Analysis of health-related quality of life during neoadjuvant endocrine therapy with letrozole in postmenopausal breast cancer patients: N-SAS BC06 trial.

Authors

null

Shoichiro Ohtani

Hiroshima City Hospital, Hiroshima, Japan

Shoichiro Ohtani , Naruto Taira , Kiyohiro Kihara , Yoshie Hasegawa , Takehiko Sakai , Takuji Iwase , Norikazu Masuda , Tomomi Fujisawa , Yasuhiro Yanagita , Shozo Ohsumi , Kenji Higaki , Takuhiro Yamaguchi , Hiroji Iwata

Organizations

Hiroshima City Hospital, Hiroshima, Japan, Okayama University Hospital, Okayama, Japan, Department of Biostatistics, The University of Tokyo, Tokyo, Japan, Hirosaki Municipal Hospital, Aomori, Japan, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan, Breast Oncology Center, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan, Osaka National Hospital, Osaka, Japan, Gunma Prefectural Cancer Center, Gunma, Japan, Gunma Prefectural Cancer Center, Gunma, Japan, NHO Shikoku Cancer Center, Department of Breast Oncology, Matsuyama, Japan, Department of Breast Surgery, Hiroshima City Hospital, Hiroshima, Japan, Tohoku University, Sendai, Japan, Aichi Cancer Center Hospital, Nagoya, Japan

Research Funding

Other Foundation

Background: The impact of neoadjuvant endocrine therapy (NET) on health-related QOL (HRQOL) has not been clarified yet. N-SAS BC 06 is a multicenter study in postmenopausal patients with hormone-sensitive primary breast cancer, two-staged (preoperative and postoperative) enrollment, and intervention. It includes a randomized controlled study of patients responding to NET, which is designed to compare chemotherapy followed by endocrine therapy, with endocrine therapy alone, as postoperative adjuvant therapy. The primary endpoint is DFS, and the secondary endpoints include adverse events, HRQOL and health economic evaluation. This report presents the planned analysis of HRQOL during 6 months of NET. Methods: The target sample size was 850 patients of whom the first 500 enrolled patients were included in HRQOL evaluation. Subjects were assessed at enrollment, and at 1 and 4 months after starting NET, using FACT-G (General), B (Breast), ES (Endocrine Symptoms) and HADS (Hospital Anxiety and Depression Scale). Results: Mean age was 63 years, mean BMI was 23.9. Results of clinical efficacy were as follows: CR: 2%; PR: 44.3%; SD: 48%; and PD: 5.7%. The questionnaire response rates at enrollment, and at 1 and 4 months were 93%, 90% and 82%, respectively, quite a high response rate. The mean scores at enrollment, and at 1 and 4 months were as follows: FACT-G: 82.9; 83.4; 82.7, FACT-B TOI (Trail outcome index): 68.3; 69.5; 68.9; ES subscale: 61.2; 60.1; 59.7 and HADS score: 10.4; 8.9; 8.8 respectively. There were no significant changes in the FACT-G or B-TOI over time, while the social domain score, ES subscale, decreased significantly (worse social well-being and ES). In the ES analysis by item, symptoms such as hot flash showed a greater decrease. HADS scores deceased significantly (improved anxiety and depression), and emotional domain scores increased significantly (better emotional well-being) at 1 month and 4 months after NET. Conclusions: NET had no impact on the overall HRQOL scores, but the anxiety and depression observed at enrollment had improved by 1 month after therapy. To our best knowledge, this is the first report of HRQOL during NET. Clinical trial information: 000001090.

Disclaimer

This material on this page is ©2024 American Society of Clinical Oncology, all rights reserved. Licensing available upon request. For more information, please contact licensing@asco.org

Abstract Details

Meeting

2013 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Health Services Research

Track

Health Services Research

Sub Track

Outcomes and Quality of Care

Clinical Trial Registration Number

000001090

Citation

J Clin Oncol 31, 2013 (suppl; abstr 6588)

DOI

10.1200/jco.2013.31.15_suppl.6588

Abstract #

6588

Poster Bd #

17D

Abstract Disclosures