[伊布替尼治疗淋巴浆细胞性淋巴瘤/瓦尔登斯特伦巨球蛋白血症的疗效和安全性]。

Y S Huang, W J Xiong, J J Yuan, Y Yu, Y X Li, Y T Yan, T Y Wang, R Lyu, W Liu, G An, Y Z Zhao, D H Zou, L G Qiu, S H Yi
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引用次数: 0

摘要

目的探讨伊布替尼治疗新近治疗和复发难治性(R/R)淋巴浆细胞性淋巴瘤(LPL)/瓦尔登斯特伦巨球蛋白血症(WM)的有效性和安全性。方法回顾性收集2016年3月至2023年6月在中国医学科学院血液病医院接受伊布替尼治疗的98例新治疗和复发难治性LPL/WM患者的临床资料,分析其疗效和安全性。结果共纳入98例LPL/WM患者,包括45例新治疗患者和53例R/R患者。其中男性 74 人(75.5%),中位年龄为 64(42-87)岁。88名患者符合疗效评估条件,中位治疗时间为20.8(2.1-55.0)个月,主要缓解率(MRR)为78.4%,总体反应率(ORR)为85.2%。新治疗患者的 MRR 和 ORR 分别为 78.4% 和 86.5%,而 R/R 患者的 MRR 和 ORR 分别为 78.4% 和 84.3%。初始治疗患者和再治疗患者的 MRR 和 ORR 差异无统计学意义(所有 P 值均大于 0.05)。中位随访时间为29.1(2.9-50.3)个月,新治疗患者和R/R患者的中位总生存时间未达标。中位无进展生存期分别为 23.5(95% CI 10.5-36.5)个月和 45.0(95% CI 34.0-56.0)个月,差异无统计学意义(所有 P 值均大于 0.05)。共有25名患者死亡,没有死亡病例与伊布替尼治疗有关。伊布替尼的主要不良反应为血小板减少(5.1%)、肺炎(8.1%)和高尿酸血症(21.4%)。心房颤动的发生率为2.0%。结论伊布替尼对新治疗和复发性LPL/WM患者具有良好的疗效和安全性。
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[The efficacy and safety of ibrutinib in the treatment of lymphoplasmacytic lymphoma/Waldenström macroglobulinemia].

Objective: To explore the efficacy and safety of ibrutinib for the treatment of newly treated and relapsed refractory (R/R) lymphoplasmacytic lymphoma (LPL) /Waldenström macroglobulinemia (WM) . Methods: Retrospectively collected clinical data of 98 cases of newly treated and R/R LPL/WM patients who received ibrutinib treatment at the Hematology & Blood Diseases Hospital of the Chinese Academy of Medical Sciences from March 2016 to June 2023, and analyzed their efficacy and safety. Results: A total of 98 LPL/WM patients were included, which consisted of 45 newly treated patients and 53 R/R patients. Of these, 74 were males (75.5%) and the cohort had a median age of 64 (42-87) years. Eighty-eight patients were eligible for efficacy evaluation with a median treatment time of 20.8 (2.1-55.0) months, a major remission rate (MRR) of 78.4%, and an overall response rate (ORR) of 85.2%. The MRR and ORR of the newly treated patients were 78.4% and 86.5%, respectively, whereas the MRR and ORR of the R/R patients were 78.4% and 84.3%, respectively. There were no statistically significant differences in MRR and ORR between the initial treatment and R/R patients (all P values >0.05) . The median follow-up period was 29.1 (2.9-50.3) months and the median overall survival time for newly treated and R/R patients was not reached. The median progression-free survival time was 23.5 (95% CI 10.5-36.5) months and 45.0 (95% CI 34.0-56.0) months, respectively, with no statistically significant differences (all P values >0.05) . There were 25 deceased patients and no deaths were related to ibrutinib treatment. The main adverse reactions of ibrutinib were thrombocytopenia (5.1%) , pneumonia (8.1%) , and hyperuricemia (21.4%) . The incidence of atrial fibrillation was 2.0%. Conclusion: Ibrutinib exhibits good efficacy and safety for newly treated and R/R LPL/WM patients.

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