Phase I/II clinical trial of brentuximab vedotin for pretreated Japanese patients with CD30‐positive cutaneous T‐cell lymphoma

Author:

Hirai Yoji1ORCID,Sakurai Jun2,Yoshida Shiho2,Kikuchi Takashi2,Mitsuhashi Toshiharu2,Miyake Tomoko1ORCID,Fujimura Taku3ORCID,Abe Riichiro4ORCID,Fujikawa Hiroki4,Boki Hikari5,Suga Hiraku5,Shibata Sayaka5ORCID,Miyagaki Tomomitsu5ORCID,Shimauchi Takatoshi6ORCID,Kiyohara Eiji7,Kawakami Yoshio1ORCID,Morizane Shin1ORCID

Affiliation:

1. Department of Dermatology Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University Okayama Japan

2. Center for Innovative Clinical Medicine Okayama University Hospital Okayama Japan

3. Department of Dermatology Tohoku University Graduate School of Medicine Sendai Japan

4. Department of Dermatology Niigata University Niigata Japan

5. Department of Dermatology Tokyo University Tokyo Japan

6. Department of Dermatology Hamamatsu University School of Medicine Hamamatsu Japan

7. Department of Dermatology Osaka University Osaka Japan

Abstract

AbstractBrentuximab vedotin (BV), a conjugate of anti‐CD30 antibody and monomethyl auristatin E, has emerged as a promising treatment option for refractory CD30+ mycosis fungoides (MF) and primary cutaneous anaplastic large‐cell lymphoma (pcALCL). BV has been shown to be safe and effective in treating Hodgkin's lymphoma and peripheral T‐cell lymphoma. This multicenter, prospective, single‐arm phase I/II study evaluated the efficacy of BV in Japanese patients with CD30+ cutaneous lymphomas, namely CD30+ cutaneous T‐cell lymphoma. Participants were divided into two groups: those with CD30+ MF or pcALCL (cohort 1, n = 13) and those with CD30+ lymphoproliferative disorders other than those in cohort 1 (cohort 2, n = 3). The studied population included the full analysis set (FAS), modified FAS (mFAS), and safety analysis set (SAF). These sets were identified in cohorts 1 and 1 + 2 and labeled FAS1 and FAS2, mFAS1 and mFAS2, and SAF1 and SAF2, respectively. Each treatment cycle lasted 3 weeks, and BV was continued for up to 16 cycles after the third cycle based on treatment response. The primary endpoint was the 4‐month objective response rate (ORR4) determined by the Independent Review Forum (IRF). ORR4 was 69.2% for FAS1 and 62.5% for FAS2 (P < 0.0001). Secondary endpoints of ORR, assessed using the global response score (53.8% in FAS1) and modified severity‐weighted assessment tool (62.5% in FAS1), using the IRF, provided results comparable to the primary findings. The incidence of ≥grade 3 adverse events (≥15%) in SAF1 was peripheral neuropathy in three patients (23%) and fever and eosinophilia in two patients (15%). In conclusion, BV showed favorable efficacy, tolerability, and safety profile in Japanese patients with relapsed or refractory CD30+ primary cutaneous T‐cell lymphoma. The trial was registered with University Hospital Medical Information Network Clinical Trials Registry, Japan (protocol ID: UMIN000034205).

Funder

Takeda Pharmaceutical Company

Publisher

Wiley

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