Key result
Cisplatin-based chemotherapy was associated with a higher risk of in-hospital venous thromboembolic events compared to carboplatin/nedaplatin-based chemotherapy (OR 1.35; 95% CI 1.08-1.68; P<0.01).
Why the study?
Does cisplatin-based chemotherapy increase the risk of in-hospital venous thromboembolic events compared to carboplatin/nedaplatin-based chemotherapy in patients with lung cancer?
Cohort (n=235,104)
Yes
Does cisplatin-based chemotherapy increase the risk of in-hospital venous thromboembolic events compared to carboplatin/nedaplatin-based chemotherapy in patients with lung cancer?
Cisplatin-based chemotherapy is a stronger risk factor for in-hospital venous thromboembolic events than carboplatin/nedaplatin-based chemotherapy in patients with lung cancer.
May warrant closer VTE monitoring with cisplatin in lung cancer; leaves open whether platinum choice should change pending randomized data.
An association between chemotherapy and venous thromboembolic events (VTEs) in patients with cancer is well established, with cisplatin (CDDP) being one of the most well-studied risk factors. However, whether CDDP is more strongly associated with occurrence of VTEs than carboplatin (CBDCA) or nedaplatin (CDGP) is controversial. Our purposes were to characterize patients with lung cancer and in-hospital VTEs, identify risk factors associated with VTEs, and compare the risks associated with CDDP-based versus CBDCA/CDGP-based chemotherapy. We retrospectively identified patients with lung cancer who underwent platinum-based chemotherapy from April 2012 to March 2015 from a national inpatient database in Japan. We used multivariable logistic regression analysis to analyze associations between various factors, including chemotherapy regimens and VTE. Of 235 104 eligible patients, 675 (0.29%) had VTEs after receiving platinum-based chemotherapy while hospitalized. Multivariable analysis showed that age, activity of daily living index, and invasive medical procedures were significant risk factors for the occurrence of VTE. Furthermore, CDDP-based chemotherapy was associated with a higher rate of VTE than CBDCA/CDGP-based chemotherapy (adjusted odds ratio: 1.35; 95% confidence interval: 1.08-1.68; P<0.01). In conclusion, CDDP-based chemotherapy is a stronger risk factor for VTEs than CBDCA/CDGP-based chemotherapy in patients with lung cancer.
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Mitani et al. (2018) conducted a cohort in Lung cancer (n=235,104). Cisplatin (CDDP)-based chemotherapy vs. Carboplatin (CBDCA) or nedaplatin (CDGP)-based chemotherapy was evaluated on In-hospital venous thromboembolic events (VTEs) (OR 1.35, 95% CI 1.08-1.68, p=<0.01). Cisplatin-based chemotherapy was associated with a higher risk of in-hospital venous thromboembolic events compared to carboplatin/nedaplatin-based chemotherapy (OR 1.35; 95% CI 1.08-1.68; P<0.01).
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