APHP, Sorbonne Université, IHU, ICM, Service de Neurologie-Mazarin, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.
Unité de Biométrie, Institut Curie, Saint-Cloud, France.
J Clin Oncol. 2022 Nov 10;40(32):3692-3698. doi: 10.1200/JCO.22.00491. Epub 2022 Jul 14.
JCO We previously reported the results of a randomized phase II study in patients with newly diagnosed primary CNS lymphoma (age 18-60 years). Patients were treated with high-dose methotrexate-based induction chemotherapy followed by whole-brain radiotherapy (WBRT) or high-dose chemotherapy (thiotepa-busulfan-cyclophosphamide) with autologous stem-cell transplantation (ASCT). The median follow-up was 33 months. In this report, we provide long-term data (median follow-up, 8 years) regarding the outcomes and toxicities. Fifty-three and 44 patients received induction chemotherapy followed by WBRT or ASCT, respectively. Their 8-year event-free survival from random assignment was 67% and 39% in the ASCT and WBRT arms, respectively ( = .03), with a significantly lower risk of relapse after ASCT (hazard ratio, 0.13; < .001). One third of patients who relapsed after WBRT were alive after salvage treatment. Five and four patients died of ASCT and WBRT-related toxicities, respectively. The 8-year overall survival was 69% and 65% in the ASCT and WBRT arms, respectively (not significant). Balance (52% 10%, ≤ 0.001) and neurocognition (64% 13%, < .001) significantly deteriorated after WBRT compared with ASCT during the follow-up. This study shows that 40 Gy WBRT should be avoided in first-line treatment because of its neurotoxicity and suboptimal efficacy in reducing relapses while ASCT appears to be highly efficient in preventing relapses.
JCO 我们之前报道了一项针对新诊断原发性中枢神经系统淋巴瘤(年龄 18-60 岁)患者的随机 II 期研究结果。患者接受高剂量甲氨蝶呤为基础的诱导化疗,随后进行全脑放疗(WBRT)或高剂量化疗(噻替哌-白消安-环磷酰胺)联合自体干细胞移植(ASCT)。中位随访时间为 33 个月。在本报告中,我们提供了关于结局和毒性的长期数据(中位随访时间 8 年)。53 例和 44 例患者分别接受诱导化疗后行 WBRT 或 ASCT。随机分组后,8 年无事件生存率在 ASCT 和 WBRT 组分别为 67%和 39%(=.03),ASCT 后复发风险显著降低(风险比,0.13; <.001)。WBRT 后复发的三分之一患者经挽救治疗后仍存活。5 例和 4 例患者分别死于 ASCT 和 WBRT 相关毒性。8 年总生存率在 ASCT 和 WBRT 组分别为 69%和 65%(无显著差异)。平衡(52% 10%, ≤ 0.001)和神经认知(64% 13%, <.001)在 WBRT 后与 ASCT 相比明显恶化。本研究表明,40 Gy WBRT 应避免用于一线治疗,因为其神经毒性和降低复发的效果不理想,而 ASCT 似乎能有效地预防复发。