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Long‐term outcomes and central nervous system relapse in extranodal natural killer/T‐cell lymphoma

医学 内科学 异环磷酰胺 依托泊苷 危险系数 中性粒细胞减少症 淋巴瘤 胃肠病学 化疗 外科 肿瘤科 置信区间
作者
Kana Miyazaki,Ritsuro Suzuki,Masahiko Oguchi,Senzo Taguchi,Jun Amaki,Takeshi Maeda,Nobuko Kubota,Dai Maruyama,Yasuhito Terui,Nodoka Sekiguchi,Jun Takizawa,Hiroyuki Tsukamoto,Tohru Murayama,Toshihiko Ando,Hiroshi Matsuoka,Masatoshi Hasegawa,Hideho Wada,Rika Sakai,Yoshihiro Kameoka,Norifumi Tsukamoto,Ilseung Choi,Yasufumi Masaki,Kazuyuki Shimada,Noriko Fukuhara,Takahiko Utsumi,Nobuhiko Uoshima,Yoshitoyo Kagami,Naoko Asano,Yasuo Ejima,Naoyuki Katayama,Motoko Yamaguchi
出处
期刊:Hematological Oncology [Wiley]
卷期号:40 (4): 667-677 被引量:1
标识
DOI:10.1002/hon.2977
摘要

To elucidate the long-term outcomes of non-anthracycline-containing therapies and central nervous system (CNS) events in patients with extranodal NK/T-cell lymphoma, nasal type (ENKTL), the clinical data of 313 patients with ENKTL diagnosed between 2000 and 2013 in a nationwide retrospective study in Japan were updated and analyzed. At a median follow-up of 8.4 years, the 5-year overall survival (OS) and progression-free survival (PFS) were 71% and 64%, respectively, in 140 localized ENKTL patients who received radiotherapy-dexamethasone, etoposide, ifosfamide, and carboplatin (RT-DeVIC) in clinical practice. Nine (6.4%) patients experienced second malignancies. In 155 localized ENKTL patients treated with RT-DeVIC, 10 (6.5%) experienced CNS relapse (median, 12.8 months after diagnosis). In five of them, the events were confined to the CNS. Nine of the 10 patients who experienced CNS relapse died within 1 year after CNS relapse. Multivariate analysis identified gingival (hazard ratio [HR], 54.35; 95% confidence interval [CI], 8.60-343.35) and paranasal involvement (HR, 7.42; 95% CI, 1.78-30.89) as independent risk factors for CNS relapse. In 80 advanced ENKTL patients, 18 received steroid (dexamethasone), methotrexate, ifosfamide, L-asparaginase, and etoposide (SMILE) chemotherapy as first-line treatment. Patients who received SMILE as their first-line treatment tended to have better OS than those who did not (p = 0.071). Six (7.5%) advanced ENKTL patients experienced isolated CNS relapse (median, 2.6 months after diagnosis) and died within 4 months of relapse. No second malignancies were documented in advanced ENKTL patients. In the entire cohort, the median OS after first relapse or progression was 4.6 months. 12 patients who survived 5 years after PFS events were disease-free at the last follow-up. Of those, 11 (92%) underwent hematopoietic stem cell transplantation. Our 8-year follow-up revealed the long-term efficacy and safety of RT-DeVIC and SMILE. The risk of CNS relapse is an important consideration in advanced ENKTL.
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