Trastuzumab-Pertuzumab Plus Eribulin or Taxane as First-Line Chemotherapy for Human Epidermal Growth Factor 2–Positive Locally Advanced/Metastatic Breast Cancer: The Randomized Noninferiority Phase III EMERALD Trial

T Toshinari Yamashita (Department of Breast Surgery and Oncology, Kanagawa Cancer Center, Yokohama, Japan) S Shigehira Saji (Department of Medical Oncology, Fukushima Medical University, Fukushima, Japan) T Toshimi Takano Y Yoichi Naito (National Cancer Center Hospital East, Kashiwa, Japan) M Michiko Tsuneizumi A Akiyo Yoshimura (Department of Breast Oncology, Aichi Cancer Center Hospital, Aichi, Japan) M Masato Takahashi J Junji Tsurutani (The Innovative Center of Translational Research and Clinical Science for Cancer Therapy, Showa Medical University Hospital, Tokyo, Japan) T Tsuguo Iwatani (Breast and Endocrine Surgery, Okayama University Hospital, Okayama, Japan) M Masahiro Kitada (Asahikawa Medical University Hospital, Asahikawa, Japan) H Hiroshi Tada N Natsuko Mori (Department of Breast Surgery, Seirei Hamamatsu General Hospital, Shizuoka, Japan) T Toru Higuchi (Department of Breast Unit, Japanese Red Cross Saitama Hospital, Saitama, Japan) T Tsutomu Iwasa (Kindai University Hospital, Osaka, Japan) K Kazuhiro Araki (Gunma Prefectural Cancer Center, Department of Clinical Oncology, Ohta, Gunma, Japan) K Kei Koizumi (Department of Surgery 1, Division of Breast Surgery, Hamamatsu University School of Medicine, Shizuoka, Japan) H Hiroki Hasegawa Y Yohei Uchida (Medical HQs, Eisai Co, Ltd, Tokyo, Japan) S Satoshi Morita N Norikazu Masuda (Graduate School of Medicine, Kyoto University, Kyoto, Japan)

Abstract

PURPOSE Trastuzumab-pertuzumab (HP) plus taxane is a current standard first-line therapy for recurrent or metastatic human epidermal growth factor 2 (HER2)+ breast cancer (BC). We investigated noninferiority of eribulin to a taxane when combined with dual HER2 blockade as first-line systemic treatment for locally advanced/metastatic HER2+ BC. METHODS In the phase III EMERALD trial (target sample size, 480; ClinicalTrials.gov identifier: NCT03264547 /UMIN000027938), patients were randomly assigned (1:1) to receive eribulin 1.4 mg/m 2 once daily on days 1 and 8 (eribulin group) or a taxane (docetaxel 75 mg/m 2 once on day 1 or paclitaxel 80 mg/m 2 once daily on days 1, 8, and 15; taxane group) intravenously in a 21-day cycle, each with HP on day 1. The primary end point was progression-free survival (PFS; intention-to-treat population). Secondary end points included objective response rate, overall survival (OS), patient-reported quality of life (QoL), and safety. Noninferiority was tested using the stratified Cox proportional hazards model to estimate hazard ratios (HRs) for PFS events, with a noninferiority HR margin of 1.33. RESULTS Between August 2017 and June 2021, 446 patients (median age, 56.0 years) were enrolled. The median PFS was 14.0 and 12.9 months in the eribulin group (n = 224) and taxane group (n = 222 [docetaxel/paclitaxel, n = 186/36]), respectively (HR, 0.95 [95% CI, 0.76 to 1.19]), which confirmed the noninferiority of the study regimen. The median OS was 65.3 months in the taxane group but has not been reached in the eribulin group. Median time to QoL deterioration was numerically longer with eribulin than with taxane. Adverse event (AE) rates were similar, despite the longer duration of eribulin use. Infusion reaction, skin-related AEs, diarrhea, and edema were more common with taxane, whereas neutropenia was more common with eribulin. CONCLUSION The results suggested that eribulin + HP is an option for first-line treatment of locally advanced/metastatic HER2+ BC.

Article Details

Volume / Issue Vol. 43, Issue 11
Published April 10, 2025
Pages 1302-1313
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

T

Toshinari Yamashita

Department of Breast Surgery and Oncology, Kanagawa Cancer Center, Yokohama, Japan

S

Shigehira Saji

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

T

Toshimi Takano

Y

Yoichi Naito

National Cancer Center Hospital East, Kashiwa, Japan

M

Michiko Tsuneizumi

A

Akiyo Yoshimura

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

M

Masato Takahashi

J

Junji Tsurutani

The Innovative Center of Translational Research and Clinical Science for Cancer Therapy, Showa Medical University Hospital, Tokyo, Japan

T

Tsuguo Iwatani

Breast and Endocrine Surgery, Okayama University Hospital, Okayama, Japan

M

Masahiro Kitada

Asahikawa Medical University Hospital, Asahikawa, Japan

H

Hiroshi Tada

N

Natsuko Mori

Department of Breast Surgery, Seirei Hamamatsu General Hospital, Shizuoka, Japan

T

Toru Higuchi

Department of Breast Unit, Japanese Red Cross Saitama Hospital, Saitama, Japan

T

Tsutomu Iwasa

Kindai University Hospital, Osaka, Japan

K

Kazuhiro Araki

Gunma Prefectural Cancer Center, Department of Clinical Oncology, Ohta, Gunma, Japan

K

Kei Koizumi

Department of Surgery 1, Division of Breast Surgery, Hamamatsu University School of Medicine, Shizuoka, Japan

H

Hiroki Hasegawa

Y

Yohei Uchida

Medical HQs, Eisai Co, Ltd, Tokyo, Japan

S

Satoshi Morita

N

Norikazu Masuda

Graduate School of Medicine, Kyoto University, Kyoto, Japan