O'Brien S, Kantarjian H, Estey E, Koller C, Robertson B, Beran M, Andreeff M, Pierce S, Keating M
Department of Hematology, University of Texas M.D. Anderson Cancer Center, Houston 77030.
N Engl J Med. 1994 Feb 3;330(5):319-22. doi: 10.1056/NEJM199402033300504.
Fludarabine and 2-chlorodeoxyadenosine are nucleoside analogues that have proved effective in patients with chronic lymphocytic leukemia (CLL). Although their mechanism of action is thought to be similar, a small number of patients who do not respond to fludarabine do respond to 2-chlorodeoxyadenosine. The extent to which 2-chlorodeoxyadenosine is effective in patients who do not respond to fludarabine is not known, however.
We treated 28 patients with CLL refractory to fludarabine therapy with a continuous infusion of 2-chlorodeoxyadenosine at a daily dose of 4 mg per square meter of body-surface area for seven days. The treatment could be repeated monthly. The number of treatments ranged from one to five; patients who responded continued to receive treatment until the maximal response was achieved.
Two patients (7 percent) had partial remissions, but no patients had complete remissions. One other patient had a substantial response but had residual thrombocytopenia. The rate of response in most affected organs was 20 percent, but anemia or thrombocytopenia rarely improved. Myelosuppression was frequent, and 65 percent of the courses of 2-chlorodeoxyadenosine therapy were accompanied by febrile episodes or infections. Ten patients died within 60 days of starting therapy with 2-chlorodeoxyadenosine; eight deaths were related to infection. The median platelet count at the start of 2-chlorodeoxyadenosine therapy in these 10 patients was 24,000 per cubic millimeter, as compared with 109,000 per cubic millimeter in the other 18 patients. Five patients were alive after a median follow-up of 24 months.
Patients with advanced CLL refractory to fludarabine therapy are unlikely to benefit from treatment with 2-chlorodeoxyadenosine. Although 20 percent of the patients have some response, thrombocytopenia and anemia are rarely corrected and may be made worse by 2-chlorodeoxyadenosine therapy.
氟达拉滨和2-氯脱氧腺苷是核苷类似物,已被证明对慢性淋巴细胞白血病(CLL)患者有效。尽管它们的作用机制被认为相似,但少数对氟达拉滨无反应的患者对2-氯脱氧腺苷有反应。然而,2-氯脱氧腺苷对氟达拉滨无反应患者的有效程度尚不清楚。
我们对28例氟达拉滨治疗难治的CLL患者进行治疗,以每日每平方米体表面积4毫克的剂量持续输注2-氯脱氧腺苷,共7天。治疗可每月重复一次。治疗次数为1至5次;有反应的患者继续接受治疗,直至达到最大反应。
2例患者(7%)部分缓解,但无患者完全缓解。另有1例患者有显著反应,但仍有血小板减少。大多数受累器官的反应率为20%,但贫血或血小板减少很少改善。骨髓抑制很常见,65%的2-氯脱氧腺苷治疗疗程伴有发热或感染。10例患者在开始2-氯脱氧腺苷治疗后60天内死亡;8例死亡与感染有关。这10例患者开始2-氯脱氧腺苷治疗时的血小板计数中位数为每立方毫米24,000,而其他18例患者为每立方毫米109,000。中位随访24个月后,5例患者存活。
氟达拉滨治疗难治的晚期CLL患者不太可能从2-氯脱氧腺苷治疗中获益。虽然20%的患者有一些反应,但血小板减少和贫血很少得到纠正,且2-氯脱氧腺苷治疗可能使其恶化。