Lüftenegger W, Ackermann D K, Futterlieb A, Kraft R, Minder C E, Nadelhaft P, Studer U E
Department of Urology, University of Berne, Switzerland.
J Urol. 1996 Feb;155(2):483-7. doi: 10.1016/s0022-5347(01)66427-9.
Intravesical instillation of bacillus Calmette-Guerin (BCG) induces various immunological reactions and decreases the recurrence rate of superficial bladder tumors. To determine whether additional immune stimulation with concomitant intradermal BCG applications could further lower the recurrence rate, 154 patients with superficial bladder tumors at high risk for recurrence were randomized to receive either 6 intravesical instillations of 120 mg. Pasteur strain BCG alone or combined with intradermal application.
A total of 76 patients received intravesical and intradermal BCG, while 78 received intravesical BCG only. Median followup was 41 months (range 2 to 89) and 36 months (range 2 to 86), respectively. Both treatment groups were comparable regarding patient age and number of previous transurethral bladder tumor resections, as well as tumor recurrence rate, stage and grade before BCG therapy.
A highly significant decrease in the monthly tumor recurrence rate was observed in both arms after BCG compared to the pretreatment recurrence rates (p < 0.0001). Recurrence rate decreased from 0.73 +/- 1.07 (standard deviation) to 0.06 +/- 0.13 in the combined treatment group and from 0.71 +/- 0.90 to 0.074 +/- 0.17 in the intravesical treatment only group. However, we were unable to find any difference between the 2 groups regarding interval to initial recurrence or recurrence rates after BCG treatment. Changes in the purified protein derivative skin test performed before and after BCG therapy were not useful to predict response to treatment because 44% of our patients already had a positive test before treatment. Also, interpretation of the skin test was difficult and not always reliable. In the multivariate analysis, however, fever was an important prognostic factor. Patients with increased body temperature greater than 37.5C had a significantly lower recurrence rate than those without fever (37.5C or less) after BCG instillation (p = 0.009). Moreover, fever after BCG instillation was observed significantly more frequently in patients with a positive purified protein derivative skin test before treatment (p = 0.021).
The therapeutic benefit from intravesical BCG apparently was not substantially improved by simultaneous intradermal BCG vaccination. Fever following intravesical BCG instillation is an important prognostic factor regarding superficial bladder tumor recurrence. Fever occurs predominantly in patients who were previously sensitized to mycobacteria (by BCG vaccination or infection) as shown by a positive pretreatment purified protein derivative skin test. This finding suggests that previously sensitized patients respond significantly better to a single course of intravesical BCG.
膀胱内灌注卡介苗(BCG)可引发多种免疫反应,并降低浅表性膀胱肿瘤的复发率。为确定同时进行皮内注射BCG带来的额外免疫刺激是否能进一步降低复发率,将154例具有高复发风险的浅表性膀胱肿瘤患者随机分为两组,一组仅接受6次膀胱内灌注120mg巴斯德菌株BCG,另一组在膀胱内灌注的基础上联合皮内注射。
76例患者接受膀胱内及皮内注射BCG,78例仅接受膀胱内注射BCG。两组的中位随访时间分别为41个月(范围2至89个月)和36个月(范围2至86个月)。两个治疗组在患者年龄、既往经尿道膀胱肿瘤切除术次数、BCG治疗前的肿瘤复发率、分期及分级方面具有可比性。
与治疗前复发率相比,两组患者在接受BCG治疗后每月肿瘤复发率均显著降低(p<0.0001)。联合治疗组的复发率从0.73±1.07(标准差)降至0.06±0.13,单纯膀胱内治疗组从0.71±0.90降至0.074±0.17。然而,我们未能发现两组在首次复发间隔时间或BCG治疗后的复发率方面存在差异。BCG治疗前后进行的纯化蛋白衍生物皮肤试验的变化对预测治疗反应并无帮助,因为44%的患者在治疗前该试验即为阳性。此外,皮肤试验的解读困难且并非总是可靠。在多因素分析中,发热是一个重要的预后因素。体温高于37.5℃的患者在接受BCG灌注后的复发率显著低于体温未升高(37.5℃及以下)的患者(p = 0.009)。此外,治疗前纯化蛋白衍生物皮肤试验呈阳性的患者在接受BCG灌注后发热的发生率明显更高(p = 0.021)。
同时进行皮内注射BCG并未显著提高膀胱内灌注BCG的治疗效果。膀胱内灌注BCG后出现发热是浅表性膀胱肿瘤复发的一个重要预后因素。发热主要发生在先前对分枝杆菌致敏的患者中(通过BCG接种或感染),治疗前纯化蛋白衍生物皮肤试验呈阳性即表明这一点。这一发现提示,先前致敏的患者对单一疗程的膀胱内BCG治疗反应明显更好。