Krown S E
AIDS Task Force, Memorial Sloan-Kettering Cancer Center, New York.
Hematol Oncol Clin North Am. 1991 Apr;5(2):311-22.
Interferon-alpha is an effective treatment for a subset of patients with AIDS-associated Kaposi's sarcoma. When given at high doses to patients who lack systemic signs, symptoms, and opportunistic infections associated with advanced HIV infection and who maintain some degree of cell-mediated immune function, tumor regression may be observed in a high proportion of patients. Although the addition of chemotherapy to IFN-alpha appears to confer no added benefits, the combination of IFN-alpha with zidovudine has induced high tumor response rates in preliminary studies, including responses in some patients considered unlikely to respond to IFN-alpha alone. IFN-alpha-induced tumor regression has also been associated with suppression of HIV, as measured by serum p24 antigen concentrations and peripheral blood virus cultures. Other biologic agents, including interferons beta and gamma, tumor necrosis factor, and IL-2, have also been tested, to a lesser extent, in patients with Kaposi's sarcoma. Although systemically administered IFN-beta and intralesional TNF injections have led to tumor regression in some cases, the role of these biologics has been incompletely defined. Additional studies of these agents in combination with nucleoside reverse transcriptase inhibitors such as zidovudine will be required to fully assess their role in the treatment of Kaposi's sarcoma and HIV infection. It can also be anticipated that newer biologic agents, which specifically inhibit the production or action of angiogenic factors believed to be involved in the genesis of Kaposi's sarcoma, will be studied in the near future.
α干扰素是治疗部分艾滋病相关卡波西肉瘤患者的有效方法。对于那些没有与晚期HIV感染相关的全身症状、体征和机会性感染且仍保持一定程度细胞介导免疫功能的患者,给予高剂量α干扰素时,很大一部分患者可能会出现肿瘤消退。虽然在α干扰素基础上加用化疗似乎并无额外益处,但在初步研究中,α干扰素与齐多夫定联合使用已诱导出较高的肿瘤反应率,包括一些被认为单独使用α干扰素不太可能有反应的患者也出现了反应。通过血清p24抗原浓度和外周血病毒培养检测发现,α干扰素诱导的肿瘤消退还与HIV抑制有关。其他生物制剂,包括β干扰素、γ干扰素、肿瘤坏死因子和白细胞介素-2,在卡波西肉瘤患者中也进行了程度较轻的试验。虽然全身给予β干扰素和病灶内注射肿瘤坏死因子在某些情况下导致了肿瘤消退,但这些生物制剂的作用尚未完全明确。需要对这些制剂与核苷类逆转录酶抑制剂如齐多夫定联合使用进行更多研究,以全面评估它们在治疗卡波西肉瘤和HIV感染中的作用。还可以预期,在不久的将来会研究能特异性抑制被认为参与卡波西肉瘤发生的血管生成因子产生或作用的新型生物制剂。