Risk of Selected Dermatological Toxicities in Cancer Patients Treated with MEK Inhibitors: A Comparative Systematic Review and Meta-Analysis
O Abdel-Rahman, H ElHalawani, H Ahmed - Future Oncology, 2015 - Taylor & Francis
O Abdel-Rahman, H ElHalawani, H Ahmed
Future Oncology, 2015•Taylor & FrancisBackground: This meta-analysis was conducted aiming at assessing the risk of selected
dermatological toxicities associated with MEK inhibitors. Methods: We considered relevant
prospective randomized Phase II and III trials of cancer patients on the three MEK inhibitors
(trametinib, selumetinib and cobimetinib), describing events of skin rash and acneiform
dermatitis, as eligible for inclusion. Results: After exclusion of ineligible studies, a total of 14
clinical trials were considered eligible for the meta-analysis. The relative risk of all-grade …
dermatological toxicities associated with MEK inhibitors. Methods: We considered relevant
prospective randomized Phase II and III trials of cancer patients on the three MEK inhibitors
(trametinib, selumetinib and cobimetinib), describing events of skin rash and acneiform
dermatitis, as eligible for inclusion. Results: After exclusion of ineligible studies, a total of 14
clinical trials were considered eligible for the meta-analysis. The relative risk of all-grade …
Background
This meta-analysis was conducted aiming at assessing the risk of selected dermatological toxicities associated with MEK inhibitors. Methods
We considered relevant prospective randomized Phase II and III trials of cancer patients on the three MEK inhibitors (trametinib, selumetinib and cobimetinib), describing events of skin rash and acneiform dermatitis, as eligible for inclusion. Results
After exclusion of ineligible studies, a total of 14 clinical trials were considered eligible for the meta-analysis. The relative risk of all-grade skin rash and acneiform dermatitis was 1.71 (95% CI: 1.07–2.72; p = 0.02) and 6.55 (95% CI: 3.42–12.56; p < 0.00001), correspondingly; while the relative risk of high-grade skin rash and acneiform dermatitis was 2.64 (95% CI: 1.42–4.91; p = 0.002) and 8.44 (95% CI: 2.39–29.81; p = 0.0009), respectively. Conclusion
Our meta-analysis has demonstrated that MEK inhibitor-based treatment is associated with an increased risk of all-grade and high-grade skin rash and acneiform dermatitis compared with control.