Evidence map›Paper›PMID 36752890›Full record

ArticleClinical and experimental medicine2023

Utility of public knowledge bases for the interpretation of comprehensive tumor molecular profiling results.

Alexandra Lebedeva, Grigory Timokhin, Ekaterina Ignatova, Alexandra Kavun, Egor Veselovsky, Margarita Sharova, Vladislav Mileyko, Valentina Yakushina, Olesya Kuznetsova, Maria Stepanova and 16 more

Abstract read
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In one paragraph

Article in Clinical and experimental medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

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

26 authors.

Alexandra LebedevaOncoAtlas LLC, Malaya Nikitskaya Str., 31, Moscow, Russia, 121069. lebedeva.alexandra.2015@post.bio.msu.ru.
Grigory TimokhinOncoAtlas LLC, Malaya Nikitskaya Str., 31, Moscow, Russia, 121069.
Ekaterina IgnatovaResearch Centre for Medical Genetics, Moskvorech'ye Ulitsa, 1, Moscow, Russia, 115478.
Alexandra KavunOncoAtlas LLC, Malaya Nikitskaya Str., 31, Moscow, Russia, 121069.
Egor VeselovskyOncoAtlas LLC, Malaya Nikitskaya Str., 31, Moscow, Russia, 121069.
Margarita SharovaOncoAtlas LLC, Malaya Nikitskaya Str., 31, Moscow, Russia, 121069.
Vladislav MileykoOncoAtlas LLC, Malaya Nikitskaya Str., 31, Moscow, Russia, 121069.
Valentina YakushinaOncoAtlas LLC, Malaya Nikitskaya Str., 31, Moscow, Russia, 121069.
Olesya KuznetsovaOncoAtlas LLC, Malaya Nikitskaya Str., 31, Moscow, Russia, 121069.
Maria StepanovaClinic "Luch'', Savushkina Str., 73, Saint-Petersburg, Russian Federation, 197183.
Polina ShiloClinic "Luch'', Savushkina Str., 73, Saint-Petersburg, Russian Federation, 197183.
Fedor MoiseenkoSaint-Petersburg Clinical Research Center of Specialized Types of Medical Care (Oncological), Leningradskaya Str., 68A, Saint-Petersburg, Russian Federation, 197758.
Nikita VolkovSaint-Petersburg Clinical Research Center of Specialized Types of Medical Care (Oncological), Leningradskaya Str., 68A, Saint-Petersburg, Russian Federation, 197758.
Igor PlaksaGENETICO LLC, Gubkina Str., 3/1, Moscow, Russian Federation, 119333.
Andrey IsaevHigher School of Oncology, Saint Petersburg, Russian Federation.
Margarita GayryanGENETICO LLC, Gubkina Str., 3/1, Moscow, Russian Federation, 119333.
Elizaveta ArtemyevaSaint-Petersburg Clinical Research Center of Specialized Types of Medical Care (Oncological), Leningradskaya Str., 68A, Saint-Petersburg, Russian Federation, 197758.
Albina ZhabinaSaint-Petersburg Clinical Research Center of Specialized Types of Medical Care (Oncological), Leningradskaya Str., 68A, Saint-Petersburg, Russian Federation, 197758.
Mikhail KramchaninovSaint-Petersburg Clinical Research Center of Specialized Types of Medical Care (Oncological), Leningradskaya Str., 68A, Saint-Petersburg, Russian Federation, 197758.
Valentina ShamrikovaClinical Hospital No. 2, "Medsi" Group of Companies, 5/4 2-Oy Botkinskiy Proezd, Moscow, Russia, 125284.
Ilya PokataevFederal State Budgetary Institution, N.N. Blokhin National Medical Research Center of Oncology, Kashira Hwy, 23, Moscow, Russian Federation, 115522.
Alexey RumyantsevFederal State Budgetary Institution, N.N. Blokhin National Medical Research Center of Oncology, Kashira Hwy, 23, Moscow, Russian Federation, 115522.
Evgeny LedinMEDSI, Moscow, Russia.
Alexey TryakinFederal State Budgetary Institution, N.N. Blokhin National Medical Research Center of Oncology, Kashira Hwy, 23, Moscow, Russian Federation, 115522.
Mikhail FedyaninFederal State Budgetary Institution, N.N. Blokhin National Medical Research Center of Oncology, Kashira Hwy, 23, Moscow, Russian Federation, 115522.
Maxim IvanovOncoAtlas LLC, Malaya Nikitskaya Str., 31, Moscow, Russia, 121069.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the growing use of comprehensive tumor molecular profiling (CTMP), the therapeutic landscape of cancer is rapidly evolving. NGS produces large amounts of genomic data requiring complex analysis and subsequent interpretation. We sought to determine the utility of publicly available knowledge bases (KB) for the interpretation of the cancer mutational profile in clinical practice. Analysis was performed across patients who previously underwent CTMP. Independent interpretation of the CTMP was performed manually, and then, the recommendations were compared to ones present in KBs (OncoKB, CIViC, CGI, CGA, VICC, MolecularMatch). A total of 222 CTMP reports from 222 patients with 932 genomic alterations (GA) were identified. For 368 targetable GA identified in 171 (77%) of the patients, 1381 therapy recommendations were compiled. Except for CGA, therapy ESCAT LOE I, II, IIIA and IIIB therapy options were equally represented in the majority of KB. Personalized treatment options with ESCAT LOE I-II were provided for 35 patients (16%); MolecularMatch/CIViC allowed to collect ESCAT I-II treatment options for 34 of them (97%), OncoKB/CGI-for 33 of them (94%). Employing VICC and CGA 6 (17%) and 20 (57%) of patients were left without ESCAT I or II treatment options. For 88 patients with ESCAT level III-B therapy recommendations: only 2 (2%), 3 (3%), 4 (5%) and 6 (7%) of patients were left without options with CIViC, MolecularMatch, CGI and OncoKB, and with VICC-12 (14%). Highest overlap ratio was observed for IIIA (0.81) biomarkers, with the comparable results for LOE I-II. Meanwhile, overlap ratio for ESCAT LOE IV was 0.22. Public KBs provide substantial information on ESCAT-I/R1 biomarkers, but the information on ESCAT II-IV and resistance biomarkers is underrepresented. Manual curation should be considered the gold standard for the CTMP interpretation.

Indexed as

NeoplasmsBiomarkersGenomicsHumansKnowledge BasesMutationBiomarkersComprehensive tumor molecular profilingGenomic alterationsMolecular diagnosticsNGSPrecision oncologyPrecision oncology knowledge bases

Identifiers

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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.