Dimopoulos M A, Kantarjian H, Weber D, O'Brien S, Estey E, Delasalle K, Rose E, Cabanillas F, Keating M, Alexanian R
Department of Hematology, University of Texas M.D. Anderson Cancer Center, Houston.
J Clin Oncol. 1994 Dec;12(12):2694-8. doi: 10.1200/JCO.1994.12.12.2694.
To assess the activity of 2-chlorodeoxyadenosine (2CdA) as primary therapy for patients with Waldenström's macroglobulinemia.
2CdA was given to 26 consecutive, previously untreated and symptomatic patients with Waldenström's macroglobulinemia. 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 up without further therapy and were scheduled to receive two additional treatments with 2CdA on disease relapse.
Twenty-two of 26 patients responded to the 2CdA therapy (85%; 95% confidence interval [CI], 65% to 96%), including three patients who achieved a complete response and 19 patients who had a partial response. Treatment was well tolerated, with no acute hematologic toxicity. A marked and sustained reduction of CD4+ lymphocytes occurred in all patients and may have contributed to a fatal infection with disseminated herpes simplex in one patient. With a median follow-up of 13 months, five patients have relapsed and all re-treated patients have responded again to 2CdA.
2CdA is highly active in previously untreated patients with Waldenström's macroglobulinemia. A limited program of treatment induced responses of good quality and long duration in more than 80% of patients.
评估2-氯脱氧腺苷(2CdA)作为原发性治疗瓦尔登斯特伦巨球蛋白血症患者的活性。
连续26例既往未接受过治疗且有症状的瓦尔登斯特伦巨球蛋白血症患者接受2CdA治疗。门诊患者接受两个疗程治疗,剂量为每天0.1mg/kg体重,使用便携式泵通过中心静脉导管连续输注7天。有反应的患者在无进一步治疗的情况下接受随访,并计划在疾病复发时再接受两个疗程的2CdA治疗。
26例患者中有22例对2CdA治疗有反应(85%;95%置信区间[CI],65%至96%),包括3例完全缓解患者和19例部分缓解患者。治疗耐受性良好,无急性血液学毒性。所有患者的CD4+淋巴细胞均出现显著且持续的减少,这可能是导致1例患者发生播散性单纯疱疹致命感染的原因。中位随访13个月时,5例患者复发,所有再次接受治疗的患者对2CdA再次产生反应。
2CdA对既往未接受过治疗的瓦尔登斯特伦巨球蛋白血症患者具有高度活性。有限疗程的治疗使超过80%的患者产生了高质量且持续时间长的反应。