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阿仑单抗治疗失败或存在巨大淋巴结病的氟达拉滨难治性慢性淋巴细胞白血病患者的自然病程。

The natural history of fludarabine-refractory chronic lymphocytic leukemia patients who fail alemtuzumab or have bulky lymphadenopathy.

作者信息

Tam Constantine S, O'Brien Susan, Lerner Susan, Khouri I, Ferrajoli A, Faderl S, Browning M, Tsimberidou Apostolia M, Kantarjian Hagop, Wierda William G

机构信息

Department of Leukemia and Stem Cell Transplantation, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA.

出版信息

Leuk Lymphoma. 2007 Oct;48(10):1931-9. doi: 10.1080/10428190701573257.

Abstract

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.

摘要

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。

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