Nelson D F
Radiation Oncology, Mayo Clinic, Rochester, MN 55905, USA.
J Neurooncol. 1999 Jul;43(3):241-7. doi: 10.1023/a:1006206602918.
The use of radiotherapy alone to treat primary central nervous system lymphoma (PCNSL) does not produce the high local control and survival rates that it does in limited extranodal non-Hodgkin's lymphoma outside the central nervous system (CNS). Even with doses of whole brain radiation therapy (WBRT) to 40+20 Gy boost, the Radiation Therapy Oncology Group (RTOG) reported a local control rate of 39%. Seventy-nine percent of recurrences were in the 60 Gy region. The median survival was 11.6 months. This response to local radiotherapy is quite different from the response of non-CNS Diffuse Large Cell Lymphoma where doses of 30-40 and >40 Gy have a 75-90% local control rate. Neither systemic lymphoma nor PCNSL have a classic radiotherapy dose response. For PCNSL there appears to be a threshold dose that ranges in the literature between 30 and > 50 Gy with a median of 40 Gy. Therefore, when radiotherapy is combined with chemotherapy that crosses the BBB, WBRT and/or boost doses may be able to be decreased, especially in patients achieving a complete response. Promising data from the Centre Leon Berard suggest that this is possible. When such chemotherapy was combined with intrathecal chemotherapy and 20 Gy WBRT, they obtained a 56% actuarial 5 year survival rate. Confirmation of single institution reports of favorable results such as these are needed. Cooperative group and intergroup trials are needed to define optimal therapy.
单独使用放射疗法治疗原发性中枢神经系统淋巴瘤(PCNSL),无法产生像在中枢神经系统(CNS)以外的局限性结外非霍奇金淋巴瘤中那样高的局部控制率和生存率。即便采用全脑放射治疗(WBRT)剂量达40 + 20 Gy的增敏方案,放射治疗肿瘤学组(RTOG)报告的局部控制率也仅为39%。79%的复发发生在60 Gy照射区域。中位生存期为11.6个月。这种对局部放疗的反应与非CNS弥漫大B细胞淋巴瘤的反应截然不同,后者采用30 - 40 Gy和>40 Gy的剂量时局部控制率可达75 - 90%。系统性淋巴瘤和PCNSL均不存在典型的放疗剂量反应。对于PCNSL,似乎存在一个阈值剂量,文献报道的范围在30至>50 Gy之间,中位数为40 Gy。因此,当放疗与能透过血脑屏障的化疗联合使用时,WBRT和/或增敏剂量可能可以降低,尤其是对于达到完全缓解的患者。里昂贝拉尔中心的有前景的数据表明这是可行的。当这种化疗与鞘内化疗及20 Gy的WBRT联合使用时,他们获得了56%的5年精算生存率。需要对这类单机构报告的良好结果进行确认。需要开展协作组和组间试验来确定最佳治疗方案。