Evidence map›Paper›PMID 35309086›Full record

ArticleTherapeutic advances in medical oncology2022

Platinum-based chemotherapy for pancreatic cancer: impact of mutations in the homologous recombination repair and Fanconi anemia genes.

Marina Emelyanova, Elena Pudova, Darya Khomich, George Krasnov, Anna Popova, Ivan Abramov, Vladimir Mikhailovich, Maxim Filipenko, Sofia Menshikova, Sergey Tjulandin and 1 more

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
2.1field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 27 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

11 authors at 4 institutions in 1 country.

Marina EmelyanovaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, Russian Federation.
Elena PudovaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russian Federation.
Darya KhomichEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russian Federation.
George KrasnovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russian Federation.
Anna PopovaN.N. Blokhin National Medical Research Center for Oncology, Ministry of Health of the Russian Federation, Moscow, Russian Federation.
Ivan AbramovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russian Federation.
Vladimir MikhailovichEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russian Federation.
Maxim FilipenkoInstitute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation.
Sofia MenshikovaK31 City Clinic, Moscow, Russian Federation.
Sergey TjulandinN.N. Blokhin National Medical Research Center for Oncology, Ministry of Health of the Russian Federation, Moscow, Russian Federation.
Ilya PokataevN.N. Blokhin National Medical Research Center for Oncology, Ministry of Health of the Russian Federation, Moscow, Russian Federation.
Engelhardt Institute of Molecular Biology · RUCity Clinical Hospital · RUMinistry of Health of the Russian Federation · RUInstitute of Chemical Biology and Fundamental Medicine · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Mutations in homologous recombination (HR) and Fanconi anemia (FA) genes may predispose to pancreatic cancer (PC) and enable the prediction of sensitivity to platinum-based chemotherapy. FOLFIRINOX is a standard treatment option for non-selected PC patients and could be effective due to undiagnosed DNA repair deficiency. Here, we aimed to determine the frequency of mutations in genes involved in the HR and FA pathways, evaluate their clinical implications, and determine the objective response rate (ORR), progression-free survival (PFS), and overall survival (OS) of PC patients treated with platinum. Methods: We performed targeted DNA sequencing of 30 genes ( Results: In Conclusion: Mutations in the

Indexed as

BRCA1/2homologous recombination deficiencymutationsPALB2pancreatic cancerplatinum-based chemotherapy

Identifiers

PMID35309086
PMCPMC8928350
OpenAlexW4220968403

What OpenQuestion holds

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LicenceCC BY-NC
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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.