Evidence map›Paper›PMID 36202909›Full record

ArticleNPJ precision oncology2022

MatchMiner: an open-source platform for cancer precision medicine.

Harry Klein, Tali Mazor, Ethan Siegel, Pavel Trukhanov, Andrea Ovalle, Catherine Del Vecchio Fitz, Zachary Zwiesler, Priti Kumari, Bernd Van Der Veen, Eric Marriott and 18 more

Abstract read
In one paragraph

Article in NPJ precision oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

23 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. AI for clinical trials in oncology.ESMO real world data and digital oncology · 2026
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Basket Trials: Past, Present, and Future.Annual review of cancer biology · 2024
    Article
  17. Article
  18. Article
  19. Review
  20. OncoCTMiner: streamlining precision oncology trial matching via molecular profile analysis.Database : the journal of biological databases and curation · 2023
    Article
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

28 authors.

Harry KleinDepartment of Data Science, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA. hrklein@ds.dfci.harvard.edu.ORCID http://orcid.org/0000-0002-3237-8943
Tali MazorDepartment of Data Science, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA. tmazor@ds.dfci.harvard.edu.ORCID http://orcid.org/0000-0002-0138-9615
Ethan SiegelDepartment of Data Science, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.
Pavel TrukhanovDepartment of Data Science, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.ORCID http://orcid.org/0000-0002-4942-5451
Andrea OvalleDepartment of Data Science, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.
Catherine Del Vecchio FitzDepartment of Data Science, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.ORCID http://orcid.org/0000-0002-9554-411X
Zachary ZwieslerDepartment of Data Science, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.
Priti KumariDepartment of Data Science, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.
Bernd Van Der VeenThe Hyve, Utrecht, The Netherlands.
Eric MarriottDepartment of Data Science, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.ORCID http://orcid.org/0000-0002-3994-9331
Jason HanselDepartment of Data Science, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.
Joyce YuDepartment of Data Science, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.
Adem AlbayrakInformatics and Analytics, Dana-Farber Cancer Institute, Boston, MA, USA.
Susan BarryDana-Farber Cancer Institute, Boston, MA, USA.
Rachel B KellerDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID http://orcid.org/0000-0001-6138-9257
Laura E MacConaillDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
Neal LindemanDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
Bruce E JohnsonDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Barrett J RollinsDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Khanh T DoDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID http://orcid.org/0000-0002-9411-8899
Brian BeardsleeDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Geoffrey ShapiroDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Suzanne Hector-BarryDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
John MethotInformatics and Analytics, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID http://orcid.org/0000-0002-7983-2154
Lynette ShollDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
James LindsayDepartment of Data Science, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.ORCID http://orcid.org/0000-0002-6295-098X
Michael J HassettDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID http://orcid.org/0000-0003-0754-3510
Ethan CeramiDepartment of Data Science, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Widespread, comprehensive sequencing of patient tumors has facilitated the usage of precision medicine (PM) drugs to target specific genomic alterations. Therapeutic clinical trials are necessary to test new PM drugs to advance precision medicine, however, the abundance of patient sequencing data coupled with complex clinical trial eligibility has made it challenging to match patients to PM trials. To facilitate enrollment onto PM trials, we developed MatchMiner, an open-source platform to computationally match genomically profiled cancer patients to PM trials. Here, we describe MatchMiner's capabilities, outline its deployment at Dana-Farber Cancer Institute (DFCI), and characterize its impact on PM trial enrollment. MatchMiner's primary goals are to facilitate PM trial options for all patients and accelerate trial enrollment onto PM trials. MatchMiner can help clinicians find trial options for an individual patient or provide trial teams with candidate patients matching their trial's eligibility criteria. From March 2016 through March 2021, we curated 354 PM trials containing a broad range of genomic and clinical eligibility criteria and MatchMiner facilitated 166 trial consents (MatchMiner consents, MMC) for 159 patients. To quantify MatchMiner's impact on trial consent, we measured time from genomic sequencing report date to trial consent date for the 166 MMC compared to trial consents not facilitated by MatchMiner (non-MMC). We found MMC consented to trials 55 days (22%) earlier than non-MMC. MatchMiner has enabled our clinicians to match patients to PM trials and accelerated the trial enrollment process.

Identifiers

PMID36202909
PMCPMC9537311

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.