O'Brien S, Kantarjian H, Talpaz M
Department of Hematology, University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.
Leuk Lymphoma. 1996 Oct;23(3-4):247-52. doi: 10.3109/10428199609054827.
Interferon-A (IFN-A) is an effective agent in the treatment of chronic myelogenous leukemia (CML). Hematologic remissions occur in the majority of patients with newly diagnosed disease, and cytogenetic remissions may occur in up to 50% of patients. Several studies have shown a correlation between the dose of IFN-A and achievement of a major cytogenetic response; this response has also been correlated with prolonged survival. However, IFN-A may be associated with significant side effects that reduce enthusiasm for the use of this drug, produce difficulties in patient compliance, and limit the dose delivered to the patient, thus resulting in ineffective use of IFN-A. Experience with this drug has led to a refinement in techniques for initiation of therapy as well as interventions to deal with side effects. These strategies are often not discussed in publications dealing with response rates and survival. In this review we discuss strategies to minimize toxicity and improve the effectiveness of IFN-A in the treatment of CML.
干扰素 -A(IFN -A)是治疗慢性粒细胞白血病(CML)的一种有效药物。大多数新诊断疾病的患者会出现血液学缓解,高达50%的患者可能会出现细胞遗传学缓解。多项研究表明,IFN -A的剂量与主要细胞遗传学反应的达成之间存在关联;这种反应也与生存期延长相关。然而,IFN -A可能会伴有显著的副作用,这降低了对使用该药物的热情,给患者依从性带来困难,并限制了给予患者的剂量,从而导致IFN -A使用无效。使用这种药物的经验促使治疗起始技术以及应对副作用的干预措施得到改进。这些策略在关于缓解率和生存期的出版物中常常未被讨论。在本综述中,我们讨论将IFN -A治疗CML时的毒性降至最低并提高其有效性的策略。