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首页> 外文期刊>Medicine. >Bacillus Calmette-Guerin (BCG) Infection Following Intravesical BCG Administration as Adjunctive Therapy For Bladder Cancer Incidence, Risk Factors, and Outcome in a Single-Institution Series and Review of the Literature
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Bacillus Calmette-Guerin (BCG) Infection Following Intravesical BCG Administration as Adjunctive Therapy For Bladder Cancer Incidence, Risk Factors, and Outcome in a Single-Institution Series and Review of the Literature

机译:膀胱内BCG施用后卡介苗芽孢杆菌(BCG)感染作为单一机构系列膀胱癌发病率,危险因素和结果的辅助疗法并进行文献复习

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摘要

Bacillus Calmette-Guerin (BCG) is the most effective intravesical immunotherapy for superficial bladder cancer. Although generally well tolerated, BCG-related infectious complications may occur following instillation. Much of the current knowledge about this complication comes from single case reports, with heterogeneous diagnostic and therapeutic approaches and no investigation on risk factors for its occurrence. We retrospectively analyzed 256 patients treated with intravesical BCG in our institution during a 6-year period, with a minimum follow-up of 6 months after the last instillation. We also conducted a comprehensive review and pooled analysis of additional cases reported in the literature since 1975. Eleven patients (4.3%) developed systemic BCG infection in our institution, with miliary tuberculosis as the most common form (6 cases). A 3-drug antituberculosis regimen was initiated in all but 1 patient, with a favorable outcome in 9/10 cases. There were no significant differences in the mean number of transurethral resections prior to the first instillation, the time interval between both procedures, the overall mean number of instillations, or the presence of underlying immunosuppression between patients with or without BCG infection. We included 282 patients in the pooled analysis (271 from the literature and 11 from our institution). Disseminated (34.4%), genitourinary (23.4%), and osteomuscular (19.9%) infections were the most common presentations of disease. Specimens for microbiologic diagnosis were obtained in 87.2% of cases, and the diagnostic performances for acid-fast staining, conventional culture, and polymerase chain reaction (PCR)-based assays were 25.3%, 40.9%, and 41.8%, respectively. Most patients (82.5%) received antituberculosis therapy for a median of 6.0 (interquartile range: 4.0-9.0) months. Patients with disseminated infection more commonly received antituberculosis therapy and adjuvant corticosteroids, whereas those with reactive arthritis were frequently treated only with nonsteroidal antiinflammatory drugs (p<0.001 for all comparisons). Attributable mortality was higher for patients aged >= 65 years (7.4% vs 2.1%; p =0.091) and those with disseminated infection (9.9% vs 3.0%; p =0.040) and vascular involvement (16.7% vs 4.6%; p =0.064). The scheduled BCG regimen was resumed in only 2 of 36 patients with available data (5.6%), with an uneventful outcome. In the absence of an apparent predictor of the development of disseminated BCG infection after intravesical therapy, and considering the protean variety of clinical manifestations, it is essential to keep a high index of suspicion to initiate adequate therapy promptly and to evaluate carefully the risk-benefit balance of resuming intravesical BCG immunotherapy.
机译:卡介苗芽孢杆菌(BCG)是浅表性膀胱癌最有效的膀胱内免疫疗法。尽管一般耐受性良好,但滴注后可能会发生BCG相关的感染并发症。目前,关于这种并发症的许多知识都来自单例报告,其诊断和治疗方法多种多样,并且没有对其发生的危险因素进行调查。我们回顾性分析了我们机构在6年期间接受膀胱内BCG治疗的256例患者,最后一次滴注后至少随访6个月。自1975年以来,我们还对文献中报道的其他病例进行了全面回顾和汇总分析。在我们机构中,有11例患者(4.3%)发生了系统性BCG感染,其中以粟粒性结核病最为常见(6例)。除一名患者外,所有患者均开始了3药抗结核治疗方案,其中9/10例结果良好。初次滴注前经尿道切除术的平均次数,两次手术之间的时间间隔,总体平均滴注次数或有或没有BCG感染的患者之间均无显着差异。在汇总分析中,我们纳入了282例患者(文献中有271例,本机构中有11例)。传播性(34.4%),泌尿生殖道(23.4%)和骨肌(19.9%)感染是最常见的疾病表现。在87.2%的病例中获得了用于微生物学诊断的标本,用于耐酸染色,常规培养和基于聚合酶链反应(PCR)的检测的诊断性能分别为25.3%,40.9%和41.8%。大多数患者(82.5%)接受了抗结核治疗,中位时间为6.0(四分位间距:4.0-9.0)个月。传播感染的患者更常接受抗结核治疗和糖皮质激素辅助治疗,而反应性关节炎患者通常仅接受非甾体类抗炎药治疗(所有比较均p <0.001)。 > = 65岁的患者的可归因死亡率较高(7.4%vs 2.1%; p = 0.091)和那些具有弥散性感染的患者(9.9%vs 3.0%; p = 0.040)和血管受累(16.7%vs 4.6%; p = 0.064)。 36例患者中只有2例恢复了既定的BCG方案(5.6%),预后良好。在缺乏膀胱内治疗后弥散性BCG感染发展的明显预测指标,并考虑到各种蛋白质的临床表现时,必须保持高度怀疑,以便迅速开始适当治疗并仔细评估风险获益恢复膀胱内BCG免疫疗法的平衡。

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