Lindsey K R, Rosenberg S A, Sherry R M
Surgery Branch, Division of Clinical Sciences, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892-1502, USA.
J Clin Oncol. 2000 May;18(9):1954-9. doi: 10.1200/JCO.2000.18.9.1954.
To determine the impact of treatment with successive courses of high-dose bolus interleukin-2 (IL-2) on the incidence of clinical responses in patients with metastatic melanoma or renal cell cancer.
A consecutive series of 350 patients with either metastatic melanoma or renal cell cancer who were treated with high-dose bolus IL-2 in the Surgery Branch, National Cancer Institute, between September 1985 and November 1996 was analyzed, with a median potential follow-up of 7.1 years. All patients were treated with 720,000 IU/kg of IL-2 administered by a 15-minute intravenous infusion every 8 hours for up to 5 days, as clinically tolerated per cycle. Patients were retreated according to clinical response and tolerance to the IL-2 therapy.
Of the 149 patients with melanoma, 10 achieved complete responses (CRs) and 13 partial responses (PRs), for an overall response rate of 15.4%. Of the 201 patients with renal cell cancer, 18 achieved CRs and 20 PRs, for an overall response rate of 19.0%. Among responding patients, 21 of 23 with melanoma and 34 of 38 with renal cell cancer developed at least PRs after the first course of IL-2.
Most patients with metastatic melanoma and renal cell cancer who achieved PRs or CRs to intravenous high-dose bolus IL-2 were identified after the first course of therapy. Those who demonstrated no response after two treatment courses failed to respond to additional IL-2 therapy. Based on this retrospective analysis, we recommend that patients who exhibit objective responses to treatment with high-dose bolus IL-2 receive additional treatment courses until either CR or IL-2 intolerance develops. Patients who do not achieve objective responses after two courses of IL-2 should receive no further treatment with this regimen.
确定连续大剂量推注白细胞介素-2(IL-2)治疗对转移性黑色素瘤或肾细胞癌患者临床反应发生率的影响。
分析了1985年9月至1996年11月期间在国立癌症研究所外科分部接受大剂量推注IL-2治疗的350例转移性黑色素瘤或肾细胞癌患者,中位潜在随访时间为7.1年。所有患者每8小时静脉输注720,000 IU/kg的IL-2,持续15分钟,每周期最多5天,具体根据临床耐受性而定。患者根据临床反应和对IL-2治疗的耐受性进行再次治疗。
149例黑色素瘤患者中,10例获得完全缓解(CR),13例获得部分缓解(PR),总缓解率为15.4%。201例肾细胞癌患者中,18例获得CR,20例获得PR,总缓解率为19.0%。在有反应的患者中,黑色素瘤患者23例中有21例、肾细胞癌患者38例中有34例在第一疗程IL-2治疗后至少达到PR。
大多数对静脉大剂量推注IL-2有PR或CR的转移性黑色素瘤和肾细胞癌患者在第一疗程治疗后即可确定。在两个疗程治疗后无反应的患者对额外的IL-2治疗无反应。基于这项回顾性分析,我们建议对大剂量推注IL-2治疗有客观反应的患者接受额外疗程的治疗,直至出现CR或IL-2不耐受。在两个疗程IL-2治疗后未达到客观反应的患者不应再接受该方案的进一步治疗。