Evidence map›Paper›PMID 37777577›Full record

ArticleBritish journal of cancer2023

Outcomes of relapsed clinical stage I versus de novo metastatic testicular cancer patients: an analysis of the IGCCCG Update database.

Jakob Lauritsen, Nicolas Sauvé, Alexey Tryakin, Di Maria Jiang, Robert Huddart, Daniel Y C Heng, Angelika Terbuch, Eric Winquist, Michal Chovanec, Marcus Hentrich and 15 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
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

25 authors at 20 institutions in 12 countries.

Jakob Lauritsen *Department of Oncology, Copenhagen University Hospital, Rigshospitalet, Denmark.ORCID 0000-0002-9985-174X
Nicolas Sauvé *European Organisation for Research and Treatment of Cancer (EORTC), Brussels, Belgium.
Alexey TryakinDepartment of Chemotherapy, N.N.Blokhin Russian Cancer Research Center, Moscow, Russia.
Di Maria JiangDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada.ORCID 0000-0002-1950-2292
Robert HuddartInstitute of Cancer Research and Royal Marsden Hospital, Downs Road, Sutton, Surrey, UK.ORCID 0000-0003-3604-1990
Daniel Y C HengDivision of Medical Oncology, Tom Baker Cancer Centre, University of Calgary, Calgary, Alberta, Canada.
Angelika TerbuchDivision of Oncology, Medical University of Graz, Graz, Austria.
Eric WinquistDepartment of Oncology, University of Western Ontario and London Health Sciences Centre, London, ON, Canada.
Michal Chovanec2nd Department of Oncology, Faculty of Medicine, Comenius University, National Cancer Institute, Bratislava, Slovakia.ORCID 0000-0002-5653-2909
Marcus HentrichDepartment of Hematology/Oncology, Red Cross Hospital, Munich, Germany.
Christian D FankhauserUniversity of Zurich, Zurich, Switzerland.ORCID 0000-0002-4073-5488
Jonathan ShamashDepartment of Oncology, St Bartholomew's Hospital, London, UK.
Xavier Garcia Del MuroDepartment of Medical Oncology, Catalan Institute of Oncology, Barcelona, Spain.ORCID 0000-0001-5571-2847
David VaughnDivision of Hematology/Oncology, Abramson Cancer Center at the University of Pennsylvania, Philadelphia, PA, USA.
Axel HeidenreichDepartment of Urology, Uro-Oncology, Robot Assisted and Specialized Urologic Surgery, University Hospital Cologne, Cologne, Germany.ORCID 0000-0002-2511-3664
Cora N SternbergEnglander Institute for Precision Medicine, Sandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York-Presbyterian, New York, NY, USA.
Christopher SweeneyDana-Farber Cancer Institute, Harvard Medical School, Boston, USA.
Andrea NecchiVita-Salute San Raffaele University, Department of Medical Oncology, IRCCS San Raffaele Hospital, Milan, Italy.
Carsten BokemeyerDepartment of Oncology, Hematology and BMT with section Pneumonology, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
Mikkel BandakDepartment of Consulting and Research, International Drug Development Institute, Louvain-la-Neuve, Belgium.
Abolghassem JandariEuropean Organisation for Research and Treatment of Cancer (EORTC), Brussels, Belgium.
Laurence ColletteEuropean Organisation for Research and Treatment of Cancer (EORTC), Brussels, Belgium.
Silke GillessenOncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland.
Joerg BeyerDepartment of Medical Onccology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland. joerg.beyer@insel.ch.ORCID 0000-0003-1755-9700
Gedske DaugaardDepartment of Oncology, Copenhagen University Hospital, Rigshospitalet, Denmark.ORCID 0000-0002-9618-9180
European Organisation for Research and Treatment of Cancer · BECopenhagen University Hospital · DKComenius University Bratislava · SKCornell University · USGerman Red Cross · DEHarvard University · USInstitut Català d'Ornitologia · ESInstitute of Oncology Research · CHInternational Drug Development Institute (Belgium) · BEMedical University of Graz · ATRoyal Marsden NHS Foundation Trust · GBRussian Cancer Research Center NN Blokhin · RUSt Bartholomew's Hospital · GBUniversität Hamburg · DEUniversity Hospital Cologne · DEUniversity of Bern · CHUniversity of Calgary · CAUniversity of Lucerne · CHUniversity of Pennsylvania · USUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundActive surveillance after orchiectomy is the preferred management in clinical stage I (CSI) germ-cell tumours (GCT) associated with a 15 to 30% relapse rate. PATIENTS AND

methodsIn the IGCCCG Update database, we compared the outcomes of gonadal disseminated GCT relapsing from initial CSI to outcomes of patients with de novo metastatic GCT.

resultsA total of 1014 seminoma (Sem) [298 (29.4%) relapsed from CSI, 716 (70.6%) de novo] and 3103 non-seminoma (NSem) [626 (20.2%) relapsed from CSI, 2477 (79.8%) de novo] were identified. Among Sem, no statistically significant differences in PFS and OS were found between patients relapsing from CSI and de novo metastatic disease [5-year progression-free survival (5y-PFS) 87.6% versus 88.5%; 5-year overall survival (5y-OS) 93.2% versus 96.1%). Among NSem, PFS and OS were higher overall in relapsing CSI patients (5y-PFS 84.6% versus 80.0%; 5y-OS 93.3% versus 88.7%), but there were no differences within the same IGCCCG prognostic groups (HR = 0.89; 95% CI: 0.70-1.12). Relapses in the intermediate or poor prognostic groups occurred in 11/298 (4%) Sem and 112/626 (18%) NSem.

conclusionRelapsing CSI GCT patients expect similar survival compared to de novo metastatic patients of the same ICCCCG prognostic group. Intermediate and poor prognosis relapses from initial CSI expose patients to unnecessary toxicity from more intensive treatments.

Indexed as

Neoplasms, Germ Cell and EmbryonalNeoplasms, Second PrimarySeminomaTesticular NeoplasmsHumansMalePrognosisProgression-Free SurvivalRecurrence

Identifiers

PMID37777577
PMCPMC10667594
OpenAlexW4387220566

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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.