Literature DB >> 23211372

Systemic treatment in unresectable metastatic well-differentiated carcinoid tumors: consensus results from a modified delphi process.

Jonathan R Strosberg1, George A Fisher, Al B Benson, Jennifer L Malin, Dasha Cherepanov, Michael S Broder, Lowell B Anthony, Bulent Arslan, George A Fisher, John F Gibbs, Edward Greeno, Renuka V Iyer, Michelle K Kim, William Maples, Philip A Philip, Jonathan Strosberg, Edward M Wolin.   

Abstract

OBJECTIVES: This study aimed to develop expert consensus for the use of systemic treatments for unresectable metastatic well-differentiated (grade 1-2) carcinoid tumors using the RAND/UCLA modified Delphi process.
METHODS: After a comprehensive literature review, 404 patient scenarios addressing the use of systemic treatments for carcinoid tumors were constructed. A multidisciplinary panel of 10 physicians assessed the scenarios as appropriate, inappropriate, or uncertain (on a 1-9 scale) or as an area of disagreement before and after an extended discussion of the evidence.
RESULTS: Experts were medical and surgical oncologists, interventional radiologists, and gastroenterologists. Among rated scenarios, disagreement decreased from 14% before the meeting to 4% after. Consensus statements about midgut carcinoids included the following: (1) Somatostatin analogs are appropriate as first-line therapy for all patients; (2) In patients with uncontrolled secretory symptoms, it is appropriate to increase the dose/frequency of octreotide long-acting repeatable up to 60 mg every 4 weeks or up to 40 mg every 3 weeks as second-line therapy for refractory carcinoid syndrome. Other options may also be appropriate. Consensus was similar for non-midgut carcinoids.
CONCLUSIONS: The Delphi process provided a structured methodological approach to assist clinician experts in reaching consensus on the appropriateness of specific medical therapies for the treatment of advanced carcinoid tumors.

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Year:  2013        PMID: 23211372     DOI: 10.1097/MPA.0b013e31826d3a17

Source DB:  PubMed          Journal:  Pancreas        ISSN: 0885-3177            Impact factor:   3.327


  13 in total

Review 1.  Appropriateness of systemic treatments in unresectable metastatic well-differentiated pancreatic neuroendocrine tumors.

Authors:  Jonathan R Strosberg; George A Fisher; Al B Benson; Lowell B Anthony; Bulent Arslan; John F Gibbs; Edward Greeno; Renuka V Iyer; Michelle K Kim; William J Maples; Philip A Philip; Edward M Wolin; Dasha Cherepanov; Michael S Broder
Journal:  World J Gastroenterol       Date:  2015-02-28       Impact factor: 5.742

2.  Whither peptide receptor radionuclide therapy for neuroendocrine tumors: an Einsteinian view of the facts and myths.

Authors:  Vikas Prasad; Lisa Bodei; Mark Kidd; Irvin M Modlin
Journal:  Eur J Nucl Med Mol Imaging       Date:  2014-10       Impact factor: 9.236

Review 3.  Gastrointestinal neuroendocrine tumors treated with high dose octreotide-LAR: a systematic literature review.

Authors:  Michael S Broder; David Beenhouwer; Jonathan R Strosberg; Maureen P Neary; Dasha Cherepanov
Journal:  World J Gastroenterol       Date:  2015-02-14       Impact factor: 5.742

4.  Follow-up intervals in patients with Cushing's disease: recommendations from a panel of experienced pituitary clinicians.

Authors:  Eliza B Geer; Alejandro Ayala; Vivien Bonert; John D Carmichael; Murray B Gordon; Laurence Katznelson; Ekaterina Manuylova; Ismat Shafiq; Vijaya Surampudi; Ronald S Swerdloff; Michael S Broder; Dasha Cherepanov; Marianne Eagan; Jackie Lee; Qayyim Said; Maureen P Neary; Beverly M K Biller
Journal:  Pituitary       Date:  2017-08       Impact factor: 4.107

Review 5.  Consensus on biomarkers for neuroendocrine tumour disease.

Authors:  Kjell Oberg; Irvin M Modlin; Wouter De Herder; Marianne Pavel; David Klimstra; Andrea Frilling; David C Metz; Anthony Heaney; Dik Kwekkeboom; Jonathan Strosberg; Timothy Meyer; Steven F Moss; Kay Washington; Edward Wolin; Eric Liu; James Goldenring
Journal:  Lancet Oncol       Date:  2015-09       Impact factor: 41.316

6.  Clinical benefits of above-standard dose of octreotide LAR in patients with neuroendocrine tumors for control of carcinoid syndrome symptoms: a multicenter retrospective chart review study.

Authors:  Jonathan R Strosberg; Al B Benson; Lynn Huynh; Mei Sheng Duh; Jamie Goldman; Vaibhav Sahai; Alfred W Rademaker; Matthew H Kulke
Journal:  Oncologist       Date:  2014-08-05

Review 7.  Octreotide and Lanreotide in Gastroenteropancreatic Neuroendocrine Tumors.

Authors:  Venkata K Pokuri; Mei Ka Fong; Renuka Iyer
Journal:  Curr Oncol Rep       Date:  2016-01       Impact factor: 5.075

8.  Comparing the Cost of Treatment with Octreotide Long-Acting Release versus Lanreotide in Patients with Metastatic Gastrointestinal Neuroendocrine Tumors.

Authors:  Rajeev Ayyagari; Maureen Neary; Shang Li; Ariel Rokito; Hongbo Yang; Jipan Xie; Al B Benson
Journal:  Am Health Drug Benefits       Date:  2017-11

9.  A Delphic consensus assessment: imaging and biomarkers in gastroenteropancreatic neuroendocrine tumor disease management.

Authors:  Kjell Oberg; Eric Krenning; Anders Sundin; Lisa Bodei; Mark Kidd; Margot Tesselaar; Valentina Ambrosini; Richard P Baum; Matthew Kulke; Marianne Pavel; Jaroslaw Cwikla; Ignat Drozdov; Massimo Falconi; Nicola Fazio; Andrea Frilling; Robert Jensen; Klaus Koopmans; Tiny Korse; Dik Kwekkeboom; Helmut Maecke; Giovanni Paganelli; Ramon Salazar; Stefano Severi; Jonathan Strosberg; Vikas Prasad; Aldo Scarpa; Ashley Grossman; Annemeik Walenkamp; Mauro Cives; Irene Virgolini; Andreas Kjaer; Irvin M Modlin
Journal:  Endocr Connect       Date:  2016-08-31       Impact factor: 3.335

Review 10.  Practical management of toxicities associated with targeted therapies for advanced gastroenteropancreatic neuroendocrine tumors.

Authors:  Pieter-Jan Cuyle; Hans Prenen
Journal:  Ann Gastroenterol       Date:  2018-01-08
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