Grever M R, Leiby J M, Kraut E H, Wilson H E, Neidhart J A, Wall R L, Balcerzak S P
J Clin Oncol. 1985 Sep;3(9):1196-201. doi: 10.1200/JCO.1985.3.9.1196.
Deoxycoformycin (dCF), a potent inhibitor of adenosine deaminase (ADA), was explored for its antineoplastic potential in 28 patients with advanced lymphoid malignancy. Both normal and malignant B lymphocytes have low levels of ADA activity, and low doses of dCF profoundly inhibit this enzyme in the peripheral blood of patients with chronic lymphocytic leukemia (CLL). The low doses of dCF administered in this trial (4 mg/m2) were not associated with prohibitive toxicity. Five of 28 patients had an objective response. Four additional patients had clinical improvement. No significant difference in the pretreatment ADA activity existed between responding patients and treatment failures. The demonstration of responses to dCF following failure on standard alkylating agents suggests that dCF may not be cross-resistant with current agents used to treat CLL. Additional studies should be pursued using low-dose dCF in patients with advanced malignancy.
去氧助间型霉素(dCF)是一种有效的腺苷脱氨酶(ADA)抑制剂,对28例晚期淋巴恶性肿瘤患者的抗肿瘤潜力进行了研究。正常和恶性B淋巴细胞的ADA活性水平都较低,低剂量的dCF能显著抑制慢性淋巴细胞白血病(CLL)患者外周血中的这种酶。本试验中给予的低剂量dCF(4mg/m²)并无严重毒性。28例患者中有5例出现客观缓解。另有4例患者有临床改善。缓解患者与治疗失败患者的预处理ADA活性无显著差异。在标准烷化剂治疗失败后对dCF有反应,这表明dCF可能与目前用于治疗CLL的药物不存在交叉耐药性。应进一步开展研究,对晚期恶性肿瘤患者使用低剂量dCF。