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Clinical, Diagnostic, and Treatment Characteristics of SDHA-Related Metastatic Pheochromocytoma and Paraganglioma

58

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47

References

2019

Year

Abstract

<b>Background:</b> Pheochromocytoma and paraganglioma (PHEO/PGL) are rare neuroendocrine tumors which may cause potentially life-threatening complications, with about a third of cases found to harbor specific gene mutations. Thus, early diagnosis, treatment, and meticulous monitoring are of utmost importance. Because of low incidence of succinate dehydrogenase complex subunit A (<i>SDHA</i>)-related metastatic PHEO/PGL, currently there exists insufficient clinical information, especially with regards to its diagnostic and treatment characteristics. <b>Methods:</b> Ten patients with <i>SDHA</i>-related metastatic PHEO/PGL were followed-up prospectively and/or retrospectively between January 2010-July 2018. They underwent biochemical tests (<i>n</i> = 10), <sup>123</sup>I-MIBG (<i>n</i> = 9) scintigraphy, and multiple whole-body positron emission tomography/computed tomography (PET/CT) scans with <sup>68</sup>Ga-DOTATATE (<i>n</i> = 10), <sup>18</sup>F-FDG (<i>n</i> = 10), and <sup>18</sup>F-FDOPA (<i>n</i> = 6). <b>Results:</b> Our findings suggest that these tumors can occur early and at extra-adrenal locations, behave aggressively, and have a tendency to develop metastatic disease within a short period of time. None of our patients had a family history of PHEO/PGL, making them appear sporadic. Nine out of 10 patients showed abnormal PHEO/PGL-specific biochemical markers with predominantly noradrenergic and/or dopaminergic phenotype, suggesting their utility in diagnosing and monitoring the disease. Per patient detection rates of <sup>68</sup>Ga-DOTATATE (<i>n</i> = 10/10), <sup>18</sup>F-FDG (<i>n</i> = 10/10), <sup>18</sup>F-FDOPA (<i>n</i> = 5/6) PET/CT, and <sup>123</sup>I-MIBG (<i>n</i> = 7/9) scintigraphy were 100, 100, 83.33, and 77.77%, respectively. Five out of 7 <sup>123</sup>I-MIBG positive patients had minimal <sup>123</sup>I-MIBG avidity or detected very few lesions compared to widespread metastatic disease on <sup>18</sup>F-FDG PET/CT, implying that diagnosis and treatment with <sup>123/131</sup>I-MIBG is not a good option. <sup>68</sup>Ga-DOTATATE PET/CT was found to be superior or equal to <sup>18</sup>F-FDG PET/CT in 7 out of 10 patients and hence, is recommended for evaluation and follow-up of these patients. All 7 out of 7 patients who received conventional therapies (chemotherapy, somatostatin analog therapy, radiation therapy, <sup>131</sup>I-MIBG, peptide receptor radionuclide therapy) in addition to surgery showed disease progression. <b>Conclusion:</b> In our cohort of patients, <i>SDHA</i>-related metastatic PHEO/PGL followed a disease-course similar to that of <i>SDHB</i>-related metastatic PHEO/PGL, showing highly aggressive behavior, similar imaging and biochemical phenotypes, and suboptimal response to conventional therapies. Therefore, we recommend careful surveillance of the affected patients and a search for effective therapies.

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