Subgroup analysis of Japanese patients in a phase III randomized, controlled study of neoadjuvant atezolizumab or placebo, combined with nab-paclitaxel and anthracycline-based chemotherapy in early triple-negative breast cancer (IMpassion031)

Author:

Saji Shigehira1,Ohsumi Shozo2ORCID,Ito Mitsuya3,Hayashi Naoki4,Kobayashi Kokoro5,Masuda Norikazu67,Niikura Naoki8,Yamashita Toshinari9ORCID,Kiyama Keiichiro10,Hasegawa Ayumi10,Nakagawa Shizuka10,Hattori Masaya11

Affiliation:

1. Department of Medical Oncology, Fukushima Medical University , Fukushima , Japan

2. Department of Breast Oncology, National Hospital Organization Shikoku Cancer Center , Ehime , Japan

3. Department of Breast Surgery, Hiroshima City Hiroshima Citizens Hospital , Hiroshima , Japan

4. Department of Breast Surgical Oncology, St. Luke's International Hospital , Tokyo , Japan

5. Department of Medical Oncology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research , Tokyo , Japan

6. Department of Surgery , Breast Oncology, , Osaka , Japan

7. National Hospital Organization Osaka National Hospital , Breast Oncology, , Osaka , Japan

8. Department of Breast and Endocrine Surgery, Tokai University School of Medicine , Kanagawa , Japan

9. Department of Breast and Endocrine Surgery, Kanagawa Cancer Center , Kanagawa , Japan

10. Chugai Pharmaceutical Co., Ltd. , Tokyo , Japan

11. Department of Breast Oncology, Aichi Cancer Center Hospital , Aichi , Japan

Abstract

Abstract Background In the global phase III IMpassion031 study, neoadjuvant atezolizumab plus nab-paclitaxel/anthracycline-based chemotherapy improved pathological complete response in patients with early stage triple-negative breast cancer. Here, we report primary analysis results from a subgroup of Japanese patients. Methods Patients with histologically documented, previously untreated, stage cT2–cT4, cN0–cN3, cM0 triple-negative breast cancer were randomized 1:1 to receive intravenous atezolizumab 840 mg or placebo every 2 weeks in combination with chemotherapy consisting of nab-paclitaxel intravenous 125 mg/m2 once a week, followed by doxorubicin intravenous 60 mg/m2 and cyclophosphamide intravenous 600 mg/m2 every 2 weeks. Patients then underwent surgery. Pathological complete response (ypT0/is ypN0) in the intention-to-treat and PD-L1-positive (≥1% PD-L1-expressing tumor-infiltrating immune cells) populations were co-primary endpoints. Results This subanalysis (data cutoff: 3 April 2020) included 36 patients from Japan (intention-to-treat; atezolizumab arm, n = 17; placebo arm, n = 19). Pathological complete response occurred in 41% (n = 7; 95% confidence interval, 18–67) of patients in the atezolizumab arm and 37% (n = 7; 95% confidence interval, 16–62) in the placebo arm. In the PD-L1-positive population, pathological complete response occurred in 50% (n = 5; 95% confidence interval, 19–81) of patients in the atezolizumab arm and 45% (n = 5; 95% confidence interval, 17–77) in the placebo arm. Treatment-related grade 3–4 adverse events occurred in 71% and 68% of patients in the respective arms. Conclusion Atezolizumab added to neoadjuvant chemotherapy numerically improved pathological complete response versus placebo in this small exploratory analysis of Japanese patients with early stage triple-negative breast cancer, a trend directionally consistent with the global study results. No new safety signals were identified.

Funder

F. Hoffmann-La Roche Ltd

Chugai Pharmaceutical Co. Ltd

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology,General Medicine

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