Saito K, Furusawa S, Yamada K, Waga K, Aoyagi A, Koike T, Arimura H, Noguchi M, Yamato H, Sakuma H
Third Department of Internal Medicine, Dokkyo University School of Medicine.
Rinsho Ketsueki. 1995 Mar;36(3):165-74.
We used a new chemotherapy regimen for the treatment of 18 consecutive patients with relapsed AML. The regimen consisted of low-dose cytosine arabinoside (Ara-C), low-dose aclarubicin and concurrent use of G-CSF (CAG regimen). Fifteen out of 18 patients (83%) achieved complete remission (CR). Median CR duration and median survival were 6 months and 15 months, respectively. These results were similar to those of previously reported salvage therapies for relapsed AML including intensive chemotherapy consisting of intermediate-dose Ara-C and sequential mitoxantrone with or without etoposide (MC/MEC), which we previously adopted. Myelosuppression and non-hematological toxicities were apparently lower and less frequent compared to MC/MEC. The CAG regimen seems promising for the treatment of relapsed AML with its low toxicity contributing to a high quality of life for the patient.
我们采用一种新的化疗方案连续治疗了18例复发急性髓系白血病(AML)患者。该方案由小剂量阿糖胞苷(Ara-C)、小剂量阿克拉霉素及同时使用粒细胞集落刺激因子(G-CSF)组成(CAG方案)。18例患者中有15例(83%)达到完全缓解(CR)。CR持续时间中位数和总生存中位数分别为6个月和15个月。这些结果与我们之前采用的包括中剂量Ara-C联合序贯米托蒽醌(含或不含依托泊苷)的强化化疗(MC/MEC)等先前报道的复发AML挽救治疗结果相似。与MC/MEC相比,骨髓抑制和非血液学毒性明显更低且更少见。CAG方案因其低毒性有助于提高患者生活质量,似乎对复发AML的治疗很有前景。