Evidence map›Paper›PMID 34205778›Full record

ArticleCancers2021

Gender-Specific Efficacy Revealed by Head-to-Head Comparison of Pasireotide and Octreotide in a Representative In Vivo Model of Nonfunctioning Pituitary Tumors.

Sebastian Gulde, Tobias Wiedemann, Mathias Schillmaier, Isabel Valença, Amelie Lupp, Katja Steiger, Hsi-Yu Yen, Stephen Bäuerle, Johannes Notni, Raul Luque and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

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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

15 authors at 6 institutions in 4 countries.

Sebastian GuldeInstitute for Diabetes and Cancer, Helmholtz Zentrum München, 85764 Neuherberg, Germany.ORCID 0000-0002-8672-010X
Tobias WiedemannInstitute for Diabetes and Cancer, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Mathias SchillmaierDepartment of Nuclear Medicine, School of Medicine, Technical University of Munich, 80333 Munich, Germany.
Isabel ValençaInstitute for Diabetes and Cancer, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Amelie LuppInstitute of Pharmacology and Toxicology, Jena University Hospital, Friedrich Schiller University Jena, 07743 Jena, Germany.ORCID 0000-0003-0141-7310
Katja SteigerInstitute of Pathology, School of Medicine, Technical University of Munich, 80333 Munich, Germany.ORCID 0000-0002-7269-5433
Hsi-Yu YenInstitute of Pathology, School of Medicine, Technical University of Munich, 80333 Munich, Germany.
Stephen BäuerleDepartment of Mathematics, Technical University of Munich, 85748 Garching, Germany.ORCID 0000-0001-8539-005X
Johannes NotniInstitute of Pathology, School of Medicine, Technical University of Munich, 80333 Munich, Germany.ORCID 0000-0002-3964-3391
Raul LuqueDepartment of Cell Biology, Physiology, and Immunology, Maimonides Institute for Biomedical Research of Córdoba (IMIBIC), University of Córdoba and Hospital Universitario Reina Sofía (HURS), 14004 Cordoba, Spain.ORCID 0000-0002-7585-1913
Herbert SchmidDepartment of Oncology Research, Novartis Institute for BioMedical Research, Novartis Pharma AG, 4033 Basel, Switzerland.
Stefan SchulzInstitute of Pharmacology and Toxicology, Jena University Hospital, Friedrich Schiller University Jena, 07743 Jena, Germany.
Donna P AnkerstDepartment of Mathematics, Technical University of Munich, 85748 Garching, Germany.
Franz SchillingDepartment of Nuclear Medicine, School of Medicine, Technical University of Munich, 80333 Munich, Germany.
Natalia S PellegataInstitute for Diabetes and Cancer, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Technical University of Munich · DEHeidelberg University · DEJena University Hospital · DEEssen University Hospital · DENovartis (Switzerland) · CHSpanish Biomedical Research Centre in Physiopathology of Obesity and Nutrition · ES

Funding

Deutsche Forschungsgemeinschaft 314061271-TRR 205Deutsche Forschungsgemeinschaft 391523415-SFB824Deutsche Krebshilfe 70112383Wilhelm Sander-Stiftung 2017.012.1
6 · The paper itself

Abstract

Invasive nonfunctioning pituitary tumors (NFPTs) are non-resectable neoplasms associated with frequent relapse and significant comorbidities. Current treatments, including somatostatin receptor 2 (SSTR2)-directed somatostatin analogs (SSAs), often fail against NFPTs. Thus, identifying effective therapies is clinically relevant. As NFPTs express SSTR3 at high levels, pasireotide, a multireceptor-targeted SSA, might be beneficial. Here we evaluated pasireotide in the only representative model of spontaneous NFPTs (MENX rats) in vivo. Octreotide long-acting release (LAR), pasireotide LAR, or placebo, were administered to age-matched, tumor-bearing MENX rats of both sexes for 28 d or 56 d. Longitudinal high-resolution magnetic resonance imaging monitored tumor growth. While tumors in placebo-treated rats increased in volume over time, PTs in drug-treated rats displayed significant growth suppression, and occasional tumor shrinkage. Pasireotide elicited stronger growth inhibition. Radiological responses correlated with tumors' proliferation rates. Both SSAs, but especially pasireotide, were more effective in female vs. male rats. Basal

Indexed as

MRInonfunctioning pituitary tumorsoctreotidepasireotidesex differences in drug responsesomatostatin receptors

Identifiers

PMID34205778
PMCPMC8235746
OpenAlexW3174892125

What OpenQuestion holds

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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.