Kawano Noriaki, Yoshida Shuro, Kuriyama Takuro, Tahara Yoshihiro, Yamashita Kiyoshi, Nagahiro Yuri, Kawano Jiro, Koketsu Hideki, Toyofuku Atsushi, Manabe Tatsuya, Beppu Kiichiro, Ono Nobuyuki, Himeji Daisuke, Yokota-Ikeda Naoko, Inoue Sanshiro, Ochiai Hidenobu, Sonoda Koh-Hei, Shimoda Kazuya, Ishikawa Fumihiko, Ueda Akira
Department of Internal Medicine, Miyazaki Prefectural Miyazaki Hospital, Japan.
Intern Med. 2015;54(12):1489-98. doi: 10.2169/internalmedicine.54.1953. Epub 2015 Jun 15.
Despite the remarkable advances in chemotherapy and allogeneic hematopoietic stem cell transplantation (HSCT), adult T-cell leukemia-lymphoma (ATL) is still associated with a high mortality rate. It is therefore essential to elucidate the current features of ATL.
We retrospectively analyzed 81 patients with aggressive type ATL at our institution over a 7-year period based on Shimoyama's diagnostic criteria.
Eighty-one patients with a median age of 67.5 years were classified as having acute (n=47), lymphoma (n=32), or chronic type (n=2) ATL. They were initially treated by either palliative therapy (n=25) or systemic chemotherapy [n=56; cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) therapy (n=25)/vincristine, cyclophosphamide, doxorubicin, and prednisone (VCAP)-doxorubicin, ranimustine, and prednisone (AMP)-vindesine, etoposide, carboplatin, and prednisone (VECP) therapy (VCAP-AMP-VECP) or CHOP-VMMV therapy (n=31)], and showed median survival durations of 16 and 277 days, respectively. Subsequent to the initial treatment, HSCT (n=6) was performed for certain patients, thus revealing that two-thirds (n=4) relapsed, and one-third (n=2) survived for 131 days and 203 days, respectively. The relapsed ATL patients were treated with conventional salvage therapy (n=29) or anti-CC chemokine receptor 4 antibody (mogamulizumab) (n=3). The patients treated with mogamulizumab demonstrated complete response (2) and partical response (1) with short duration periods of 82 days, 83 days, and 192 days, respectively. Among the five long-term survivors (>5 years) who received chemotherapy, most showed a low and intermediate risk according to the ATL prognostic index.
In our study, the overall survival of ATL remains poor due to the advanced age of the patients at diagnosis, a high proportion of patients receiving palliative therapy, and a small proportion of long-term survivors receiving chemotherapy and undergoing HSCT. This study illustrates the current clinical features, treatment strategies, and outcomes in clinical practice.
尽管化疗和异基因造血干细胞移植(HSCT)取得了显著进展,但成人T细胞白血病淋巴瘤(ATL)的死亡率仍然很高。因此,阐明ATL的当前特征至关重要。
我们根据Shimoyama诊断标准,回顾性分析了我院7年间81例侵袭性ATL患者。
81例患者的中位年龄为67.5岁,分为急性(n = 47)、淋巴瘤(n = 32)或慢性型(n = 2)ATL。他们最初接受姑息治疗(n = 25)或全身化疗[n = 56;环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)疗法(n = 25)/长春新碱、环磷酰胺、阿霉素和泼尼松(VCAP)-阿霉素、雷莫司汀和泼尼松(AMP)-长春地辛、依托泊苷、卡铂和泼尼松(VECP)疗法(VCAP-AMP-VECP)或CHOP-VMMV疗法(n = 31)],中位生存期分别为16天和277天。初始治疗后,部分患者接受了HSCT(n = 6),结果显示三分之二(n = 4)复发,三分之一(n = 2)分别存活131天和203天。复发的ATL患者接受了传统挽救治疗(n = 29)或抗CC趋化因子受体4抗体(莫加莫单抗)(n = 3)治疗。接受莫加莫单抗治疗的患者分别在82天、83天和192天的短时间内表现出完全缓解(2例)和部分缓解(1例)。在接受化疗的5例长期存活者(>5年)中,根据ATL预后指数,大多数表现为低风险和中风险。
在我们的研究中,由于诊断时患者年龄较大、接受姑息治疗的患者比例较高以及接受化疗和HSCT的长期存活者比例较小,ATL的总体生存率仍然很低。本研究阐明了当前临床实践中的临床特征、治疗策略和结果。