Treatment with epcoritamab in 10 patients in real-world clinical practice

As the experience of the Epcoritamab (epcor) is not well described in a real-world setting, we herein retrospectively analyzed patients who received treatment of epcor.The drug was administered to 10 patients at Saitama Cancer Center (SCC).Patients who completed at least one treatment cycle were included in the clinical study.This clinical study was conducted in accordance with the principles of the Declaration of Helsinki, and the protocol and related documents were approved by the Ethics Committee of SCC on March 13, 2024.Informed consent from the patients was obtained in the form of opt-out on the website.Patient listing and baseline characteristics at the start of epcor are shown in Table 1 (cytokine-release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) were symptoms after epcor start).The median duration of observation was 2.8 months (0.5-6.5 months), and the median number of treatment cycles was 2.5 (1-5 cycles)(Figure 1).Chimeric Antigen Receptor T-Cell (CAR-T) therapy was none.The median time from the last dose of bendamustine (benda) to the start of epcor was 7.6 months (1-21 months).The median time from the last dose of rituximab to the start of epcor was 3.3 months (1-36 months).The overall response rate was 70.0%, better than the rates reported from clinical studies. 1,2Complete response (CR) was evaluated in each cycle.The median time to response was 1.86 months (0.5-4.5 months) and CR was 2.5 months (1-4.5 months), which were comparable to the corresponding times reported from clinical studies. 1,2 Patients who showed a clinical response included elderly patients aged 75 years, high-risk patients with stage III disease and patients who had received 4 or more prior regimens (Table 1).These results were similar to those reported from clinical studies. 1,2Items not analyzed in clinical studies were the presence/absence of response in patients with decreased serum albumin, Perfomance status 2, central nervous system Treatment with epcoritamab in 10 patients in real-world clinical practice

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Publication Details

Journal
Journal of Clinical and Experimental Hematopathology
Published
2024-11-27
DOI
https://doi.org/10.3960/jslrt.24054
Citations
4
Primary Topic
Pancreatic and Hepatic Oncology Research
Type
article
Field-Weighted Citation Impact
1.13
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article

Treatment with epcoritamab in 10 patients in real-world clinical practice

Kazuhiko Kobayashi, Daisuke Takei, Hiroaki Kanda, Toshiaki Nakayama et al.
4 citations
Journal of Clinical and Experimental Hematopathology
Pancreatic and Hepatic Oncology Research
1.13
article

Treatment with epcoritamab in 10 patients in real-world clinical practice

Kazuhiko Kobayashi, Daisuke Takei, Hiroaki Kanda, Toshiaki Nakayama, Yasumasa Shimano, Yu Nishimura, Tomoya Abe, Hiroki Tsutsumi, Nobuo Maseki, M Kawamura, Yoshie Iizaki, Hirofumi Kobayashi, Masahisa Kudo, Yasunobu Sekiguchi
article en
4 citations

Abstract

As the experience of the Epcoritamab (epcor) is not well described in a real-world setting, we herein retrospectively analyzed patients who received treatment of epcor.The drug was administered to 10 patients at Saitama Cancer Center (SCC).Patients who completed at least one treatment cycle were included in the clinical study.This clinical study was conducted in accordance with the principles of the Declaration of Helsinki, and the protocol and related documents were approved by the Ethics Committee of SCC on March 13, 2024.Informed consent from the patients was obtained in the form of opt-out on the website.Patient listing and baseline characteristics at the start of epcor are shown in Table 1 (cytokine-release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) were symptoms after epcor start).The median duration of observation was 2.8 months (0.5-6.5 months), and the median number of treatment cycles was 2.5 (1-5 cycles)(Figure 1).Chimeric Antigen Receptor T-Cell (CAR-T) therapy was none.The median time from the last dose of bendamustine (benda) to the start of epcor was 7.6 months (1-21 months).The median time from the last dose of rituximab to the start of epcor was 3.3 months (1-36 months).The overall response rate was 70.0%, better than the rates reported from clinical studies. 1,2Complete response (CR) was evaluated in each cycle.The median time to response was 1.86 months (0.5-4.5 months) and CR was 2.5 months (1-4.5 months), which were comparable to the corresponding times reported from clinical studies. 1,2 Patients who showed a clinical response included elderly patients aged 75 years, high-risk patients with stage III disease and patients who had received 4 or more prior regimens (Table 1).These results were similar to those reported from clinical studies. 1,2Items not analyzed in clinical studies were the presence/absence of response in patients with decreased serum albumin, Perfomance status 2, central nervous system Treatment with epcoritamab in 10 patients in real-world clinical practice

Journal of Clinical and Experimental HematopathologyVol. 64(4)
Saitama Cancer Center (JP)
Openalex Percentile: Top 18%
Pancreatic and Hepatic Oncology Research
1.13
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Treatment with epcoritamab in 10 patients in real-world clinical practice — Kazuhiko Kobayashi, Daisuke Takei, et al. · Journal of Clinical and Experimental Hematopathology (2024) | TGRS Research Map | TGRS