Adjunctive Statistical Standardization of Adjuvant Estrogen Receptor and Progesterone Receptor in Canadian Cancer Trials Group MA.27 Postmenopausal Breast Cancer Trial of Exemestane Versus Anastrozole.

IF 42.1 1区 医学 Q1 ONCOLOGY Journal of Clinical Oncology Pub Date : 2024-08-20 Epub Date: 2024-06-02 DOI:10.1200/JCO.24.00835
Judith-Anne W Chapman, Jane Bayani, Sandip SenGupta, John M S Bartlett, Tammy Piper, Mary Anne Quintayo, Shakeel Virk, Paul E Goss, James N Ingle, Matthew J Ellis, George W Sledge, G Thomas Budd, Manuela Rabaglio, Rafat H Ansari, Richard Tozer, David P D'Souza, Haji Chalchal, Silvana Spadafora, Vered Stearns, Edith A Perez, Karen A Gelmon, Timothy J Whelan, Catherine Elliott, Lois E Shepherd, Bingshu E Chen, Karen J Taylor
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Abstract

Purpose: ASCO/College of American Pathologists guidelines recommend reporting estrogen receptor (ER) and progesterone receptor (PgR) as positive with (1%-100%) staining. Statistically standardized quantitated positivity could indicate differential associations of positivity with breast cancer outcomes.

Methods: MA.27 (ClinicalTrials.gov identifier: NCT00066573) was a phase III adjuvant trial of exemestane versus anastrozole in postmenopausal women with early-stage breast cancer. Immunochemistry ER and PgR HSCORE and % positivity (%+) were centrally assessed by machine image quantitation and statistically standardized to mean 0 and standard deviation (SD) 1 after Box-Cox variance stabilization transformations of square for ER; for PgR, (1) natural logarithm (0.1 added to 0 HSCOREs and 0%+) and (2) square root. Our primary end point was MA.27 distant disease-free survival (DDFS) at a median 4.1-year follow-up, and secondary end point was event-free survival (EFS). Univariate survival with cut points at SDs about a mean of 0 (≤-1; (-1, 0]; (0, 1]; >1) was described with Kaplan-Meier plots and examined with Wilcoxon (Peto-Prentice) test statistic. Adjusted Cox multivariable regressions had two-sided Wald tests and nominal significance P < .05.

Results: Of 7,576 women accrued, 3,048 women's tumors had machine-quantitated image analysis results: 2,900 (95%) for ER, 2,726 (89%) for PgR, and 2,582 (85% of 3,048) with both ER and PgR. Higher statistically standardized ER and PgR HSCORE and %+ were associated with better univariate DDFS and EFS (P < .001). In multivariable assessments, ER HSCORE and %+ were not significantly associated (P = .52-.88) with DDFS in models with PgR, whereas higher PgR HSCORE and %+ were significantly associated with better DDFS (P = .001) in models with ER.

Conclusion: Adjunctive statistical standardization differentiated quantitated levels of ER and PgR. Patients with higher ER- and PgR-standardized units had superior DDFS compared with those with HSCOREs and %+ ≤-1.

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加拿大癌症试验小组 MA.27 绝经后乳腺癌试验中依西美坦与阿那曲唑的辅助雌激素受体和孕激素受体的辅助统计标准化。
目的:ASCO/美国病理学家学会指南建议报告雌激素受体(ER)和孕激素受体(PgR)染色阳性率为(1%-100%)。统计标准化的定量阳性率可表明阳性率与乳腺癌预后的不同关联:MA.27(ClinicalTrials.gov标识符:NCT00066573)是一项在绝经后早期乳腺癌妇女中进行的依西美坦与阿那曲唑的III期辅助试验。免疫化学ER和PgR的HSCORE和阳性率(%+)由机器图像定量集中评估,经过Box-Cox方差稳定变换后,ER的统计标准化为均值0和标准差(SD)1;PgR为(1)自然对数(0 HSCORE和0%+加0.1)和(2)平方根。我们的主要终点是中位随访 4.1 年的 MA.27 无远处疾病生存期(DDFS),次要终点是无事件生存期(EFS)。用 Kaplan-Meier 图描述以平均值 0 的 SDs 为切点(≤-1;(-1,0];(0,1];>1)的单变量生存率,并用 Wilcoxon (Peto-Prentice) 检验统计量进行检验。调整后的 Cox 多变量回归采用双侧 Wald 检验,标称显著性 P <.05:在累积的 7576 名妇女中,3048 名妇女的肿瘤有机器量化的图像分析结果:2900 名妇女(95%)有 ER,2726 名妇女(89%)有 PgR,2582 名妇女(3048 名妇女中的 85%)同时有 ER 和 PgR。较高的ER和PgR HSCORE和%+统计标准化值与较好的单变量DDFS和EFS相关(P < .001)。在多变量评估中,ER HSCORE和%+与PgR模型中的DDFS无显著相关性(P = .52-.88),而在ER模型中,较高的PgR HSCORE和%+与较好的DDFS有显著相关性(P = .001):结论:辅助统计标准化可区分ER和PgR的量化水平。与 HSCOREs 和 %+ ≤-1 的患者相比,ER 和 PgR 标准化单位越高的患者 DDFS 越好。
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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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