Pharmaceutical Care Division, King Faisal Specialist Hospital and Research Centre, College of Medicine, Alfaisal University, MBC# 11, P.O Box 3354, Riyadh, 11211, Saudi Arabia.
College of Pharmacy, Prince Noura bent Abdulrahman University, Riyadh, Saudi Arabia.
Cancer Chemother Pharmacol. 2018 Apr;81(4):697-704. doi: 10.1007/s00280-018-3537-4. Epub 2018 Feb 10.
Cytopenia after hyperthermic intraperitoneal chemotherapy (HIPEC) with cytoreductive surgery (CRS) has been reported in non-comparative studies with various chemotherapeutic regimens. This study compared the incidence of leukopenia and thrombocytopenia in patients who underwent CRS/HIPEC and received melphalan or cisplatin plus mitomycin-c (CIS + MMC).
This retrospective study included patients who underwent CRS/HIPEC at King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia from March 2011 to March 2017 and received melphalan 60 mg/m or CIS 100 mg/m combined with MMC 30 mg/m. Incidences and severity of leukopenia, neutropenia, thrombocytopenia, and anemia were compared between groups.
This study included 46 patients who received CIS + MMC and 35 patients who received melphalan. The leukopenia incidence was 25.7% in the melphalan group and 17.3% in the CIS + MMC group (P = 0.362), with one patient (2.8%) in the melphalan group developed grade V leukopenia. The number of days to leukocyte nadir was 32.8 days for CIS + MMC group compared to 9.8 days for melphalan group(P = 0.035). Thrombocytopenia occurred at a similar rate in the melphalan (60%) and CIS + MMC (68.8%) groups (P = 0.4). Grade III thrombocytopenia developed in 3.2% and 5% of patients in the melphalan and the CIS + MMC groups, respectively. Neutropenia did not occur in any patient. In multivariate analysis, leukopenia predictors were female gender (P = 0.047) and baseline leukocyte counts (P = 0.029). Baseline platelet count predicted thrombocytopenia (P < 0.001).
Melphalan and CIS + MMC regimens were associated with comparable incidences of leukopenia and thrombocytopenia. Severe leukopenia and severe thrombocytopenia were rare following CRS/HIPEC using both chemotherapy regimens.
在非对照研究中,已经报道了接受细胞减灭术(CRS)联合高温腹腔化疗(HIPEC)后出现细胞减少症,且使用了各种化疗方案。本研究比较了接受 CRS/HIPEC 并接受美法仑或顺铂加丝裂霉素-C(CIS+MMC)治疗的患者白细胞减少症和血小板减少症的发生率。
本回顾性研究纳入了 2011 年 3 月至 2017 年 3 月在沙特阿拉伯利雅得法赫德国王专科医院和研究中心接受 CRS/HIPEC 治疗且接受美法仑 60mg/m2 或 CIS100mg/m2 联合 MMC30mg/m2 治疗的患者。比较两组白细胞减少症、中性粒细胞减少症、血小板减少症和贫血的发生率和严重程度。
本研究纳入了 46 例接受 CIS+MMC 治疗的患者和 35 例接受美法仑治疗的患者。美法仑组白细胞减少症的发生率为 25.7%,CIS+MMC 组为 17.3%(P=0.362),美法仑组有 1 例(2.8%)患者发生 5 级白细胞减少症。CIS+MMC 组白细胞减少症的最低值出现时间为 32.8 天,而美法仑组为 9.8 天(P=0.035)。美法仑组(60%)和 CIS+MMC 组(68.8%)血小板减少症的发生率相似(P=0.4)。美法仑组和 CIS+MMC 组分别有 3.2%和 5%的患者发生 3 级血小板减少症。无患者发生中性粒细胞减少症。多变量分析显示,女性(P=0.047)和基线白细胞计数(P=0.029)是白细胞减少症的预测因素。基线血小板计数预测血小板减少症(P<0.001)。
美法仑和 CIS+MMC 方案引起的白细胞减少症和血小板减少症发生率相似。两种化疗方案行 CRS/HIPEC 后,严重白细胞减少症和严重血小板减少症均罕见。