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Treatment of older patients with HER2-positive metastatic breast cancer with pertuzumab trastuzumab and docetaxel: subgroup analyses from a randomized double-blind placebo-controlled phase III trial (CLEOPATRA)

机译:帕妥珠单抗曲妥珠单抗和多西他赛治疗HER2阳性转移性乳腺癌的老年患者:亚组分析来自一项随机双盲安慰剂对照的III期临床试验(CLEOPATRA)

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摘要

Although the incidence of cancer increases with age, older patients are under-represented in cancer treatment trials, resulting in limited data availability in this patient population. Here we present results from pre-defined subgroup analyses conducted by age group (<65 vs ≥65 years) from a randomized, double-blind, placebo-controlled phase III trial in patients with HER2-positive metastatic breast cancer. Patients who had not received previous chemotherapy or biological therapy for HER2-positive locally recurrent, unresectable or metastatic breast cancer were randomly assigned to treatment with placebo, trastuzumab, and docetaxel or with pertuzumab, trastuzumab, and docetaxel. Primary endpoint was independently assessed progression-free survival. We performed pre-specified subgroup analyses of progression-free survival according to age. The study is registered with ClinicalTrials.gov, . 808 patients were enrolled. Of those, 127 patients were 65 years of age or older (placebo arm: 67, pertuzumab arm: 60). Patients in both age groups experienced progression-free survival benefit with treatment in the pertuzumab arm (<65 years: HR: 0.65; 95 % CI 0.53–0.80; ≥65 years: HR: 0.52; 95 % CI 0.31–0.86). Diarrhoea, fatigue, asthenia, decreased appetite, vomiting, and dysgeusia were reported more frequently in patients 65 years of age or older compared with younger patients. Neutropenia and febrile neutropenia were reported less frequently in the older age group. The efficacy and safety data reported in CLEOPATRA suggest that the combined use of pertuzumab, trastuzumab, and docetaxel should not be limited by patient age.Electronic supplementary materialThe online version of this article (doi:10.1007/s10549-013-2710-z) contains supplementary material, which is available to authorized users.
机译:尽管癌症的发病率随年龄增长而增加,但老年患者在癌症治疗试验中的代表性不足,导致该患者群体的数据可用性有限。在这里,我们介绍了针对HER2阳性转移性乳腺癌患者的按年龄分组(<65岁或≥65岁)进行的预先定义的亚组分析的结果,来自一项随机,双盲,安慰剂对照的III期临床试验。未曾接受过针对HER2阳性局部复发,不可切除或转移性乳腺癌的先前化学疗法或生物疗法的患者被随机分配接受安慰剂,曲妥珠单抗和多西他赛或培妥珠单抗,曲妥珠单抗和多西他赛的治疗。主要终点是独立评估的无进展生存期。我们根据年龄对无进展生存期进行了预先指定的亚组分析。该研究已在ClinicalTrials.gov上注册。招募了808名患者。其中127名患者年龄在65岁或以上(安慰剂组67名,帕妥珠单抗组60名)。两个年龄段的患者在帕妥珠单抗治疗中均获得无进展生存获益(<65岁:HR:0.65; 95%CI 0.53-0.80;≥65岁:HR:0.52; 95%CI 0.31-0.86)。与年轻患者相比,65岁或65岁以上患者腹泻,乏力,乏力,食欲下降,呕吐和消化不良的报道更为频繁。老年组中性粒细胞减少和高热性中性粒细胞减少的报道较少。 CLEOPATRA中报道的功效和安全性数据表明,帕妥珠单抗,曲妥珠单抗和多西他赛的组合使用不应受到患者年龄的限制。电子补充材料本文的在线版本(doi:10.1007 / s10549-013-2710-z)包含补充材料,授权用户可以使用。

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