Fushimi Atsushi, Tabei Isao, Fuke Azusa, Okamoto Tomoyoshi, Takeyama Hiroshi
Department of Surgery, The Jikei University School of Medicine Daisan Hospital, Japan.
Department of Breast & Endocrine Surgery, The Jikei University School of Medicine, Japan.
Int J Breast Cancer. 2020 Feb 12;2020:7156574. doi: 10.1155/2020/7156574. eCollection 2020.
There are currently no established second- and later-line therapies for postmenopausal women with hormone receptor-positive advanced or metastatic breast cancer. We examined the efficacy of high-dose toremifene (HD-TOR) for this patient group and whether aromatase inhibitor (AI) resistance influences HD-TOR treatment outcome. This retrospective analysis investigated the outcomes of 19 women with postmenopausal hormone-sensitive recurrent or metastatic breast cancer who received HD-TOR, defined as 120 mg daily from 2012 to 2016. The median follow-up duration was 9.67 months. The overall response rate (ORR) and clinical benefit rate (CBR) were compared between various clinical subgroups, including patients exhibiting primary or secondary AI resistance as defined by the timing of recurrence or progression. Time to treatment failure (TTF) was estimated by the Kaplan-Meier method and compared between subgroups by the log-rank test. The overall ORR was 21.1%, and the CBR was 31.6%. CBR was significantly higher for patients without liver metastasis (50% vs. 0%, = 0.044). Nine cases exhibited primary and eight cases secondary AI resistance. Both ORR and CBR were higher in patients with secondary AI resistance (25% vs. 0%, = 0.087; 38% vs. 11%, = 0.29). The median TTF was 6.2 months in the entire AI-resistant group ( = 17) and was longer in the secondary resistance subgroup than in the primary resistance subgroup (8.40 vs. 4.87 months; log-rank: = 0.159). High-dose TOR appears to be most effective for postmenopausal breast cancer cases with secondary resistance to AIs, cases without prior AI treatment, and cases without liver metastasis. The detailed mechanisms of AI resistance and the clinical features of responsive cases need to be further clarified to identify the best candidates for HD-TOR.
目前,对于激素受体阳性的晚期或转移性绝经后乳腺癌女性患者,尚无既定的二线及后续治疗方案。我们研究了高剂量托瑞米芬(HD-TOR)对此类患者群体的疗效,以及芳香化酶抑制剂(AI)耐药性是否会影响HD-TOR的治疗效果。这项回顾性分析调查了19例绝经后激素敏感性复发或转移性乳腺癌女性患者接受HD-TOR治疗的结果,HD-TOR定义为2012年至2016年期间每日服用120毫克。中位随访时间为9.67个月。比较了不同临床亚组的总缓解率(ORR)和临床获益率(CBR),包括根据复发或进展时间定义为原发性或继发性AI耐药的患者。采用Kaplan-Meier方法估计治疗失败时间(TTF),并通过对数秩检验在亚组之间进行比较。总体ORR为21.1%,CBR为31.6%。无肝转移患者的CBR显著更高(50%对0%,P = 0.044)。9例表现为原发性AI耐药,8例表现为继发性AI耐药。继发性AI耐药患者的ORR和CBR均更高(25%对0%,P = 0.087;38%对11%,P = 0.29)。整个AI耐药组(n = 17)的中位TTF为6.2个月,继发性耐药亚组的TTF长于原发性耐药亚组(8.40对4.87个月;对数秩检验:P = 0.159)。高剂量TOR似乎对继发性AI耐药的绝经后乳腺癌病例、未接受过AI治疗的病例以及无肝转移的病例最为有效。需要进一步阐明AI耐药的详细机制以及反应性病例的临床特征,以确定HD-TOR的最佳候选者。