Gill P S, Lunardi-Ishkandar Y, Louie S, Tulpule A, Zheng T, Espina B M, Besnier J M, Hermans P, Levine A M, Bryant J L, Gallo R C
Department of Internal Medicine, University of Southern California School of Medicine, Los Angeles 90033, USA.
N Engl J Med. 1996 Oct 24;335(17):1261-9. doi: 10.1056/NEJM199610243351702.
Kaposi's sarcoma is the most common cancer in patients with the acquired immunodeficiency syndrome (AIDS). Recently, certain preparations of human chorionic gonadotropin (hCG) have been shown to inhibit the growth of Kaposi's sarcoma cell lines in vitro and in immunodeficient mice.
After in vitro evaluation of four commercially available hCG preparations, the most active product was evaluated in 36 patients with AIDS-related Kaposi's sarcoma. In a phase 1-2 trial, 24 patients received intralesional injections of hCG three times a week for two weeks at doses of 250, 500, 1000, or 2000 IU (6 patients each). In each patient three nodular lesions were injected, two with the drug and one with diluent alone. In a double-blind trial, 12 additional patients were randomly assigned to receive intralesional injections of 2000 IU of hCG or diluent alone (6 patients each; two lesions per patient). At the conclusion of therapy, the lesions were measured, their gross appearance assessed, and biopsy specimens evaluated.
A.P.L. (Wyeth-Ayerst), which had the most in vitro activity against Kaposi's sarcoma cell lines, was selected for the clinical investigation. Treatment with A.P.L. was well tolerated at all doses. In the cohorts given 250, 500, 1000, and 2000 IU, 1, 5, 5, and 10 of the 12 injected lesions responded, respectively (P=0.03 for trend). Complete tumor regression was observed in one lesion each at the 250-IU and 500-IU doses, in two lesions given the 1000-IU dose, and in five lesions given the 2000-IU dose. In the double-blind study, none of the 12 lesions in the six patients injected with diluent had responses, as compared with 10 of the 12 lesions in the six patients injected with hCG (P=0.015). Microscopical evidence of apoptosis was observed only in hCG-treated lesions. The percentage of cells that died increased in a dose-dependent manner (P<0.001). Serum levels of follicle-stimulating hormone (P=0.002) and luteinizing hormone (P=0.001) declined after the last injection of hCG, but there was no effect on these hormones in the diluent-treated patients.
The intralesional injection of hCG induces the regression of AIDS-related Kaposi's sarcoma lesions in a dose-dependent manner. The response of these tumors appears to be mediated by the induction of apoptosis.
卡波西肉瘤是获得性免疫缺陷综合征(艾滋病)患者中最常见的癌症。最近,已证明某些人绒毛膜促性腺激素(hCG)制剂在体外和免疫缺陷小鼠中可抑制卡波西肉瘤细胞系的生长。
在对四种市售hCG制剂进行体外评估后,对最具活性的产品在36例艾滋病相关卡波西肉瘤患者中进行了评估。在一项1-2期试验中,24例患者每周接受三次病灶内注射hCG,持续两周,剂量分别为250、500、1000或2000国际单位(每组6例)。在每位患者中,对三个结节性病变进行注射,两个注射药物,一个仅注射稀释剂。在一项双盲试验中,另外12例患者被随机分配接受病灶内注射2000国际单位hCG或仅注射稀释剂(每组6例;每位患者两个病变)。治疗结束时,测量病变大小,评估其总体外观,并对活检标本进行评估。
A.P.L.(惠氏-艾尔斯特公司)在体外对卡波西肉瘤细胞系活性最强,被选用于临床研究。所有剂量的A.P.L.治疗耐受性良好。在给予250、500、1000和2000国际单位的队列中,12个注射病变中分别有1、5、5和10个有反应(趋势P=0.03)。在250国际单位和500国际单位剂量下,各有一个病变完全肿瘤消退;1000国际单位剂量下有两个病变;2000国际单位剂量下有五个病变。在双盲研究中,注射稀释剂的6例患者的12个病变均无反应,而注射hCG的6例患者的12个病变中有10个有反应(P=0.015)。仅在hCG治疗的病变中观察到凋亡的微观证据。死亡细胞的百分比呈剂量依赖性增加(P<0.001)。最后一次注射hCG后,血清促卵泡激素水平(P=0.002)和促黄体生成素水平(P=0.001)下降,但在注射稀释剂的患者中对这些激素无影响。
病灶内注射hCG可使艾滋病相关卡波西肉瘤病变呈剂量依赖性消退。这些肿瘤的反应似乎是由凋亡诱导介导的。