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DOI 10.1080/08880018.2017.1338806

Медицинская библиотека · Pediatric hematology and oncology · 2017

Pilot study of propranolol premedication to reduce FDG uptake in brown adipose tissue on PET scans of adolescent and young adult oncology patients.

George Anil, Sinha Partha, Conrad Gary, Memon Aum A, Dressler Emily V, Wagner Lars M

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Аннотация

OBJECTIVE

Physiologic uptake of 18F-fluorodeoxyglucose (FDG) in brown adipose tissue (adipose tissue) of cancer patients may confound interpretation of positron emission tomography (PET) scans. Uptake in adipose tissue occurs in up to half of pediatric oncology patients undergoing PET scans, and is especially common in adolescents. adipose tissue is innervated by the sympathetic nervous system, and beta blockers such as propranolol have shown efficacy in reducing adipose tissue uptake on PET scans done in older adult oncology patients.

PARTICIPANTS

Because propranolol may cause hypoglycemia or other side effects in fasting patients, we prospectively assessed the safety of a single dose of 20 mg propranolol in adolescent and young adult oncology patients undergoing FDG-PET imaging.

METHODS

Ten patients (median age 18 years, range 14-24) received propranolol premedication prior to FDG-PET.

RESULTS

No adverse effects or clinically significant changes in serum glucose, heart rate, or blood pressure were observed. Five of the 10 patients had adipose tissue identified on previous PET scans. However, following propranolol administration only, one patient had persistent uptake in adipose tissue.

CONCLUSIONS

Propranolol was convenient and safe in fasting adolescent and young adult oncology patients undergoing PET scans. Larger studies are warranted to better define the effectiveness of this approach.

Для цитирования: George Anil, Sinha Partha, Conrad Gary, Memon Aum A, Dressler Emily V, Wagner Lars M. Pilot study of propranolol premedication to reduce FDG uptake in brown adipose tissue on PET scans of adolescent and young adult oncology patients.. Pediatric hematology and oncology. 2017. DOI: 10.1080/08880018.2017.1338806.

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