Dimopoulos M A, Weber D, Delasalle K B, Keating M, Alexanian R
Department of Hematology, University of Texas, M.D. Anderson Cancer Center, Houston, USA.
Ann Oncol. 1995 Jan;6(1):49-52. doi: 10.1093/oxfordjournals.annonc.a059040.
Few effective treatments are available for patients with Waldenstrom's macroglobulinemia that is resistant to standard therapies. We assessed the activity of 2-chlorodeoxyadenosine (2CdA) in patients with resistant macroglobulinemia in order to identify those most likely to benefit.
2-chlorodeoxyadenosine was given to 46 consecutive patients with Waldenstrom's macroglobulinemia resistant to a combination of an alkylating agent and a glucocorticoid. Two courses were administered to outpatients at a dose of 0.1 mg/kg body weight per day for a 7-day continuous infusion using a portable pump through a central venous catheter. Responding patients were followed without further therapy.
Twenty of 46 patients responded to 2CdA therapy (43%; 95 CI; 29 to 60%) with a significantly higher frequency of benefit among patients with disease relapsing off therapy (78%) or with primary resistant disease within the first year (57%) than in those with later phases of disease (22%). The median survival after treatment was 28 months and the median progression-free survival of responding patients was 12 months. The longest survival was measured in patients with primary refractory disease (projected median 36 months) and the shortest in those with disease in refractory relapse (median 13 months).
2-Chlorodeoxyadenosine is active against macroglobulinemic lymphoma resistant to standard regimens and most effective in patients with disease relapsing off treatment or during the first year of primary refractory disease. Little benefit was observed among patients with later phases of resistant disease who should receive alternative treatments.
对于对标准疗法耐药的华氏巨球蛋白血症患者,几乎没有有效的治疗方法。我们评估了2-氯脱氧腺苷(2CdA)对耐药性巨球蛋白血症患者的活性,以确定最可能从中受益的患者。
连续46例对烷化剂和糖皮质激素联合治疗耐药的华氏巨球蛋白血症患者接受2-氯脱氧腺苷治疗。门诊患者接受两个疗程的治疗,剂量为每天0.1mg/kg体重,通过中心静脉导管使用便携式泵持续输注7天。有反应的患者在不进行进一步治疗的情况下接受随访。
46例患者中有20例对2CdA治疗有反应(43%;95%置信区间:29%至60%),治疗后复发的患者(78%)或第一年原发性耐药疾病患者(57%)的获益频率明显高于疾病晚期患者(22%)。治疗后的中位生存期为28个月,有反应患者的中位无进展生存期为12个月。原发性难治性疾病患者的生存期最长(预计中位生存期36个月),难治性复发患者的生存期最短(中位生存期13个月)。
2-氯脱氧腺苷对耐药的巨球蛋白血症淋巴瘤有活性,对治疗后复发或原发性难治性疾病第一年的患者最有效。在耐药疾病晚期患者中观察到的益处很少,这些患者应接受替代治疗。