A phase 2 trial of CHOP with anti-CCR4 antibody mogamulizumab for older patients with adult T-cell leukemia/lymphoma

M Makoto Yoshimitsu I Ilseung Choi (33National Hospital Organization Kyushu Cancer Center, Department of Hematology, Fukuoka, Japan) S Shigeru Kusumoto (4Aichi Cancer Center, Department of Hematology and Cell Therapy, Nagoya, Japan) M Mototsugu Shimokawa A Atae Utsunomiya (3Imamura General Hospital, Kagoshima, Japan) Y Youko Suehiro (8NHO Kyushu Cancer Center, Department of Hematology and Cell Therapy, Fukuoka, Japan) T Tomonori Hidaka (7Division of Hematology, Diabetes, and Endocrinology, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan) K Kisato Nosaka (Department of Hematology, Rheumatology and Infectious Diseases, Faculty of Life Sciences, Kumamoto University) H Hidenori Sasaki (9Division of Medical Oncology, Hematology, and Infectious Diseases, Faculty of Medicine, Fukuoka University, Fukuoka, Japan) S Shinya Rai (2British Columbia Cancer, Centre for Lymphoid Cancer, Vancouver, Canada) S Shinobu Tamura S Satsuki Owatari K Ki-Ryang Koh D Daisuke Nakamura M Masahito Tokunaga M Masaaki Sekine (7Division of Hematology, Diabetes, and Endocrinology, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan) Y Yuma Sakamoto (14Department of Pathology and Molecular Diagnostics, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan) H Hiroshi Inagaki (14Department of Pathology and Molecular Diagnostics, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan) T Takashi Ishida K Kenji Ishitsuka

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

Journal Blood
Volume / Issue Vol. 146, Issue 12
Published September 18, 2025
Pages 1440-1449
ISSN 0006-4971
Publisher Elsevier BV

Journal Info

Blood

Elsevier BV

ISSN: 0006-4971 Health Sciences

Authors (20)

M

Makoto Yoshimitsu

I

Ilseung Choi

33National Hospital Organization Kyushu Cancer Center, Department of Hematology, Fukuoka, Japan

S

Shigeru Kusumoto

4Aichi Cancer Center, Department of Hematology and Cell Therapy, Nagoya, Japan

M

Mototsugu Shimokawa

A

Atae Utsunomiya

3Imamura General Hospital, Kagoshima, Japan

Y

Youko Suehiro

8NHO Kyushu Cancer Center, Department of Hematology and Cell Therapy, Fukuoka, Japan

T

Tomonori Hidaka

7Division of Hematology, Diabetes, and Endocrinology, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan

K

Kisato Nosaka

Department of Hematology, Rheumatology and Infectious Diseases, Faculty of Life Sciences, Kumamoto University

H

Hidenori Sasaki

9Division of Medical Oncology, Hematology, and Infectious Diseases, Faculty of Medicine, Fukuoka University, Fukuoka, Japan

S

Shinya Rai

2British Columbia Cancer, Centre for Lymphoid Cancer, Vancouver, Canada

S

Shinobu Tamura

S

Satsuki Owatari

K

Ki-Ryang Koh

D

Daisuke Nakamura

M

Masahito Tokunaga

M

Masaaki Sekine

7Division of Hematology, Diabetes, and Endocrinology, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan

Y

Yuma Sakamoto

14Department of Pathology and Molecular Diagnostics, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan

H

Hiroshi Inagaki

14Department of Pathology and Molecular Diagnostics, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan

T

Takashi Ishida

K

Kenji Ishitsuka