Sawada Ken-ichi, Hirokawa Makoto, Fujishima Naohito, Teramura Masanao, Bessho Masami, Dan Kazuo, Tsurumi Hisashi, Nakao Shinji, Urabe Akio, Omine Mitsuhiro, Ozawa Keiya
Division of Haematologyand Oncology, Department of Medicine,Akita University School of Medicine,1-1-1 Hondo, Akita, Japan.
Haematologica. 2007 Aug;92(8):1021-8. doi: 10.3324/haematol.11192. Epub 2007 Jul 20.
Cyclosporine A (CsA) has become one of the leading agents for the treatment of pure red cell aplasia (PRCA). However, further studies are necessary to determine the relapse-free survival (RFS) and overall survival (OS) of patients treated with this drug, the minimum duration of therapy for induction of remission, and whether or not there is need for maintenance treatment.
We conducted a nationwide survey in Japan. From a total of 185 patients (with 73 primary idiopathic PRCA and 112 with secondary PRCA), we evaluated 62 patients with primary idiopathic PRCA for this report.
The remission induction therapy for these patients included CsA (n=31), corticosteroids (CS) (n=20) or other drugs (n=11). CsA and CS produced remissions in 23 (74%) and 12 (60%) patients, respectively. The salvage treatment produced remissions in 58 patients (94%). Forty-one and 15 patients were maintained on CsA+/-CS (CsA-containing group) or CS alone (CS group), respectively. The median RFS in the CsA-containing group was 103 months, longer than that seen in the CS group (33 months) (p<0.01). Of 14 patients whose CsA was discontinued, 12 patients (86%) relapsed after a median of 3 months (range 1.5 to 40 months), while only 3 of 27 patients (11%) relapsed during CsA-containing maintenance therapy. Thus, the discontinuance of maintenance therapy was strongly correlated with relapse (p<0.001). Four patients in the CsA-containing group died; however, the OS of this group was not significantly different from that of the CS-groups (p=0.104).
CsA-containing regimens sustain prolonged RFS more effectively than CS in primary idiopathic PRCA and seem to be important to prevent relapse.
环孢素A(CsA)已成为治疗纯红细胞再生障碍性贫血(PRCA)的主要药物之一。然而,有必要进一步研究接受该药物治疗患者的无复发生存期(RFS)和总生存期(OS)、诱导缓解的最短治疗持续时间,以及是否需要维持治疗。
我们在日本进行了一项全国性调查。在总共185例患者(73例原发性特发性PRCA和112例继发性PRCA)中,本报告评估了62例原发性特发性PRCA患者。
这些患者的缓解诱导治疗包括CsA(n = 31)、皮质类固醇(CS)(n = 20)或其他药物(n = 11)。CsA和CS分别使23例(74%)和12例(60%)患者获得缓解。挽救性治疗使58例患者(94%)获得缓解。分别有41例和15例患者接受CsA±CS(含CsA组)或仅接受CS(CS组)维持治疗。含CsA组的中位RFS为103个月,长于CS组(33个月)(p<0.01)。在14例停用CsA的患者中,12例(86%)在中位3个月(范围1.5至40个月)后复发,而在含CsA维持治疗期间,27例患者中只有3例(11%)复发。因此,维持治疗的中断与复发密切相关(p<0.001)。含CsA组有4例患者死亡;然而,该组的OS与CS组无显著差异(p = 0.104)。
在原发性特发性PRCA中,含CsA方案比CS更有效地维持较长的RFS,且似乎对预防复发很重要。