Evidence map›Paper›PMID 28343336›Full record

ArticleMedical oncology (Northwood, London, England)2017

Sunitinib-induced hypothyroidism predicts progression-free survival in metastatic renal cell carcinoma patients.

Anna Buda-Nowak, Jakub Kucharz, Paulina Dumnicka, Marek Kuzniewski, Roman Maria Herman, Aneta L Zygulska, Beata Kusnierz-Cabala

Open access · hybridAbstract read
In one paragraph

Article in Medical oncology (Northwood, London, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it, 41 citations in OpenAlex.

  1. Higher thyroid hormone levels and cancer.European journal of nuclear medicine and molecular imaging · 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

7 authors at 2 institutions in 1 country.

Anna Buda-NowakDepartment of Oncology, University Hospital in Krakow, Sniadeckich 10, 31-531, Cracow, Poland.
Jakub KucharzDepartment of Experimental and Clinical Surgery, Jagiellonian University Medical College, Michalowskiego 12, Cracow, 31-126, Poland. jakub.kucharz@uj.edu.pl.
Paulina DumnickaDepartment of Medical Diagnostics, Jagiellonian University Medical College, Medyczna 9, 30-688, Cracow, Poland.
Marek KuzniewskiDepartment of Nephrology, Jagiellonian University Medical College, Kopernika 15, 31-501, Cracow, Poland.
Roman Maria HermanDepartment of Experimental and Clinical Surgery, Jagiellonian University Medical College, Michalowskiego 12, Cracow, 31-126, Poland.
Aneta L ZygulskaDepartment of Oncology, University Hospital in Krakow, Sniadeckich 10, 31-531, Cracow, Poland.
Beata Kusnierz-CabalaDepartment of Diagnostics, Chair of Clinical Biochemistry, Jagiellonian University Medical College, Kopernika 15A, 31-501, Cracow, Poland.
Jagiellonian University · PLKrakow Cardiovascular Research Institute · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sunitinib is a tyrosine kinase inhibitor (TKI) used in treatment of metastatic renal cell carcinoma (mRCC), gastrointestinal stromal tumors and pancreatic neuroendocrine tumors. One of the most common side effects related to sunitinib is hypothyroidism. Recent trials suggest correlation between the incidence of hypothyroidism and treatment outcome in patients treated with TKI. This study evaluates whether development of hypothyroidism is a predictive marker of progression-free survival (PFS) in patients with mRCC treated with sunitinib. Twenty-seven patients diagnosed with clear cell mRCC, after nephrectomy and in 'good' or 'intermediate' MSKCC risk prognostic group, were included in the study. All patients received sunitinib as a first-line treatment on a standard schedule (initial dose 50 mg/day, 4 weeks on, 2 weeks off). The thyroid-stimulating hormone serum levels were obtained at the baseline and every 12 weeks of treatment. In statistic analyses, we used Kaplan-Meier method for assessment of progression-free survival; for comparison of survival, we used log-rank test. In our study, the incidence of hypothyroidism was 44%. The patients who had developed hypothyroidism had better median PFS to patients with normal thyroid function 28,3 months [95% (CI) 20.4-36.2 months] versus 9.8 months (6.4-13.1 months). In survival analysis, we perceive that thyroid dysfunction is a predictive factor of a progression-free survival (PFS). In the unified group of patients, the development of hypothyroidism during treatment with sunitinib is a positive marker for PFS. During that treatment, thyroid function should be evaluated regularly.

Indexed as

AgedCarcinoma, Renal CellDisease-Free SurvivalFemaleHumansHypothyroidismIndolesKaplan-Meier EstimateKidney NeoplasmsMaleMiddle AgedProtein Kinase InhibitorsPyrrolesRetrospective StudiesSunitinibIndolesProtein Kinase InhibitorsPyrrolesSunitinibHypothyroidismPredictive factorPrognosisProgression-free survivalRenal cell carcinomaSunitinib

Identifiers

PMID28343336
PMCPMC5366170
OpenAlexW2598071289

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Registered trials

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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.