A phase 2 trial of CHOP with anti-CCR4 antibody mogamulizumab for older patients with adult T-cell leukemia/lymphoma
Abstract
Abstract No standard of care for older patients with aggressive adult T-cell leukemia/lymphoma (ATL) has been established. We evaluated the efficacy of CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisolone) every 2 weeks with mogamulizumab (Moga; Moga-CHOP-14) for older patients with untreated ATL. In this multicenter phase 2 trial, patients aged ≥66 years and those aged 56 to 65 years ineligible for transplantation received 6 cycles of Moga-CHOP-14, followed by 2 cycles of Moga monotherapy. The primary end point was 1-year progression-free survival (PFS). Secondary end points were the complete response (CR) rate, overall response rate (ORR), overall survival (OS), 1-year event-free survival (EFS), and safety. We also investigated the impact of CC chemokine receptor 4 (CCR4) mutation and Moga-associated cutaneous adverse events (cAEs) on PFS and OS. The study protocol was amended to allow the dosing interval to be extended to 21 days at the physician’s discretion. Among 48 evaluable patients, the 1-year PFS was 36.2% (90% confidence interval, 24.9-47.6), with a median follow-up of 1.6 years. The 1-year OS and EFS were 66.0% and 29.9%, respectively. CR and ORR were 64.6% and 91.7%. No unexpected toxicities were observed. Of 47 patients who received ≥2 cycles of CHOP, 20 (42.6%) received CHOP-14, among whom 12 (25.5%) completed 6 cycles. CCR4 mutation and Moga-associated cAEs were associated with better OS. This study showed that Moga-CHOP significantly improved PFS, although the optimal interval for CHOP remains undetermined. Moga-CHOP is now considered a preferable first-line treatment for this patient population. This trial was registered at https://jrct.mhlw.go.jp/en-top as #jRCTs041180130.
Article Details
Authors (20)
Makoto Yoshimitsu
Ilseung Choi
33National Hospital Organization Kyushu Cancer Center, Department of Hematology, Fukuoka, Japan
Shigeru Kusumoto
4Aichi Cancer Center, Department of Hematology and Cell Therapy, Nagoya, Japan
Mototsugu Shimokawa
Atae Utsunomiya
3Imamura General Hospital, Kagoshima, Japan
Youko Suehiro
8NHO Kyushu Cancer Center, Department of Hematology and Cell Therapy, Fukuoka, Japan
Tomonori Hidaka
7Division of Hematology, Diabetes, and Endocrinology, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan
Kisato Nosaka
Department of Hematology, Rheumatology and Infectious Diseases, Faculty of Life Sciences, Kumamoto University
Hidenori Sasaki
9Division of Medical Oncology, Hematology, and Infectious Diseases, Faculty of Medicine, Fukuoka University, Fukuoka, Japan
Shinya Rai
2British Columbia Cancer, Centre for Lymphoid Cancer, Vancouver, Canada
Shinobu Tamura
Satsuki Owatari
Ki-Ryang Koh
Daisuke Nakamura
Masahito Tokunaga
Masaaki Sekine
7Division of Hematology, Diabetes, and Endocrinology, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan
Yuma Sakamoto
14Department of Pathology and Molecular Diagnostics, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan
Hiroshi Inagaki
14Department of Pathology and Molecular Diagnostics, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan
Takashi Ishida
Kenji Ishitsuka