Belldegrun A, Pierce W, Kaboo R, Tso C L, Shau H, Turcillo P, Moldawer N, Golub S, deKernion J, Figlin R
Department of Surgery, UCLA School of Medicine.
J Urol. 1993 Nov;150(5 Pt 1):1384-90. doi: 10.1016/s0022-5347(17)35785-3.
Murine models demonstrate therapeutic synergy for the combination of interleukin-2, interferon-alpha and tumor-infiltrating lymphocytes. We treated 11 patients with metastatic renal cell carcinoma with a novel regimen consisting of in vivo primed tumor-infiltrating lymphocytes, interferon-alpha and interleukin-2. Patients received interferon-alpha before radical nephrectomy; in vivo primed tumor-infiltrating lymphocytes were isolated and expanded in vitro. Low dose continuous infusion interleukin-2 at a dose of 2 x 10(6) units per m.2 per day was administered for 96 hours during each treatment week and interferon-alpha was administered as a subcutaneous injection at a dose of 6 x 10(6) units per m.2 per day on days 1 and 4 of the interleukin-2 infusion. No therapy was given during the last 3 days of a treatment week. One course of therapy consisted of 3 weeks of therapy followed by 3 weeks of rest. Patients were treated until maximal response, disease progression or dose limiting toxicity. A maximum of 6 courses of therapy were administered. Eleven patients underwent interferon-alpha priming and subsequent radical nephrectomy. In vivo primed tumor-infiltrating lymphocytes were successfully expanded in all 11 patients with an expansion index of greater than 170. In vivo primed tumor-infiltrating lymphocytes maintained their lytic activity for greater than 5 to 8 weeks in culture as demonstrated in the 4-hour 51chromium release assay. Ten patients underwent multimodality biological therapy and 3 (30%, 95% confidence interval 6 to 65%) have achieved complete response (2 clinical and 1 surgical) with durations of 24+, 23+ and 5+ months. Patients with stable disease received no additional therapy. No deaths and no grade 4 toxicities occurred. Immunotherapy using a combination of interferon-alpha primed tumor-infiltrating lymphocytes, low dose continuous infusion interleukin-2 and interferon-alpha can induce significant and durable antitumor responses in some patients with advanced renal cell carcinoma.
小鼠模型证明白细胞介素 -2、α干扰素和肿瘤浸润淋巴细胞联合使用具有治疗协同作用。我们用一种新方案治疗了11例转移性肾细胞癌患者,该方案包括体内致敏的肿瘤浸润淋巴细胞、α干扰素和白细胞介素 -2。患者在根治性肾切除术前行α干扰素治疗;分离出体内致敏的肿瘤浸润淋巴细胞并在体外进行扩增。在每个治疗周期间,以每天每平方米2×10⁶单位的剂量持续低剂量输注白细胞介素 -2,共96小时,α干扰素在白细胞介素 -2输注的第1天和第4天以每天每平方米6×10⁶单位的剂量皮下注射。在治疗周的最后3天不进行治疗。一个疗程包括3周治疗,随后休息3周。患者持续接受治疗,直至出现最大反应、疾病进展或剂量限制性毒性。最多给予6个疗程的治疗。11例患者接受了α干扰素预处理及随后的根治性肾切除术。所有11例患者体内致敏的肿瘤浸润淋巴细胞均成功扩增,扩增指数大于170。如4小时⁵¹铬释放试验所示,体内致敏的肿瘤浸润淋巴细胞在培养中保持其溶解活性超过5至8周。10例患者接受了多模式生物治疗,3例(30%,95%置信区间6%至65%)获得完全缓解(2例临床缓解和1例手术缓解),缓解持续时间分别为24个月以上、23个月以上和5个月以上。病情稳定的患者未接受额外治疗。未发生死亡病例,也未出现4级毒性反应。使用α干扰素致敏的肿瘤浸润淋巴细胞、低剂量持续输注白细胞介素 -2和α干扰素联合进行免疫治疗可在一些晚期肾细胞癌患者中诱导显著且持久的抗肿瘤反应。