Mark Bishton
The safety and clinical effectiveness of rapid infusion with CT‐P10 in patients with non‐Hodgkin's lymphoma or chronic lymphocytic leukemia: A retrospective non‐interventional post‐authorization safety study in Europe
Bishton, Mark; Marshall, Scott; Harchowal, Jatinder; Salles, Gilles; Golfier, Camille; Tucci, Alessandra; Fernández, Alicia Rodriguez; Sanchez Blanco, Jose Javier; Bocchia, Monica; Kim, Soo Kyoung; Lee, Young Nam; Zinzani, Pier Luigi
Authors
Scott Marshall
Jatinder Harchowal
Gilles Salles
Camille Golfier
Alessandra Tucci
Alicia Rodriguez Fernández
Jose Javier Sanchez Blanco
Monica Bocchia
Soo Kyoung Kim
Young Nam Lee
Pier Luigi Zinzani
Abstract
Rapid infusion (RI) of the rituximab biosimilar CT-P10 is currently only an approved treatment regimen for the treatment of rheumatoid arthritis. Although both CT-P10 and reference rituximab are known to be frequently administered using a RI regimen (≤90 min) in clinical practice, published data on the safety of RI of CT-P10 in patients with NHL and CLL are limited. Hence, this study collected real-world safety and effectiveness data on RI-CT-P10 from the medical records of 196 patients with NHL or CLL in 10 European centers, 6 months after the date of the first RI (index date); the infusion-related reaction (IRR) rate was compared to previously published data. Ten percent (95% confidence interval 6%–15%; n = 20/196) of patients experienced an infusion-related reaction (IRR) on day 1–2 post-index, which was not significantly different (p = 0.45) to the IRR rate for rituximab described in a previous meta-analysis (8.8%). During the observation period, 2% of patients experienced grade 3–5 IRRs and 85% (n = 166) experienced an adverse event (non-IRR). The most common reason for discontinuation of first-line CT-P10 was planned treatment completion (81%; n = 158). Complete response and partial response to CT-P10 was observed in 74% (n = 142/192) and 22% (n = 42/192) of patients, respectively. The results of this real-world study demonstrate that the safety and effectiveness profile of RI-CT-P10 is similar to RI of reference rituximab and therefore support the current use of RI-CT-P10 in patients with NHL and CLL.
Citation
Bishton, M., Marshall, S., Harchowal, J., Salles, G., Golfier, C., Tucci, A., Fernández, A. R., Sanchez Blanco, J. J., Bocchia, M., Kim, S. K., Lee, Y. N., & Zinzani, P. L. (2022). The safety and clinical effectiveness of rapid infusion with CT‐P10 in patients with non‐Hodgkin's lymphoma or chronic lymphocytic leukemia: A retrospective non‐interventional post‐authorization safety study in Europe. Hematological Oncology, 40(3), 370-380. https://doi.org/10.1002/hon.2978
Journal Article Type | Article |
---|---|
Acceptance Date | Jan 21, 2022 |
Online Publication Date | Mar 17, 2022 |
Publication Date | 2022-08 |
Deposit Date | Nov 24, 2022 |
Publicly Available Date | Nov 24, 2022 |
Journal | Hematological Oncology |
Print ISSN | 0278-0232 |
Electronic ISSN | 1099-1069 |
Publisher | Wiley |
Peer Reviewed | Peer Reviewed |
Volume | 40 |
Issue | 3 |
Pages | 370-380 |
DOI | https://doi.org/10.1002/hon.2978 |
Public URL | https://nottingham-repository.worktribe.com/output/14036214 |
Publisher URL | https://onlinelibrary.wiley.com/doi/10.1002/hon.2978 |
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