Literature DB >> 19609217

Metastatic carcinoid tumor: changing patterns of care over two decades.

Amanda Townsend1, Tim Price, Sue Yeend, Ken Pittman, Kevin Patterson, Colin Luke.   

Abstract

BACKGROUND: Metastatic carcinoid tumors (MCTs), an important subgroup of neuroendocrine tumors, occur infrequently and often have an indolent course, limiting data on long-term treatment outcomes. We aimed to assess treatment trends at a single center over time and the impact on the outcome. STUDY: Patients diagnosed with carcinoid tumors in the North West Adelaide Health Service between January 1, 1985 and March 1, 2007 were identified from the South Australian Cancer Registry.
RESULTS: We identified 92 patients with carcinoid tumors; 49 had MCT. Although treatment options increased over time, the most significant change was to access octreotide therapy, with 24 receiving long-acting somatostatin analogs. Survival improved over time and the median overall survival for patients receiving long-acting somatostatin analogs was 112 months compared with 53 months for those who did not (P=0.021, hazard ratio: 2.46). Ten year survival was 40% and 22%, respectively. About 75% of evaluable patients had a biochemical response to initial therapy and a measurable response occurred in 3 of 24 (13%) patients.
CONCLUSIONS: This single center experience has provided insight into current treatment options for MCT, and suggests the use of long-acting somatostatin analogs may impact on disease control and survival. However, the uptake of other treatment options seems limited and there is a need for agents that target tumor progression.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 19609217     DOI: 10.1097/MCG.0b013e3181a9f10a

Source DB:  PubMed          Journal:  J Clin Gastroenterol        ISSN: 0192-0790            Impact factor:   3.062


  5 in total

1.  [Primary metastatic well-differentiated neuroendocrine tumor arising in a tailgut cyst].

Authors:  M Wöhlke; J Sauer; K Dommisch; S Görling; A Valdix; R Hinze
Journal:  Pathologe       Date:  2011-03       Impact factor: 1.011

Review 2.  Potential synergies for combined targeted therapy in the treatment of neuroendocrine cancer.

Authors:  Ramon Salazar; Diane Reidy-Lagunes; James Yao
Journal:  Drugs       Date:  2011-05-07       Impact factor: 9.546

3.  Multidisciplinary reference centers: the care of neuroendocrine tumors.

Authors:  Simron Singh; Calvin Law
Journal:  J Oncol Pract       Date:  2010-11       Impact factor: 3.840

4.  Incidence, survival, and prevalence of neuroendocrine tumors versus neuroblastoma in children and young adults: nine standard SEER registries, 1975-2006.

Authors:  Pournima Navalkele; M Sue O'Dorisio; Thomas M O'Dorisio; Gideon K D Zamba; Charles F Lynch
Journal:  Pediatr Blood Cancer       Date:  2011-01       Impact factor: 3.167

5.  [Surgical management of a retrorectal tumor with consideration of a rare differential diagnosis].

Authors:  K Krückemeier; P Barth; U Peitz; M W Hoffmann; E H Allemeyer
Journal:  Chirurg       Date:  2012-07       Impact factor: 0.955

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.