Thalmann G N, Sermier A, Rentsch C, Möhrle K, Cecchini M G, Studer U E
Department of Urology, University of Berne, Berne, Switzerland.
J Urol. 2000 Dec;164(6):2129-33.
We evaluate the predictive value of urinary cytokine levels of interleukin (IL) 8 and 18 for response in patients receiving intravesical bacillus Calmette-Guerin (BCG) for prevention of recurrences of superficial bladder cancer and treatment of carcinoma in situ.
In 28 patients with superficial bladder cancer treated with BCG IL-8 expression in the urine during the first 6 hours after the first BCG instillation was determined. In 17 patients IL-18 levels were also evaluated during the first 12 hours after BCG instillation. IL-8 and 18 levels were determined by solid phase double ligand enzyme-linked immunosorbent assay.
In 12 of the 28 patients assessed for IL-8 expression disease recurred after a median followup of 66 months. Median IL-8 expression during the first 6 hours for these patients was 851 ng. (range 232 to 8,497). Median IL-8 expression during the first 6 hours in patients without recurrence was 4,200 ng. (range 432 to 12, 232). Of 8 patients with a followup of greater than 36 months 7 (88%) had no recurrent disease and IL-8 levels greater than 4,000 ng. Patients secreting more than 4,000 ng. IL-8 into the urine after BCG have a significantly higher chance of remaining disease-free (p <0.05), and those with elevated IL-18 expression have a significantly longer disease-free survival (p <0.05). After a median followup of 23 months (range 7 to 93) 6 of the 17 patients assessed for IL-18 expression had treatment failure. Median IL-18 expression in those patients during the first 12 hours was 2,632 pg. (range 860 to 8,298). Median IL-18 expression during the first 12 hours in patients without recurrence was 12,258 pg. (range 1,727 to 151,495).
In this study we confirmed the value of quantitative IL-8 expression in the urine during the first 6 hours after BCG instillation for superficial bladder cancer to predict freedom of disease. Furthermore, to our knowledge we report for the first time the potential value of IL-18 expression in the urine during the first 12 hours after BCG to predict freedom from disease. These findings may help improve the treatment of patients with superficial bladder cancer, especially by identifying those with a high risk of disease recurrence and progression after BCG therapy.
我们评估了白细胞介素(IL)-8和IL-18尿细胞因子水平对接受膀胱内卡介苗(BCG)预防浅表性膀胱癌复发及原位癌治疗患者反应的预测价值。
对28例接受BCG治疗的浅表性膀胱癌患者,测定首次BCG灌注后最初6小时尿液中的IL-8表达。对17例患者还评估了BCG灌注后最初12小时的IL-18水平。采用固相双配体酶联免疫吸附测定法测定IL-8和IL-18水平。
在评估IL-8表达的28例患者中,12例在中位随访66个月后疾病复发。这些患者最初6小时的IL-中位数为851 ng(范围232至8497)。未复发患者最初6小时的IL-8中位数为4200 ng(范围432至12232)。在随访超过36个月的8例患者中,7例(88%)无疾病复发且IL-8水平大于4000 ng。BCG灌注后尿液中分泌IL-8超过4000 ng的患者无病生存几率显著更高(p<0.05),且IL-18表达升高的患者无病生存期显著更长(p<0.05)。在中位随访23个月(范围7至93个月)后,评估IL-18表达的17例患者中有6例治疗失败。这些患者最初12小时的IL-18中位数为2632 pg(范围860至8298)。未复发患者最初12小时的IL-18中位数为12258 pg(范围1727至151495)。
在本研究中,我们证实了BCG灌注后最初6小时尿液中定量IL-8表达对预测浅表性膀胱癌无病状态的价值。此外,据我们所知,我们首次报告了BCG灌注后最初12小时尿液中IL-18表达对预测无病状态的潜在价值。这些发现可能有助于改善浅表性膀胱癌患者的治疗,特别是通过识别BCG治疗后疾病复发和进展风险高的患者。