Association between skeletal muscle loss and the response to neoadjuvant chemotherapy for breast cancer

Byung Min Lee, Yeona Cho, Jun Won Kim, Sung Gwe Ahn, Jee Hung Kim, Hei Cheul Jeung, Joon Jeong, Ik Jae Lee

Research output: Contribution to journalArticlepeer-review

Abstract

There are no means to predict patient response to neoadjuvant chemotherapy (NAC); the impact of skeletal muscle loss on the response to NAC remains undefined. We investigated the association between response to chemotherapy and skeletal muscle loss in breast cancer patients. Patients diagnosed with invasive breast cancer who were treated with NAC, surgery, and radiotherapy were analyzed. We quantified skeletal muscle loss using pre‐NAC and post‐NAC computed tomography scans. The response to treatment was determined using the Response Evaluation Criteria in Solid Tumors. We included 246 patients in this study (median follow‐up, 28.85 months). The median age was 48 years old (interquartile range 42–54) and 115 patients were less than 48 years old (46.7%). Patients showing a complete or partial response were categorized into the responder group (208 patients); the rest were categorized into the non‐responder group (38 patients). The skeletal muscle mass cut‐off value was determined using a receiver operating characteristic curve; it showed areas under the curve of 0.732 and 0.885 for the pre‐NAC and post‐NAC skeletal muscle index (p < 0.001 for both), respectively. Skeletal muscle loss and cancer stage were significantly associated with poor response to NAC in locally advanced breast cancer patients. Accurately measuring muscle loss to guide treatment and delaying muscle loss through various interventions would help enhance the response to NAC and improve clinical outcomes.

Original languageEnglish
Article number1806
JournalCancers
Volume13
Issue number8
DOIs
Publication statusPublished - 2021 Apr 2

Bibliographical note

Funding Information:
Funding: This research was supported by a project grant funded by the Ministry of Health & Wel‐ fare, Republic of Korea (grant number: HI19C1330) and a National Research Foundation of Korea Grant funded by the Korean Government (No. NRF‐2019R1A2C1085958).

Funding Information:
This research was supported by a project grant funded by the Ministry of Health & Welfare, Republic of Korea (grant number: HI19C1330) and a National Research Foundation of Korea Grant funded by the Korean Government (No. NRF?2019R1A2C1085958).

Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

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