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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)
BACKGROUND: Metastatic 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. METHODS: Data were collected from mGCT patients receiving f...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943085/ https://www.ncbi.nlm.nih.gov/pubmed/31715650 http://dx.doi.org/10.1002/cam4.2674 |
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author | Tran, Ben Ruiz‐Morales, Jose M. Gonzalez‐Billalabeitia, Enrique Patrikidou, Anna Amir, Eitan Seidel, Christoph Bokemeyer, Carsten Fankhauser, Christian Hermanns, Thomas Rumyantsev, Alexey Tryakin, Alexey Brito, Margarida Fléchon, Aude Kwan, Edmond Michael Cheng, Tina Castellano, Daniel Garcia del Muro, Xavier Hamid, Anis A. Ottaviano, Margaret Palmieri, Giovannella Kitson, Robert Reid, Alison Heng, Daniel Y. C. Bedard, Philippe L. |
author_facet | Tran, Ben Ruiz‐Morales, Jose M. Gonzalez‐Billalabeitia, Enrique Patrikidou, Anna Amir, Eitan Seidel, Christoph Bokemeyer, Carsten Fankhauser, Christian Hermanns, Thomas Rumyantsev, Alexey Tryakin, Alexey Brito, Margarida Fléchon, Aude Kwan, Edmond Michael Cheng, Tina Castellano, Daniel Garcia del Muro, Xavier Hamid, Anis A. Ottaviano, Margaret Palmieri, Giovannella Kitson, Robert Reid, Alison Heng, Daniel Y. C. Bedard, Philippe L. |
author_sort | Tran, Ben |
collection | PubMed |
description | BACKGROUND: Metastatic 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. METHODS: 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. RESULTS: 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). CONCLUSIONS: 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. |
format | Online Article Text |
id | pubmed-6943085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69430852020-01-07 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) Tran, Ben Ruiz‐Morales, Jose M. Gonzalez‐Billalabeitia, Enrique Patrikidou, Anna Amir, Eitan Seidel, Christoph Bokemeyer, Carsten Fankhauser, Christian Hermanns, Thomas Rumyantsev, Alexey Tryakin, Alexey Brito, Margarida Fléchon, Aude Kwan, Edmond Michael Cheng, Tina Castellano, Daniel Garcia del Muro, Xavier Hamid, Anis A. Ottaviano, Margaret Palmieri, Giovannella Kitson, Robert Reid, Alison Heng, Daniel Y. C. Bedard, Philippe L. Cancer Med Clinical Cancer Research BACKGROUND: Metastatic 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. METHODS: 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. RESULTS: 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). CONCLUSIONS: 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. John Wiley and Sons Inc. 2019-11-12 /pmc/articles/PMC6943085/ /pubmed/31715650 http://dx.doi.org/10.1002/cam4.2674 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Cancer Research Tran, Ben Ruiz‐Morales, Jose M. Gonzalez‐Billalabeitia, Enrique Patrikidou, Anna Amir, Eitan Seidel, Christoph Bokemeyer, Carsten Fankhauser, Christian Hermanns, Thomas Rumyantsev, Alexey Tryakin, Alexey Brito, Margarida Fléchon, Aude Kwan, Edmond Michael Cheng, Tina Castellano, Daniel Garcia del Muro, Xavier Hamid, Anis A. Ottaviano, Margaret Palmieri, Giovannella Kitson, Robert Reid, Alison Heng, Daniel Y. C. Bedard, Philippe L. 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) |
title | 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) |
title_full | 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) |
title_fullStr | 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) |
title_full_unstemmed | 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) |
title_short | 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) |
title_sort | 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) |
topic | Clinical Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943085/ https://www.ncbi.nlm.nih.gov/pubmed/31715650 http://dx.doi.org/10.1002/cam4.2674 |
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