Ellis Matthew J, Suman Vera J, Hoog Jeremy, Goncalves Rodrigo, Sanati Souzan, Creighton Chad J, DeSchryver Katherine, Crouch Erika, Brink Amy, Watson Mark, Luo Jingqin, Tao Yu, Barnes Michael, Dowsett Mitchell, Budd G Thomas, Winer Eric, Silverman Paula, Esserman Laura, Carey Lisa, Ma Cynthia X, Unzeitig Gary, Pluard Timothy, Whitworth Pat, Babiera Gildy, Guenther J Michael, Dayao Zoneddy, Ota David, Leitch Marilyn, Olson John A, Allred D Craig, Hunt Kelly
Matthew J. Ellis and Chad J. Creighton, Baylor College of Medicine; Gildy Babiera and Kelly Hunt, MD Anderson Cancer Center, Houston; Gary Unzeitig, Doctor's Hospital of Laredo, Laredo; Marilyn Leitch, University of Texas Southwestern Campus, Dallas, TX; Vera J. Suman, Mayo Clinic, Rochester MN; Jeremy Hoog, Rodrigo Goncalves, Souzan Sanati, Katherine DeSchryver, Erika Crouch, Amy Brink, Mark Watson, Jingqin Luo, Yu Tao, Cynthia X. Ma, and D. Craig Allred, Washington University School of Medicine, St Louis; Timothy Pluard, St Lukes Hospital, Kansas City, MO; Michael Barnes, Roche Diagnostics, Mountain View; Laura Esserman, University of California San Francisco, San Francisco, CA; Mitchell Dowsett, Royal Marsden Hospital, London, UK; G. Thomas Budd, Cleveland Clinic; Paula Silverman, Case Western Reserve University, Cleveland OH; Eric Winer, Dana-Farber Cancer Institute, Boston MA; Lisa Carey, University of North Carolina, Chapel Hill; David Ota, Duke University, Durham, NC; Pat Whitworth, Nashville Breast Center, Nashville, TN; J. Michael Guenther, St Elizabeth Medical Center, Edgewood, KY; Zoneddy Dayao, University of New Mexico, Albuquerque, NM; and John A. Olson Jr, University of Maryland School of Medicine and Greenebaum Cancer Center, Baltimore, MD.
J Clin Oncol. 2017 Apr 1;35(10):1061-1069. doi: 10.1200/JCO.2016.69.4406. Epub 2017 Jan 3.
Purpose To determine the pathologic complete response (pCR) rate in estrogen receptor (ER) -positive primary breast cancer triaged to chemotherapy when the protein encoded by the MKI67 gene (Ki67) level was > 10% after 2 to 4 weeks of neoadjuvant aromatase inhibitor (AI) therapy. A second objective was to examine risk of relapse using the Ki67-based Preoperative Endocrine Prognostic Index (PEPI). Methods The American College of Surgeons Oncology Group (ACOSOG) Z1031A trial enrolled postmenopausal women with stage II or III ER-positive (Allred score, 6 to 8) breast cancer whose treatment was randomly assigned to neoadjuvant AI therapy with anastrozole, exemestane, or letrozole. For the trial ACOSOG Z1031B, the protocol was amended to include a tumor Ki67 determination after 2 to 4 weeks of AI. If the Ki67 was > 10%, patients were switched to neoadjuvant chemotherapy. A pCR rate of > 20% was the predefined efficacy threshold. In patients who completed neoadjuvant AI, stratified Cox modeling was used to assess whether time to recurrence differed by PEPI = 0 score (T1 or T2, N0, Ki67 < 2.7%, ER Allred > 2) versus PEPI > 0 disease. Results Only two of the 35 patients in ACOSOG Z1031B who were switched to neoadjuvant chemotherapy experienced a pCR (5.7%; 95% CI, 0.7% to 19.1%). After 5.5 years of median follow-up, four (3.7%) of the 109 patients with a PEPI = 0 score relapsed versus 49 (14.4%) of 341 of patients with PEPI > 0 (recurrence hazard ratio [PEPI = 0 v PEPI > 0], 0.27; P = .014; 95% CI, 0.092 to 0.764). Conclusion Chemotherapy efficacy was lower than expected in ER-positive tumors exhibiting AI-resistant proliferation. The optimal therapy for these patients should be further investigated. For patients with PEPI = 0 disease, the relapse risk over 5 years was only 3.6% without chemotherapy, supporting the study of adjuvant endocrine monotherapy in this group. These Ki67 and PEPI triage approaches are being definitively studied in the ALTERNATE trial (Alternate Approaches for Clinical Stage II or III Estrogen Receptor Positive Breast Cancer Neoadjuvant Treatment in Postmenopausal Women: A Phase III Study; clinical trial information: NCT01953588).
确定在新辅助芳香化酶抑制剂(AI)治疗2至4周后,MKI67基因(Ki67)编码蛋白水平>10%而接受化疗的雌激素受体(ER)阳性原发性乳腺癌患者的病理完全缓解(pCR)率。第二个目的是使用基于Ki67的术前内分泌预后指数(PEPI)来检查复发风险。方法:美国外科医师学会肿瘤学组(ACOSOG)Z1031A试验纳入了II期或III期ER阳性(Allred评分6至8)的绝经后乳腺癌女性患者,其治疗被随机分配接受阿那曲唑、依西美坦或来曲唑的新辅助AI治疗。对于ACOSOG Z1031B试验,方案进行了修订,以纳入AI治疗2至4周后的肿瘤Ki67测定。如果Ki67>10%,患者则转为新辅助化疗。pCR率>20%是预先设定的疗效阈值。在完成新辅助AI治疗的患者中,采用分层Cox模型评估复发时间在PEPI = 0评分(T1或T2,N0,Ki67<2.7%,ER Allred>2)与PEPI>0疾病之间是否存在差异。结果:ACOSOG Z1031B试验中转为新辅助化疗的35例患者中只有2例实现了pCR(5.7%;95%CI,0.7%至19.1%)。经过5.5年的中位随访,PEPI = 0评分的109例患者中有4例(3.7%)复发,而PEPI>0的341例患者中有49例(14.4%)复发(复发风险比[PEPI = 0对PEPI>0],0.27;P = 0.014;95%CI,0.092至0.764)。结论:在表现出AI抵抗性增殖的ER阳性肿瘤中,化疗疗效低于预期。这些患者的最佳治疗方案应进一步研究。对于PEPI = 0疾病的患者,不进行化疗时5年复发风险仅为3.6%,支持对该组患者进行辅助内分泌单药治疗的研究。这些Ki67和PEPI分类方法正在ALTERNATE试验(绝经后女性临床II期或III期雌激素受体阳性乳腺癌新辅助治疗的替代方法:一项III期研究;临床试验信息:NCT01953588)中进行明确研究。