictive biomarker for paclitaxel benefit.

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