Gill P S, Harrington W, Kaplan M H, Ribeiro R C, Bennett J M, Liebman H A, Bernstein-Singer M, Espina B M, Cabral L, Allen S
Department of Internal Medicine, University of Southern California School of Medicine, Los Angeles, USA.
N Engl J Med. 1995 Jun 29;332(26):1744-8. doi: 10.1056/NEJM199506293322603.
Infection with the human T-cell lymphotropic virus type I, a retrovirus, can cause a distinctive cancer, adult T-cell leukemia-lymphoma. The median survival of patients with the acute and lymphomatous forms of the disease is short, despite the use of cytotoxic chemotherapy.
We treated 19 patients with acute or lymphomatous forms of adult T-cell leukemia-lymphoma with oral zidovudine (200 mg five times daily) and interferon alfa (Intron A, 5 to 10 million units subcutaneously each day). Seven of these patients had either relapsed after multiagent cytotoxic chemotherapy or failed to respond to that treatment.
Major responses were achieved in 58 percent of the patients (11 of 19), including complete remission in 26 percent (5 of 19). Four patients in whom prior cytotoxic therapy had failed had major responses, two of which were complete remissions. Six patients have survived for more than 12 months, with the longest remission since the discontinuation of treatment lasting more than 59 months.
The combination of zidovudine and interferon alfa has activity against adult T-cell leukemia-lymphoma, even in patients in whom prior cytotoxic therapy has failed. This regimen should be evaluated further for its role in the treatment of adult T-cell leukemia-lymphoma.
感染I型人类嗜T细胞病毒(一种逆转录病毒)可引发一种独特的癌症——成人T细胞白血病-淋巴瘤。尽管使用了细胞毒性化疗,但该疾病急性和淋巴瘤形式患者的中位生存期较短。
我们用口服齐多夫定(每日5次,每次200毫克)和干扰素α(重组干扰素α-2b,每天皮下注射500万至1000万单位)治疗了19例成人T细胞白血病-淋巴瘤急性或淋巴瘤形式的患者。其中7例患者在多药细胞毒性化疗后复发或对该治疗无反应。
58%的患者(19例中的11例)取得了主要缓解,包括26%(19例中的5例)完全缓解。4例先前细胞毒性治疗失败的患者取得了主要缓解,其中2例为完全缓解。6例患者存活超过12个月,自停止治疗以来最长缓解期超过59个月。
齐多夫定和干扰素α联合用药对成人T细胞白血病-淋巴瘤有活性,即使在先前细胞毒性治疗失败的患者中也是如此。该方案在成人T细胞白血病-淋巴瘤治疗中的作用应进一步评估。