Evidence map›Paper›PMID 41657564›Full record

ArticleFrontiers in medicine2025

Treatment of metastatic bladder paraganglioma with cadonilimab plus radiotherapy: a case report and literature review.

RiHan Wu, ZiRui Wang, YuanRui Bai, Yihui Liu, Chunhui Dong, Ling Chen

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Article in Frontiers in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

RiHan Wu *Department of Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
ZiRui Wang *Health Science Center, Xi'an Jiaotong University, Xi'an, China.
YuanRui BaiDepartment of Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Yihui LiuRadiotherapy Oncology, People's Hospital of Ningxia Hui Autonomous Region, Yinchuan, China.
Chunhui DongCardiovascular Hospital, Ninth Hospital of Xi'an, Xi'an, China.
Ling ChenDepartment of Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Bladder paraganglioma (PPGL) is a rare neuroendocrine tumor associated with a lower survival rate compared to paragangliomas originating in other anatomical locations. Surgical resection is still the primary treatment modality for bladder paraganglioma; however, this approach carries a significant risk of malignant metastasis. Once metastasis occurs, therapeutic options become notably limited. The response rate and 5-year overall survival for bladder paraganglioma treated with cyclophosphamide, vincristine, and dacarbazine (CVD) chemotherapy are relatively low. Recent advancements in tumor immunotherapy, particularly antibodies targeting CTLA-4 and PD-1/PD-L1, have effectively treated various cancers, including neuroendocrine tumors. These immunotherapeutic approaches offer promising alternatives and potentially improve outcomes for patients with metastatic bladder paraganglioma. Case description: A 44-year-old male presented with intermittent hematuria, abdominal pain, and frequent urination. Pre-operative computed tomography (CT) revealed a neuroendocrine tumor and a laparoscopic partial cystectomy was subsequently performed. Post-operative pathology confirmed paraganglioma of the bladder, with immunohistochemical results showing SYN (+), P504S (+/-), and Ki-67 (+20%). The patient's post-operative symptoms resolved, returning to normal. However, recurrence occurred 33 months post-surgery. The patient later received 11 cycles of cadonilimab and local radiation therapy, with tumor progression evaluated via imaging every 2 months. During the follow-up period, the patient maintained stable disease for 12 months. After local progression, the patient received targeted therapy, chemotherapy, and palliative treatment. Survival time after recurrence is 25 months. Overall survival from diagnosis is 58 months. Conclusions: We report, for the first time, a case of metastatic bladder paraganglioma in which a patient treated with cadonilimab in combination with radiotherapy maintained stable disease for 12 months. These results demonstrate that this combination therapy may be a potential treatment option for bladder paraganglioma.

Indexed as

bladder paragangliomacadonilimabcase reportliterature reviewradiotherapy

Identifiers

PMID41657564
PMCPMC12872470

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.