Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/22144
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dc.contributor.authorTran, Ben-
dc.contributor.authorRuiz-Morales, Jose M-
dc.contributor.authorGonzalez-Billalabeitia, Enrique-
dc.contributor.authorPatrikidou, Anna-
dc.contributor.authorAmir, Eitan-
dc.contributor.authorSeidel, Christoph-
dc.contributor.authorBokemeyer, Carsten-
dc.contributor.authorFankhauser, Christian-
dc.contributor.authorHermanns, Thomas-
dc.contributor.authorRumyantsev, Alexey-
dc.contributor.authorTryakin, Alexey-
dc.contributor.authorBrito, Margarida-
dc.contributor.authorFléchon, Aude-
dc.contributor.authorKwan, Edmond Michael-
dc.contributor.authorCheng, Tina-
dc.contributor.authorCastellano, Daniel-
dc.contributor.authorGarcia Del Muro, Xavier-
dc.contributor.authorHamid, Anis A-
dc.contributor.authorOttaviano, Margaret-
dc.contributor.authorPalmieri, Giovannella-
dc.contributor.authorKitson, Robert-
dc.contributor.authorReid, Alison-
dc.contributor.authorHeng, Daniel Y C-
dc.contributor.authorBedard, Philippe L-
dc.date2019-11-12-
dc.date.accessioned2019-12-04T01:53:27Z-
dc.date.available2019-12-04T01:53:27Z-
dc.date.issued2020-01-
dc.identifier.citationCancer medicine 2020; 9(1): 116-124-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/22144-
dc.description.abstractMetastatic 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. Data 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. Data 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). Large 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.-
dc.language.isoeng-
dc.subjectdeep vein thrombosis-
dc.subjectgerm cell tumor-
dc.subjectpulmonary embolism-
dc.subjecttesticular cancer-
dc.subjectvascular access device-
dc.subjectvenous thromboembolism-
dc.titleLarge 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).-
dc.typeJournal Article-
dc.identifier.journaltitleCancer medicine-
dc.identifier.affiliationDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia-
dc.identifier.affiliationTom Baker Cancer Centre, Calgary, AB, Canada-
dc.identifier.affiliationHospital Universitario Morales Meseguer - IMIB, UCAM, Murcia, Spain-
dc.identifier.affiliationRoyal Marsden Hospital, London, UK-
dc.identifier.affiliationDivision of Medical Oncology and Hematology, Department of Medicine, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada-
dc.identifier.affiliationDepartment of Oncology, Hematology, BMT with Section Pneumology, Hubertus Wald Tumorzentrum, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany-
dc.identifier.affiliationUniversity Hospital Zurich, University of Zurich, Zurich, Switzerland-
dc.identifier.affiliationNN Blokhin Russian Cancer Research Centre and Research Institute of Oncology at BSMU, Moskva, Russia-
dc.identifier.affiliationInstituto Português de Oncologia de Lisboa Francisco Gentil, Lisbon, Portugal-
dc.identifier.affiliationCentre Léon Bérard, Lyon, France-
dc.identifier.affiliationHospital Universitario 12 de Octubre, Madrid, Spain-
dc.identifier.affiliationInstitut Catala d'Oncologia, Idibell, University of Barcelona, Barcelona, Spain-
dc.identifier.affiliationOlivia Newton-John Cancer Wellness and Research Centre, Austin Health, Heidelberg, Victoria, Australia-
dc.identifier.affiliationCRTR Rare Tumors Reference Center, Università Degli Studi di Napoli Federico II, Napoli, Italy-
dc.identifier.doi10.1002/cam4.2674-
dc.identifier.orcid0000-0001-9124-354X-
dc.identifier.orcid0000-0003-3143-3143-
dc.identifier.orcid0000-0002-6771-2999-
dc.identifier.orcid0000-0002-0376-2559-
dc.identifier.pubmedid31715650-
dc.type.austinJournal Article-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
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