Laurencet F M, Zulian G B, Guetty-Alberto M, Iten P A, Betticher D C, Alberto P
Division of Oncology, Geneva University Hospitals, Switzerland.
Br J Cancer. 1999 Mar;79(7-8):1215-9. doi: 10.1038/sj.bjc.6690195.
The feasibility of combining cladribine with cyclophosphamide and prednisone in the management of indolent lymphoid malignancies was determined. Nineteen patients [nine chronic lymphocytic leukaemia (CLL), seven non-Hodgkin's lymphoma (NHL) and three macroglobulinaemia (M))] received cladribine 0.1 mg kg(-1) per day as a subcutaneous bolus injection on days 1-3 (up to 5 injections) with intravenous cyclophosphamide 500 mg m(-2) on day 1 and oral prednisone 40 mg (m-2) on days 1-5 at 4-weekly intervals up to a maximum of six courses. A total of 80 courses were given. Overall response rate was 88%, with four patients achieving a complete clinical and haematological response and 12 achieving a partial response. Neutropenia WHO grade 4 in two patients and WHO grade 3 infection in one patient were the limiting toxicities on treatment. During the follow-up, WHO grade >3 haematological complications occurred in five patients and WHO grade >3 non-haematological complications in five patients. There were no treatment-related deaths. This study demonstrates the feasibility of the cladribine/cyclophosphamide/prednisone (CCP) combination that appears highly active and safe in the management of indolent lymphoid malignancies.
确定了将克拉屈滨与环磷酰胺和泼尼松联合用于惰性淋巴恶性肿瘤治疗的可行性。19例患者[9例慢性淋巴细胞白血病(CLL)、7例非霍奇金淋巴瘤(NHL)和3例巨球蛋白血症(M)]在第1 - 3天接受皮下推注注射克拉屈滨0.1 mg·kg⁻¹(最多5次注射),第1天静脉注射环磷酰胺500 mg·m⁻²,第1 - 5天口服泼尼松40 mg·m⁻²,每4周为一个疗程,最多6个疗程。共给予80个疗程。总缓解率为88%,4例患者实现完全临床和血液学缓解,12例患者实现部分缓解。2例患者出现4级中性粒细胞减少,1例患者出现3级感染是治疗的限制性毒性。在随访期间,5例患者发生>3级血液学并发症,5例患者发生>3级非血液学并发症。无治疗相关死亡。本研究证明了克拉屈滨/环磷酰胺/泼尼松(CCP)联合方案在惰性淋巴恶性肿瘤治疗中具有高活性和安全性的可行性。