Thalmann G N, Dewald B, Baggiolini M, Studer U E
Department of Urology, Inselspital and Theodor-Kocher Institute, University of Berne, Switzerland.
J Urol. 1997 Oct;158(4):1340-4.
We assessed whether interleukin-8 (IL-8), one of the first cytokines expressed in the urine after bacillus Calmette-Guerin (BCG) therapy for superficial urothelial tumors, may serve as a prognostic factor for treatment response.
Of 20 patients with superficial urothelial cancer of the urinary tract treated with BCG 13 had superficial bladder cancer and 7 received BCG perfusion of the upper urinary tract due to inoperability, solitary kidney, renal insufficiency or bilateral disease. After intravesical instillation of 120 mg. BCG or after 2-hour perfusion of the upper urinary tract with 360 mg. BCG urine was collected at 6-hour intervals. IL-8 was determined by solid phase double ligand enzyme-linked immunosorbent assay.
IL-8 was stable in the urine for more than 48 hours. At a median followup of 36.5 months treatment failure occurred in 10 of the 20 patients, including 3 with recurrence, 6 with progressive disease and 1 with extensive carcinoma in situ. IL-8 excretion was more than 4,000 ng. in the first 6 hours after BCG therapy in all 10 patients who remained disease-free. In 9 of the 10 patients with recurrent disease IL-8 excretion was less than 4,000 ng. in the first 6 hours after BCG therapy. Patients secreting less than 4,000 ng. IL-8 into the urine during the first 6 hours after BCG therapy had a significantly higher risk of tumor recurrence and progression (p <0.0002).
Due to its stability and kinetics IL-8 determined in urine collected during the first 6 hours after BCG therapy may prove to be a prognostic factor for tumor recurrence and progression after BCG therapy.
我们评估了白细胞介素-8(IL-8),即卡介苗(BCG)治疗浅表性尿路上皮肿瘤后尿液中最早表达的细胞因子之一,是否可作为治疗反应的预后因素。
20例接受BCG治疗的浅表性尿路尿路上皮癌患者中,13例患有浅表性膀胱癌,7例因无法手术、孤立肾、肾功能不全或双侧疾病接受上尿路BCG灌注。膀胱内灌注120mg BCG后或上尿路用360mg BCG灌注2小时后,每隔6小时收集尿液。通过固相双配体酶联免疫吸附测定法测定IL-8。
IL-8在尿液中稳定超过48小时。中位随访36.5个月时,20例患者中有10例出现治疗失败,包括3例复发、6例疾病进展和1例广泛原位癌。在所有10例无疾病复发的患者中,BCG治疗后的前6小时IL-8排泄量超过4000ng。在10例复发疾病患者中的9例中,BCG治疗后的前6小时IL-8排泄量小于4000ng。BCG治疗后前6小时尿液中IL-8分泌量小于4000ng的患者肿瘤复发和进展风险显著更高(p<0.0002)。
由于其稳定性和动力学特性,BCG治疗后前6小时收集的尿液中测定的IL-8可能被证明是BCG治疗后肿瘤复发和进展的预后因素。