Evidence map›Paper›PMID 29661166›Full record

ArticleBMC cancer2018

High OX40 expression in recurrent ovarian carcinoma is indicative for response to repeated chemotherapy.

Michaela Ramser, Simone Eichelberger, Silvio Däster, Benjamin Weixler, Marko Kraljević, Robert Mechera, Athanasios Tampakis, Tarik Delko, Uwe Güth, Sylvia Stadlmann and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 72 citations in OpenAlex.

  1. Pooled it
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  7. The CD8PeerJ · 2025
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  18. Activation of the TGF-Disease markers · 2022
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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

13 authors at 2 institutions in 1 country.

Michaela RamserDepartment of Surgery, University Hospital Basel, Spitalstrasse 21, 4031, Basel, Switzerland.
Simone EichelbergerDepartment of Surgery, University Hospital Basel, Spitalstrasse 21, 4031, Basel, Switzerland.
Silvio DästerDepartment of Surgery, University Hospital Basel, Spitalstrasse 21, 4031, Basel, Switzerland.
Benjamin WeixlerDepartment of Surgery, University Hospital Basel, Spitalstrasse 21, 4031, Basel, Switzerland.
Marko KraljevićSpital Limmattal, Urdorferstrasse 100, 8952, Schlieren, Switzerland.
Robert MecheraDepartment of Surgery, University Hospital Basel, Spitalstrasse 21, 4031, Basel, Switzerland.
Athanasios TampakisDepartment of Surgery, University Hospital Basel, Spitalstrasse 21, 4031, Basel, Switzerland.
Tarik DelkoDepartment of Surgery, University Hospital Basel, Spitalstrasse 21, 4031, Basel, Switzerland.
Uwe GüthBrustzentrum Zürich, Seefeldstrasse 214, 8008, Zürich, Switzerland.
Sylvia StadlmannInstitute of Pathology, Kantonsspital Baden AG, Im Ergel 1, 5404, Baden, Switzerland.
Luigi TerraccianoInstitute of Pathology, University Hospital Basel, Schönbeinstrasse 40, 4031, Basel, Switzerland.
Raoul A DroeserDepartment of Surgery, University Hospital Basel, Spitalstrasse 21, 4031, Basel, Switzerland. raoul.droeser@usb.ch.
Gad SingerInstitute of Pathology, Kantonsspital Baden AG, Im Ergel 1, 5404, Baden, Switzerland.
University Hospital of Basel · CHSpital Limmattal · CH

Funding

Oncosuisse OCS 01506-02-2004
6 · The paper itself

Abstract

backgroundOvarian carcinoma (OC) is the fifth most common female cancer and mostly diagnosed at an advanced stage. Surgical debulking is usually followed by adjuvant platinum-based chemotherapy. Only few biomarkers are known to be related to chemosensitivity. OX40 is a TNF receptor member and expressed on activated CD4+ and CD8+ T cells. It is known that OX40 signaling promotes survival and responds to various immune cells of the innate and adaptive immune system. Therefore we investigated the indicative value of OX40 expression for recurrence and survival in OC.

methodsA tissue microarray of biopsies of mostly high-grade primary serous OC and matched recurrences of 47 patients was stained with OX40. Recurrence within 6 months of the completion of platinum-based chemotherapy was defined as chemoresistance.

resultsChemosensitivity correlated significantly with high OX40 positive immune cell density in primary cancer biopsies (p = 0.027). Furthermore patients with a higher OX40 expression in recurrent cancer biopsies showed a better outcome in recurrence free survival (RFS) (p = 0.017) and high OX40 expression was associated with chemosensitivity (p = 0.008). OX40 positive TICI in recurrent carcinomas significantly correlated with IL-17 positive tumor infiltrating immune cells in primary carcinomas (r

conclusionHigh OX40 expression in OC is correlated with chemosensitivity and improved RFS in OC. Patients might therefore benefit from a second line therapy.

Indexed as

AdultAgedBiomarkers, TumorCarcinomaDisease-Free SurvivalDrug-Related Side Effects and Adverse ReactionsDrug TherapyFemaleGene Expression Regulation, NeoplasticHumansMiddle AgedNeoplasm StagingOvarian NeoplasmsOX40 LigandPrognosisBiomarkers, TumorOX40 LigandTNFSF4 protein, humanCD134ChemosensitivityOvarian cancerOX40

Identifiers

PMID29661166
PMCPMC5903007
OpenAlexW2802033457

What OpenQuestion holds

Textmetadata
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.