Evidence map›Paper›PMID 32101329›Full record

Trial reportHematological oncology2020

Immunohistochemistry for c-myc and bcl-2 overexpression improves risk stratification in primary central nervous system lymphoma.

Stefan Hatzl, Florian Posch, Alexander Deutsch, Christine Beham-Schmid, Herbert Stöger, Hildegard Greinix, Martin Pichler, Peter Neumeister, Katharina T Prochazka

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Hematological oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 28 citations in OpenAlex.

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  6. Assessment of Expressor Lymphoma Prevalence in High-Grade Large B-cell Lymphomas: An Observational Analysis From a Tertiary Care Centre.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2025
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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

9 authors at 2 institutions in 2 countries.

Stefan HatzlDivision of Hematology, Department of Internal Medicine, Medical University of Graz (MUG), Austria.ORCID https://orcid.org/0000-0001-6266-0512
Florian PoschDivision of Oncology, Department of Internal Medicine, Medical University of Graz (MUG), Austria.
Alexander DeutschDivision of Hematology, Department of Internal Medicine, Medical University of Graz (MUG), Austria.
Christine Beham-SchmidInstitute of Pathology, Medical University of Graz (MUG), Austria.
Herbert StögerDivision of Oncology, Department of Internal Medicine, Medical University of Graz (MUG), Austria.
Hildegard GreinixDivision of Hematology, Department of Internal Medicine, Medical University of Graz (MUG), Austria.
Martin PichlerDivision of Oncology, Department of Internal Medicine, Medical University of Graz (MUG), Austria.
Peter NeumeisterDivision of Hematology, Department of Internal Medicine, Medical University of Graz (MUG), Austria.
Katharina T ProchazkaDivision of Hematology, Department of Internal Medicine, Medical University of Graz (MUG), Austria.
Medical University of Graz · ATThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of bcl-2 and c-myc are defining features of double-expressor-lymphoma (DEL) but may also occur separately in patients with primary central nervous system lymphoma (PCNSL). Despite all progress in optimizing treatment regimen, there is lack of sufficient risk stratification models. Here, we first describe the relationship between DEL biology, the National Comprehensive Cancer Network International Prognostic Index (NCCN-IPI), treatment response, disease progression, and mortality in PCNSL. In this study, we determined c-myc and bcl-2 status immunohistochemically in samples of 48 patients with newly diagnosed PCNSL and followed these patients for a median interval of 6.2 years. Twelve, 18, and 17 patients harbored none, one, or both DEL features. Corresponding overall response rates after first-line therapy were strongly associated with DEL biology (100%, 42%, and 44% in patients with 0, 1, or 2 DEL features). Patients with one or both DEL features had a 5-fold and 13-fold higher 5-year risk of progression and/or death than patients without DEL features. These associations prevailed after adjusting for the NCCN-IPI. DEL improved the discriminatory capability of the NCCN-IPI (P = .0001). Furthermore, we could show that addition of DEL biology to the NCCN-IPI significantly improved the score's discriminatory potential both toward progression-free survival (increase in Harell's c = 0.15, P = .005) and overall survival (increase in Harell's c = 0.11, P = .029). In conclusion, DEL biology is a strong and simple-to-use predictor of adverse outcome in PCNSL. Addition of DEL to the NCCN-IPI improves its prognostic potential. Disease progression from PCNSL harboring both DEL features is invariably fatal. This defines a novel PCNSL patient subset with a great unmet need for improved therapy.

Indexed as

AgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorCentral Nervous System NeoplasmsCytarabineDisease ProgressionFemaleFollow-Up StudiesHumansImmunohistochemistryMaleMethotrexateMiddle AgedNeoplasm Recurrence, LocalPrognosisBCL2 protein, humanBiomarkers, TumorCytarabineMethotrexateMYC protein, humanProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mycbcl-2c-mycdouble expressor lymphomaPCNSLprimary CNS lymphoma

Identifiers

PMID32101329
PMCPMC7496545
OpenAlexW3008037436

What OpenQuestion holds

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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.