Literature DB >> 32141667

Abnormal Pretreatment Liver Function Tests Are Associated with Discontinuation of Peptide Receptor Radionuclide Therapy in a U.S.-Based Neuroendocrine Tumor Cohort.

Jason M Heckert1, Sarit T Kipnis1, Shria Kumar2, Samuel Botterbusch2, Alice Alderson2, Bonita Bennett2, Caroline Creamer2, Jennifer R Eads3, Michael C Soulen4, Daniel A Pryma4, David A Mankoff4, David C Metz2, Bryson W Katona2.   

Abstract

BACKGROUND: Peptide receptor radionuclide therapy (PRRT) is effective for treating midgut neuroendocrine tumors (NETs); however, incorporation of PRRT into routine practice in the U.S. is not well studied. Herein we analyze the first year of PRRT implementation to determine tolerance of PRRT and factors that increase risk of PRRT discontinuation.
MATERIALS AND METHODS: Medical records were reviewed and data were abstracted on all patients with NETs scheduled for PRRT during the first year of PRRT implementation at a U.S. NET referral center (August 2018 through July 2019). Logistic regression was used to identify factors associated with PRRT discontinuation.
RESULTS: Fifty-five patients (56% male) were scheduled for PRRT over the study period. The most common primary NET location was small bowel (47%), followed by pancreas (26%), and 84% of the NETs were World Health Organization grade 1 or 2. The cohort was heavily pretreated with somatostatin analog (SSA) therapy (98%), non-SSA systemic therapy (64%), primary tumor resection (73%), and liver-directed therapy (55%). At the time of analysis, 52 patients completed at least one PRRT treatment. Toxicities including bone marrow suppression and liver function test (LFT) abnormalities were comparable to prior publications. Eleven patients (21%) prematurely discontinued PRRT because of toxicity or an adverse event. Pretreatment LFT abnormality was associated with increased risk of PRRT cancellation (odds ratio: 12; 95% confidence interval: 2.59-55.54; p < .001).
CONCLUSION: PRRT can be administered to a diverse NET population at a U.S. NET referral center. Baseline liver function test abnormality increases the likelihood of PRRT discontinuation. IMPLICATIONS FOR PRACTICE: Peptide receptor radionuclide therapy (PRRT) can be successfully implemented at a U.S. neuroendocrine tumor (NET) referral center in a NET population that is diverse in tumor location, grade, and prior treatment history. Toxicity and adverse effects of PRRT are comparable to prior reports; however, 21% of individuals prematurely discontinued PRRT. Patients with baseline liver function test abnormalities were more likely to discontinue PRRT than patients with normal liver function tests, which should be taken into consideration when selecting treatment options for NETs. © AlphaMed Press 2020.

Entities:  

Keywords:  DOTATATE; Lu-177; Neuroendocrine tumor; Peptide receptor radionuclide therapy

Mesh:

Substances:

Year:  2020        PMID: 32141667      PMCID: PMC7356755          DOI: 10.1634/theoncologist.2019-0743

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  22 in total

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Authors:  Seong-Jang Kim; Kyoungjune Pak; Phillip J Koo; Jennifer J Kwak; Samuel Chang
Journal:  Eur J Nucl Med Mol Imaging       Date:  2015-08-09       Impact factor: 9.236

2.  Peptide Receptor Radionuclide Therapy With 177Lu-Octreotate in Patients With Somatostatin Receptor Expressing Neuroendocrine Tumors: Six Years' Assessment.

Authors:  Mohammadali Hamiditabar; Muzammil Ali; Joseph Roys; Edward M Wolin; Thomas M OʼDorisio; David Ranganathan; Izabela Tworowska; Jonathan R Strosberg; Ebrahim S Delpassand
Journal:  Clin Nucl Med       Date:  2017-06       Impact factor: 7.794

3.  Long-term results and tolerability of tandem peptide receptor radionuclide therapy with 90Y/177Lu-DOTATATE in neuroendocrine tumors with respect to the primary location: a 10-year study.

Authors:  Jolanta Kunikowska; Dariusz Pawlak; Marianna I Bąk; Beata Kos-Kudła; Renata Mikołajczak; Leszek Królicki
Journal:  Ann Nucl Med       Date:  2017-03-18       Impact factor: 2.668

4.  Phase 3 Trial of 177Lu-Dotatate for Midgut Neuroendocrine Tumors.

Authors:  Jonathan Strosberg; Ghassan El-Haddad; Edward Wolin; Andrew Hendifar; James Yao; Beth Chasen; Erik Mittra; Pamela L Kunz; Matthew H Kulke; Heather Jacene; David Bushnell; Thomas M O'Dorisio; Richard P Baum; Harshad R Kulkarni; Martyn Caplin; Rachida Lebtahi; Timothy Hobday; Ebrahim Delpassand; Eric Van Cutsem; Al Benson; Rajaventhan Srirajaskanthan; Marianne Pavel; Jaime Mora; Jordan Berlin; Enrique Grande; Nicholas Reed; Ettore Seregni; Kjell Öberg; Maribel Lopera Sierra; Paola Santoro; Thomas Thevenet; Jack L Erion; Philippe Ruszniewski; Dik Kwekkeboom; Eric Krenning
Journal:  N Engl J Med       Date:  2017-01-12       Impact factor: 91.245

5.  Specific efficacy of peptide receptor radionuclide therapy with (177)Lu-octreotate in advanced neuroendocrine tumours of the small intestine.

Authors:  Amir Sabet; Kristina Dautzenberg; Torjan Haslerud; Anas Aouf; Amin Sabet; Birgit Simon; Karin Mayer; Hans-Jürgen Biersack; Samer Ezziddin
Journal:  Eur J Nucl Med Mol Imaging       Date:  2015-03-26       Impact factor: 9.236

6.  Predictors of long-term outcome in patients with well-differentiated gastroenteropancreatic neuroendocrine tumors after peptide receptor radionuclide therapy with 177Lu-octreotate.

Authors:  Samer Ezziddin; Mared Attassi; Charlotte J Yong-Hing; Hojjat Ahmadzadehfar; Winfried Willinek; Frank Grünwald; Stefan Guhlke; Hans-Jürgen Biersack; Amir Sabet
Journal:  J Nucl Med       Date:  2014-01-16       Impact factor: 10.057

7.  Changes in the Epidemiology of Neuroendocrine Tumours.

Authors:  Isabel Huguet; Ashley B Grossman; Dermot O'Toole
Journal:  Neuroendocrinology       Date:  2015-10-28       Impact factor: 4.914

8.  Prospective observational study of 177Lu-DOTA-octreotate therapy in 200 patients with advanced metastasized neuroendocrine tumours (NETs): feasibility and impact of a dosimetry-guided study protocol on outcome and toxicity.

Authors:  Ulrike Garske-Román; Mattias Sandström; Katarzyna Fröss Baron; Lars Lundin; Per Hellman; Staffan Welin; Silvia Johansson; Tanweera Khan; Hans Lundqvist; Barbro Eriksson; Anders Sundin; Dan Granberg
Journal:  Eur J Nucl Med Mol Imaging       Date:  2018-03-01       Impact factor: 9.236

Review 9.  Current best practice in the management of neuroendocrine tumors.

Authors:  Marina Tsoli; Eleftherios Chatzellis; Anna Koumarianou; Dionysia Kolomodi; Gregory Kaltsas
Journal:  Ther Adv Endocrinol Metab       Date:  2018-10-31       Impact factor: 3.565

10.  Salvage peptide receptor radionuclide therapy with [177Lu-DOTA,Tyr3]octreotate in patients with bronchial and gastroenteropancreatic neuroendocrine tumours.

Authors:  W A van der Zwan; T Brabander; B L R Kam; J J M Teunissen; R A Feelders; J Hofland; E P Krenning; W W de Herder
Journal:  Eur J Nucl Med Mol Imaging       Date:  2018-09-28       Impact factor: 9.236

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  2 in total

1.  Laboratory, Clinical, and Survival Outcomes Associated With Peptide Receptor Radionuclide Therapy in Patients With Gastroenteropancreatic Neuroendocrine Tumors.

Authors:  Sarit T Kipnis; Matthew Hung; Shria Kumar; Jason M Heckert; Hwan Lee; Bonita Bennett; Michael C Soulen; Daniel A Pryma; David A Mankoff; David C Metz; Jennifer R Eads; Bryson W Katona
Journal:  JAMA Netw Open       Date:  2021-03-01

2.  Application of FLIC model to predict adverse events onset in neuroendocrine tumors treated with PRRT.

Authors:  F Scalorbi; G Argiroffi; M Baccini; L Gherardini; V Fuoco; N Prinzi; S Pusceddu; E M Garanzini; G Centonze; M Kirienko; E Seregni; M Milione; M Maccauro
Journal:  Sci Rep       Date:  2021-09-30       Impact factor: 4.379

  2 in total

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