Braverman A S
State University of New York-Health Science Center, Brooklyn.
Ann Intern Med. 1993 Apr 15;118(8):630-2. doi: 10.7326/0003-4819-118-8-199304150-00010.
Immunocyte and germ cell neoplasms, often curable by chemotherapy, arise from normal tissues most vulnerable to the effects of cytotoxic drugs; generalizing from these results to treating other tumors with such agents may not be entirely valid. Our limited success in treating epithelial neoplasms may be due to insensitivity rather than to drug resistance. Well-designed attempts to overcome resistance have been unsuccessful. The acquired immunodeficiency syndrome has not confirmed the putative role of immune surveillance in the pathogenesis of most neoplasms. The limited success of the most elaborate immunotherapies suggests that they, too, are nonspecific cell-killing techniques. Immunologic and cytotoxic drug therapies deserve further investigation but on a smaller scale. Neoplastic cell molecular biology, unknown when these therapies were developed, is being rapidly elucidated and may make it possible to treat malignancies by modulating cell physiology. Success of therapies based on the advances, in molecular biology, is not more uncertain than that of traditional treatments. Differentiation-induction techniques have already induced remissions in patients with acute promyelocytic leukemia and squamous cell carcinomas.
免疫细胞和生殖细胞肿瘤通常可用化疗治愈,它们起源于对细胞毒性药物作用最敏感的正常组织;将这些结果推广到用此类药物治疗其他肿瘤可能并不完全有效。我们在治疗上皮性肿瘤方面取得的有限成功可能是由于不敏感而非耐药性。精心设计的克服耐药性的尝试均未成功。获得性免疫缺陷综合征并未证实免疫监视在大多数肿瘤发病机制中的假定作用。最复杂的免疫疗法取得的有限成功表明,它们同样也是非特异性的细胞杀伤技术。免疫疗法和细胞毒性药物疗法值得进一步研究,但规模要小一些。肿瘤细胞分子生物学在这些疗法开发时尚不为人知,目前正在迅速阐明,这可能使通过调节细胞生理学来治疗恶性肿瘤成为可能。基于分子生物学进展的疗法的成功并不比传统治疗更不确定。分化诱导技术已经在急性早幼粒细胞白血病和鳞状细胞癌患者中诱导了缓解。