Open Access

Additional effect of anthracycline in preoperative chemotherapy with a sequential anthracycline‑containing regimen preceded by pertuzumab, trastuzumab and docetaxel combination therapy

  • Authors:
    • Hiroaki Shima
    • Goro Kutomi
    • Yoko Kuga
    • Asaka Wada
    • Fukino Satomi
    • Kiminori Sato
    • Daisuke Kyuno
    • Noriko Nishikawa
    • Satoko Uno
    • Hidekazu Kameshima
    • Tosei Ohmura
    • Tadashi Hasegawa
    • Ichiro Takemasa
  • View Affiliations

  • Published online on: December 13, 2022     https://doi.org/10.3892/etm.2022.11767
  • Article Number: 68
  • Copyright: © Shima et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

The proper use of anthracycline‑containing regimens in combination with anti‑HER2‑targeted therapy in a neoadjuvant setting for patients with HER2‑positive breast cancer has not been resolved. Regimens preceded by anthracyclines have become the standard of care, and although the order has no significant impact on HER2‑negative breast cancer, it is inconclusive as to whether a taxane‑first sequence would have a similar effect on HER2‑positive breast cancer. The present study aimed to investigate the benefit of a taxane‑first sequence and of adriamycin and cyclophosphamide (AC) in patients with non‑clinical complete response (non‑cCR) to pertuzumab, trastuzumab and docetaxel (PTD). The present single‑center prospective observational study was performed to investigate PTD followed by AC, and aimed to clarify the cCR rate after PTD alone and the pathological clinical response (pCR) rate after subsequent AC in patients without cCR after PTD alone. A total 24 patients were analyzed; of these, 14 achieved pCR (pCR rate, 58.3%). While four of 14 patients (28.6%) in the intention‑to‑treat population achieved pCR, nine of 14 patients (64.3%) achieved pCR with AC but not cCR after PTD. The median tumor reduction rate after four cycles of PTD was 58.9% (range, 20.8‑100%) in all 24 patients, whereas the reduction rate after PTD‑AC was 76.9% (range, 31.1‑100%). Cardiac serious adverse events occurred in three patients (12.5%). In conclusion, a high pCR rate was observed for the taxane‑first sequence. Patients were highly responsive to PTD, but some cases achieved additional antitumor effects after AC, which resulted in pCR without cCR after PTD alone. Since cardiotoxicity remains a significant problem, a higher risk‑benefit treatment strategy is required to aim for AC omission. Trial registration number: UMIN000046338, name of registry: UMIN‑CTR, date of registration: December 10, 2021.
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January-2023
Volume 25 Issue 1

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Spandidos Publications style
Shima H, Kutomi G, Kuga Y, Wada A, Satomi F, Sato K, Kyuno D, Nishikawa N, Uno S, Kameshima H, Kameshima H, et al: Additional effect of anthracycline in preoperative chemotherapy with a sequential anthracycline‑containing regimen preceded by pertuzumab, trastuzumab and docetaxel combination therapy. Exp Ther Med 25: 68, 2023
APA
Shima, H., Kutomi, G., Kuga, Y., Wada, A., Satomi, F., Sato, K. ... Takemasa, I. (2023). Additional effect of anthracycline in preoperative chemotherapy with a sequential anthracycline‑containing regimen preceded by pertuzumab, trastuzumab and docetaxel combination therapy. Experimental and Therapeutic Medicine, 25, 68. https://doi.org/10.3892/etm.2022.11767
MLA
Shima, H., Kutomi, G., Kuga, Y., Wada, A., Satomi, F., Sato, K., Kyuno, D., Nishikawa, N., Uno, S., Kameshima, H., Ohmura, T., Hasegawa, T., Takemasa, I."Additional effect of anthracycline in preoperative chemotherapy with a sequential anthracycline‑containing regimen preceded by pertuzumab, trastuzumab and docetaxel combination therapy". Experimental and Therapeutic Medicine 25.1 (2023): 68.
Chicago
Shima, H., Kutomi, G., Kuga, Y., Wada, A., Satomi, F., Sato, K., Kyuno, D., Nishikawa, N., Uno, S., Kameshima, H., Ohmura, T., Hasegawa, T., Takemasa, I."Additional effect of anthracycline in preoperative chemotherapy with a sequential anthracycline‑containing regimen preceded by pertuzumab, trastuzumab and docetaxel combination therapy". Experimental and Therapeutic Medicine 25, no. 1 (2023): 68. https://doi.org/10.3892/etm.2022.11767