Evidence map›Paper›PMID 31715650›Full record

ArticleCancer medicine2020

Large retroperitoneal lymphadenopathy and increased risk of venous thromboembolism in patients receiving first-line chemotherapy for metastatic germ cell tumors: A study by the global germ cell cancer group (G3).

Ben Tran, Jose M Ruiz-Morales, Enrique Gonzalez-Billalabeitia, Anna Patrikidou, Eitan Amir, Christoph Seidel, Carsten Bokemeyer, Christian Fankhauser, Thomas Hermanns, Alexey Rumyantsev and 14 more

Abstract readMulticenter Study
In one paragraph

Article in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Canadian Urological Association consensus guideline: Management of testicular germ cell cancer.Canadian Urological Association journal = Journal de l'Association des urologues du Canada · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. 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

24 authors.

Ben TranDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Vic., Australia.ORCID 0000-0001-9124-354X
Jose M Ruiz-MoralesTom Baker Cancer Centre, Calgary, AB, Canada.
Enrique Gonzalez-BillalabeitiaHospital Universitario Morales Meseguer - IMIB, UCAM, Murcia, Spain.ORCID 0000-0003-3143-3143
Anna PatrikidouRoyal Marsden Hospital, London, UK.
Eitan AmirDivision of Medical Oncology and Hematology, Department of Medicine, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada.
Christoph SeidelDepartment of Oncology, Hematology, BMT with Section Pneumology, Hubertus Wald Tumorzentrum, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Carsten BokemeyerDepartment of Oncology, Hematology, BMT with Section Pneumology, Hubertus Wald Tumorzentrum, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Christian FankhauserUniversity Hospital Zurich, University of Zurich, Zurich, Switzerland.
Thomas HermannsUniversity Hospital Zurich, University of Zurich, Zurich, Switzerland.
Alexey RumyantsevNN Blokhin Russian Cancer Research Centre and Research Institute of Oncology at BSMU, Moskva, Russia.
Alexey TryakinNN Blokhin Russian Cancer Research Centre and Research Institute of Oncology at BSMU, Moskva, Russia.
Margarida BritoInstituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal.
Aude FléchonCentre Léon Bérard, Lyon, France.
Edmond Michael KwanDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Vic., Australia.
Tina ChengTom Baker Cancer Centre, Calgary, AB, Canada.
Daniel CastellanoHospital Universitario 12 de Octubre, Madrid, Spain.
Xavier Garcia Del MuroInstitut Catala d'Oncologia, Idibell, University of Barcelona, Barcelona, Spain.
Anis A HamidOlivia Newton John Cancer, Wellness and Research Centre, Heidelberg, Vic., Australia.
Margaret OttavianoCRTR Rare Tumors Reference Center, Università Degli Studi di Napoli Federico II, Napoli, Italy.
Giovannella PalmieriCRTR Rare Tumors Reference Center, Università Degli Studi di Napoli Federico II, Napoli, Italy.
Robert KitsonRoyal Marsden Hospital, London, UK.
Alison ReidRoyal Marsden Hospital, London, UK.
Daniel Y C HengTom Baker Cancer Centre, Calgary, AB, Canada.
Philippe L BedardDivision of Medical Oncology and Hematology, Department of Medicine, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada.ORCID 0000-0002-6771-2999

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetastatic germ cell tumor (mGCT) patients receiving chemotherapy have increased risk of life-threatening venous thromboembolism (VTE). Identifying VTE risk factors may guide thromboprophylaxis in this highly curable population.

methodsData were collected from mGCT patients receiving first-line platinum-based chemotherapy at 22 centers. Predefined variables included International Germ Cell Cancer Collaborative Group (IGCCCG) risk classification, long-axis diameter of largest retroperitoneal lymph node (RPLN), Khorana score, and use of indwelling vascular access device (VAD). VTE occurring at baseline, during chemotherapy and within 90 days, was analyzed.

resultsData from 1135 patients were collected. Median age was 31 years (range 10-74). IGCCCG risk was 64% good, 20% intermediate, and 16% poor. VTE occurred in 150 (13%) patients. RPLN >3.5 cm demonstrated highest discriminatory accuracy for VTE (AUC 0.632, P < .001) and was associated with significantly higher risk of VTE in univariable analysis (22% vs 8%, OR 3.0, P < .001) and multivariable analysis (OR 1.8, P = .02). Other significant risk factors included, Khorana score ≥3 (OR 2.6, P = .008) and VAD use (OR 2.7, P < .001).

conclusionsLarge RPLN and VAD use are independent risk factors for VTE in mGCT patients receiving chemotherapy. VAD use should be minimized in this population and thromboprophylaxis might be considered for large RPLN.

Indexed as

AdolescentAdultAgedAntineoplastic Combined Chemotherapy ProtocolsCatheters, IndwellingChildCisplatinHumansLymphatic MetastasisLymph NodesMaleMiddle AgedNeoplasms, Germ Cell and EmbryonalRetroperitoneal NeoplasmsRetroperitoneal SpaceRetrospective StudiesCisplatindeep vein thrombosisgerm cell tumorpulmonary embolismtesticular cancervascular access devicevenous thromboembolism

Identifiers

PMID31715650
PMCPMC6943085

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.