Evidence map›Paper›PMID 31423337›Full record

ArticleESMO open2019

Interim analysis of a real-world precision medicine platform for molecular profiling of metastatic or advanced cancers: MONDTI.

Markus Kieler, Matthias Unseld, Daniela Bianconi, Fredrik Waneck, Robert Mader, Fritz Wrba, Thorsten Fuereder, Christine Marosi, Markus Raderer, Philipp Staber and 7 more

Open access · goldAbstract read
In one paragraph

Article in ESMO open, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Precision Oncology in Older Cancer Patients: A Single-Center Experience.International journal of molecular sciences · 2024
    Article
  3. Article
  4. Article
  5. Review
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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

17 authors at 2 institutions in 1 country.

Markus KielerDepartment of Medicine I, Division of Oncology, Medical University of Vienna, Wien, Austria.ORCID 0000-0002-4082-5731
Matthias UnseldDepartment of Medicine I, Division of Oncology, Medical University of Vienna, Wien, Austria.
Daniela BianconiDepartment of Medicine I, Division of Oncology, Medical University of Vienna, Wien, Austria.
Fredrik WaneckDepartment of Biomedical Imaging and Image-guided Therapy, Division of Cardiovascular and Interventional Radiology, Medical University of Vienna, Wien, Austria.
Robert MaderDepartment of Medicine I, Division of Oncology, Medical University of Vienna, Wien, Austria.
Fritz WrbaDepartment of Pathology, Medical University of Vienna, Wien, Austria.
Thorsten FuerederDepartment of Medicine I, Division of Oncology, Medical University of Vienna, Wien, Austria.
Christine MarosiDepartment of Medicine I, Division of Oncology, Medical University of Vienna, Wien, Austria.
Markus RadererDepartment of Medicine I, Division of Oncology, Medical University of Vienna, Wien, Austria.
Philipp StaberDepartment of Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Wien, Austria.
Walter BergerInstitute of Cancer Research, Department of Medicine I, Comprehensive Cancer Center, Medical University of Vienna, Wien, Austria.
Maria SibiliaInstitute of Cancer Research, Department of Medicine I, Comprehensive Cancer Center, Medical University of Vienna, Wien, Austria.
Stephan PolterauerDepartment of Obstetrics and Gynecology, Division of General Gynecology and Gynecologic Oncology, Medical University of Vienna, Wien, Austria.
Leonhard MüllauerDepartment of Pathology, Medical University of Vienna, Wien, Austria.
Matthias PreusserDepartment of Medicine I, Division of Oncology, Medical University of Vienna, Wien, Austria.ORCID 0000-0003-3541-2315
Christoph C ZielinskiDepartment of Medicine I, Division of Oncology, Medical University of Vienna, Wien, Austria.
Gerald W PragerDepartment of Medicine I, Division of Oncology, Medical University of Vienna, Wien, Austria.ORCID 0000-0002-4751-6595
Medical University of Vienna · ATComprehensive Cancer Center Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHigh-throughput genomic profiling of tumour specimens facilitates the identification of individual actionable mutations which could be used for individualised targeted therapy. This approach is becoming increasingly more common in the clinic; however, the interpretation of results from molecular profiling tests and efficient guiding of molecular therapies to patients with advanced cancer offer a significant challenge to the oncology community. EXPERIMENTAL

designMONDTI is a precision medicine platform for molecular characterisation of metastatic solid tumours to identify actionable genomic alterations. From 2013 to 2016, comprehensive molecular profiles derived from real-time biopsy specimens and archived tumour tissue samples of 295 patients were performed. Results and treatment suggestions were discussed within multidisciplinary tumour board meetings.

resultsThe mutational profile was obtained from 293 (99%) patients and a complete immunohistochemical (IHC) and cytogenetic profile was obtained in 181 (61%) and 188 (64%) patients. The most frequent cancer types were colorectal cancer (12%), non-Hodgkin's lymphomas (9.8%) and head and neck cancers (7.8%). The most commonly detected mutations were

conclusionsThe results reveal that the open concept for all solid tumours characterised for molecular profile and immunotherapy could not only match individualised treatment concepts at a high rate but also underscores the challenges encountered when offering molecularly matched therapies to a patient population with an advanced stage cancer.

Indexed as

precision medicine – molecular profile – targeted treatment

Identifiers

PMID31423337
PMCPMC6677998
OpenAlexW2962862689

What OpenQuestion holds

Textmetadata
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.