Rossi Sabrina, Cassano Alessandra, Strippoli Antonia, Schinzari Giovanni, D'Argento Ettore, Basso Michele, Barone Carlo
Department of Oncology and Hematology, Humanitas Clinical and Research Center, Rozzano (MI), Italy.
Department of Medical Oncology, Catholic University of Sacred Heart, Rome, Italy.
Drugs Context. 2017 Nov 8;6:212506. doi: 10.7573/dic.212506. eCollection 2017.
Eribulin mesylate is currently approved in the United States and Europe for the treatment of metastatic breast cancer (MBC).
The objective of this retrospective study is to find specific predictive criteria related to patient or tumor characteristics in order to select patients that might benefit the most from eribulin and define the correct treatment sequence.
Forty-four patients with MBC who received eribulin in third or subsequent lines of therapy in a single Italian center were considered eligible. Patients were stratified by body mass index, hormonal/HER2 status, and previous therapies. Primary endpoint was progression free survival (PFS), whereas secondary endpoint was disease control rate (DCR).A longer PFS was found in patients with hormone-positive tumors (=0.0051), in HER2-negative cases (=0.037), and in overweight patients (=0.0015). No difference in efficacy was observed when eribulin was administered in third or subsequent lines of therapy. Significantly longer PFS (<0.0001) and higher DCR (=0.035) were achieved by patients previously treated with paclitaxel-bevacizumab in comparison to those pretreated with other drug combinations or with anthracyclines. Prior treatment with nab-paclitaxel seems to have a detrimental effect on PFS (=0.0008).
Hormone and HER2 status seems a good predictive and prognostic indicator of response to eribulin. Efficacy seems independent from the number of prior therapies, and it is not influenced by prior endocrine treatments and anthracyclines-containing regimens. On the other hand, sensitivity to a prior treatment with paclitaxel-bevacizumab might be predictive of response to eribulin.
甲磺酸艾瑞布林目前在美国和欧洲被批准用于治疗转移性乳腺癌(MBC)。
本回顾性研究的目的是寻找与患者或肿瘤特征相关的特定预测标准,以便选择可能从艾瑞布林中获益最大的患者,并确定正确的治疗顺序。
在意大利的一个中心,44例在三线或后续治疗中接受艾瑞布林治疗的MBC患者被认为符合条件。患者根据体重指数、激素/HER2状态和既往治疗进行分层。主要终点是无进展生存期(PFS),次要终点是疾病控制率(DCR)。激素阳性肿瘤患者(P=0.0051)、HER2阴性患者(P=0.037)和超重患者(P=0.0015)的PFS更长。在三线或后续治疗中使用艾瑞布林时,未观察到疗效差异。与接受其他药物组合或蒽环类药物预处理的患者相比,先前接受紫杉醇-贝伐单抗治疗的患者的PFS显著更长(P<0.0001),DCR更高(P=0.035)。先前接受白蛋白结合型紫杉醇治疗似乎对PFS有不利影响(P=0.0008)。
激素和HER2状态似乎是对艾瑞布林反应的良好预测指标和预后指标。疗效似乎与既往治疗的次数无关,且不受既往内分泌治疗和含蒽环类药物方案的影响。另一方面,对先前紫杉醇-贝伐单抗治疗的敏感性可能预测对艾瑞布林的反应。