Soussain Carole, Hoang-Xuan Khê, Taillandier Luc, Fourme Emmanuelle, Choquet Sylvain, Witz Francis, Casasnovas Olivier, Dupriez Brigitte, Souleau Bertrand, Taksin Anne-Laure, Gisselbrecht Christian, Jaccard Arnaud, Omuro Antonio, Sanson Marc, Janvier Maud, Kolb Brigitte, Zini Jean-Marc, Leblond Véronique
Department of Hematology, Biostatistics Unit, Centre René Huguenin, Saint-Cloud, France.
J Clin Oncol. 2008 May 20;26(15):2512-8. doi: 10.1200/JCO.2007.13.5533. Epub 2008 Apr 14.
The prognosis of relapsing primary CNS lymphoma (PCNSL) is poor. We report the results of a prospective multicenter trial of intensive chemotherapy followed by autologous hematopoietic stem-cell rescue (IC + HCR) in immunocompetent adult patients with PCNSL or intraocular lymphoma (IOL) after failure of high-dose methotrexate-based treatment.
Salvage treatment consisted of two cycles of high-dose cytarabine and etoposide (CYVE). Intensive chemotherapy combined thiotepa, busulfan, and cyclophosphamide. Forty-three patients (median age, 52 years; range, 23 to 65 years) were included, with relapse (n = 22), refractory disease (n = 17), or a partial response to first-line treatment (n = 4). The response to CYVE was not assessable in three cases because of treatment-related death. Twenty patients (47%) were chemosensitive to CYVE: 15 of them proceeded to IC + HCR. IC + HCR was also administered to 12 patients who did not respond to CYVE. All but one of the 27 patients who underwent IC + HCR entered complete remission.
With a median follow-up of 36 months, the median overall survival was 18.3 months in the overall population, and 58.6 months among patients who completed IC + HCR. The respective median progression-free survival (PFS) times after IC + HCR were 11.6 and 41.1 months. The 2-year overall survival probability was 45% in the whole population and 69% among the 27 patients who received IC + HCR. The 2-year PFS probability was 43% among all the patients and 58% in the IC + HCR subpopulation.
IC + HCR is an effective treatment for refractory and recurrent PCNSL.
复发性原发性中枢神经系统淋巴瘤(PCNSL)的预后较差。我们报告了一项前瞻性多中心试验的结果,该试验针对免疫功能正常的成年PCNSL或眼内淋巴瘤(IOL)患者,在基于大剂量甲氨蝶呤的治疗失败后,采用强化化疗继以自体造血干细胞挽救(IC + HCR)。
挽救治疗包括两个周期的大剂量阿糖胞苷和依托泊苷(CYVE)。强化化疗联合了噻替派、白消安和环磷酰胺。纳入43例患者(中位年龄52岁;范围23至65岁),其中复发患者(n = 22)、难治性疾病患者(n = 17)或对一线治疗部分缓解的患者(n = 4)。3例患者因治疗相关死亡而无法评估对CYVE的反应。20例患者(47%)对CYVE化疗敏感:其中15例继续接受IC + HCR。12例对CYVE无反应的患者也接受了IC + HCR。接受IC + HCR的27例患者中,除1例之外均进入完全缓解。
中位随访36个月,总体人群的中位总生存期为18.3个月,完成IC + HCR的患者为58.6个月。IC + HCR后的中位无进展生存期(PFS)分别为11.6个月和41.1个月。总体人群的2年总生存概率为45%,接受IC + HCR的27例患者为69%。所有患者的2年PFS概率为43%,IC + HCR亚组为58%。
IC + HCR是治疗难治性和复发性PCNSL的有效方法。