D.C.H. van Dorst , M.M. Hofman , R.M. de Waal , E. Oomen-de Hoop , K. de Joode , S. Bins , S.L.W. Koolen , A. Joosse , J. Versmissen , M.J.H.A. Kruip , A.A.M. van der Veldt , R.H.J. Mathijssen
{"title":"接受免疫检查点抑制剂的黑色素瘤患者的血栓栓塞:发病率和危险因素","authors":"D.C.H. van Dorst , M.M. Hofman , R.M. de Waal , E. Oomen-de Hoop , K. de Joode , S. Bins , S.L.W. Koolen , A. Joosse , J. Versmissen , M.J.H.A. Kruip , A.A.M. van der Veldt , R.H.J. Mathijssen","doi":"10.1016/j.iotech.2025.101063","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Immune checkpoint inhibitors (ICIs) may increase the incidence of thromboembolisms (TEs). In patients with melanoma, the risk of TE and its association with the disease setting remains largely unknown. This study investigated the incidences of arterial thromboembolism (ATE) and venous thromboembolism (VTE) and associated risk factors in ICI-treated patients with melanoma in the advanced and adjuvant disease settings.</div></div><div><h3>Patients and methods</h3><div>ATE and VTE incidences were retrospectively collected from patients receiving ICI in the advanced (irresectable stage III/IV) or adjuvant (stage III/IV, after complete resection) disease setting until 2 years or after censoring. Associations between characteristics and ATE/VTE were analyzed using the Fine–Gray model, with all-cause death as competing risk.</div></div><div><h3>Results</h3><div>In the advanced disease cohort, 7 (2.2%) and 16 (5.1%) of 315 included patients developed ATE and VTE, respectively. In the adjuvant cohort, 3 (2.1%) and 2 (1.4%) of 143 included patients developed ATE and VTE, respectively. In the advanced cohort, ICI combination therapy was associated with VTE [standardized hazard ration (sHR) 4.42, 95% confidence interval (CI) 1.58-12.38, <em>P</em> = 0.005] and higher body mass index (BMI) with ATE (sHR 1.09 per point BMI increase, 95% CI 1.02-1.17, <em>P</em> = 0.017), with a trend toward VTE (sHR 1.06, 95% CI 1.00-1.13, <em>P</em> = 0.055). In the adjuvant cohort, VTE history was associated with increased combined TE (sHR 11.22, 95% CI 1.83-68.68, <em>P</em> = 0.009) and higher BMI with a trend toward increased TE (sHR 1.19, 95% CI 0.97-1.46, <em>P</em> = 0.091).</div></div><div><h3>Conclusions</h3><div>Both ATE and VTE incidences seem to be modest in patients with melanoma receiving ICI in both disease settings. Patients with higher BMI and who are prescribed ICI combination therapy might be at increased thrombotic risk.</div></div>","PeriodicalId":73352,"journal":{"name":"Immuno-oncology technology","volume":"27 ","pages":"Article 101063"},"PeriodicalIF":0.0000,"publicationDate":"2025-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Thromboembolism in patients with melanoma receiving immune checkpoint inhibitors: incidence and risk factors\",\"authors\":\"D.C.H. van Dorst , M.M. Hofman , R.M. de Waal , E. Oomen-de Hoop , K. de Joode , S. Bins , S.L.W. Koolen , A. Joosse , J. Versmissen , M.J.H.A. Kruip , A.A.M. van der Veldt , R.H.J. Mathijssen\",\"doi\":\"10.1016/j.iotech.2025.101063\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Immune checkpoint inhibitors (ICIs) may increase the incidence of thromboembolisms (TEs). In patients with melanoma, the risk of TE and its association with the disease setting remains largely unknown. This study investigated the incidences of arterial thromboembolism (ATE) and venous thromboembolism (VTE) and associated risk factors in ICI-treated patients with melanoma in the advanced and adjuvant disease settings.</div></div><div><h3>Patients and methods</h3><div>ATE and VTE incidences were retrospectively collected from patients receiving ICI in the advanced (irresectable stage III/IV) or adjuvant (stage III/IV, after complete resection) disease setting until 2 years or after censoring. Associations between characteristics and ATE/VTE were analyzed using the Fine–Gray model, with all-cause death as competing risk.</div></div><div><h3>Results</h3><div>In the advanced disease cohort, 7 (2.2%) and 16 (5.1%) of 315 included patients developed ATE and VTE, respectively. In the adjuvant cohort, 3 (2.1%) and 2 (1.4%) of 143 included patients developed ATE and VTE, respectively. In the advanced cohort, ICI combination therapy was associated with VTE [standardized hazard ration (sHR) 4.42, 95% confidence interval (CI) 1.58-12.38, <em>P</em> = 0.005] and higher body mass index (BMI) with ATE (sHR 1.09 per point BMI increase, 95% CI 1.02-1.17, <em>P</em> = 0.017), with a trend toward VTE (sHR 1.06, 95% CI 1.00-1.13, <em>P</em> = 0.055). In the adjuvant cohort, VTE history was associated with increased combined TE (sHR 11.22, 95% CI 1.83-68.68, <em>P</em> = 0.009) and higher BMI with a trend toward increased TE (sHR 1.19, 95% CI 0.97-1.46, <em>P</em> = 0.091).</div></div><div><h3>Conclusions</h3><div>Both ATE and VTE incidences seem to be modest in patients with melanoma receiving ICI in both disease settings. 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引用次数: 0
摘要
免疫检查点抑制剂(ICIs)可能增加血栓栓塞(TEs)的发生率。在黑色素瘤患者中,TE的风险及其与疾病环境的关系在很大程度上仍然未知。本研究调查了在晚期和辅助疾病环境下接受ici治疗的黑色素瘤患者动脉血栓栓塞(ATE)和静脉血栓栓塞(VTE)的发生率及相关危险因素。患者和方法回顾性收集晚期(不可切除的III/IV期)或辅助(完全切除后的III/IV期)接受ICI的患者的ate和VTE发生率,直至2年或切除后。使用Fine-Gray模型分析特征与ATE/VTE之间的关联,并将全因死亡作为竞争风险。结果在晚期疾病队列中,315例患者中分别有7例(2.2%)和16例(5.1%)发生ATE和VTE。在辅助治疗组中,143例患者中分别有3例(2.1%)和2例(1.4%)发生ATE和VTE。在晚期队列中,ICI联合治疗与VTE相关[标准化危险比(sHR) 4.42, 95%可信区间(CI) 1.58-12.38, P = 0.005],较高的体重指数(BMI)与ATE相关(BMI每增加一点sHR 1.09, 95% CI 1.02-1.17, P = 0.017),并有发生VTE的趋势(sHR 1.06, 95% CI 1.00-1.13, P = 0.055)。在辅助组中,VTE病史与合并TE升高(sHR 11.22, 95% CI 1.83-68.68, P = 0.009)和BMI升高相关(sHR 1.19, 95% CI 0.97-1.46, P = 0.091)。结论:在两种疾病情况下接受ICI的黑色素瘤患者中,ATE和VTE的发生率似乎都不大。BMI较高的患者和接受ICI联合治疗的患者可能有更高的血栓形成风险。
Thromboembolism in patients with melanoma receiving immune checkpoint inhibitors: incidence and risk factors
Background
Immune checkpoint inhibitors (ICIs) may increase the incidence of thromboembolisms (TEs). In patients with melanoma, the risk of TE and its association with the disease setting remains largely unknown. This study investigated the incidences of arterial thromboembolism (ATE) and venous thromboembolism (VTE) and associated risk factors in ICI-treated patients with melanoma in the advanced and adjuvant disease settings.
Patients and methods
ATE and VTE incidences were retrospectively collected from patients receiving ICI in the advanced (irresectable stage III/IV) or adjuvant (stage III/IV, after complete resection) disease setting until 2 years or after censoring. Associations between characteristics and ATE/VTE were analyzed using the Fine–Gray model, with all-cause death as competing risk.
Results
In the advanced disease cohort, 7 (2.2%) and 16 (5.1%) of 315 included patients developed ATE and VTE, respectively. In the adjuvant cohort, 3 (2.1%) and 2 (1.4%) of 143 included patients developed ATE and VTE, respectively. In the advanced cohort, ICI combination therapy was associated with VTE [standardized hazard ration (sHR) 4.42, 95% confidence interval (CI) 1.58-12.38, P = 0.005] and higher body mass index (BMI) with ATE (sHR 1.09 per point BMI increase, 95% CI 1.02-1.17, P = 0.017), with a trend toward VTE (sHR 1.06, 95% CI 1.00-1.13, P = 0.055). In the adjuvant cohort, VTE history was associated with increased combined TE (sHR 11.22, 95% CI 1.83-68.68, P = 0.009) and higher BMI with a trend toward increased TE (sHR 1.19, 95% CI 0.97-1.46, P = 0.091).
Conclusions
Both ATE and VTE incidences seem to be modest in patients with melanoma receiving ICI in both disease settings. Patients with higher BMI and who are prescribed ICI combination therapy might be at increased thrombotic risk.