Evidence map›Paper›PMID 27698832›Full record

ArticleOncology letters2016

Prognostic value of serum carbonic anhydrase IX in testicular germ cell tumor patients.

Katarina Kalavska, Michal Chovanec, Miriam Zatovicova, Martina Takacova, Paulina Gronesova, Daniela Svetlovska, Magdalena Baratova, Vera Miskovska, Jana Obertova, Patrik Palacka and 9 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

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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

19 authors at 4 institutions in 1 country.

Katarina KalavskaTranslational Research Unit, Faculty of Medicine, Comenius University, 811 02 Bratislava, Slovakia; Department of Oncology, National Cancer Institute, 833 10 Bratislava, Slovakia; Cancer Research Institute, Biomedical Research Center, Slovak Academy of Sciences, 811 04 Bratislava, Slovakia.
Michal ChovanecTranslational Research Unit, Faculty of Medicine, Comenius University, 811 02 Bratislava, Slovakia; Department of Oncology, National Cancer Institute, 833 10 Bratislava, Slovakia; Second Department of Oncology, Faculty of Medicine, Comenius University and National Cancer Institute, 833 10 Bratislava, Slovakia.
Miriam ZatovicovaDepartment of Molecular Medicine, Institute of Virology, Biomedical Research Center, Slovak Academy of Sciences, 811 04 Bratislava, Slovakia.
Martina TakacovaDepartment of Molecular Medicine, Institute of Virology, Biomedical Research Center, Slovak Academy of Sciences, 811 04 Bratislava, Slovakia.
Paulina GronesovaCancer Research Institute, Biomedical Research Center, Slovak Academy of Sciences, 811 04 Bratislava, Slovakia.
Daniela SvetlovskaTranslational Research Unit, Faculty of Medicine, Comenius University, 811 02 Bratislava, Slovakia; Department of Oncology, National Cancer Institute, 833 10 Bratislava, Slovakia.
Magdalena BaratovaDepartment of Molecular Medicine, Institute of Virology, Biomedical Research Center, Slovak Academy of Sciences, 811 04 Bratislava, Slovakia.
Vera MiskovskaFirst Department of Oncology, Faculty of Medicine, Comenius University and St. Elizabeth Cancer Institute, 81 250 Bratislava, Slovakia; Department of Oncology, St. Elizabeth Cancer Institute, 81 250 Bratislava, Slovakia.
Jana ObertovaTranslational Research Unit, Faculty of Medicine, Comenius University, 811 02 Bratislava, Slovakia.
Patrik PalackaTranslational Research Unit, Faculty of Medicine, Comenius University, 811 02 Bratislava, Slovakia.
Jan RajecTranslational Research Unit, Faculty of Medicine, Comenius University, 811 02 Bratislava, Slovakia.
Zuzana Sycova-MilaTranslational Research Unit, Faculty of Medicine, Comenius University, 811 02 Bratislava, Slovakia.
Zuzana CiernaDepartment of Pathology, Faculty of Medicine, Comenius University, 811 02 Bratislava, Slovakia.
Karol KajoDepartment of Pathology, Slovak Medical University, 833 03 Bratislava, Slovakia.
Stanislav SpanikFirst Department of Oncology, Faculty of Medicine, Comenius University and St. Elizabeth Cancer Institute, 81 250 Bratislava, Slovakia; Department of Oncology, St. Elizabeth Cancer Institute, 81 250 Bratislava, Slovakia.
Pavel BabalDepartment of Pathology, Faculty of Medicine, Comenius University, 811 02 Bratislava, Slovakia.
Jozef MardiakTranslational Research Unit, Faculty of Medicine, Comenius University, 811 02 Bratislava, Slovakia; Second Department of Oncology, Faculty of Medicine, Comenius University and National Cancer Institute, 833 10 Bratislava, Slovakia.
Silvia PastorekovaDepartment of Molecular Medicine, Institute of Virology, Biomedical Research Center, Slovak Academy of Sciences, 811 04 Bratislava, Slovakia.
Michal MegoTranslational Research Unit, Faculty of Medicine, Comenius University, 811 02 Bratislava, Slovakia; Department of Oncology, National Cancer Institute, 833 10 Bratislava, Slovakia; Second Department of Oncology, Faculty of Medicine, Comenius University and National Cancer Institute, 833 10 Bratislava, Slovakia.
Comenius University Bratislava · SKBiomedical Research Center of the Slovak Academy of Sciences · SKInstitute of Virology of the Slovak Academy of Sciences · SKSlovak Medical University · SK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the fact that testicular germ cell tumors (TGCTs) are one of the most chemosensitive solid tumors, a small proportion of patients fail to be cured following cisplatin-based first line chemotherapy. Upregulation of carbonic anhydrase IX (CA IX) in various solid tumors is associated with poor outcome. The current prospective study investigated the prognostic value of serum CA IX level in TGCTs. In total, 83 patients (16 non-metastatic following orchiectomy with no evidence of disease, 57 metastatic chemotherapy-naïve and 10 metastatic relapsed chemotherapy-pretreated) starting adjuvant and/or new line of chemotherapy and 35 healthy controls were enrolled in the study. Serum CA IX values were determined using an enzyme-linked immunosorbent assay, and intratumoral CA IX was analyzed by immunohistochemistry. Metastatic chemotherapy-naïve patients had significantly higher mean CA IX serum levels than healthy controls (490.6 vs. 249.6 pg/ml, P=0.005), while there was no difference in serum CA IX levels in non-metastatic or relapsed TGCT patients compared with healthy controls. There was no significant difference in the mean serum CA IX levels between different groups of patients and between the first and second cycle of chemotherapy, nor association with patients/tumor characteristics. Serum CA IX was not prognostic for progression-free survival [hazard ratio (HR)=0.81, P=0.730] or overall survival (HR=0.64, P=0.480). However, there was a significant association between intratumoral CA IX expression and serum CA IX concentration (rho=0.51, P=0.040). These results suggest that serum CA IX level correlates with tumor CA IX expression in TGCT patients, but fails to exhibit either a prognostic value or an association with patients/tumor characteristics.

Indexed as

carbonic anhydrase IXhypoxiaprognostic valuetesticular germ cell tumors

Identifiers

PMID27698832
PMCPMC5038507
OpenAlexW2515806010

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.