# Rare Case of Collecting Duct Carcinoma With Complete Response to Nivolumab

**Authors:** Muhammed Hajmusa, Gi Eun Kim, Mohammed Ussama Al Homsi, Ahmed Abdalhadi

PMC · DOI: 10.1155/crom/9619945 · 2025-10-28

## TL;DR

A rare kidney cancer case showed complete remission after treatment with nivolumab and radiotherapy.

## Contribution

Demonstrates a durable complete response to nivolumab in a rare and aggressive kidney cancer subtype.

## Key findings

- The patient achieved a complete radiographic remission lasting over 5 years with nivolumab.
- Combining nivolumab with stereotactic radiotherapy led to sustained tumor regression.
- Genomic profiling identified CDKN2A deletion, guiding targeted therapy.

## Abstract

Collecting duct carcinoma (CDC) is a rare, aggressive subtype of renal cell carcinoma originating in the renal medulla. We report a unique case of metastatic CDC in a patient with prior breast ductal carcinoma in situ. Genomic profiling revealed a homozygous deletion of CDKN2A (encoding p16). After progression on systemic therapies, the patient received stereotactic body radiotherapy (SBRT) to metastatic lesions concurrently with nivolumab (anti-PD-1). This regimen achieved a rapid complete radiographic remission of all lesions. We present a 63-year-old Sudanese woman with metastatic CDC who achieved a complete remission of over 5 years following nivolumab therapy. The patient initially presented with right flank pain and hematuria. Imaging revealed an exophytic renal mass, and she underwent radical nephrectomy in June 2019. Pathology confirmed high-grade CDC (pT3aN1) with clear margins; immunohistochemistry was notable for positive vimentin, PAX8, CK19, and patchy AMACR, with loss of CDKN2A. Postoperative PET/CT was clear, but by October 2019, three intra-abdominal metastases were seen (liver and retroperitoneum). She was first treated with palbociclib and letrozole, but progression occurred after 3 months. Given reports of immunotherapy efficacy in CDC, she began nivolumab in May 2020. Imaging in October 2020 showed marked tumor regression, sustained on repeat scans. In September 2021, isolated para-aortic lymph node recurrence was treated with stereotactic radiation (20–25 Gy/5 fractions) while continuing nivolumab. Subsequent PET/CT scans (Feb 2022, Feb 2023, June 2023, March 2024, and January 2025) demonstrated continued complete metabolic response. This combined modality approach achieved an unprecedented durable response, underscoring that personalized multimodal therapy—linking radiotherapy, immunotherapy and targeted cell-cycle inhibition—can yield long-term control in CDC. For a disease as lethal as CDC, this outcome demonstrates that genomically informed therapy can achieve extraordinary benefit.

## Linked entities

- **Genes:** CDKN2A (cyclin dependent kinase inhibitor 2A) [NCBI Gene 1029]
- **Chemicals:** palbociclib (PubChem CID 5330286), letrozole (PubChem CID 3902)
- **Diseases:** collecting duct carcinoma (MONDO:0005220), breast ductal carcinoma in situ (MONDO:0005023)

## Full-text entities

- **Genes:** SPATA2 (spermatogenesis associated 2) [NCBI Gene 9825] {aka PD1, PPP1R145, tamo}, VIM (vimentin) [NCBI Gene 7431], CDKN2A (cyclin dependent kinase inhibitor 2A) [NCBI Gene 1029] {aka ARF, CAI2, CDK4I, CDKN2, CMM2, INK4}, AMACR (alpha-methylacyl-CoA racemase) [NCBI Gene 23600] {aka AMACRD, CBAS4, P504S, RACE, RM}, KRT19 (keratin 19) [NCBI Gene 3880] {aka CK19, K19, K1CS}, PAX8 (paired box 8) [NCBI Gene 7849] {aka PAX-8}
- **Diseases:** flank pain (MESH:D021501), hematuria (MESH:D006417), metastases (MESH:D009362), tumor (MESH:D009369), CDC (MESH:D002292), breast ductal carcinoma in situ (MESH:D018270), renal mass (MESH:C536030)
- **Chemicals:** letrozole (MESH:D000077289), palbociclib (MESH:C500026), Nivolumab (MESH:D000077594)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12585813/full.md

---
Source: https://tomesphere.com/paper/PMC12585813