Evidence map›Paper›PMID 31189618›Full record

Trial reportThe oncologist2019

TELEPRO: Patient-Reported Carcinoid Syndrome Symptom Improvement Following Initiation of Telotristat Ethyl in the Real World.

Jonathan Strosberg, Vijay N Joish, Susan Giacalone, Raul Perez-Olle, Ann Fish-Steagall, Kanika Kapoor, Sam Dharba, Pablo Lapuerta, Al B Benson

Open access · hybridAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The oncologist, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Progress in the Treatment of Small Intestine Cancer.Current treatment options in oncology · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 1 country.

Jonathan StrosbergMoffitt Cancer Center, Tampa, Florida, USA jonathan.strosberg@moffitt.org.
Vijay N JoishLexicon Pharmaceuticals, Inc., The Woodlands, Texas, USA.
Susan GiacaloneLexicon Pharmaceuticals, Inc., The Woodlands, Texas, USA.
Raul Perez-OlleLexicon Pharmaceuticals, Inc., The Woodlands, Texas, USA.
Ann Fish-SteagallBiologics McKesson, Inc., Raleigh, North Carolina, USA.
Kanika KapoorDiplomat, Flint, Michigan, USA.
Sam DharbaDatawave Solutions, Cranbury, New Jersey, USA.
Pablo LapuertaLexicon Pharmaceuticals, Inc., The Woodlands, Texas, USA.
Al B BensonFeinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Lexicon Pharmaceuticals (United States) · USMcKesson (United States) · USMoffitt Cancer Center · USNorthwestern University · USUniversity of Michigan–Flint · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhen carcinoid syndrome (CS) diarrhea (CSD) is inadequately controlled with long-acting somatostatin analogs (SSAs), clinical practice guidelines recommend addition of the tryptophan hydroxylase inhibitor telotristat ethyl (TE). In a 12-week multinational, randomized controlled trial, TE added to SSA reduced peripheral serotonin and the frequency of CSD. We evaluated real-world effectiveness of TE using patient-reported data from a nurse support program over 3 months. MATERIALS AND

methodsThis study used a deidentified data set of patients initiating TE who opted into a nurse support program between March and November 2017 and reported CS symptom burden at baseline and at least one follow-up time point at months 1, 2, and 3. Patients reported demographic and medical history information as well as frequency of bowel movements (BMs) and flushing episodes, severity of nausea, urgency and abdominal pain (0 "no/not at all" to 100 "worst imaginable/very urgent"), and stool form (1 "very hard" to 10 "watery"). Mean changes from baseline in CS symptom burden were reported using paired-sample

resultsMost patients initiating TE enrolled in the nurse program (791/898, 88%), of whom 369 (47%) were included in the analysis. Patients treated with TE reported significant reductions in CSD and other CS symptoms (all

conclusionPatients taking SSA therapy showed substantial burden of disease before initiating TE and significant improvements with the addition of TE treatment in this real-world effectiveness study. IMPLICATIONS FOR PRACTICE: Patients with carcinoid syndrome diarrhea uncontrolled by high doses of long-acting somatostatin analogs may be candidates for additional therapy with the tryptophan hydroxylase inhibitor telotristat ethyl. Understanding the real-world prevalence of uncontrolled symptoms and the effectiveness of telotristat ethyl in clinical practice may further support clinical and policy decisions for these patients. This study investigated self-reported carcinoid syndrome symptom burden and improvements among patients initiating telotristat ethyl and participating in a voluntary nurse support program. Disease burden and off-label somatostatin analog treatment before initiating telotristat ethyl were high, and symptoms improved markedly over 1, 2, and 3 months of treatment.

Indexed as

Patient Reported Outcome MeasuresAgedCohort StudiesDiarrheaFemaleFollow-Up StudiesHumansInternational AgenciesMaleMalignant Carcinoid SyndromePhenylalaninePrognosisPyrimidinesPhenylalaninePyrimidinestelotristat ethylCarcinoid tumorLanreotideMalignant carcinoid syndromeNeuroendocrine tumorsOctreotideTelotristat ethyl

Identifiers

PMID31189618
PMCPMC6853091
OpenAlexW2949365824

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

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.