Evidence map›Paper›PMID 18780869›Full record

ArticleJournal of the National Cancer Institute2008

Priorities for improving the management of gastroenteropancreatic neuroendocrine tumors.

Irvin M Modlin, Steven F Moss, Daniel C Chung, Robert T Jensen, Elizabeth Snyderwine

2 registry-linked trialsAbstract readConference Proceedings
In one paragraph

Article in Journal of the National Cancer Institute, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 104 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01873248 early_phase1completednot on this mapstarted 2013, after this paper: background citation

Impact of 68Ga-DOTATATE PET/CT on the Management of Neuroendocrine Tumors: The Referring Physician's Perspective

TypeinterventionalSponsorJonsson Comprehensive Cancer CenterRan2013 to 2017Enrolled100ConditionsNeuroendocrine TumorsArms68Ga-DOTATATE
NCT04339036 phase2recruitingnot on this mapstarted 2021, after this paper: background citation

UPCC 04219 Phase 2 Study of Capecitabine-Temozolomide(CapTem) With Yttrium-90 Radioembolization in the Treatment of Patients With Unresectable Metastatic Grade 2/3 Neuroendocrine Tumors

TypeinterventionalSponsorAbramson Cancer Center at Penn MedicineRan2021 to 2028Enrolled70ConditionsNeuroendocrine Tumor Grade 2, Neuroendocrine TumorsArmsCapecitabine Oral Product, Temozolomide Oral Product, transarterial radioembolization
3 · Its place in the literature

Who cites it

104 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  10. Circulating hsa-miR-5096 predictsFrontiers in oncology · 2023
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44 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Irvin M ModlinDepartment of Gastroenterological Surgery, Yale University School of Medicine, New Haven, CT 06520-8062, USA. imodlin@optonline.net
Steven F Moss
Daniel C Chung
Robert T Jensen
Elizabeth Snyderwine

Funding

Diagnosis, Natural History, Management,tumor biology of Gastrinomas/PETs/Neuroendocrine tumorsZIADK053200 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI JENSEN, ROBERT · 2009 to 2025
$4.3M
Molecular aspects of gastrinomaZ01DK053215 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI JENSEN, ROBERT · 2007 to 2008
$709k
MANAGEMENT OF ISLET CELL TUMORSZ01DK053200 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI JENSEN, ROBERT · 1990 to 2008
$667k
6 · The paper itself

Abstract

A National Cancer Institute summit meeting on gastroenteropancreatic neuroendocrine and carcinoid tumors was held in September 2007 to present the currently accepted standards of care for patients with these tumors and to identify areas requiring investigation and development. These tumors are clinically and pathologically heterogeneous, present commonly with obscure symptoms that lead to delays in diagnosis of years, and have an incidence in the United States of 2.5 to 5 cases per 100,000. The 5-year survival rates range between 15% and 95%, depending on the site and extent of disease. This report delineates the main conclusions of the meeting, including the best practice diagnosis and treatment strategies for gastropancreatic neuroendocrine tumors, and the identification of clinical and scientific areas that are most in need of attention. The most pressing needs were public and physician education, identification of molecular markers for early diagnosis and therapeutic monitoring, improved imaging modalities and molecular prognostication, development of a standardized pathological classification system, and creation of regional centers of expertise with tumor and laboratory data banks. In addition, adequately validated neuroendocrine tumor models and cell lines should be established to investigate the molecular mechanisms involved in the control of their growth and secretion, and to facilitate the development of specific therapies that should be examined in well-designed multicenter studies of defined patient groups.

Indexed as

Carcinoid TumorGastrointestinal NeoplasmsNeuroendocrine TumorsPancreatic NeoplasmsAnimalsBiomarkers, TumorBiomedical ResearchDisease Models, AnimalEarly DiagnosisHumansIncidenceInterdisciplinary CommunicationNational Cancer Institute (U.S.)Neoplasm StagingPrevalencePrognosisBiomarkers, Tumor

Identifiers

PMID18780869
PMCPMC2538549

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.