Evidence map›Paper›PMID 33675399›Full record

ArticleJournal of cancer research and clinical oncology2021

Microsatellite instability (MSI-H) is associated with a high immunoscore but not with PD-L1 expression or increased survival in patients (pts.) with metastatic colorectal cancer (mCRC) treated with oxaliplatin (ox) and fluoropyrimidine (FP) with and without bevacizumab (bev): a pooled analysis of the AIO KRK 0207 and RO91 trials.

Stefanie Noepel-Duennebacke, Hendrik Juette, Karsten Schulmann, Ulrich Graeven, Rainer Porschen, Jan Stoehlmacher, Susanna Hegewisch-Becker, Arne Raulf, Dirk Arnold, Anke Reinacher-Schick and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

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  12. CD8Clinical & translational immunology · 2020
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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 6 institutions in 1 country.

Stefanie Noepel-Duennebacke *Department for Hematology, Oncology und Palliative Care, St. Josef-Hospital, Ruhr-University, Bochum, Germany.ORCID http://orcid.org/0000-0002-8360-6715
Hendrik Juette *Institute of Pathology, Ruhr-University Bochum, Bürkle-de-la-Camp-Platz 1, 44789, Bochum, Germany.
Karsten SchulmannDepartment for Hematology and Oncology, Klinikum Hochsauerland, Meschede, Germany.
Ulrich GraevenDepartment for Hematology, Oncology and Gastroenterology, Kliniken Maria-Hilf Mönchengladbach, Mönchengladbach, Germany.
Rainer PorschenMedical Department, Klinikum Bremen-Ost, Bremen, Germany.
Jan StoehlmacherIndividuelle Krebsberatung, Bonn, Germany.
Susanna Hegewisch-BeckerHOPE-Practice for Oncology, Hamburg, Germany.
Arne RaulfCenter for Protein Diagnostics, Bioinformatics Group, Faculty of Biology and Biotechnology, Ruhr-University, Bochum, Germany.
Dirk ArnoldAsklepios Cancer Center, Department for Hematology, Oncology and Palliative Care, Asklepios Klinikum Altona Hamburg, Hamburg, Germany.
Anke Reinacher-Schick *Department for Hematology, Oncology und Palliative Care, St. Josef-Hospital, Ruhr-University, Bochum, Germany.
Aandrea Tannapfel *Institute of Pathology, Ruhr-University Bochum, Bürkle-de-la-Camp-Platz 1, 44789, Bochum, Germany. andrea.tannapfel@pathologie-bochum.de.
Ruhr University Bochum · DESt. Josef-Hospital · DEAsklepios Klinik Altona · DEInstitute for Prevention and Occupational Medicine · DEKliniken Maria Hilf · DEKlinikum Bremen-Mitte · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionIn a retrospective analysis of two randomized phase III trials in mCRC patients treated first line with oxaliplatin, fluoropyrimidine with and without Bevacizumab (the AIO KRK 0207 and R091 trials) we evaluated the association of high microsatellite instability (MSI-H), immunoscore (IS) and PD-L1 expression in relation to overall survival (OS).

methodsIn total, 550 samples were analysed. Immunohistochemical analysis of the MMR proteins and additionally fragment length analysis was performed, molecular examinations via allele-discriminating PCR in combination with DNA sequencing. Furthermore PD-L1 and IS were assessed.

resultsMSI-H tumors were more frequent in right sided tumors (13.66% vs. 4.14%) and were correlated with mutant BRAF (p = 0.0032), but not with KRAS nor NRAS mutations (MT). 3.1% samples were found to be PD-L1 positive, there was no correlation of PDL1 expression with MSI-H status, but in a subgroup analysis of MSI-H tumors the percentage of PD-L1 positive tumors was higher than in MSS tumors (9.75% vs. 2.55%). 8.5% of samples showed a positive IS, MSI-H was associated with a high IS. The mean IS of the pooled population was 0.57 (SD 0.97), while the IS of MSI-H tumors was significantly higher (mean of 2.4; SD 1.4; p =< 0.0001). DISCUSSION: Regarding OS in correlation with MSI-H, PD-L1 and IS status we did not find a significant difference. However, PD-L1 positive mCRC tended to exhibit a longer OS compared to PD-L1 negative cancers (28.9 vs. 22.1 months).

Indexed as

Microsatellite InstabilityAntineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenBevacizumabBiomarkers, TumorClinical Trials, Phase III as TopicColorectal NeoplasmsFemaleFluorouracilFollow-Up StudiesHumansMaleMiddle AgedNeoplasm InvasivenessOxaliplatinPrognosisB7-H1 AntigenBevacizumabBiomarkers, TumorCD274 protein, humanFluorouracilOxaliplatinBevacizumabImmunoscoreMetastatic colorectal cancerMicrosatellite instabilityOverall survivalPD-L1

Identifiers

PMID33675399
PMCPMC8397637
OpenAlexW3135592633

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.