Department of Pulmonary Circulation, Thromboembolic Diseases and Cardiology, Centre of Postgraduate Medical Education, European Health Centre, Borowa 14/18, 05-400, Otwock, Poland.
Clinic of Clinical Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, Cracow Branch, Kraków, Poland.
Sci Rep. 2020 Oct 28;10(1):18481. doi: 10.1038/s41598-020-75614-4.
Cardiovascular diseases (CVDs) are the major cause of morbidity/mortality among breast cancer (BC) patients. Observation of the daily practice in eight experienced Polish oncology centers was conducted to find all possible predictors of new cases of heart failure (HF) and overall survival (OS) of metastatic BC patients treated with liposomal doxorubicin, taking into account the impact of pre-existing CVDs. HF was the cause of premature discontinuation of liposomal doxorubicin therapy in 13 (3.2%) of 402 patients. The probability of developing HF was higher in women with pre-existing CVDs (HR 4.61; 95%CI 1.38-15.38). Independent of CVDs history, a lower risk of HF was observed in those treated with a cumulative dose of liposomal doxorubicin > 300 mg/m2 (HR 0.14; 95% CI 0.04-0.54) and taxane-naive (HR 0.26; 95% CI 0.07-0.96). Multivariate analysis including the presence of pre-existing CVDs and occurrence of new HF, revealed a liposomal doxorubicin in cumulative doses of > 300 mg/m2 as a beneficial predictor for OS (HR 0.61; 95% CI 0.47-0.78) independently of subsequent chemotherapy (HR 0.72; 95% CI 0.57-0.92) or endocrine therapy (HR 0.65; 95% CI 0.49-0.87). Higher doses of liposomal doxorubicin can decrease mortality in metastatic BC without increasing the risk of HF. The clinical benefit is achieved regardless of pre-existing CVDs and subsequent anticancer therapy.
心血管疾病 (CVDs) 是乳腺癌 (BC) 患者发病率/死亡率的主要原因。观察了 8 个经验丰富的波兰肿瘤中心的日常实践,以寻找所有可能预测接受脂质体多柔比星治疗的转移性 BC 患者新发心力衰竭 (HF) 和总生存 (OS) 的因素,同时考虑到预先存在的 CVDs 的影响。在 402 名患者中,有 13 名(3.2%)因 HF 而提前停止脂质体多柔比星治疗。预先存在 CVDs 的女性发生 HF 的可能性更高(HR 4.61;95%CI 1.38-15.38)。独立于 CVDs 病史,累积剂量超过 300mg/m2 的患者(HR 0.14;95%CI 0.04-0.54)和紫杉烷初治患者(HR 0.26;95%CI 0.07-0.96)发生 HF 的风险较低。包括预先存在的 CVDs 和新发 HF 在内的多变量分析显示,累积剂量超过 300mg/m2 的脂质体多柔比星是 OS 的有益预测因子(HR 0.61;95%CI 0.47-0.78),独立于随后的化疗(HR 0.72;95%CI 0.57-0.92)或内分泌治疗(HR 0.65;95%CI 0.49-0.87)。更高剂量的脂质体多柔比星可以降低转移性 BC 的死亡率,而不会增加 HF 的风险。无论是否存在预先存在的 CVDs 以及随后的抗癌治疗,都可以获得临床获益。