Department of Radiology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, The Netherlands.
GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre, P.O. Box 5800, 6202 AZ, Maastricht, The Netherlands.
Breast Cancer Res Treat. 2019 Aug;176(3):597-605. doi: 10.1007/s10549-019-05254-4. Epub 2019 May 7.
The aim of this study was to determine the safety and efficacy of Mitomycin C (MMC) infusion in a large cohort of advanced liver metastatic breast cancer patients (LMBC) and to determine factors influencing overall survival (OS).
We retrospectively analysed LMBC patients, treated with MMC infusion between 2000 and 2017. Hepatic response was measured with baseline CT scans and first available CT scan after MMC infusion by RECIST 1.1 criteria. Adverse events were registered by the CTCAE version 5.0. OS and hepatic progression free survival (hPFS) were evaluated using Kaplan-Meier estimates. After univariable analysis, a stepwise forward multivariable (MV) prediction analysis was developed to select independent pre-treatment factors associated with OS.
We included 176 patients with a total of 599 MMC infusions, mostly heavily pre-treated patients with a median time from diagnosis of MBC to MMC infusion of 36.9 months. RECIST evaluation of liver lesions (n = 132) showed a partial response rate of 15%, stable disease of 43% and progressive disease in 17%. Adverse events grade 3 and 4 were reported in 17.5%. Median PFS was 5.5 months and median OS was 7.8 months. Significant independent baseline predictors of worse OS included number of prior systemic chemotherapy lines, prior liver ablation, higher liver tumour burden and elevated levels of bilirubin and ALT.
MMC infusion is safe and effective in advanced LMBC patients. An increased number of prior therapies, a higher liver tumour burden and elevated levels of bilirubin and ALT were associated with a worse OS.
本研究旨在确定丝裂霉素 C(MMC)输注在大量晚期肝转移性乳腺癌(LMBC)患者中的安全性和疗效,并确定影响总生存期(OS)的因素。
我们回顾性分析了 2000 年至 2017 年间接受 MMC 输注治疗的 LMBC 患者。基线 CT 扫描和 MMC 输注后首次可获得的 CT 扫描通过 RECIST 1.1 标准测量肝反应。通过 CTCAE 版本 5.0 登记不良事件。使用 Kaplan-Meier 估计评估 OS 和肝无进展生存期(hPFS)。在单变量分析后,采用逐步向前多变量(MV)预测分析来选择与 OS 相关的独立治疗前因素。
我们纳入了 176 例患者,共接受了 599 次 MMC 输注,大多数是经过大量预处理的患者,从 MBC 诊断到 MMC 输注的中位时间为 36.9 个月。对肝脏病变的 RECIST 评估(n=132)显示部分缓解率为 15%,稳定疾病为 43%,进展性疾病为 17%。报告了 17.5%的 3 级和 4 级不良事件。中位 PFS 为 5.5 个月,中位 OS 为 7.8 个月。总生存期较差的独立基线预测因素包括先前系统化疗线数、先前肝消融术、较高的肝肿瘤负担以及胆红素和 ALT 水平升高。
MMC 输注在晚期 LMBC 患者中是安全有效的。先前治疗次数增加、肝肿瘤负担增加以及胆红素和 ALT 水平升高与 OS 较差相关。