Venous thromboembolism incidence and risk assessment in lung cancer patients treated with immune checkpoint inhibitors. (16th March 2021)

• Record Type: Journal Article
• Authors: Icht, Oded; Darzi, Naama; Shimony, Shai; Jacobi, Oded; Reinhorn, Daniel; Landman, Yosef; Mutai, Raz; Averbuch, Itamar; Shochat, Tzippy; Spectre, Galia; Raanani, Pia; Rotem, Ofer; Dudnik, Elizabeth; Peled, Nir; Zer, Alona; Leader, Avi
• Is Part Of: Journal of thrombosis and haemostasis. Volume 19:Number 5(2021)
• Page Start: 1250
• Page End: 1258
• Publication Date: 2021-03-16
• Subjects: immune‐checkpoint inhibitors -- Khorana score -- lung cancer -- thromboprophylaxis -- venous thrombo‐embolism; Thrombosis -- Periodicals; Hemostasis -- Periodicals; Blood coagulation disorders -- Periodicals; 616.1
• DOI: 10.1111/jth.15272
• Languages: English
• ISSNs: 1538-7933

Abstract

Abstract: Background: There are scarce data on venous thromboembolism (VTE) rates among non‐small cell lung cancer (NSCLC) patients treated with immune‐checkpoint inhibitors (ICI). The Khorana Score (KS), used to guide thromboprophylaxis in cancer patients, was validated in patients receiving chemotherapy. Objective: To assess VTE rates and KS performance among NSCLC patients treated with ICI or chemotherapy. Methods: We performed a retrospective cohort study of NSCLC patients starting either ICI or platinum‐based chemotherapy. The 6‐month cumulative incidence of VTE in the ICI and chemotherapy cohorts and hazard ratios (HR) with 95% confidence intervals (CI) were calculated, using death as a competing risk. Subgroup analysis of low (0‐1) and high (≥2) KS risk groups was performed. Results: The study included 345 NSCLC patients receiving single agent ICI ( n = 176) or chemotherapy ( n = 169). The 6‐month cumulative incidence of VTE was 7.1% in the chemotherapy cohort and 4.5% in the ICI cohort (HR for chemotherapy = 1.6, 95% CI 0.66‐3.9). Among chemotherapy treated patients, the high‐risk KS group had a trend toward a higher VTE incidence, compared with patients with a low‐risk KS (HR 3.04, 95% CI 0.82‐11.22). Among ICI‐treated patients, the high‐risk KS group had a trend toward a lower VTE incidence compared with the low‐risk group (HR 0.17, 95% CI 0.02‐1.36). Conclusions: VTE rates were higher among NSCLC patients treated with platinum‐based chemotherapy than those treated with ICI alone, though the precision of the relative estimate is low. The KS did not identify high‐risk ICI‐treated patients, suggesting that an ICI‐specific risk model is warranted.