Cancer Treatment and Research Communications (Jan 2023)

Multi-gene assay 95- and 155-gene classifiers for prognosis prediction and chemotherapy omission in lymphnode positive luminal-type breast cancer

  • Saya Matsumoto,
  • Ryo Tsunashima,
  • Sae Kitano,
  • Akira Watanabe,
  • Chikage Kato,
  • Midori Morita,
  • Koichi Sakaguchi,
  • Balázs Győrffy,
  • Yasuto Naoi

Journal volume & issue
Vol. 36
p. 100711

Abstract

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Background: The prognosis of lymphnode positive breast cancer is worse than that of lymph node negative breast cancer but some cases may not require chemotherapy. We investigated the ability of the new multi-gene assays, 95GC and 155GC, to identify patients with lymphnode positive Luminal-type breast cancer whose chemotherapy can be omitted relatively safely. Patients and Methods: We extracted 1721 cases of lymphnode positive Luminal-type breast cancer from 22 public database Caucasoid cohorts and 3 Asian cohorts, and performed recurrence prognosis analysis with 95GC and 155GC. Results: Using 95GC, the cases were stratified as the high (n = 917) and low (n = 202) groups according to the prognosis of lymphnode positive Luminal-type endocrine only breast cancer. The 5 years DRFS in the low risk group was relatively good at 90%, and no additional effect of chemotherapy was observed, suggesting omission of chemotherapy. The recurrence prognosis was also significantly dichotomized into the high and low risks by 95GC in 21GC RS 0–25 cases. Here, we found a group with poor prognosis even in post-menopause RS 0–25 and requiring chemotherapy. Additionally, a group in which the prognosis was good in pre-menopause RS 0–25, and the omission of chemotherapy could be considered. Patients in the high-risk group at 155GC had poor prognosis after chemotherapy. 155GC also showed a group that chemotherapy alone was not sufficient. Conclusion: In this study, we demonstrated the possibility of accurately selecting patient groups for which chemotherapy can be omitted from lymphnode positive Luminal-type breast cancer.

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