# The first real-world evidence on dose-dense methotrexate, vinblastine, doxorubicin, and cisplatin followed by switch maintenance avelumab in advanced urothelial carcinoma: a propensity score-matched study

**Authors:** Satoru Taguchi, Taketo Kawai, Yoshiaki Kurokawa, Naoki Saegusa, Masahiro Yamamoto, Yoshiki Ambe, Kazuki Honda, Kazuki Maki, Yoichi Fujii, Jimpei Miyakawa, Yuumi Tokura, Hazuki Inoue, Tomoyuki Kaneko, Takehiro Tanaka, Katsuhiko Nara, Jun Kamei, Shigenori Kakutani, Yuta Yamada, Aya Niimi, Daisuke Yamada, Tappei Takada, Tohru Nakagawa, Haruki Kume

PMC · DOI: 10.1007/s10147-025-02729-x · 2025-03-03

## TL;DR

This study shows that using dd-MVAC followed by avelumab improves survival in patients with advanced urothelial carcinoma.

## Contribution

First real-world evidence of dd-MVAC followed by avelumab in advanced urothelial carcinoma.

## Key findings

- Median overall survival was 24 months and progression-free survival was 7 months.
- Patients receiving avelumab had significantly longer survival compared to those who did not.
- dd-MVAC followed by avelumab remains a valid treatment option in the new treatment landscape.

## Abstract

Dose-dense methotrexate, vinblastine, doxorubicin, and cisplatin (dd-MVAC) is an established regimen for advanced urothelial carcinoma (aUC). Although platinum-based chemotherapy, typically gemcitabine and cisplatin, followed by switch maintenance avelumab has been a recommended strategy for aUC, no study has evaluated outcomes of dd-MVAC followed by avelumab therapy.

We reviewed 71 patients treated with first-line dd-MVAC for aUC at two university hospitals between 2018 and 2024. Overall survival (OS) and progression-free survival (PFS) were assessed as endpoints. Additionally, among patients who achieved ≥ stable disease, we performed propensity score matching between patients with and without avelumab to balance their background characteristics.

Of 71 patients, 49 (69%) experienced disease progression and 30 (42%) died during the median follow-up of 13 months. Median OS and PFS were 24 and 7 months, respectively. Among 59 patients who achieved ≥ stable disease after completion of dd-MVAC, 35 received switch maintenance avelumab, while the remaining 24 did not. After propensity score matching, patients with avelumab had significantly longer OS and PFS (both: not reached) than those without (OS: 28 months; PFS: 7 months).

We herein report outcomes of dd-MVAC followed by switch maintenance avelumab in real-world patients with aUC for the first time. Avelumab therapy was significantly associated with longer survival in patients who achieved ≥ stable disease after first-line dd-MVAC. Given the excellent survival outcomes, dd-MVAC followed by switch maintenance avelumab may still be a valid option for aUC even in the new treatment paradigm as typified by enfortumab vedotin and pembrolizumab.

The online version contains supplementary material available at 10.1007/s10147-025-02729-x.

## Linked entities

- **Chemicals:** methotrexate (PubChem CID 4112), vinblastine (PubChem CID 13342), doxorubicin (PubChem CID 31703), cisplatin (PubChem CID 5460033)

## Full-text entities

- **Diseases:** aUC (MESH:D014523)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12014834/full.md

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Source: https://tomesphere.com/paper/PMC12014834