Defucosylated Anti-CCR4 Monoclonal Antibody (KW-0761) for Relapsed Adult T-Cell Leukemia-Lymphoma: A Multicenter Phase II Study

Takashi Ishida(Nagasaki University), Tatsuro Joh(Nagasaki University), Naokuni Uike(Nagasaki University), Kazuhito Yamamoto(Nagasaki University), Atae Utsunomiya(Nagasaki University), Shinichiro Yoshida(Nagasaki University), Yoshio Saburi(Nagasaki University), Toshihiro Miyamoto(Nagasaki University), Shigeki Takemoto(Nagasaki University), Hitoshi Suzushima(Nagasaki University), Kunihiro Tsukasaki(Nagasaki University), Kisato Nosaka(Nagasaki University), Hiroshi Fujiwara(Nagasaki University), Kenji Ishitsuka(Nagasaki University), Hiroshi Inagaki(Nagasaki University), Michinori Ogura(Nagasaki University), Shiro Akinaga(Nagasaki University), Masao Tomonaga(Nagasaki University), Kensei Tobinai(Nagasaki University), Ryuzo Ueda(Nagasaki University)
Journal of Clinical Oncology
February 7, 2012
Cited by 648Open Access
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Abstract

PURPOSE: Adult T-cell leukemia-lymphoma (ATL) is usually resistant to conventional chemotherapies, and there are few other treatment options. Because CC chemokine receptor 4 (CCR4) is expressed on tumor cells from most patients with ATL, KW-0761, a humanized anti-CCR4 monoclonal antibody, which markedly enhances antibody-dependent cellular cytotoxicity, was evaluated in the treatment of patients with relapsed ATL. PATIENTS AND METHODS: A multicenter phase II study of KW-0761 for patients with relapsed, aggressive CCR4-positive ATL was conducted to evaluate efficacy, pharmacokinetic profile, and safety. The primary end point was overall response rate, and secondary end points included progression-free and overall survival from the first dose of KW-0761. Patients received intravenous infusions of KW-0761 once per week for 8 weeks at a dose of 1.0 mg/kg. RESULTS: Of 28 patients enrolled onto the study, 27 received at least one infusion of KW-0761. Objective responses were noted in 13 of 26 evaluable patients, including eight complete responses, with an overall response rate of 50% (95% CI, 30% to 70%). Median progression-free and overall survival were 5.2 and 13.7 months, respectively. The mean half-life period after the eighth infusion was 422 ± 147 hours (± standard deviation). The most common adverse events were infusion reactions (89%) and skin rashes (63%), which were manageable and reversible in all cases. CONCLUSION: KW-0761 demonstrated clinically meaningful antitumor activity in patients with relapsed ATL, with an acceptable toxicity profile. Further investigation of KW-0761 for treatment of ATL and other T-cell neoplasms is warranted.


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