Lu Charles, Perez-Soler Roman, Piperdi Bilal, Walsh Garrett L, Swisher Stephen G, Smythe W Roy, Shin Hyung J, Ro Jae Y, Feng Lei, Truong Mylene, Yalamanchili Adiseshu, Lopez-Berestein Gabriel, Hong Waun K, Khokhar Abdul R, Shin Dong M
Department of Thoracic/Head & Neck Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
J Clin Oncol. 2005 May 20;23(15):3495-501. doi: 10.1200/JCO.2005.00.802.
To determine pathologic response rates to liposome-entrapped cis-bisneodecanoato-trans-R,R-1,2-diaminocyclohexane platinum(II) (L-NDDP) administered intrapleurally in patients with malignant pleural mesothelioma.
Thirty-three patients with malignant pleural mesothelioma and free-flowing pleural effusions received intrapleural L-NDDP once every 3 weeks at a dose of 450 mg/m2. Thoracoscopic evaluation with pleural biopsies was performed before therapy and then after every two cycles. The primary end point was pathologic response as determined by thoracoscopic biopsy.
After at least two cycles, post-treatment pleural biopsy analysis was negative in 14 patients for a pathologic response rate of 42% (95% CI, 25% to 61%). Median survival was 11.2 months. There were three treatment-related deaths secondary to peritonitis, cellulitis at the thoracoscopy site, and empyema. Grade 3 nonhematologic toxicities included infection, fever, dyspnea, and anorexia, which occurred in five (15%), one (3%), one (3%), and one (3%) patients, respectively. There were no grade 4 nonhematologic toxicities. Grade 3 or 4 neutropenia, thrombocytopenia, and anemia occurred in five (15%), three (9%), and two (6%) patients, respectively. Two patients with pathologic responses subsequently underwent pleural decortication. Both surgical specimens revealed residual tumor in regions that were not in direct communication with the pleural space.
Intrapleural L-NDDP therapy in this patient population is feasible with significant but manageable toxicity. Although pathologic responses are highly encouraging, areas of mesothelioma that are not in direct communication with the pleural space will evade drug exposure and limit efficacy in some patients. The optimal role of intrapleural L-NDDP therapy currently remains to be determined.
确定脂质体包裹的顺 - 双新癸酸 - 反式 -R,R - 1,2 - 二氨基环己烷铂(II)(L - NDDP)经胸膜腔内给药治疗恶性胸膜间皮瘤患者的病理缓解率。
33例伴有自由流动胸腔积液的恶性胸膜间皮瘤患者,每3周接受一次胸膜腔内L - NDDP治疗,剂量为450mg/m²。在治疗前以及每两个周期后进行胸腔镜评估及胸膜活检。主要终点是通过胸腔镜活检确定的病理缓解情况。
至少两个周期后,14例患者治疗后的胸膜活检分析结果为阴性,病理缓解率为42%(95%置信区间,25%至61%)。中位生存期为11.2个月。有3例与治疗相关的死亡,分别继发于腹膜炎、胸腔镜检查部位蜂窝织炎和脓胸。3级非血液学毒性包括感染、发热、呼吸困难和厌食,分别发生在5例(15%)、1例(3%)、1例(3%)和1例(3%)患者中。无4级非血液学毒性。3级或4级中性粒细胞减少、血小板减少和贫血分别发生在5例(15%)、3例(9%)和2例(6%)患者中。2例有病理缓解的患者随后接受了胸膜剥脱术。两份手术标本均显示在与胸膜腔无直接连通的区域存在残留肿瘤。
该患者群体接受胸膜腔内L - NDDP治疗是可行的,毒性显著但可控。尽管病理缓解情况非常令人鼓舞,但与胸膜腔无直接连通的间皮瘤区域会逃避药物暴露,从而在某些患者中限制疗效。胸膜腔内L - NDDP治疗的最佳作用目前仍有待确定。