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Metz, David C.

https://orcid.org/0000-0001-7717-1762

Mayo Clinic

University of Pennsylvania

Citations 3

Consensus guideline for the management of peritoneal metastases from neuroendocrine neoplasms
Su, David , Brown, Leanne , Bansal, Varun , Bakkila, Baylee , Turaga, Kiran K. , Gunderson, Craig G. , Bergsland, Emily K. , Metz, David C. , Kunz, Pamela L. , Gangi, Alexandra , Ly, Quan P. , Fackche, Nadege , Chan, Carlos H.F. , Sundar, Raghav , Hoehn, Richard S. , Dillon, Joseph S. , Su, David G , Brown, Leanne M , Bansal, Varun V , Turaga, Kiran K , Chan, Carlos H F , Dillon, Joseph S , Hoehn, Richard , Concors, Seth Jason , Strosberg, Jonathan , Hálfdánarson, Þorvarður R. , Kunstman, John W.

Cancer | June 25, 2025 | Volume: 131 | Issue: 13 | Pages: No page available

10.1002/cncr.35871 Get It

AbstractNeuroendocrine neoplasms (NENs) with peritoneal metastases (PM) represent a complex clinical challenge because of low incidence and heterogeneous phenotypes. This commentary describes the results of a national consensus aimed at addressing clinical management of patients with NENs and PM. An update of the 2018 Chicago consensus guidelines was conducted with a modified Delphi technique, which encompassed two rounds of voting. The levels of agreement for various pathway blocks were assessed, and key systemic therapy concepts were summarized by content experts. Supporting evidence was evaluated via a rapid literature review. Overall, the level of evidence for the management of PM in this disease was universally low. In total, 107 participants responded in the first round, with 88 of 107 (82%) participating in the second round. Strong consensus (>90%) was achieved in five of seven (71%) and seven of seven (100%) blocks in rounds 1 and 2, respectively. A multidisciplinary approach including psychosocial and wellness assessments received a strong positive recommendation. Management of NENs with PM was organized according to disease grade and symptom profiles. In grade 1 and 2 well‐differentiated NENs, cytoreductive surgery received strong support (>95%) after the management of functional syndromes (if present). For grade 3 well‐differentiated NENs, systemic therapy is the primary recommendation, with surgical resection considered in select cases. Given the limited evidence, the consensus‐driven clinical pathway offers vital clinical guidance for the management of NENs with PM. The need for high‐quality evidence remains critical to the field.
Differential Diagnosis of Diarrhea in Patients With Neuroendocrine Tumors
Eads, Jennifer R. , Reidy‐Lagunes, Diane , Chan, Jennifer A. , Anthony, Lowell , Hálfdánarson, Þorvarður R. , Naraev, Boris G., Wolin, Edward M. , Halperin, Daniel M. , Pommier, Rodney F. , Zacks, Jerome, Morse, Michael A. , Metz, David C. , Collaborative, from the Carcinoid Syndrome Control, Halfdanarson, Thorvardur R , Soares, Heloisa P. , Li, Daneng , Collaborative, from the Carcinoid Syndrome Control

Pancreas | September 29, 2020 | Volume: 49 | Issue: 9 | Pages: 1123-1130

10.1097/mpa.0000000000001658 Get It

Abstract Patients with neuroendocrine tumors (NETs) and carcinoid syndrome experience diarrhea that can have a debilitating effect on quality of life. Diarrhea also may develop in response to other hormonal syndromes associated with NETs, surgical complications, medical comorbidities, medications, or food sensitivities. Limited guidance on the practical approach to the differential diagnosis of diarrhea in these patients can lead to delays in appropriate treatment. This clinical review and commentary underscore the complexity in identifying the etiology of diarrhea in patients with NETs. Based on our collective experience and expertise, we offer a practical algorithm to guide medical oncologists and other care providers to expedite effective management of diarrhea and related symptoms in patients with NETs.
The North American Neuroendocrine Tumor Society Consensus Guidelines for Surveillance and Medical Management of Pancreatic Neuroendocrine Tumors
Hálfdánarson, Þorvarður R. , Tang, Laura , Bellizzi, Andrew M. , Bergsland, Emily K. , Halperin, Daniel M. , Eads, Jennifer R. , Singh, Simron , Metz, David C. , Naraev, Boris G., Reidy‐Lagunes, Diane , Howe, James R. , Pommier, Rodney F. , Menda, Yusuf , Chan, Jennifer A. , Halfdanarson, Thorvardur R , Bellizzi, Andrew M , Howe, James R , Menda, Yusuf , Strosberg, Jonathan , O’Dorisio, Thomas M. , Fishbein, Lauren , Hope, Thomas A. , Salem, Riad

Pancreas | July 14, 2020 | Volume: 49 | Issue: 7 | Pages: 863-881

10.1097/mpa.0000000000001597 Get It

AbstractThis article is the result of the North American Neuroendocrine Tumor Society consensus conference on the medical management of pancreatic neuroendocrine tumors from July 19 to 20, 2018. The guidelines panel consisted of medical oncologists, pathologists, gastroenterologists, endocrinologists, and radiologists. The panel reviewed a series of questions regarding the medical management of patients with pancreatic neuroendocrine tumors as well as questions regarding surveillance after resection. The available literature was reviewed for each of the question and panel members voted on controversial topics, and the recommendations were included in a document circulated to all panel members for a final approval.