Ishida Takashi, Utsunomiya Atae, Jo Tatsuro, Yamamoto Kazuhito, Kato Koji, Yoshida Shinichiro, Takemoto Shigeki, Suzushima Hitoshi, Kobayashi Yukio, Imaizumi Yoshitaka, Yoshimura Kenichi, Kawamura Kouichi, Takahashi Takeshi, Tobinai Kensei, Ueda Ryuzo
Department of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Department of Hematology, Imamura Bun-in Hospital, Kagoshima, Japan.
Cancer Sci. 2017 Oct;108(10):2022-2029. doi: 10.1111/cas.13343. Epub 2017 Aug 28.
The present study sought to elucidate the prognosis of adult T-cell leukemia-lymphoma (ATL) patients receiving mogamulizumab, a defucosylated anti-CCR4 monoclonal antibody. Progression-free survival (PFS) and overall survival (OS) of ATL patients enrolled in two studies are herein updated, namely NCT00355472 (phase I study of mogamulizumab in relapsed patients with ATL and peripheral T-cell lymphoma) and NCT00920790 (phase II study for relapsed ATL). Of 13 patients with relapsed aggressive ATL in the phase I study, four (31%) survived >3 years. For 26 relapsed patients with aggressive ATL in the phase II study, median PFS was 5.2 months and 1-year PFS was 26%, whereas median OS was 14.4 months, and 3-year OS was 23%. For patients without a rash or who developed a grade 1 rash only, median PFS was 0.8 months, and 1-year PFS was zero, with a median OS of 6.0 months, and 3-year OS of 8%. In contrast, for patients who developed a rash ≥grade 2, median PFS was 11.7 months, and 1-year PFS was 50%, with a median OS of 25.6 months, and 3-year OS of 36%. Thus, we conclude that mogamulizumab monotherapy may improve PFS and OS in some patients with relapsed aggressive ATL, especially those who develop a skin rash as a moderate immune-related adverse event. Therefore, further investigation is warranted to validate the present observations and to clarify the mechanisms involved in the activity of mogamulizumab.
本研究旨在阐明接受莫加穆利单抗(一种去岩藻糖基化抗CCR4单克隆抗体)治疗的成人T细胞白血病-淋巴瘤(ATL)患者的预后。本文更新了两项研究中ATL患者的无进展生存期(PFS)和总生存期(OS),这两项研究分别是NCT00355472(莫加穆利单抗用于复发ATL和外周T细胞淋巴瘤患者的I期研究)和NCT00920790(复发ATL的II期研究)。在I期研究的13例复发侵袭性ATL患者中,4例(31%)存活超过3年。在II期研究的26例复发侵袭性ATL患者中,中位PFS为5.2个月,1年PFS为26%,而中位OS为14.4个月,3年OS为23%。对于没有皮疹或仅出现1级皮疹的患者,中位PFS为0.8个月,1年PFS为零,中位OS为6.0个月,3年OS为8%。相比之下,对于出现≥2级皮疹的患者,中位PFS为11.7个月,1年PFS为50%,中位OS为25.6个月,3年OS为36%。因此,我们得出结论,莫加穆利单抗单药治疗可能改善部分复发侵袭性ATL患者的PFS和OS,尤其是那些出现皮疹作为中度免疫相关不良事件的患者。因此,有必要进一步研究以验证目前的观察结果并阐明莫加穆利单抗活性所涉及的机制。