Evidence map›Paper›PMID 24037980›Full record

ReviewThe oncologist2013

Current understanding and management of medullary thyroid cancer.

Madhuchhanda Roy, Herbert Chen, Rebecca S Sippel

Open access · bronzeAbstract readReview
In one paragraph

Review in The oncologist, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

53 citing papers in PubMed, 121 citations in OpenAlex.

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  9. Correlation ofArchives of endocrinology and metabolism · 2024
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  16. [European journal of nuclear medicine and molecular imaging · 2023
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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

3 authors at 1 institution in 1 country.

Madhuchhanda RoyDepartment of Surgery, University of Wisconsin, Madison, Wisconsin, USA.
Herbert Chen
Rebecca S Sippel
University of Wisconsin–Madison · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Medullary thyroid cancer (MTC) typically accounts for 3%-4% of all thyroid cancers. Although the majority of MTCs are sporadic, 20% of cases are hereditary. Hereditary MTC can be found in multiple endocrine neoplasia 2A or 2B or as part of familial MTC based on a specific germline mutation in the RET proto-oncogene. This article discusses the current approaches available for the diagnosis, evaluation, and management of patients and their family members with suspected MTC. The disease is predominantly managed surgically and typically requires a total thyroidectomy and lymph node dissection. A review of recent guidelines on the extent and timing of surgical excision is discussed. There are not very many effective systemic treatment options for MTC, but several emerging therapeutic targets have promise.

Indexed as

ThyroidectomyCalcitoninCarcinoma, MedullaryCarcinoma, NeuroendocrineGerm-Line MutationHumansLymph Node ExcisionMultiple Endocrine Neoplasia Type 2aProto-Oncogene MasProto-Oncogene Proteins c-retThyroid NeoplasmsCalcitoninMAS1 protein, humanProto-Oncogene MasProto-Oncogene Proteins c-retRET protein, humanFamilial Medullary Thyroid Cancer (FMTC)Medullary Thyroid Cancer (MTC)Multiple Endocrine Neoplasia SyndromeProphylactic surgery in MTCRET proto-oncogeneSerum calcitonin

Identifiers

PMID24037980
PMCPMC3805151
OpenAlexW2116862985

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.