Literature DB >> 26063632

Population-based analysis of the impact and generalizability of the NSABP-B24 study on endocrine therapy for patients with ductal carcinoma in situ of the breast.

A C Lo1, P T Truong2, E S Wai2, A Nichol3, L Weir3, C Speers4, M M Hayes5, C Baliski6, S Tyldesley7.   

Abstract

BACKGROUND: In 1999, the National Surgical Adjuvant Breast and Bowel Project (NSABP)-B24 trial demonstrated that tamoxifen reduced relapse risk in women with ductal carcinoma in situ (DCIS) treated with breast-conserving surgery (BCS) and radiotherapy (RT). In 2002, Allred's subgroup analysis showed that tamoxifen mainly benefitted estrogen receptor (ER)-positive disease. This study evaluates the impact and generalizability of these trial findings at the population level. PATIENTS AND METHODS: From 1989 to 2009, 2061 women with DCIS underwent BCS + RT in British Columbia. The following cohorts were analyzed: (1) pre-NSABP-B24 era (1989-1998, N = 417); (2) post-NSABP-B24 era (2000-2009, N = 1548). Cohort 2 was further divided into pre- and post-Allred eras.
RESULTS: Endocrine therapy (ET) was used in 404/2061 (20%) patients. Median age of patients treated with compared with without ET, was 53 versus 57 years, (P < 0.0005). One of 417 (0.2%) versus 399/1548 (26%) patients took ET before versus after NSABP-B24. Among the post-Allred era cohort treated with ET (N = 227), tumors were ER-positive in 65%, ER-negative in 1%, and ER-unknown in 33%; whereas of those treated without ET (N = 801), ER was positive in 43%, negative in 15%, and unknown in 42% (P < 0.0005). On multivariable analysis of the post-NSABP-B24 era, ET was associated with improved event-free survival (EFS) (hazard ratio 0.6; P = 0.02); 5-year EFS were 96.9% with ET versus 94.5% without ET.
CONCLUSIONS: ET use in DCIS patients treated with BCS + RT increased significantly after the NSABP-B24 study. ER+ disease and younger age were associated with increased ET use. ET was associated with improved EFS, confirming the generalizability of trial data at a population level.
© The Author 2015. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  breast; ductal carcinoma in situ; endocrine therapy; hormonal therapy; tamoxifen

Mesh:

Substances:

Year:  2015        PMID: 26063632     DOI: 10.1093/annonc/mdv251

Source DB:  PubMed          Journal:  Ann Oncol        ISSN: 0923-7534            Impact factor:   32.976


  5 in total

1.  Prescribing practices of endocrine therapy for ductal carcinoma in situ in British Columbia.

Authors:  A T Chaudhry; T A Koulis; C Speers; R A Olson
Journal:  Curr Oncol       Date:  2018-04-30       Impact factor: 3.677

Review 2.  The Role of MicroRNAs as Predictors of Response to Tamoxifen Treatment in Breast Cancer Patients.

Authors:  Nina G Egeland; Siri Lunde; Kristin Jonsdottir; Tone H Lende; Deirdre Cronin-Fenton; Bjørnar Gilje; Emiel A M Janssen; Håvard Søiland
Journal:  Int J Mol Sci       Date:  2015-10-14       Impact factor: 5.923

Review 3.  A retrospective alternative for active surveillance trials for ductal carcinoma in situ of the breast.

Authors:  Mieke R Van Bockstal; Marie C Agahozo; Linetta B Koppert; Carolien H M van Deurzen
Journal:  Int J Cancer       Date:  2019-05-08       Impact factor: 7.396

4.  Clinicopathological Characteristics of Breast Ductal Carcinoma In Situ: An Analysis of Chinese Population of 617 Patients.

Authors:  Guangmin Mao; Xiu-Hua Shi; Xiaofang Wang; Xiaomeng Zhang; Xingxing Chen; Jinli Ma; Xiaoli Yu; Zhen Zhang; Xiaomao Guo
Journal:  J Oncol       Date:  2021-01-05       Impact factor: 4.375

Review 5.  Paradigm Shift toward Reducing Overtreatment of Ductal Carcinoma In Situ of Breast.

Authors:  Yasuaki Sagara; Wong Julia; Mehra Golshan; Masakazu Toi
Journal:  Front Oncol       Date:  2017-08-28       Impact factor: 6.244

  5 in total

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