Tsurusawa M, Katano N, Asami K, Watanabe A, Koizumi S, Miyake M, Kikuta A, Iwai A, Yamamura Y, Kawano Y, Mugishima H, Sekine I, Matsushita T, Horikoshi Y, Kikuchi M, Anami K, Fujimoto T
Dept. of Pediatrics, Aichi Medical University.
Gan To Kagaku Ryoho. 2000 Oct;27(11):1695-702.
To address the issue of salvageability in relapsed children with NHL who had all received the same frontline therapy, we retrospectively studied the treatment response and the outcome of 27 children who relapsed following the CCLSG-NHL890 protocol. The reinduction rates and 3-year survival rates (mean +/- SD) were as follows: lymphoblastic lymphoma (LB, n = 9), 44% & 17 +/- 14%; leukemia lymphoma syndrome (LLS, n = 8), 25% & 0%; large cell lymphoma (LC, n = 3) 100% & 67 +/- 27%; Burkitt's lymphoma (B, n = 7) 0% & 0%. Thus, the salvageability of LC lymphoma was good, but the outcome of Burkitt's lymphoma was very poor. CCLSG-NHL960 protocol for LB lymphomas and intensive multiagent regimens for LC lymphomas produced favorable response rates, but the effect of the high-dose Ara-C regimen for Burkitt's lymphoma was not determined. The initial stages of the disease seemed to be associated with the patient outcome: the outcome of the patients in stage IV was inferior to that of patients in stages II or III. Other clinical variables, such as relapse sites, relapse time and BM rescue did not affect the patients' outcome.
为了探讨接受相同一线治疗的复发性非霍奇金淋巴瘤(NHL)儿童的挽救治疗问题,我们回顾性研究了27例按照CCLSG-NHL890方案治疗后复发的儿童的治疗反应和结局。再诱导率和3年生存率(均值±标准差)如下:淋巴细胞淋巴瘤(LB,n = 9),44%和17±14%;白血病淋巴瘤综合征(LLS,n = 8),25%和0%;大细胞淋巴瘤(LC,n = 3),100%和67±27%;伯基特淋巴瘤(B,n = 7),0%和0%。因此,LC淋巴瘤的挽救性良好,但伯基特淋巴瘤的结局非常差。针对LB淋巴瘤的CCLSG-NHL960方案和针对LC淋巴瘤的强化多药方案产生了良好的反应率,但高剂量阿糖胞苷方案对伯基特淋巴瘤的效果尚未确定。疾病的初始阶段似乎与患者结局相关:IV期患者的结局不如II期或III期患者。其他临床变量,如复发部位、复发时间和骨髓挽救,并未影响患者的结局。