# Complete Response to Pembrolizumab After Progression on Avelumab Maintenance in Metastatic Urothelial Carcinoma

**Authors:** Fumihiro Ito, Koki Kobayashi, Gaku Hayashi, Shunsuke Kamijo, Takashi Fujita

PMC · DOI: 10.1002/iju5.70160 · IJU Case Reports · 2026-03-08

## TL;DR

A patient with advanced bladder cancer achieved a complete response to pembrolizumab after progressing on avelumab, suggesting that switching immunotherapy drugs can overcome resistance.

## Contribution

Demonstrates that switching from PD-L1 to PD-1 inhibitors may overcome resistance in metastatic urothelial carcinoma.

## Key findings

- The patient achieved a complete response to pembrolizumab after progressing on avelumab.
- He remained recurrence-free for three years without immune-related adverse events.
- The case suggests that PD-L2 assessment and biomarker strategies may guide rechallenge decisions.

## Abstract

Avelumab maintenance after response to platinum chemotherapy improves outcomes in metastatic urothelial carcinoma. Progression during maintenance presents a therapeutic dilemma.

A 72‐year‐old man underwent radical cystectomy and left nephroureterectomy for high‐grade urothelial carcinoma. Two and a half years later, a solitary pelvic nodal recurrence achieved complete response to gemcitabine–cisplatin, after which avelumab maintenance was started. After 16 cycles, the same node regrew, indicating progression. Pembrolizumab was initiated and induced a second complete response after four cycles. He remains recurrence‐free for three years without immune‐related adverse events.

Durable remission with pembrolizumab following progression on avelumab suggests that switching from PD‐L1 to PD‐1 blockade can overcome resistance in selected patients; prospective studies and biomarker strategies, including PD‐L2 assessment, are warranted and may guide individualized rechallenge strategies.

## Linked entities

- **Chemicals:** gemcitabine (PubChem CID 60750), cisplatin (PubChem CID 5460033)
- **Diseases:** urothelial carcinoma (MONDO:0040679)

## Full-text entities

- **Genes:** PDCD1LG2 (programmed cell death 1 ligand 2) [NCBI Gene 80380] {aka B7DC, Btdc, CD273, PD-L2, PDCD1L2, PDL2}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, TENM1 (teneurin transmembrane protein 1) [NCBI Gene 10178] {aka ODZ1, ODZ3, TEN-M1, TEN1, TNM, TNM1}
- **Diseases:** Urothelial Carcinoma (MESH:D014523), hypertension (MESH:D006973), nodal lesion (MESH:D013611), melanoma (MESH:D008545), malignancies (MESH:D009369), lung cancer (MESH:D008175)
- **Chemicals:** cisplatin (MESH:D002945), EV-301 (-), Pembrolizumab (MESH:C582435), gemcitabine (MESH:D000093542), formalin (MESH:D005557), paraffin (MESH:D010232), platinum (MESH:D010984), Avelumab (MESH:C000609138), PS (MESH:D010758), Enfortumab vedotin (MESH:C000632577)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12967568/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12967568/full.md

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Source: https://tomesphere.com/paper/PMC12967568