Clinical Outcomes of Avelumab Maintenance Following Full-Dose, Reduced-Dose Cisplatin, or Carboplatin-Based Chemotherapy in Advanced Urothelial Carcinoma.

IF 2.7 Q2 UROLOGY & NEPHROLOGY
Research and Reports in Urology Pub Date : 2025-09-25 eCollection Date: 2025-01-01 DOI:10.2147/RRU.S554029
Nobuki Furubayashi, Jiro Tsujita, Azusa Takayama, Shin Nakashima, Motonobu Nakamura, Takahito Negishi
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引用次数: 0

Abstract

Background: Avelumab maintenance therapy is a standard of care for patients with advanced urothelial carcinoma (UC) who achieve disease control following platinum-based chemotherapy. However, the influence of induction chemotherapy intensity on avelumab outcomes remains unclear.

Materials and methods: This retrospective study included 26 patients with advanced UC who received avelumab maintenance after first-line platinum-based chemotherapy between March 2021 and June 2025. Patients were grouped by induction regimen: full-dose gemcitabine/cisplatin (GC), reduced-dose GC, or gemcitabine/carboplatin (GCarbo). Survival outcomes from the start of avelumab treatment and from chemotherapy initiation were analyzed using the Kaplan-Meier method and compared using the Log rank test.

Results: The median patient age was 72 years, with a significant difference among groups (P < 0.01). The objective response rates to induction chemotherapy were 60.0% (full-dose GC), 80.0% (reduced-dose GC), and 45.5% (GCarbo) (P=0.458), with respective disease control rates during avelumab maintenance of 50.0%, 100.0%, and 54.5% (P=0.188). The median progression-free survival (PFS) values from avelumab initiation were 4.0, 12.1, and 5.7 months, respectively (P=0.636). The median overall survival (OS) values from avelumab initiation were 21.7, 18.6, and 18.4 months (P=0.587), while those from chemotherapy initiation were 28.8, 28.7, and 29.0 months (P=0.496), in the respective groups. No significant differences in PFS or OS were observed among the three groups or between the GC-based and GCarbo regimens.

Conclusion: Avelumab maintenance showed comparable efficacy across the full-dose GC, reduced-dose GC, and GCarbo groups, highlighting the potential feasibility of personalized induction chemotherapy strategies. These findings may provide reassurance in clinical situations where full-dose cisplatin is not feasible due to patient frailty or renal dysfunction.

晚期尿路上皮癌全剂量、减剂量顺铂或卡铂化疗后Avelumab维持的临床结果
背景:Avelumab维持治疗是晚期尿路上皮癌(UC)患者在铂基化疗后实现疾病控制的标准护理。然而,诱导化疗强度对阿韦单抗结果的影响尚不清楚。材料和方法:该回顾性研究纳入了26例晚期UC患者,这些患者在2021年3月至2025年6月期间接受一线铂类化疗后接受了avelumab维持治疗。患者按诱导方案分组:全剂量吉西他滨/顺铂(GC)、减少剂量GC或吉西他滨/卡铂(GCarbo)。使用Kaplan-Meier方法分析avelumab治疗开始和化疗开始的生存结果,并使用Log rank检验进行比较。结果:患者中位年龄为72岁,组间差异有统计学意义(P < 0.01)。诱导化疗的客观有效率分别为60.0%(全剂量GC)、80.0%(减少剂量GC)和45.5% (GCarbo) (P=0.458), avelumab维持期间的疾病控制率分别为50.0%、100.0%和54.5% (P=0.188)。avelumab起始的中位无进展生存期(PFS)值分别为4.0个月、12.1个月和5.7个月(P=0.636)。在两组中,avelumab起始的中位总生存期(OS)值分别为21.7、18.6和18.4个月(P=0.587),而化疗起始的中位总生存期(OS)值分别为28.8、28.7和29.0个月(P=0.496)。在三组之间或基于gc和GCarbo的方案之间,PFS或OS未观察到显著差异。结论:Avelumab维持在全剂量GC组、减剂量GC组和GCarbo组均显示出相当的疗效,突出了个性化诱导化疗策略的潜在可行性。这些发现可能为临床情况提供保证,在全剂量顺铂是不可行的,因为病人虚弱或肾功能不全。
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来源期刊
Research and Reports in Urology
Research and Reports in Urology UROLOGY & NEPHROLOGY-
CiteScore
3.40
自引率
0.00%
发文量
60
审稿时长
16 weeks
期刊介绍: Research and Reports in Urology is an international, peer-reviewed, open access, online journal. Publishing original research, reports, editorials, reviews and commentaries on all aspects of adult and pediatric urology in the clinic and laboratory including the following topics: Pathology, pathophysiology of urological disease Investigation and treatment of urological disease Pharmacology of drugs used for the treatment of urological disease Although the main focus of the journal is to publish research and clinical results in humans; preclinical, animal and in vitro studies will be published where they will shed light on disease processes and potential new therapies. Issues of patient safety and quality of care will also be considered.
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