SDHx mutations and temozolomide in malignant pheochromocytoma and paraganglioma

Kimberly Perez1,2, Heather Jacene2,3,4, Jason L Hornick2,5

  • 1Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.

Insights

Malignant pheochromocytomas/paragangliomas (PHEOs/PGLs) treated with temozolomide (TMZ) showed limited association between succinate dehydrogenase (SDHx) mutations and treatment response. Further research is needed to clarify outcomes for these rare tumors.

Area of Science:

  • Oncology
  • Genetics
  • Pharmacology

Background:

  • Malignant pheochromocytomas (PHEOs) and paragangliomas (PGLs) are rare neuroendocrine tumors with limited treatment options and poorly defined clinical outcomes.
  • A subset of these tumors (approx. 27%) harbor pathogenic germline succinate dehydrogenase (SDHx) mutations, which have been anecdotally linked to temozolomide (TMZ) sensitivity.

Purpose of the Study:

  • To investigate the association between germline SDHx mutations and response to temozolomide (TMZ)-based chemotherapy in patients with metastatic malignant PHEO/PGL.
  • To evaluate clinical outcomes, including progression-free survival (PFS) and overall survival (OS), in relation to SDHx mutation status.

Main Methods:

  • Retrospective analysis of metastatic malignant PHEO/PGL patients treated with TMZ chemotherapy from 2003-2020.
  • Assessment of treatment response using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 and PET Response Criteria in Solid Tumors (PERCIST).
  • Germline DNA analysis to identify pathogenic SDHx mutations.

Main Results:

  • Of 19 patients treated with TMZ, 9 (53%) had pathogenic germline SDHx mutations.
  • Fifteen patients were evaluable for RECIST 1.1 response: 6 (40%) partial response, 4 (27%) stable disease, 5 (33%) progressive disease.
  • Median PFS was 1.3 years for SDHx mutation carriers versus 5.5 years for non-carriers; 3-year OS was 58% (median OS 1.5 years for carriers, not estimable for non-carriers).

Conclusions:

  • While SDHx mutations are common in malignant PHEO/PGL, this study suggests a limited association between these mutations and response to TMZ chemotherapy.
  • Clinical outcomes, including PFS and OS, appear to differ between SDHx mutation carriers and non-carriers, warranting further investigation.

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