Prognostic and Predictive Value of Centrally Reviewed Expression of Estrogen and Progesterone Receptors in a Randomized Trial Comparing Letrozole and Tamoxifen Adjuvant Therapy for Postmenopausal Early Breast Cancer: BIG 1-98

来曲唑 三苯氧胺 医学 乳腺癌 雌激素受体 孕酮受体 内科学 肿瘤科 辅助治疗 佐剂 激素受体 雌激素 癌症 妇科
作者
Giuseppe Viale,Meredith M. Regan,Eugenio Maiorano,Mauro G. Mastropasqua,Patrizia Dell’Orto,Birgitte Rasmussen,Johnny Raffoul,Patrick Neven,Zsolt Horváth,Stephen Braye,Christian Öhlschlegel,Beat Thürlimann,Richard D. Gelber,Monica Castiglione‐Gertsch,Karen N. Price,Aron Goldhirsch,Barry A. Gusterson,Alan S. Coates
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
卷期号:25 (25): 3846-3852 被引量:417
标识
DOI:10.1200/jco.2007.11.9453
摘要

Purpose To evaluate locally versus centrally assessed estrogen (ER) and progesterone (PgR) receptor status and the impact of PgR on letrozole adjuvant therapy compared with tamoxifen in postmenopausal women with early breast cancer. Patients and Methods Breast International Group (BIG) 1-98 randomly assigned 8,010 patients to four arms comparing letrozole and tamoxifen with sequences of each agent. The Central Pathology Office received material for 6,549 patients (82%), of which 79% were assessable (6,291 patients). Prognostic and predictive value of both local and central hormone receptor expression on disease-free survival (DFS) were evaluated among 3,650 assessable patients assigned to the monotherapy arms. Prognostic value and the treatment effect were estimated for centrally assessed ER and PgR expression levels using the Subpopulation Treatment Effect Pattern Plot. Results Central review confirmed 97% of tumors as hormone receptor–positive (ER and/or PgR ≥10%). Of 105 tumors locally ER-negative, 73 were found to have more than 10% positive cells, and eight had 1% to 9%. Of 6,100 tumors locally ER positive, 66 were found to have no staining, and 54 had only 1% to 9%. Discordance was more marked for PgR than ER. Patients with tumors reclassified centrally as ER-negative, or as hormone receptor–negative, had poor DFS. Centrally assessed ER and PgR showed prognostic value. Among patients with centrally assessed ER-expressing tumors, letrozole showed better DFS than tamoxifen, irrespective of PgR expression level. Conclusion Central review changed the assessment of receptor status in a substantial proportion of patients, and should be performed whenever possible in similar trials. PgR expression did not affect the relative efficacy of letrozole over tamoxifen.
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