TY - JOUR
T1 - Growth differentiation factor-15 for prediction of bleeding in cancer patients
AU - Mulder, Frits I.
AU - Bosch, Floris T. M.
AU - Carrier, Marc
AU - Mallick, Ranjeeta
AU - Middeldorp, Saskia
AU - van Es, Nick
AU - Kamphuisen, Pieter Willem
AU - Wells, Phill S.
N1 - Funding Information: This study was supported by a research grant from Roche Diagnostics for the laboratory measurements. The AVERT trial was funded by the Canadian Institute for Health Research and the BMS‐Pfizer Alliance. The sponsor had no role in the data collection, the analysis, data interpretation, or writing of the manuscript. Funding Information: Dr. Mulder and Dr. Bosch declare no conflict of interest. Dr. Carrier declares research funding from LEO Pharma, BMS, and Pfizer; advisory board honoraria from Bayer, BMS, LEO Pharma, Pfizer, Servier, and Sanofi. Dr. Kamphuisen declares research funding from Daiichi Sankyo and Roche Diagnostics. Dr. van Es reports receiving advisory board honoraria from Daiichi‐Sankyo, LEO Pharma, and Bayer. Dr. Middeldorp declares grants and fees paid to her institution from GSK, BMS/Pfizer, Aspen, Daiichi Sankyo, Bayer, Boehringer Ingelheim, Sanofi, and Portola. Dr. Wells reports receiving grant support, lecture fees, and advisory board fees from Bayer HealthCare; lecture fees from Medscape, Pfizer, and Daiichi Sankyo; fees for serving on a writing committee from Itreas; grant support from Bristol‐Myers Squibb/Pfizer; consulting fees from Janssen Scientific; and fees for serving on a roundtable from Sanofi. DR. Kamphuisen declares research funding from Daiichi Sankyo and Roche Diagnostics. Publisher Copyright: © 2021 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis
PY - 2022/1
Y1 - 2022/1
N2 - Background: Growth differentiation factor-15 (GDF-15) is a strong predictor for bleeding in patients with atrial fibrillation, but there are no data on cardiovascular outcomes for this biomarker in cancer patients. Bleeding risk assessment is important in cancer patients when considering primary thromboprophylaxis because it is associated with an increased bleeding risk. Objectives: To evaluate GDF-15 as predictor for bleeding events in cancer patients previously enrolled in the AVERT trial. Patients/Methods: In this trial, 574 participants were randomized to prophylactic apixaban or placebo and followed for 180 days for venous thromboembolism, major bleeding, clinically relevant nonmajor bleeding, and any bleeding. Plasma concentrations of GDF-15 were measured centrally with the Elecsys GDF-15 commercial assay kit (Roche Diagnostics GmbH). Results: In apixaban recipients, the area under the receiver operator characteristic curve of GDF-15 for major bleeding was 0.73 (95% confidence interval [CI], 0.44–1.00). Compared with the lowest GDF-15 tertile (<1470 ng/L), major bleeding risk was significantly higher in the highest tertile (≥2607 ng/L; hazard ratio [HR] 3.19; 95% CI, 2.41–4.22), also when adjusting for sex, age, antiplatelet use, and gastrointestinal cancer (adjusted HR 2.80; 95% CI, 1.91–4.11). GDF-15 was also significantly associated with clinically relevant nonmajor bleeding (adjusted HR 1.67; 95% CI, 1.08–2.58) and any bleeding (adjusted HR 2.12; 95% CI, 1.38–3.25). Conclusions: Although hypothesis generating, this is the first study to show that GDF-15 predicts bleeding in cancer patients receiving thromboprophylaxis.
AB - Background: Growth differentiation factor-15 (GDF-15) is a strong predictor for bleeding in patients with atrial fibrillation, but there are no data on cardiovascular outcomes for this biomarker in cancer patients. Bleeding risk assessment is important in cancer patients when considering primary thromboprophylaxis because it is associated with an increased bleeding risk. Objectives: To evaluate GDF-15 as predictor for bleeding events in cancer patients previously enrolled in the AVERT trial. Patients/Methods: In this trial, 574 participants were randomized to prophylactic apixaban or placebo and followed for 180 days for venous thromboembolism, major bleeding, clinically relevant nonmajor bleeding, and any bleeding. Plasma concentrations of GDF-15 were measured centrally with the Elecsys GDF-15 commercial assay kit (Roche Diagnostics GmbH). Results: In apixaban recipients, the area under the receiver operator characteristic curve of GDF-15 for major bleeding was 0.73 (95% confidence interval [CI], 0.44–1.00). Compared with the lowest GDF-15 tertile (<1470 ng/L), major bleeding risk was significantly higher in the highest tertile (≥2607 ng/L; hazard ratio [HR] 3.19; 95% CI, 2.41–4.22), also when adjusting for sex, age, antiplatelet use, and gastrointestinal cancer (adjusted HR 2.80; 95% CI, 1.91–4.11). GDF-15 was also significantly associated with clinically relevant nonmajor bleeding (adjusted HR 1.67; 95% CI, 1.08–2.58) and any bleeding (adjusted HR 2.12; 95% CI, 1.38–3.25). Conclusions: Although hypothesis generating, this is the first study to show that GDF-15 predicts bleeding in cancer patients receiving thromboprophylaxis.
KW - biomarkers
KW - hemorrhage
KW - neoplasms
KW - risk
KW - venous thromboembolism
UR - http://www.scopus.com/inward/record.url?scp=85118404471&partnerID=8YFLogxK
U2 - https://doi.org/10.1111/jth.15559
DO - https://doi.org/10.1111/jth.15559
M3 - Article
C2 - 34662498
VL - 20
SP - 138
EP - 144
JO - Journal of Thrombosis and Haemostasis
JF - Journal of Thrombosis and Haemostasis
SN - 1538-7933
IS - 1
ER -