Managing Catecholamine Release Syndrome During and Following Lu-177-DOTATATE in High-Risk Pheochromocytoma Patients.

التفاصيل البيبلوغرافية
العنوان: Managing Catecholamine Release Syndrome During and Following Lu-177-DOTATATE in High-Risk Pheochromocytoma Patients.
المؤلفون: Phelps TE; Molecular Imaging Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA., Del Rivero J; Developmental Therapeutics Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA., Chertow DS; Critical Care Medicine Department, Clinical Center, National Institutes of Health, Bethesda, MD 20892, USA., Rosing D; Cardiovascular Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA., Pacak K; Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA., Lin FI; Molecular Imaging Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
المصدر: JCEM case reports [JCEM Case Rep] 2024 Apr 10; Vol. 2 (4), pp. luae049. Date of Electronic Publication: 2024 Apr 10 (Print Publication: 2024).
نوع المنشور: Case Reports
اللغة: English
بيانات الدورية: Publisher: Oxford University Press on behalf of the Endocrine Society Country of Publication: England NLM ID: 9918609886906676 Publication Model: eCollection Cited Medium: Internet ISSN: 2755-1520 (Electronic) Linking ISSN: 27551520 NLM ISO Abbreviation: JCEM Case Rep Subsets: PubMed not MEDLINE
أسماء مطبوعة: Publication: Oxford : Oxford University Press on behalf of the Endocrine Society, [2023]-
مستخلص: Pheochromocytomas and paragangliomas (PPGLs) are rare catecholamine-producing tumors that express somatostatin receptors (SSTR) that can be treated with lutetium-177 DOTATATE (Lu-177-TRT); however, treatment can be associated with life-threatening cardiovascular events. A patient case with management strategies for high-risk PPGL patients receiving Lu-177-TRT is described. The 78-year-old patient with metastatic paraganglioma was enrolled and treated under NCT03206060. Deemed to be at high risk, the patient was preemptively admitted to the intensive care unit (ICU) with central line access placed. Due to comorbidities, a reduced dose of 100 mCi x 4 cycles was used for this patient. Vital signs, blood work, and serum catecholamine levels were obtained at various time points. Despite reduced dosing, the patient still developed a severe hypertensive reaction with systolic blood pressure of 240 mmHg within minutes of Lu-177-TRT infusion, which was controlled with an intravenous nicardipine drip. The patient remained in the ICU for 24 hours post Lu-177-TRT before moving to an inpatient ward for an additional 24 hours. All subsequent infusions were performed using reduced doses with elective ICU admissions and were well-tolerated. Despite the increased risk, metastatic PPGL patients can be safely treated with proper staff training, monitoring, and preparation for intravenous medications, especially nicardipine.
(Published by Oxford University Press on behalf of the Endocrine Society 2024.)
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معلومات مُعتمدة: ZIA BC011789 United States ImNIH Intramural NIH HHS
فهرسة مساهمة: Keywords: Lu-177-DOTATATE; catecholamine release syndrome; paraganglioma; peptide receptor radionuclide therapy; pheochromocytoma; targeted radionuclide therapy
تواريخ الأحداث: Date Created: 20240411 Latest Revision: 20240425
رمز التحديث: 20240425
مُعرف محوري في PubMed: PMC11005828
DOI: 10.1210/jcemcr/luae049
PMID: 38601063
قاعدة البيانات: MEDLINE
الوصف
تدمد:2755-1520
DOI:10.1210/jcemcr/luae049