Literature DB >> 30606883

Real-World Treatment Patterns and Clinical Outcomes in Advanced Gastrointestinal Neuroendocrine Tumors (GI NET): A Multicenter Retrospective Chart Review Study.

Matthew H Kulke1,2, Al B Benson3, Arvind Dasari4, Lynn Huynh5, Beilei Cai6, Todor Totev5, Nina Roesner5, Mei Sheng Duh5, Maureen P Neary6, Victoria E Maurer3, Brandon E Shih7, Cecile G Dagohoy4, Jennifer Chan8, Emily K Bergsland7.   

Abstract

BACKGROUND: We assessed treatment patterns and outcomes of patients with advanced gastrointestinal (GI) neuroendocrine tumors (NET) at four large tertiary referral centers in the U.S. PATIENTS AND METHODS: We performed a retrospective chart review of patients aged ≥18 years at advanced GI NET diagnosis, treated between July 2011 and December 2014. Index date was the histologically confirmed diagnosis date of locally advanced/metastatic GI NET. Data included baseline characteristics, treatment patterns, progression, death, and GI NET-related health care resource utilization from index date through last contact or death. Time-to-event analyses, including treatment discontinuation, progression, and overall survival (OS), were performed using Kaplan-Meier analysis.
RESULTS: We identified 273 patients; 156 (57%) had primary ileum NET, and 174 (64%) had functional NET. First-line treatments included somatostatin analog (SSA) alone (89%) or in combination (2%), liver-directed therapy (LDT; 8%), and cytotoxic chemotherapy or interferon (2%). One hundred fifty-five patients continued with second-line therapy, including SSA alone (17%) or in combination (75%, with 3% combined with peptide receptor radionuclide therapy), LDT (4%), and other treatments (3%). Median time (months) to first-line discontinuation was 154.0 for SSAs and 3.8 for cytotoxic chemotherapy. Overall median time to investigator-assessed progression following treatment initiation was 30.3 months. Median OS (months) following first-line initiation was 151.8 for all patients and 178.9 for first-line SSA.
CONCLUSION: Our study illustrates the common use of SSAs in both first-line and subsequent treatment of patients with GI NETs, as well as the relatively long survival durations and multiple additional treatments received by patients with this condition. Treatment pattern assessment at later times, following approval of newer treatments, is warranted. IMPLICATIONS FOR PRACTICE: This study, assessing treatment patterns over a period of up to 30 years, showed that SSAs, LDT, cytotoxic chemotherapy, and interferon are common treatments for advanced GI NETs. SSAs alone or in combination with other treatments were the most frequent therapy in first and subsequent lines. Patients in this study remained on SSAs long-term, with median treatment duration of 12.8 years in first line. Treatment patterns should be assessed beyond this study's time period, given recent U.S. Food and Drug Administration approvals for additional treatments for GI NET, which will likely be incorporated in the continuum of care of patients. © AlphaMed Press 2019.

Entities:  

Keywords:  Gastrointestinal neuroendocrine tumor; Real‐world analysis; Somatostatin analogs; Treatment patterns

Year:  2019        PMID: 30606883      PMCID: PMC6693731          DOI: 10.1634/theoncologist.2018-0519

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


  12 in total

1.  Frequency of carcinoid syndrome at neuroendocrine tumour diagnosis: a population-based study.

Authors:  Daniel M Halperin; Chan Shen; Arvind Dasari; Ying Xu; Yiyi Chu; Shouhao Zhou; Ya-Chen Tina Shih; James C Yao
Journal:  Lancet Oncol       Date:  2017-02-24       Impact factor: 41.316

2.  Neuroendocrine tumors.

Authors:  Matthew H Kulke; Al B Benson; Emily Bergsland; Jordan D Berlin; Lawrence S Blaszkowsky; Michael A Choti; Orlo H Clark; Gerard M Doherty; James Eason; Lyska Emerson; Paul F Engstrom; Whitney S Goldner; Martin J Heslin; Fouad Kandeel; Pamela L Kunz; Boris W Kuvshinoff; Jeffrey F Moley; Venu G Pillarisetty; Leonard Saltz; David E Schteingart; Manisha H Shah; Stephen Shibata; Jonathan R Strosberg; Jean-Nicolas Vauthey; Rebekah White; James C Yao; Deborah A Freedman-Cass; Mary A Dwyer
Journal:  J Natl Compr Canc Netw       Date:  2012-06-01       Impact factor: 11.908

3.  Clinical characteristics, treatment patterns, and economic burden in patients treated for neuroendocrine tumors in the United States: a retrospective cohort study.

Authors:  Chien-Chia Chuang; Sharvari Bhurke; Shin-Yin Chen; Siham Brulais; Sylvie Gabriel
Journal:  J Med Econ       Date:  2014-11-05       Impact factor: 2.448

Review 4.  One hundred years after "carcinoid": epidemiology of and prognostic factors for neuroendocrine tumors in 35,825 cases in the United States.

Authors:  James C Yao; Manal Hassan; Alexandria Phan; Cecile Dagohoy; Colleen Leary; Jeannette E Mares; Eddie K Abdalla; Jason B Fleming; Jean-Nicolas Vauthey; Asif Rashid; Douglas B Evans
Journal:  J Clin Oncol       Date:  2008-06-20       Impact factor: 44.544

5.  United States-based practice patterns and resource utilization in advanced neuroendocrine tumor treatment.

Authors:  Jonathan Strosberg; Roman Casciano; Lee Stern; Rohan Parikh; Maruit Chulikavit; Jacob Willet; Zhimei Liu; Xufang Wang; Krzysztof J Grzegorzewski
Journal:  World J Gastroenterol       Date:  2013-04-21       Impact factor: 5.742

Review 6.  The diagnosis and medical management of advanced neuroendocrine tumors.

Authors:  Gregory A Kaltsas; G Michael Besser; Ashley B Grossman
Journal:  Endocr Rev       Date:  2004-06       Impact factor: 19.871

7.  Trends in the Incidence, Prevalence, and Survival Outcomes in Patients With Neuroendocrine Tumors in the United States.

Authors:  Arvind Dasari; Chan Shen; Daniel Halperin; Bo Zhao; Shouhao Zhou; Ying Xu; Tina Shih; James C Yao
Journal:  JAMA Oncol       Date:  2017-10-01       Impact factor: 31.777

8.  Trends of incidence and survival of gastrointestinal neuroendocrine tumors in the United States: a seer analysis.

Authors:  Vassiliki L Tsikitis; Betsy C Wertheim; Marlon A Guerrero
Journal:  J Cancer       Date:  2012-07-01       Impact factor: 4.207

Review 9.  Management Options for Advanced Low or Intermediate Grade Gastroenteropancreatic Neuroendocrine Tumors: Review of Recent Literature.

Authors:  Vladimir Neychev; Electron Kebebew
Journal:  Int J Surg Oncol       Date:  2017-05-16

10.  Association Between Tumor Progression Endpoints and Overall Survival in Patients with Advanced Neuroendocrine Tumors.

Authors:  Monica Ter-Minassian; Sui Zhang; Nichole V Brooks; Lauren K Brais; Jennifer A Chan; David C Christiani; Xihong Lin; Sylvie Gabriel; Jérôme Dinet; Matthew H Kulke
Journal:  Oncologist       Date:  2017-02-08
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