Department of Surgery, Oncology, and Gastroenterology, University of Padova, Padova, Italy.
Medical Oncology 2, Istituto Oncologico Veneto - IRCCS, Padova, Italy.
Oncologist. 2018 Mar;23(3):297-305. doi: 10.1634/theoncologist.2017-0322. Epub 2017 Nov 13.
The Breast DX Italy prospective study evaluated the impact of the 21-gene recurrence score (RS) result on adjuvant treatment decisions for patients with early breast cancer.
Nine centers (two Hub and seven Spoke centers of the Veneto Oncology Network) participated. Consecutive patients with estrogen receptor positive, human epidermal growth receptor negative, T1-T3, N0-N1 early breast cancer were prospectively registered; only those meeting protocol-defined clinicopathological "intermediate risk" criteria were eligible for the RS test. Pre-RS and post-RS physicians' treatment recommendations and treatment actually received were collected.
A total of = 124 N0 and = 126 N1 patients underwent the RS assay. The majority had Grade 2 tumors (71%); median age was 55 years, median tumor size was 16 mm, and median Ki67 expression was 20%. Patients enrolled at Hub centers presented higher-risk features. The distribution of RS results was <18 (60.8%), 18-30 (32.4%), and >30 (6.8%). The indication before RS was hormonal therapy (HT) alone in 52% of cases. An indication before RS of chemotherapy (CT)+HT was more frequent for patients with N1 versus N0 tumors (57% vs. 39%, = .0035) and for patients enrolled at Hub versus Spoke centers (54% vs. 36%, = .007).The overall rate of change in treatment decision was 16% ( = 40), mostly from CT+HT to HT ( = 30). According to nodal status, rate of change in treatment decision was 12% for the N0 cohort and 20% for the N1 cohort. The proportion of patients recommended to CT+HT was significantly reduced from before to after RS (48% to 40%, < .0016), especially in the N1 cohort (57% to 45%, = .0027) and at Hub centers (54% to 44%, = .001).
Despite frequent indication of HT before RS, the use of the RS assay further contributed to sparing CT, especially for patients with N1 tumors and at Hub centers.
This study shows that, although a high proportion of patients were recommended to receive endocrine treatment alone before knowing the recurrence score (RS) assay, the RS test further contributed in sparing chemotherapy for some of these patients, especially in case of the N1 stage or for patients enrolled at referral centers. These data highlight the need for further work in collaboration with health authorities and companies in order to define strategies for the implementation of the use of RS testing in clinical practice in the Italian setting.
意大利乳腺 DX 前瞻性研究评估了 21 基因复发评分(RS)结果对早期乳腺癌患者辅助治疗决策的影响。
9 家中心(威尼托肿瘤网络的两个中心和 7 个辐条中心)参与了该项前瞻性研究。连续登记了雌激素受体阳性、人表皮生长因子受体阴性、T1-T3、N0-N1 期早期乳腺癌患者;仅符合方案定义的临床病理“中危”标准的患者才有资格进行 RS 检测。收集了 RS 检测前和 RS 检测后医生的治疗建议和实际接受的治疗。
共纳入了 124 例 N0 期和 126 例 N1 期患者进行 RS 检测。大多数患者为 II 级肿瘤(71%);中位年龄为 55 岁,中位肿瘤大小为 16mm,中位 Ki67 表达为 20%。中心中心登记的患者具有更高的风险特征。RS 结果分布为<18(60.8%)、18-30(32.4%)和>30(6.8%)。在 RS 检测之前,52%的患者的治疗指征为单独激素治疗(HT)。与 N0 期肿瘤相比,N1 期肿瘤患者在 RS 检测之前接受化疗(CT)+HT 的治疗指征更为常见(57% vs. 39%, = .0035),且在中心中心登记的患者比在辐条中心登记的患者更为常见(54% vs. 36%, = .007)。治疗决策改变的总体比率为 16%( = 40),主要是从 CT+HT 改为 HT( = 30)。根据淋巴结状态,N0 队列和 N1 队列的治疗决策改变率分别为 12%和 20%。在 RS 检测之后,推荐 CT+HT 的患者比例显著降低(48%降至 40%, < .0016),尤其是在 N1 队列(57%降至 45%, = .0027)和中心中心(54%降至 44%, = .001)。
尽管在 RS 检测之前经常建议使用 HT,但 RS 检测进一步有助于避免 CT,特别是对于 N1 期肿瘤和中心中心的患者。
本研究表明,尽管在进行复发评分(RS)检测之前,很大一部分患者被建议单独接受内分泌治疗,但 RS 检测进一步有助于为其中一些患者节省化疗,特别是在 N1 期或在转诊中心登记的患者中。这些数据强调需要与卫生当局和公司进一步合作,以制定在意大利临床实践中实施 RS 检测使用的策略。