Evidence map›Paper›PMID 32172368›Full record

ReviewCurrent treatment options in oncology2020

Patient Selection and Toxicities of PRRT for Metastatic Neuroendocrine Tumors and Research Opportunities.

Shagufta Shaheen, Farshad Moradi, Gerardo Gamino, Pamela L Kunz

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current treatment options in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  8. Clinical Utility ofCancers · 2021
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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

4 authors at 2 institutions in 1 country.

Shagufta ShaheenDepartment of Medicine, Division of Oncology, Stanford University, School of Medicine, Stanford, CA, 94305, USA.
Farshad MoradiDepartment of Radiology, Division of Nuclear Medicine, Stanford University, School of Medicine, Stanford, CA, 94305, USA.
Gerardo GaminoBrigham Young University, 22234 S Vermont Ave. #203, Torrance, CA, 90502, USA.
Pamela L KunzDepartment of Medicine, Division of Oncology, Stanford University, School of Medicine, Stanford, CA, 94305, USA. pkunz@stanford.edu.
Stanford University · USBrigham Young University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

opinion statementNeuroendocrine tumors (NETs) are a heterogenous group of neoplasms characterized by varied biological hallmarks and behavior, ranging from indolent to aggressive. For many decades, somatostatin analogues and few targeted therapies were available for NETs and these therapies had minimal response rates. However, there have been a number of recent treatment advances. Peptide receptor radionuclide therapy (PRRT) is a novel approach to treatment of NETs and has changed the landscape of treatment for NETs. It is a form of targeted therapy in which a radiolabeled somatostatin analogue delivers radiation specifically to tumor cells expressing the somatostatin receptor.

Indexed as

Patient SelectionBiomedical ResearchBrachytherapyCombined Modality TherapyDisease ManagementHumansNeoplasm MetastasisNeoplasm StagingNeuroendocrine TumorsPractice Guidelines as TopicRadiation DosageRadiopharmaceuticalsReceptors, PeptideTreatment OutcomeRadiopharmaceuticalsReceptors, PeptideMyelodysplastic syndrome (MDSPeptide receptor radionuclide therapy (PRRT)Salvage therapySomatostatin analogues (SSAs)Somatostatin receptors (SSTRs)Toxicity

Identifiers

PMID32172368
OpenAlexW3012260471

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.