Efficacy of brachytherapy for locally advanced bladder cancer: a single-center retrospective clinical study.

IF 4.4 4区 医学 Q2 ONCOLOGY
Cancer Biology & Therapy Pub Date : 2025-12-01 Epub Date: 2025-05-22 DOI:10.1080/15384047.2025.2509200
Xuebing Han, Huiqing Chen, Bin Wang
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引用次数: 0

Abstract

To explore the feasibility, safety, and effectiveness of brachytherapy of locally advanced bladder cancer, clinical data of 86 patients with locally advanced bladder cancer treated in the Department of Urology Surgery, Shanxi Provincial Cancer Hospital, between January 2015 and June 2019 were analyzed retrospectively. The patients were categorized into the study (n = 45) and control (n = 41) groups according to the treatment methods. Patients in the study group were treated with brachytherapy (intraoperative implantation of radioactive particles) + neoadjuvant chemotherapy (NAC), and those in the control group were treated with NAC. Patients in both groups underwent radical cystectomy (RC) + pelvic lymph node dissection. Postoperative pathological examinations proved that patients in both groups had urothelial carcinoma at stage pT3-pT4. The endpoints included 3-y locoregional recurrence-free survival (LRFS), distant metastasis-free survival (DMFS), disease-free survival (DFS), overall survival (OS), and adverse events after treatment. The efficacy and safety of interstitial implantation of radioactive particles for the treatment of locally advanced bladder cancer were assessed. The patients were followed up for 9-42 months. The 3-y LRFS was significantly higher in the study group (88.9%) than in the control group (60.9%) (p = .003). The 3-y DMFS in the study group (71.1%) and the control group (73.2%) was statistically similar (p = .945). The 3-y DFS and OS were not statistically significant between the two groups (DFS: study group 64.4% vs. control group 51.2%, p = .073; OS: study group 66.7% vs. control group 58.5%, p = .180). Local shifting of the particles was detected in three patients at 1 week to 1 month after the operations in the study group, but no related complications were observed. Blood events (anemia, leukocytopenia, and thrombocytopenia), liver and renal dysfunction, vomiting, diarrhea, and weakness were the major adverse reactions, which were alleviated after symptomatic treatments. The results have not statistically significant differences between the two groups in major adverse reactions. Compared to the NAC group, brachytherapy + NAC significantly prolongs the LRFS of patients with locally advanced urothelial bladder carcinoma who underwent RC + pelvic lymph node dissection. This surgery increases the LRFS, develops better personalized treatment plans, and improves treatment effectiveness. In addition, the treatment is safe and effective, with only limited adverse effects.

近距离放疗治疗局部晚期膀胱癌的疗效:单中心回顾性临床研究。
为探讨近距离放射治疗局部晚期膀胱癌的可行性、安全性和有效性,回顾性分析2015年1月至2019年6月山西省肿瘤医院泌尿外科收治的86例局部晚期膀胱癌患者的临床资料。根据治疗方法将患者分为研究组(n = 45)和对照组(n = 41)。研究组采用近距离放疗(术中植入放射性粒子)+新辅助化疗(NAC)治疗,对照组采用NAC治疗。两组患者均行根治性膀胱切除术+盆腔淋巴结清扫术。术后病理检查证实两组患者均为pT3-pT4期尿路上皮癌。终点包括3-y局部无复发生存期(LRFS)、远端无转移生存期(DMFS)、无病生存期(DFS)、总生存期(OS)和治疗后不良事件。评价放射性粒子间质植入治疗局部晚期膀胱癌的疗效和安全性。随访9 ~ 42个月。研究组3-y LRFS(88.9%)显著高于对照组(60.9%)(p = 0.003)。研究组3-y DMFS(71.1%)与对照组(73.2%)差异有统计学意义(p = .945)。两组患者3-y DFS和OS差异无统计学意义(DFS:研究组64.4% vs对照组51.2%,p = 0.073;OS:研究组66.7% vs.对照组58.5%,p = 0.180)。研究组3例患者术后1周至1个月出现颗粒局部移位,未见相关并发症。血液事件(贫血、白细胞减少、血小板减少)、肝肾功能障碍、呕吐、腹泻、虚弱为主要不良反应,对症治疗后症状减轻。结果两组在主要不良反应方面差异无统计学意义。与NAC组相比,近距离放疗+ NAC可显著延长局部晚期尿路上皮性膀胱癌行RC +盆腔淋巴结清扫的患者LRFS。这种手术增加了LRFS,制定了更好的个性化治疗计划,提高了治疗效果。此外,治疗是安全有效的,只有有限的副作用。
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来源期刊
Cancer Biology & Therapy
Cancer Biology & Therapy 医学-肿瘤学
CiteScore
7.00
自引率
0.00%
发文量
60
审稿时长
2.3 months
期刊介绍: Cancer, the second leading cause of death, is a heterogenous group of over 100 diseases. Cancer is characterized by disordered and deregulated cellular and stromal proliferation accompanied by reduced cell death with the ability to survive under stresses of nutrient and growth factor deprivation, hypoxia, and loss of cell-to-cell contacts. At the molecular level, cancer is a genetic disease that develops due to the accumulation of mutations over time in somatic cells. The phenotype includes genomic instability and chromosomal aneuploidy that allows for acceleration of genetic change. Malignant transformation and tumor progression of any cell requires immortalization, loss of checkpoint control, deregulation of growth, and survival. A tremendous amount has been learned about the numerous cellular and molecular genetic changes and the host-tumor interactions that accompany tumor development and progression. It is the goal of the field of Molecular Oncology to use this knowledge to understand cancer pathogenesis and drug action, as well as to develop more effective diagnostic and therapeutic strategies for cancer. This includes preventative strategies as well as approaches to treat metastases. With the availability of the human genome sequence and genomic and proteomic approaches, a wealth of tools and resources are generating even more information. The challenge will be to make biological sense out of the information, to develop appropriate models and hypotheses and to translate information for the clinicians and the benefit of their patients. Cancer Biology & Therapy aims to publish original research on the molecular basis of cancer, including articles with translational relevance to diagnosis or therapy. We will include timely reviews covering the broad scope of the journal. The journal will also publish op-ed pieces and meeting reports of interest. The goal is to foster communication and rapid exchange of information through timely publication of important results using traditional as well as electronic formats. The journal and the outstanding Editorial Board will strive to maintain the highest standards for excellence in all activities to generate a valuable resource.
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