Hopkins Ashley M, Rowland Andrew, McKinnon Ross A, Sorich Michael J
College of Medicine and Public Health, Flinders University, Adelaide, SA, Australia.
Front Oncol. 2019 Aug 22;9:789. doi: 10.3389/fonc.2019.00789. eCollection 2019.
HER2-positive advanced breast cancer (ABC) is associated with significant heterogeneity in long-term disease control and survival. Prognostic models for HER2-positive ABC patients considering first-line pertuzumab, trastuzumab, and docetaxel have not been evaluated. A pre-treatment prognostic model for progression-free survival (PFS) and overall survival (OS) was developed for HER2-positive ABC patients initiating first-line pertuzumab, trastuzumab, and docetaxel using clinicopathological data from the randomized clinical trial CLEOPATRA ( = 408). Cox proportional hazard analysis with a backwards deletion process was used. Metastatic sites count (<3 vs. ≥ 3) and lactate dehydrogenase (LDH) (≤ ULN vs. >ULN) were identified as common pre-treatment risk predictors for PFS and OS ( < 0.05). Based on these two factors, patients can be characterized as one of three prognostic groups (good = 0 factors; intermediate = 1 factor; poor = 2 factors). The prognostic groups were associated with significantly different PFS ( < 0.001), with 3-year PFS probabilities of 44% (36-55), 28% (22-36), and 17% (11-29) for the good, intermediate and poor prognostic groups, respectively. Similarly, there was significant differences in OS ( < 0.001), with 4-year OS probabilities of 75% (95% CI: 67-84), 60% (53-68) and 31% (21-45) for the good, intermediate and poor prognostic groups, respectively. Pre-treatment prognostic groups identified for HER2-positive ABC patients initiating first-line pertuzumab, trastuzumab, and docetaxel had significantly different long-term disease control and survival outcomes.
人表皮生长因子受体2(HER2)阳性晚期乳腺癌(ABC)在长期疾病控制和生存方面存在显著异质性。尚未对考虑一线使用帕妥珠单抗、曲妥珠单抗和多西他赛的HER2阳性ABC患者的预后模型进行评估。利用随机临床试验CLEOPATRA(n = 408)的临床病理数据,为开始一线使用帕妥珠单抗、曲妥珠单抗和多西他赛的HER2阳性ABC患者建立了无进展生存期(PFS)和总生存期(OS)的治疗前预后模型。采用向后删除法进行Cox比例风险分析。转移部位计数(<3个 vs. ≥3个)和乳酸脱氢酶(LDH)(≤正常上限 vs. >正常上限)被确定为PFS和OS常见的治疗前风险预测因素(P < 0.05)。基于这两个因素,患者可被分为三个预后组之一(良好 = 0个因素;中等 = 1个因素;不良 = 2个因素)。预后组与显著不同的PFS相关(P < 0.001),良好、中等和不良预后组的3年PFS概率分别为44%(36 - 55)、28%(22 - 36)和17%(11 - 29)。同样,OS也存在显著差异(P < 0.00I),良好、中等和不良预后组的4年OS概率分别为75%(95%CI:67 - 84)、60%(53 - 68)和31%(21 - 45)。为开始一线使用帕妥珠单抗、曲妥珠单抗和多西他赛的HER2阳性ABC患者确定的治疗前预后组在长期疾病控制和生存结果方面存在显著差异。