Tam Constantine S, O'Brien Susan, Lerner Susan, Khouri I, Ferrajoli A, Faderl S, Browning M, Tsimberidou Apostolia M, Kantarjian Hagop, Wierda William G
Department of Leukemia and Stem Cell Transplantation, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA.
Leuk Lymphoma. 2007 Oct;48(10):1931-9. doi: 10.1080/10428190701573257.
The natural history and outcome of salvage treatment for patients with fludarabine-refractory chronic lymphocytic leukemia who are either refractory to alemtuzumab ("double-refractory") or ineligible for alemtuzumab due to bulky lymphadenopathy ("bulky fludarabine-refractory") have not been described. We present the outcomes of 99 such patients (double-refractory n = 58, bulky fludarabine-refractory n = 41) undergoing their first salvage treatment at our center. Patients received a variety of salvage regimens including monoclonal antibodies (n = 15), single-agent cytotoxic drugs (n = 14), purine analogue combination regimens (n = 21), intensive combination chemotherapy (n = 36), allogeneic stem cell transplantation (SCT; n = 4), or other therapies (n = 9). Overall response to first salvage therapy other than SCT was 23%, with no complete responses. All four patients who underwent SCT as first salvage achieved complete remission. Early death (within 8 weeks of commencing first salvage) occurred in 13% of patients, and 54% of patients experienced a major infection during therapy. Overall survival was 9 months, with hemoglobin < 11 g/dL (hazard ratio 2.3), hepatomegaly (hazard ratio 2.4), and performance status > or = 2 (hazard ratio 1.9) being significant independent predictors of inferior survival.
对于氟达拉滨难治性慢性淋巴细胞白血病患者,若对阿仑单抗难治(“双重难治”)或因巨大淋巴结病而不符合阿仑单抗治疗条件(“巨大氟达拉滨难治性”),其挽救治疗的自然病程和结果尚未见描述。我们报告了99例此类患者(双重难治58例,巨大氟达拉滨难治性41例)在本中心接受首次挽救治疗的结果。患者接受了多种挽救方案,包括单克隆抗体(15例)、单药细胞毒性药物(14例)、嘌呤类似物联合方案(21例)、强化联合化疗(36例)、异基因干细胞移植(SCT;4例)或其他治疗(9例)。除SCT外,首次挽救治疗的总体缓解率为23%,无完全缓解。作为首次挽救治疗接受SCT的4例患者均实现完全缓解。13%的患者发生早期死亡(在开始首次挽救治疗后8周内),54%的患者在治疗期间发生严重感染。总生存期为9个月,血红蛋白<11 g/dL(风险比2.3)、肝肿大(风险比2.4)和体能状态≥2(风险比1.9)是生存较差的显著独立预测因素。