TY - JOUR
T1 - Consensus report of the 2021 National Cancer Institute neuroendocrine tumor clinical trials planning meeting
AU - NET CTPM participants
AU - Singh, Simron
AU - Hope, Thomas A.
AU - Bergsland, Emily B.
AU - Bodei, Lisa
AU - Bushnell, David L.
AU - Chan, Jennifer A.
AU - Chasen, Beth R.
AU - Chauhan, Aman
AU - Das, Satya
AU - Dasari, Arvind
AU - Del Rivero, Jaydira
AU - El-Haddad, Ghassan
AU - Goodman, Karyn A.
AU - Halperin, Daniel M.
AU - Lewis, Mark A.
AU - Lindwasser, O. Wolf
AU - Myrehaug, Sten
AU - Raj, Nitya P.
AU - Reidy-Lagunes, Diane L.
AU - Soares, Heloisa P.
AU - Strosberg, Jonathan R.
AU - Kohn, Elise C.
AU - Kunz, Pamela L.
N1 - Publisher Copyright:
© The Author(s) 2023. Published by Oxford University Press. All rights reserved. For permissions, please email: [email protected].
PY - 2023/9/7
Y1 - 2023/9/7
N2 - Important progress has been made over the last decade in the classification, imaging, and treatment of neuroendocrine neoplasm (NENs), with several new agents approved for use. Although the treatment options available for patients with well-differentiated neuroendocrine tumors (NETs) have greatly expanded, the rapidly changing landscape has presented several unanswered questions about how best to optimize, sequence, and individualize therapy. Perhaps the most important development over the last decade has been the approval of 177Lu-DOTATATE for treatment of gastroenteropancreatic-NETs, raising questions around optimal sequencing of peptide receptor radionuclide therapy (PRRT) relative to other therapeutic options, the role of re-treatment with PRRT, and whether PRRT can be further optimized through use of dosimetry among other approaches. The NET Task Force of the National Cancer Institute GI Steering Committee convened a clinical trial planning meeting in 2021 with multidisciplinary experts from academia, the federal government, industry, and patient advocates to develop NET clinical trials in the era of PRRT. Key clinical trial recommendations for development included 1) PRRT re-treatment, 2) PRRT and immunotherapy combinations, 3) PRRT and DNA damage repair inhibitor combinations, 4) treatment for liver-dominant disease, 5) treatment for PRRT-resistant disease, and 6) dosimetry-modified PRRT.
AB - Important progress has been made over the last decade in the classification, imaging, and treatment of neuroendocrine neoplasm (NENs), with several new agents approved for use. Although the treatment options available for patients with well-differentiated neuroendocrine tumors (NETs) have greatly expanded, the rapidly changing landscape has presented several unanswered questions about how best to optimize, sequence, and individualize therapy. Perhaps the most important development over the last decade has been the approval of 177Lu-DOTATATE for treatment of gastroenteropancreatic-NETs, raising questions around optimal sequencing of peptide receptor radionuclide therapy (PRRT) relative to other therapeutic options, the role of re-treatment with PRRT, and whether PRRT can be further optimized through use of dosimetry among other approaches. The NET Task Force of the National Cancer Institute GI Steering Committee convened a clinical trial planning meeting in 2021 with multidisciplinary experts from academia, the federal government, industry, and patient advocates to develop NET clinical trials in the era of PRRT. Key clinical trial recommendations for development included 1) PRRT re-treatment, 2) PRRT and immunotherapy combinations, 3) PRRT and DNA damage repair inhibitor combinations, 4) treatment for liver-dominant disease, 5) treatment for PRRT-resistant disease, and 6) dosimetry-modified PRRT.
UR - http://www.scopus.com/inward/record.url?scp=85170111871&partnerID=8YFLogxK
U2 - 10.1093/jnci/djad096
DO - 10.1093/jnci/djad096
M3 - Article
C2 - 37255328
AN - SCOPUS:85170111871
SN - 0027-8874
VL - 115
SP - 1001
EP - 1010
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
IS - 9
ER -