PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
September 5, 2025The Oncologist0 citationsOpen Access

IUC24432-80 Neoadjuvant or induction chemotherapy (N/IC) for bladder cancer: updated “real-world” experience from Croatia

View Full Paper
JMJure MurgićMJMarijana JazvićITIgor Tomašković

Key Points

  • Pathologic complete response was associated with improved disease-free and overall survival in bladder cancer patients.
  • In a cohort of 289 patients, the overall survival was a median of 41 months, with 34% experiencing recurrence.
  • Cox regression analysis indicated that pathologic complete response significantly impacts survival outcomes.
  • Real-world data highlights the need for broader adoption of neoadjuvant chemotherapy in the treatment of muscle-invasive bladder cancer.

Abstract

Abstract Background Despite level I evidence and known overall survival (OS) benefit of cisplatin-based neoadjuvant chemotherapy (NAC) for muscle-invasive bladder cancer (MIBC), its use remains suboptimal and varies geographically. We report treatment patterns and outcomes in patients (pts) receiving N/IC within the Croatian Uro-Oncology Network. Methods We retrospectively reviewed records of consecutive patients treated with N/IC. Endpoints included pathologic complete response (pCR, ypT0N0), major pathologic response (MPR, ypT ≤ 1N0), disease-free survival (DFS), and OS. Survival was estimated from the N/IC start using Kaplan–Meier and log-rank tests. Clinical variables were assessed via Cox regression. Results A total of 289 patients received N/IC across 9 sites. Clinical stage: II (45%), IIIA (29%), IIIB (24%). Median age was 66 years (range 40-83); 76% were male; 18% had ECOG PS 1; 23% had histologic variants. Regimens included cisplatin/gemcitabine (70%), dose-dense MVAC (24%), carboplatin/gemcitabine (3%), and cisplatin/etoposide (2%). Median duration was 2 months; median 4 cycles. Grade ≥3 toxicity occurred in 45%, including neutropenia (G3 18%, G4 10%), anemia (G3 7%), thrombocytopenia (G3 13%), and mucositis (G3 7%). Cystectomy was performed in 226 patients (78%). The median time from N/IC start to surgery was 4 months; from N/IC end to surgery, 2 months. Reasons for non-surgical management included progression (n = 13), refusal (n = 14), bladder preservation (n = 8), or ECOG deterioration (n = 4). Among operated patients, pCR and MPR were achieved in 23% and 38%, respectively. After a median follow-up of 35 months, 34% had a recurrence (22% distant, 7% locoregional, 6% both). Median DFS was 33 months (95% CI, 15-56), and OS was 41 months (95% CI, 25-91). On multivariable analysis, only pCR was independently associated with improved DFS (HR 0.2; P .0001) and OS (HR 0.3; P = .0002). Nine pts (4%) received adjuvant radiotherapy; none received adjuvant nivolumab. Conclusions In this national real-world cohort, pCR was associated with improved survival, consistent with clinical trial data. Broader adoption of N/IC will require multidisciplinary care and structured patient counseling.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Murgić et al. (2025) studied this question.

synapsesocial.com/papers/68bb5f7a6d6d5674bcd03c23https://doi.org/10.1093/oncolo/oyaf248.028
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Real-world neoadjuvant therapy utilization and outcomes in patients with muscle-invasive bladder cancer ineligible for cisplatin treatment.2026
  2. 2Neoadjuvant cisplatin-based chemotherapy followed by selective bladder preservation chemoradiotherapy in muscle-invasive urothelial carcinoma of the bladder: Post hoc analysis of two prospective studies.2024
  3. 3Bladder-sparing chemoradiotherapy following neoadjuvant chemotherapy for muscle-invasive bladder cancer: a retrospective cohort study2026
  4. 4ddMVAC versus gemcitabine–cisplatin as neoadjuvant treatment for muscle-invasive urothelial bladder cancer: a multicenter real-world study2026
  5. 5Neoadjuvant chemotherapy of node-positive M0 urothelial bladder cancer.2026