# Adjuvant treatment preferences in high-risk upper tract urothelial carcinoma: the perspective of Portuguese medical oncologists

**Authors:** Guilherme Vilhais, Mário Fontes-Sousa

PMC · DOI: 10.1093/oncolo/oyaf365 · The Oncologist · 2025-10-30

## TL;DR

Portuguese medical oncologists prefer platinum-based chemotherapy for high-risk upper tract urothelial carcinoma, even when PD-L1 status varies.

## Contribution

This study reveals adjuvant treatment preferences of Portuguese oncologists for high-risk UTUC based on PD-L1 status and cisplatin eligibility.

## Key findings

- Cisplatin plus gemcitabine is the preferred regimen for cisplatin-eligible patients regardless of PD-L1 status.
- In cisplatin-ineligible PD-L1-positive patients, carboplatin plus gemcitabine is preferred over immune checkpoint inhibitors.
- Preferences reflect reliance on UTUC-specific evidence and limited perceived benefit from ICIs in this subgroup.

## Abstract

Although upper tract urothelial carcinoma (UTUC) and bladder urothelial carcinoma (BUC) share histological features, they differ in clinical behavior and management. Valid adjuvant options include surveillance, platinum-based chemotherapy, and immune checkpoint inhibitors (ICIs). To assess real-world practice, we conducted a survey among Portuguese medical oncologists dedicated to genitourinary malignancies, exploring their preferences for adjuvant therapy in high-risk UTUC (illustrated as pT2N1M0) across three clinical scenarios that differed by PD-L1 status and renal function. Among 34 respondents, cisplatin plus gemcitabine was the preferred regimen in cisplatin-eligible patients, regardless of PD-L1 status (94% in PD-L1-negative and 85% in PD-L1-positive tumors). In PD-L1-positive, cisplatin-ineligible patients, carboplatin plus gemcitabine was preferred (47%), followed by ICIs (44%). These findings suggest a consistent preference for platinum-based chemotherapy, likely reflecting UTUC-specific evidence from the POUT trial and apparent limited ICI benefit in this subgroup, underscoring the need for dedicated prospective trials.

## Linked entities

- **Chemicals:** cisplatin (PubChem CID 5460033), gemcitabine (PubChem CID 60750), carboplatin (PubChem CID 426756)
- **Diseases:** upper tract urothelial carcinoma (MONDO:0020654), urothelial carcinoma (MONDO:0040679)

## Full-text entities

- **Genes:** CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}
- **Diseases:** UTUC (MESH:D012141), BUC (MESH:D001749), tumors (MESH:D009369), genitourinary malignancies (MESH:D014565)
- **Chemicals:** carboplatin (MESH:D016190), gemcitabine (MESH:D000093542), platinum (MESH:D010984), cisplatin (MESH:D002945)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12619994/full.md

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Source: https://tomesphere.com/paper/PMC12619994