Department of Clinical Oncology, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
Department of Pathology, National Liver Institute, Menoufyia University, Al Minufya, Egypt.
JAMA Netw Open. 2020 Jul 1;3(7):e209486. doi: 10.1001/jamanetworkopen.2020.9486.
There is no proven test that can guide the optimal treatment, either endocrine therapy or chemotherapy, for estrogen receptor-positive breast cancer.
To investigate the associations of sperm-associated antigen 5 (SPAG5) transcript and SPAG5 protein expressions with treatment response in systemic therapy for estrogen receptor-positive breast cancer.
DESIGN, SETTINGS, AND PARTICIPANTS: This retrospective cohort study included patients with estrogen receptor-positive breast cancer who received 5 years of adjuvant endocrine therapy with or without neoadjuvant anthracycline-based combination chemotherapy (NACT) derived from 11 cohorts from December 1, 1986, to November 28, 2019. The associations of SPAG5 transcript and SPAG5 protein expression with pathological complete response to NACT were evaluated, as was the association of SPAG5 mRNA expression with response to neoadjuvant endocrine therapy. The associations of distal relapse-free survival with SPAG5 transcript or SPAG5 protein expressions were analyzed. Data were analyzed from September 9, 2015, to November 28, 2019.
The primary outcomes were breast cancer-specific survival, distal relapse-free survival, pathological complete response, and clinical response. Outcomes were examined using Kaplan-Meier, multivariable logistic, and Cox regression models.
This study included 12 720 women aged 24 to 78 years (mean [SD] age, 58.46 [12.45] years) with estrogen receptor-positive breast cancer, including 1073 women with SPAG5 transcript expression and 361 women with SPAG5 protein expression of locally advanced disease stage IIA through IIIC. Women with SPAG5 transcript and SPAG5 protein expressions achieved higher pathological complete response compared with those without SPAG5 transcript or SPAG5 protein expressions (transcript: odds ratio, 2.45 [95% CI, 1.71-3.51]; P < .001; protein: odds ratio, 7.32 [95% CI, 3.33-16.22]; P < .001). Adding adjuvant anthracycline chemotherapy to adjuvant endocrine therapy for SPAG5 mRNA expression in estrogen receptor-positive breast cancer was associated with prolonged 5-year distal relapse-free survival in patients without lymph node involvement (hazard ratio, 0.34 [95% CI, 0.14-0.87]; P = .03) and patients with lymph node involvement (hazard ratio, 0.35 [95% CI, 0.18-0.68]; P = .002) compared with receiving 5-year endocrine therapy alone. Mean (SD) SPAG5 transcript was found to be downregulated after 2 weeks of neoadjuvant endocrine therapy compared with pretreatment levels in 68 of 92 patients (74%) (0.23 [0.18] vs 0.34 [0.24]; P < .001).
These findings suggest that SPAG5 transcript and SPAG5 protein expressions could be used to guide the optimal therapies for estrogen receptor-positive breast cancer. Retrospective and prospective clinical trials are warranted.
目前尚无经过验证的检测方法可以指导雌激素受体阳性乳腺癌患者的最佳治疗方法,无论是内分泌治疗还是化疗。
研究精子相关抗原 5(SPAG5)转录本和 SPAG5 蛋白表达与雌激素受体阳性乳腺癌患者接受系统治疗的应答之间的关系。
设计、地点和参与者:这是一项回顾性队列研究,纳入了 1986 年 12 月 1 日至 2019 年 11 月 28 日期间来自 11 个队列的接受 5 年辅助内分泌治疗且接受或未接受新辅助蒽环类联合化疗(NACT)的雌激素受体阳性乳腺癌患者。评估了 SPAG5 转录本和 SPAG5 蛋白表达与 NACT 病理完全缓解的关系,以及 SPAG5mRNA 表达与新辅助内分泌治疗应答的关系。分析了远处无复发生存与 SPAG5 转录本或 SPAG5 蛋白表达之间的关系。数据分析于 2015 年 9 月 9 日至 2019 年 11 月 28 日进行。
主要结局是乳腺癌特异性生存、远处无复发生存、病理完全缓解和临床应答。使用 Kaplan-Meier、多变量逻辑和 Cox 回归模型来检查结果。
这项研究纳入了 12720 名年龄在 24 岁至 78 岁(平均[标准差]年龄为 58.46[12.45]岁)的雌激素受体阳性乳腺癌患者,其中 1073 名患者的局部晚期疾病 IIA 期至 IIIIC 期有 SPAG5 转录本表达,361 名患者有 SPAG5 蛋白表达。与无 SPAG5 转录本或 SPAG5 蛋白表达的患者相比,有 SPAG5 转录本和 SPAG5 蛋白表达的患者达到更高的病理完全缓解率(转录本:比值比,2.45[95%CI,1.71-3.51];P<0.001;蛋白:比值比,7.32[95%CI,3.33-16.22];P<0.001)。在雌激素受体阳性乳腺癌患者中,将辅助蒽环类化疗联合辅助内分泌治疗用于 SPAG5mRNA 表达,与无淋巴结受累患者(风险比,0.34[95%CI,0.14-0.87];P=0.03)和有淋巴结受累患者(风险比,0.35[95%CI,0.18-0.68];P=0.002)的 5 年远处无复发生存延长相关,与单独接受 5 年内分泌治疗相比。在 92 例患者中有 68 例(74%)在接受新辅助内分泌治疗 2 周后发现 SPAG5 转录本下调,与治疗前水平相比(0.23[0.18]vs 0.34[0.24];P<0.001)。
这些发现表明 SPAG5 转录本和 SPAG5 蛋白表达可用于指导雌激素受体阳性乳腺癌的最佳治疗方法。需要进行前瞻性临床试验。