Evidence map›Paper›PMID 30373609›Full record

ArticleBMC medical informatics and decision making2018

SwissMTB: establishing comprehensive molecular cancer diagnostics in Swiss clinics.

Franziska Singer, Anja Irmisch, Nora C Toussaint, Linda Grob, Jochen Singer, Thomas Thurnherr, Niko Beerenwinkel, Mitchell P Levesque, Reinhard Dummer, Luca Quagliata and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMC medical informatics and decision making, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Circulating tumor-reactive KIRNature immunology · 2025
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  13. Bioinformatics for precision oncology.Briefings in bioinformatics · 2019
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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

14 authors at 4 institutions in 1 country.

Franziska SingerNEXUS Personalized Health Technologies, ETH Zurich, Otto-Stern-Weg 7, 8093, Zurich, Switzerland.
Anja IrmischDepartment of Dermatology, University Hospital Zurich, 8091, Zurich, Switzerland.
Nora C ToussaintNEXUS Personalized Health Technologies, ETH Zurich, Otto-Stern-Weg 7, 8093, Zurich, Switzerland.
Linda GrobNEXUS Personalized Health Technologies, ETH Zurich, Otto-Stern-Weg 7, 8093, Zurich, Switzerland.
Jochen SingerSIB Swiss Institute of Bioinformatics, 4058, Basel, Switzerland.
Thomas ThurnherrSIB Swiss Institute of Bioinformatics, 4058, Basel, Switzerland.
Niko BeerenwinkelSIB Swiss Institute of Bioinformatics, 4058, Basel, Switzerland.
Mitchell P LevesqueDepartment of Dermatology, University Hospital Zurich, 8091, Zurich, Switzerland.
Reinhard DummerDepartment of Dermatology, University Hospital Zurich, 8091, Zurich, Switzerland.
Luca QuagliataDepartment of Pathology, University Hospital Basel, Schönbeinstrasse 40, 4056, Basel, Switzerland.
Sacha I RothschildDivision of Oncology, Department of Biomedicine, University Hospital Basel, Petersgraben 4, 4031, Basel, Switzerland.
Andreas WickiDivision of Oncology, Department of Biomedicine, University Hospital Basel, Petersgraben 4, 4031, Basel, Switzerland.
Christian BeiselDepartment of Biosystems Science and Engineering, ETH Zurich, 4058, Basel, Switzerland.
Daniel J StekhovenNEXUS Personalized Health Technologies, ETH Zurich, Otto-Stern-Weg 7, 8093, Zurich, Switzerland. stekhoven@nexus.ethz.ch.ORCID 0000-0003-3163-3161
SIB Swiss Institute of Bioinformatics · CHUniversity Hospital of Basel · CHUniversity Hospital of Zurich · CHETH Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMolecular precision oncology is an emerging practice to improve cancer therapy by decreasing the risk of choosing treatments that lack efficacy or cause adverse events. However, the challenges of integrating molecular profiling into routine clinical care are manifold. From a computational perspective these include the importance of a short analysis turnaround time, the interpretation of complex drug-gene and gene-gene interactions, and the necessity of standardized high-quality workflows. In addition, difficulties faced when integrating molecular diagnostics into clinical practice are ethical concerns, legal requirements, and limited availability of treatment options beyond standard of care as well as the overall lack of awareness of their existence.

methodsTo the best of our knowledge, we are the first group in Switzerland that established a workflow for personalized diagnostics based on comprehensive high-throughput sequencing of tumors at the clinic. Our workflow, named SwissMTB (Swiss Molecular Tumor Board), links genetic tumor alterations and gene expression to therapeutic options and clinical trial opportunities. The resulting treatment recommendations are summarized in a clinical report and discussed in a molecular tumor board at the clinic to support therapy decisions.

resultsHere we present results from an observational pilot study including 22 late-stage cancer patients. In this study we were able to identify actionable variants and corresponding therapies for 19 patients. Half of the patients were analyzed retrospectively. In two patients we identified resistance-associated variants explaining lack of therapy response. For five out of eleven patients analyzed before treatment the SwissMTB diagnostic influenced treatment decision.

conclusionsSwissMTB enables the analysis and clinical interpretation of large numbers of potentially actionable molecular targets. Thus, our workflow paves the way towards a more frequent use of comprehensive molecular diagnostics in Swiss hospitals.

Indexed as

Pathology, MolecularPrecision MedicineHigh-Throughput Nucleotide SequencingHumansMutationNeoplasmsPilot ProjectsRetrospective StudiesSwitzerlandCancer diagnosticsMolecular diagnosticsMolecular tumor boardNGSPersonalized medicine

Identifiers

PMID30373609
PMCPMC6206832
OpenAlexW2899401372

What OpenQuestion holds

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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.