Rier Hánah N, Levin Mark-David, van Rosmalen Joost, Bos Monique M E M, Drooger Jan C, de Jong Paul, Portielje Johanneke E A, Elsten Elisabeth M P, Ten Tije Albert-Jan, Sleijfer Stefan, Jager Agnes
Department of Internal Medicine, Albert Schweitzer Hospital, Dordrecht, The Netherlands
Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Oncologist. 2017 Aug;22(8):901-909. doi: 10.1634/theoncologist.2016-0448. Epub 2017 May 22.
Survival of patients with human epidermal growth receptor 2 (HER2)-positive metastatic breast cancer (MBC) has improved dramatically since trastuzumab has become available, although the disease eventually progresses in most patients. This study investigates the outcome (overall survival [OS] and time to next treatment [TNT]) in MBC patients pretreated with trastuzumab in the adjuvant setting (TP-group) compared with trastuzumab-naïve patients (TN-group) in order to investigate the possibility of trastuzumab resistance.
Patients treated with first-line HER2-targeted-containing chemotherapy were eligible for the study. A power analysis was performed to estimate the minimum size of the TP-group. OS and TNT were estimated using Kaplan-Meier curves and multivariable Cox proportional hazards models.
Between January 1, 2000, and June 1, 2014, 469 patients were included, of whom 82 were in the TP-group and 387 were in the TN-group. Median OS and TNT were significantly worse in the TP-group compared with the TN-group (17 vs. 30 months, adjusted hazard ratio [HR] 1.84 [1.15-2.96], = .01 and 7 vs. 13 months, adjusted HR 1.65 [1.06-2.58], = .03) after adjustment for age, year of diagnosis, disease-free interval, hormone receptor status, metastatic site, and cytotoxic regimens.
First-line trastuzumab-containing treatment regimens are less effective in patients with failure of adjuvant trastuzumab compared with trastuzumab-naïve patients and might be due to trastuzumab resistance. The impact of trastuzumab resistance on the response on dual HER2 blockade with trastuzumab and pertuzumab and how resistance mechanisms can be used in the optimization of HER2-targeted treatment lines need further investigation.
Evidence on the efficacy of palliative trastuzumab-based therapy after failure of trastuzumab in the adjuvant setting is limited because of a minority of patients treated with adjuvant trastuzumab in clinical trials. In this study, less clinical benefit of palliative trastuzumab-based therapy was observed in patients relapsing after adjuvant trastuzumab compared with no adjuvant trastuzumab treatment. Subgroup analyses and multivariable analyses revealed that this was independent of possible confounding factors, including adjuvant taxane-treatment. This might suggest a clinically meaningful impaired efficacy of trastuzumab after previous, in this case adjuvant, trastuzumab therapy. These results could have implications for treatment decision-making after short progression-free intervals on trastuzumab-containing regimens in the palliative setting.
自曲妥珠单抗问世以来,人表皮生长因子受体2(HER2)阳性转移性乳腺癌(MBC)患者的生存率有了显著提高,尽管大多数患者的疾病最终仍会进展。本研究调查了在辅助治疗中接受过曲妥珠单抗治疗的MBC患者(TP组)与未接受过曲妥珠单抗治疗的患者(TN组)的预后(总生存期[OS]和至下次治疗时间[TNT]),以研究曲妥珠单抗耐药的可能性。
接受一线含HER2靶向治疗的化疗患者符合本研究条件。进行了功效分析以估计TP组的最小样本量。使用Kaplan-Meier曲线和多变量Cox比例风险模型估计OS和TNT。
在2000年1月1日至2014年6月1日期间,共纳入469例患者,其中82例在TP组,387例在TN组。在对年龄、诊断年份、无病间期、激素受体状态、转移部位和细胞毒性治疗方案进行调整后,TP组的中位OS和TNT显著低于TN组(分别为17个月对30个月,调整后风险比[HR]为1.84[1.15 - 2.96],P = 0.01;7个月对13个月,调整后HR为1.65[1.06 - 2.58],P = 0.03)。
与未接受过曲妥珠单抗治疗的患者相比,一线含曲妥珠单抗的治疗方案对辅助治疗中曲妥珠单抗治疗失败的患者疗效较差,这可能是由于曲妥珠单抗耐药。曲妥珠单抗耐药对曲妥珠单抗和帕妥珠单抗双重HER2阻断反应的影响以及耐药机制如何用于优化HER2靶向治疗方案尚需进一步研究。
由于临床试验中接受辅助曲妥珠单抗治疗的患者较少,关于辅助治疗中曲妥珠单抗治疗失败后基于曲妥珠单抗的姑息治疗疗效的证据有限。在本研究中,与未接受辅助曲妥珠单抗治疗的患者相比,辅助曲妥珠单抗治疗后复发的患者接受基于曲妥珠单抗的姑息治疗的临床获益较少。亚组分析和多变量分析显示,这与包括辅助紫杉烷治疗在内的可能混杂因素无关。这可能表明先前(在本病例中为辅助)曲妥珠单抗治疗后曲妥珠单抗的疗效在临床上有意义地受损。这些结果可能对姑息治疗中含曲妥珠单抗方案短期无进展间期后疾病进展的治疗决策产生影响。