Evidence map›Paper›PMID 37685988›Full record

ArticleInternational journal of molecular sciences2023

Report on the Effect of the Implementation of an Early Detection and Prevention of Cancer Program on Families at High Hereditary Risk-Concentrating on Patients Undergoing Genetic Diagnostics and Counseling in Central Poland.

Tadeusz Kałużewski, Izabela Kubiak, Michał Bednarek, Jordan Sałamunia, Dorota Kucharska, Łukasz Kępczyński, Marek Stempień, Tobiasz Kubicki, Radzisław Trzciński, Zofia Gordon-Sönmez and 3 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 80% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

13 authors at 3 institutions in 1 country.

Tadeusz KałużewskiDepartment of Genetics, Polish Mother's Memorial Hospital Research Institute, 93-338 Lodz, Poland.ORCID 0000-0001-6118-696X
Izabela KubiakR&D Department, Laboratory of Medical Genetics, GENOS Sp. z o.o., 91-033 Lodz, Poland.
Michał BednarekR&D Department, Laboratory of Medical Genetics, GENOS Sp. z o.o., 91-033 Lodz, Poland.
Jordan SałamuniaR&D Department, Laboratory of Medical Genetics, GENOS Sp. z o.o., 91-033 Lodz, Poland.
Dorota KucharskaR&D Department, Laboratory of Medical Genetics, GENOS Sp. z o.o., 91-033 Lodz, Poland.
Łukasz KępczyńskiDepartment of Genetics, Polish Mother's Memorial Hospital Research Institute, 93-338 Lodz, Poland.ORCID 0000-0002-2882-5448
Marek StempieńDepartment of General and Colorectal Surgery with the Subdepartment of Oncological Surgery, Provincial Hospital John Paul II in Bełchatów, 97-400 Belchatow, Poland.
Tobiasz KubickiSokrates Medical Center, 98-200 Sieradz, Poland.
Radzisław TrzcińskiDepartment of General and Colorectal Surgery with the Subdepartment of Oncological Surgery, Provincial Hospital John Paul II in Bełchatów, 97-400 Belchatow, Poland.
Zofia Gordon-SönmezDepartment of Gynecology and Obstetrics, Zduńska Wola District Hospital Sp. z o.o., 98-220 Zdunska Wola, Poland.
Anna Bartosińska-DycDepartment of Gynecology and Obstetrics, Zduńska Wola District Hospital Sp. z o.o., 98-220 Zdunska Wola, Poland.
Agnieszka GachDepartment of Genetics, Polish Mother's Memorial Hospital Research Institute, 93-338 Lodz, Poland.ORCID 0000-0002-6590-5797
Bogdan KałużewskiR&D Department, Laboratory of Medical Genetics, GENOS Sp. z o.o., 91-033 Lodz, Poland.
Polish Mother’s Memorial Hospital Research Institute · PLJan Kochanowski University · PLJohn Paul II Hospital · PL

Funding

Polish Mother's Memorial Hospital Research Institute 2021.2/3/3-GW
6 · The paper itself

Abstract

Over a 46-month period, the objectives of the National Cancer Control Program (NCCP, pol. Narodowy Program Zwalczania Chorób Nowotworowych), coordinated by the Ministry of Health, were pursued by conducting genetic diagnostics on individuals at high risk of developing cancer. A total of 1097 individuals were enrolled in the study, leading to the identification of 128 cases of germline mutations. The implementation of the NCCP led to the identification of genetic mutations in 4.43% of the patients qualified for

Indexed as

Endometrial NeoplasmsOvarian NeoplasmsCounselingEarly Detection of CancerFemaleHumansPolandBRCA1BRCA2breast cancerCHEK2colorectal cancerendometrial cancerhereditary breast ovarian cancerhereditary colorectal cancerhereditary endometrial cancerovarian cancerPALB2

Identifiers

PMID37685988
PMCPMC10488022
OpenAlexW4386121597

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.