Durable and deep response to CVD chemotherapy in SDHB-mutated metastatic paraganglioma: case report

Front Endocrinol (Lausanne). 2024 Dec 18:15:1483516. doi: 10.3389/fendo.2024.1483516. eCollection 2024.

Abstract

Introduction: Succinate dehydrogenase subunit B (SDHB)-mutated paragangliomas (PGLs) are rare neuroendocrine tumors characterized by increased malignancy, readily metastasizing, and poorer prognosis. Here we report a case of SDHB-mutated metastatic PGL, wherein the patient showed significant tumor shrinkage and complete symptom remission following chemotherapy. We aim to contribute additional evidence to the existing knowledge associated with SDHB-mutated PGLs.

Case report: A 40-year-old male patient presented with recurrent hypoglycemia and hypertension crisis. Imaging revealed a huge left retroperitoneal tumor and multiple diffuse metastases in lungs. Catecholamine was also elevated, aligning with a diagnosis of metastatic PGL. Pathology also confirmed this diagnosis. Additionally, the immunohistochemistry indicated negative expression of SDHB and gene test showed somatic SDHB mutation. Given the SDHB mutation, cyclophosphamide-vincristine-dacarbazine (CVD) chemotherapy was initiated in critical conditions. Subsequently, a significant tumor shrinkage and complete biochemical response were observed after two treatment cycles. In September 2024, CT scan revealed new pulmonary lesions. The progression-free survival (PFS) with CVD chemotherapy was 24 months.

Conclusion: This report reviews the distinct clinical and biochemical characteristics and treatment approaches of SDHB-mutated paragangliomas, emphasizing that the significance of incorporating both genetic testing and immunohistochemical analysis in clinical practice.

Keywords: CVD chemotherapy; SDHB-mutation; case report; hypoglycemia; metastatic paraganglioma.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Antineoplastic Combined Chemotherapy Protocols* / therapeutic use
  • Cyclophosphamide* / administration & dosage
  • Cyclophosphamide* / therapeutic use
  • Dacarbazine
  • Humans
  • Lung Neoplasms / drug therapy
  • Lung Neoplasms / genetics
  • Lung Neoplasms / pathology
  • Lung Neoplasms / secondary
  • Male
  • Mutation*
  • Paraganglioma* / drug therapy
  • Paraganglioma* / genetics
  • Paraganglioma* / pathology
  • Prognosis
  • Succinate Dehydrogenase* / genetics
  • Vincristine* / therapeutic use

Substances

  • SDHB protein, human
  • Succinate Dehydrogenase
  • Cyclophosphamide
  • Vincristine
  • Dacarbazine

Supplementary concepts

  • CVD protocol

Grants and funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.