Neoadjuvant Chemotherapy with Concurrent Letrozole for Estrogen Receptor-Positive and HER2-Negative Breast Cancer: An Open-Label, Single-Center, Nonrandomized Phase II Study (NeoCHAI)

Author:

Chae Heejung12ORCID,Sim Sung Hoon13,Kwon Youngmi4,Lee Eun-Gyeong5ORCID,Han Jai Hong5,Jung So-Youn56,Lee Seeyoun5ORCID,Kang Han-Sung5,Kim Yeon-Joo7,Kim Tae Hyun7ORCID,Lee Keun Seok1ORCID

Affiliation:

1. Department of Internal Medicine, Center for Breast Cancer, Hospital, National Cancer Center, 323 Ilsanro, Goyang 10408, Republic of Korea

2. Cancer Data Center, National Cancer Control Institute, National Cancer Center, 323 Ilsanro, Goyang 10408, Republic of Korea

3. Division of Rare and Refractory Cancer, Research Institute, National Cancer Center, 323 Ilsanro, Goyang 10408, Republic of Korea

4. Department of Pathology, National Cancer Center, Hospital, 323 Ilsanro, Goyang 10408, Republic of Korea

5. Department of Surgery, Center for Breast Cancer, Hospital, National Cancer Center, 323 Ilsanro, Goyang 10408, Republic of Korea

6. Division of Clinical Research, Research Institute, National Cancer Center, 323 Ilsanro, Goyang 10408, Republic of Korea

7. Center for Proton Therapy, National Cancer Center, 323 Ilsanro, Goyang 10408, Republic of Korea

Abstract

The role of combining neoadjuvant endocrine therapy with conventional chemotherapy remains unclear; therefore, we conducted an open-label, single-center, nonrandomized phase II trial to assess the effect of this combination. Patients with previously untreated stage II or III HR-positive, HER2-negative breast cancer received concurrent letrozole 2.5 mg with standard neoadjuvant chemotherapy. The primary endpoint was pathologic complete response (pCR) at the time of surgery. We used Simon’s minimax two-stage design; a pCR rate > 6% was necessary at the first stage to continue. Between November 2017 and November 2020, 53 women were enrolled in the first stage of the trial. Their median age was 49 years (range, 33–63), and 60% of them were premenopausal. Subsequently, 66% and 34% of patients with clinical stages II and III, respectively, were included; 93% had clinically node-positive disease. Two patients (4%) achieved pCR after neoadjuvant chemo–endocrine treatment, which did not satisfy the criteria for continuing to the second stage. The overall response rate was 83%. During the median follow-up of 53.7 months, the 3-year disease-free survival and overall survival rates were 87% and 98%, respectively. Neutropenia was the most common grade 3/4 adverse event (40%), but rarely led to febrile neutropenic episodes (4%). Myalgia (32%), nausea (19%), constipation (17%), heartburn (11%), oral mucositis (9%), and sensory neuropathy (9%) were frequently observed, but classified as grade 1 or 2. No deaths occurred during preoperative treatment. The addition of letrozole to standard neoadjuvant chemotherapy was safe and beneficial in terms of overall response rate, but did not provide a higher pCR rate in locally advanced HR-positive, HER2-negative breast cancer. Further research is needed to enhance neoadjuvant treatment strategies for this cancer subtype.

Funder

National Cancer Center, Republic of Korea

Dong-A ST

Publisher

MDPI AG

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