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Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
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.
Abstract:
Malignant pheochromocytomas (PHEOs)/paragangliomas (PGLs) are rare tumors for which clinical outcomes remain poorly defined and therapeutic options are limited. Approximately 27% carry pathogenic germline succinate dehydrogenase (SDHx) mutations; the presence of such mutations has been correlated with response to temozolomide (TMZ). We aimed to investigate the association between germline mutations in SDHx and response to TMZ. We retrospectively identified patients with metastatic malignant PHEO/PGLs treated with TMZ- based chemotherapy at Dana-Farber Cancer Institute between 2003 and 2020. The correlation between response by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 and PET Response Criteria in Solid Tumors (PERCIST) and the presence of SDHx mutations in the germline and tumor was evaluated. Nineteen patients received TMZ. Seventeen underwent germline assessment: 9 (53%) carried a pathogenic SDHx germline mutation. Fifteen patients were evaluable for response by RECIST 1.1: 6 (40%) partial response, 4 (27%) stable disease, and 5 (33%) progressive disease. Overall median progression-free survival was 2.2 years. Three-year overall survival (OS) was 58%. Median PFS was 1.3 years and 5.5 years for carriers and non-carriers, respectively and OS was 1.5 years and not estimable for carriers and non-carriers, respectively. The response by PERCIST criteria in nine patients correlated with the RECIST 1.1 assessment. Our series represents one of the largest analyses of patients with malignant PHEOs/PGLs treated with TMZ who have available germline data. The incidence of pathogenic germline SDHx mutations was similar to what has been previously published, though our analysis suggests that there may be a limited association between response to TMZ and pathogenic germline SDHx mutations.
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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