TY - JOUR
T1 - The impact of somatostatin receptor-directed PET/CT on the management of patients with neuroendocrine tumor
T2 - A systematic review and meta-analysis
AU - Barrio, Martin
AU - Czernin, Johannes
AU - Fanti, Stefano
AU - Ambrosini, Valentina
AU - Binse, Ina
AU - Du, Lin
AU - Eiber, Matthias
AU - Herrmann, Ken
AU - Fendler, Wolfgang P.
N1 - Publisher Copyright:
COPYRIGHT © 2017 by the Society of Nuclear Medicine and Molecular Imaging.
PY - 2017/5/1
Y1 - 2017/5/1
N2 - Somatostatin receptor (SSTR) imaging is widely used for guiding the management of neuroendocrine tumor (NET) patients. 68Ga-DOTATATE approval by the U.S. Food and Drug Administration has triggered widespread clinical interest in SSTR PET/CT throughout the United States. Here, we performed a systematic review and meta-analysis to evaluate the impact of SSTR PET/CT on the management of patients with NETs. Methods: A comprehensive literature search was performed using The National Center for Biotechnology Information PubMed online database, applying the following key words: "management" AND "PET" AND "neuroendocrine". Fourteen of 190 studies were deemed suitable based on the following inclusion criteria: original research, cohort study, number of patients 10 or more, and reported change in management after SSTR PET/CT. Change in management across studies was determined by a random-effects model. Results: A total of 1,561 patients were included. Overall, change in management occurred in 44% (range, 16%-71%) of NET patients after SSTR PET/CT. In 4 of 14 studies, SSTR PET/CT was performed after an 111In-Octreotide scan. In this subgroup, additional information by SSTR PET/CT led to a change in management in 39% (range, 16%-71%) of patients. Seven of 14 studies differentiated between inter- and intramodality changes, with most changes being intermodality (77%; intramodality, 23%). Conclusion: The management was changed in more than one third of patients undergoing SSTR PET/CT even when performed after an 111In-Octreotide scan. Intermodality changes were 3 times more likely than intramodality changes, underlining the clinical impact of SSTR PET/CT.
AB - Somatostatin receptor (SSTR) imaging is widely used for guiding the management of neuroendocrine tumor (NET) patients. 68Ga-DOTATATE approval by the U.S. Food and Drug Administration has triggered widespread clinical interest in SSTR PET/CT throughout the United States. Here, we performed a systematic review and meta-analysis to evaluate the impact of SSTR PET/CT on the management of patients with NETs. Methods: A comprehensive literature search was performed using The National Center for Biotechnology Information PubMed online database, applying the following key words: "management" AND "PET" AND "neuroendocrine". Fourteen of 190 studies were deemed suitable based on the following inclusion criteria: original research, cohort study, number of patients 10 or more, and reported change in management after SSTR PET/CT. Change in management across studies was determined by a random-effects model. Results: A total of 1,561 patients were included. Overall, change in management occurred in 44% (range, 16%-71%) of NET patients after SSTR PET/CT. In 4 of 14 studies, SSTR PET/CT was performed after an 111In-Octreotide scan. In this subgroup, additional information by SSTR PET/CT led to a change in management in 39% (range, 16%-71%) of patients. Seven of 14 studies differentiated between inter- and intramodality changes, with most changes being intermodality (77%; intramodality, 23%). Conclusion: The management was changed in more than one third of patients undergoing SSTR PET/CT even when performed after an 111In-Octreotide scan. Intermodality changes were 3 times more likely than intramodality changes, underlining the clinical impact of SSTR PET/CT.
KW - DOTATATE
KW - DOTATOC
KW - GI
KW - Management
KW - Neuroendocrine
KW - Oncology
KW - PET/CT
KW - Peptides
KW - SSTR
UR - http://www.scopus.com/inward/record.url?scp=85018983826&partnerID=8YFLogxK
U2 - 10.2967/jnumed.116.185587
DO - 10.2967/jnumed.116.185587
M3 - Article
C2 - 28082438
AN - SCOPUS:85018983826
SN - 0161-5505
VL - 58
SP - 756
EP - 761
JO - Journal of Nuclear Medicine
JF - Journal of Nuclear Medicine
IS - 5
ER -