Kim Tong-Yoon, Min Gi-June, Jeon Young-Woo, Yahng Seung-Ah, Cho Seok-Goo, Lee Jong-Mi, Kim Myungshin, Eom Ki-Seong
Department of Hematology, Catholic Hematology Hospital, Yeouido St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 07345, Republic of Korea.
Department of Hematology, Catholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.
Biomedicines. 2025 Jan 14;13(1):194. doi: 10.3390/biomedicines13010194.
: Anti-CD20 monoclonal antibodies combined with alkylator-based chemotherapy enhance survival in chronic lymphocytic leukemia (CLL). However, the risks of infection and bone marrow suppression may mean that new, targeted therapies are more appropriate for some patients than fludarabine-cyclophosphamide-rituximab (FCR). In the Republic of Korea, where insurance limits coverage to novel agents, FCR therapy should be carefully considered for patients with CLL. : Using clinical data from 144 FCR-treated patients with CLL, we retrospectively analyzed clinical characteristics impacting survival outcomes, the impact of cytopenia after FCR, and the durable remission status in terms of measurable residual disease (MRD). We compared the impact of bicytopenia with those of other hematologic conditions. : The 5-year overall survival (OS) and 5-year progression-free survival (PFS) for all patients were 84.4% and 68.3%, respectively. FCR-treated patients in the bicytopenia and -positive groups exhibited poor OS and PFS; in particular, the bicytopenia group often experienced prolonged anemia and thrombocytopenia (6-12 months). The responder group achieved sustained remission for a median of 5 years for MRD negativity. : In bicytopenia, FCR can induce prolonged cytopenia, making it difficult to switch to second-line therapy or complete cycles of chemoimmunotherapy, directly affecting poor survival outcomes. The cautious application of FCR therapy in CLL without bicytopenia or positivity can achieve long-term remission.
抗CD20单克隆抗体联合基于烷化剂的化疗可提高慢性淋巴细胞白血病(CLL)患者的生存率。然而,感染和骨髓抑制的风险可能意味着,对于某些患者而言,新的靶向治疗比氟达拉滨-环磷酰胺-利妥昔单抗(FCR)更合适。在韩国,保险仅覆盖新型药物,对于CLL患者应谨慎考虑FCR治疗。
我们利用144例接受FCR治疗的CLL患者的临床数据,回顾性分析了影响生存结果的临床特征、FCR治疗后血细胞减少的影响以及可测量残留疾病(MRD)方面的持久缓解状态。我们比较了双血细胞减少与其他血液学状况的影响。
所有患者的5年总生存率(OS)和5年无进展生存率(PFS)分别为84.4%和68.3%。双血细胞减少和阳性组中接受FCR治疗的患者OS和PFS较差;特别是双血细胞减少组经常出现长期贫血和血小板减少(6 - 12个月)。缓解组MRD阴性的持续缓解中位时间为5年。
在双血细胞减少的情况下,FCR可诱导长期血细胞减少,导致难以转换至二线治疗或完成化疗免疫治疗周期,直接影响不良生存结果。在无双血细胞减少或阳性的CLL患者中谨慎应用FCR治疗可实现长期缓解。