Evaluation of the Sensitivity to Endocrine Therapy Index and 21-Gene Breast Recurrence Score in the SWOG S8814 Trial

被引:11
作者
Speers, Corey W. [1 ,9 ]
Symmans, W. Fraser [2 ]
Barlow, William E. [3 ]
Trevarton, Alex [2 ]
The, Stephanie [1 ]
Du, Lili [2 ]
Rae, James M. [1 ]
Shak, Steven [4 ]
Baehner, Rick [4 ]
Sharma, Priyanka [5 ]
Pusztai, Lajos [6 ]
Hortobagyi, Gabriel N. [2 ]
Hayes, Daniel F. [1 ]
Albain, Kathy S. [7 ]
Godwin, Andrew [5 ]
Thompson, Alastair [8 ]
机构
[1] Univ Michigan, Ann Arbor, MI USA
[2] Univ Texas MD Anderson Canc Ctr, Houston, TX USA
[3] SWOG Stat & Data Management Ctr, Seattle, WA USA
[4] Exact Sci, Madison, WI USA
[5] Univ Kansas, Med Ctr, Kansas City, KS USA
[6] Yale Univ Canc Ctr, New Haven, CT USA
[7] Loyola Univ Chicago, Cardinal Bernardin Canc Ctr, Stritch Sch Med, Maywood, IL USA
[8] Baylor Coll Med, Houston, TX USA
[9] Univ Hosp Case Western Reserve Univ, 11100 Euclid Ave, Cleveland, OH 44106 USA
关键词
GENE-EXPRESSION; CANCER; CHEMOTHERAPY; ASSAY;
D O I
10.1200/JCO.22.01499
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE Chemotherapy has not demonstrated benefit over adjuvant endocrine therapy alone for postmenopausal patients with node-positive breast cancer with a 21-gene breast recurrence score (RS) of 25 or below (RS <= 25). We tested whether combined results from RS and the sensitivity to endocrine therapy (SET2,3) index of endocrine-related transcription (SETER/PR) adjusted for baseline prognostic index (BPI) improve prognostic assessment, and whether SET2,3 predicted benefit from anthracycline-based chemotherapy. METHODS A blinded retrospective clinical validation of SET2,3 in two randomized treatment arms from the SWOG S8814 trial comparing adjuvant anthracycline-based chemotherapy followed by tamoxifen endocrine therapy for 5 years, versus tamoxifen alone. SET2,3 assay was calibrated and measured using whole-transcriptome RNA sequence of tumor samples already tested for RS. The primary end point was disease-free survival (DFS). RESULTS There were 106 events in 283 patients over a median follow-up of 8.99 years. Proportional hazards assumptions were met during the first 5 years only. SET2,3 index and RS were not correlated (r = -0.04) and were independently prognostic (SET2,3: hazard ratio [HR], 0.48 per unit; 95% CI, 0.34 to 0.68; P < .001; RS: HR, 1.28 per 10 units; 95% CI, 1.14 to 1.44; P < .001). SET2,3 index did not predict chemotherapy benefit (interaction P = .77). SET2,3 was high in 93/175 (53%) patients with RS <= 25 (concordant low-risk), with 5-year DFS 97%. SET2,3 was low in 55/108 (51%) patients with RS > 25 (concordant high-risk), with 5-year DFS 53%. Both components of SET2,3 index were prognostic after adjustment for RS: SETER/PR (HR, 0.65; 95% CI, 0.46 to 0.92) and BPI (HR, 0.45; 95% CI, 0.31 to 0.64). CONCLUSION SET2,3 index was not correlated with RS, demonstrated additive prognostic performance, and was not chemopredictive in this subset of patients from S8814. The SETER/PR and BPI components of SET2,3 each added prognostic information to RS. (c) 2023 by American Society of Clinical Oncology
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收藏
页码:1841 / +
页数:12
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