Hematology and Bone Marrow Transplant Department, Hospital de Santa Maria, Centro Hospitalar Universitário Lisboa Norte, Lisbon, Portugal.
Instituto de Medicina Molecular João Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa, Lisbon, Portugal.
Cancer Med. 2021 Dec;10(24):8768-8776. doi: 10.1002/cam4.4374. Epub 2021 Nov 16.
High-dose methylprednisolone plus rituximab (R-HDMP) is a useful treatment in chronic lymphocytic leukaemia/small lymphocytic lymphoma (CLL/SLL) patients unfit for chemo-immunotherapy and has proven its utility on the treatment of CLL/SLL complicated by auto-immune cytopenias. We performed a retrospective, single-centre study, of CLL/SLL patients treated with R-HDMP for 9 years. Thirty-nine patients were included, median age at time of treatment was 77 years. Most patients had stage Rai III/IV and Binet C disease. Twenty-eight patients had relapsed/refractory disease at time of treatment with a median of 1 previous line of therapy; 53.8% had prior exposure to fludarabine and 25% to rituximab. Grade 3-4 neutropenia and thrombocytopenia were recorded in 10.2% and 17.9% patients, respectively. While on treatment, 51.3% had documented infectious complications, but no other non-haematological toxicities grades 3-4 were identified. Overall response rate was 64%. Median overall survival and progression-free survival were 24 and 13 months, respectively. Twenty four patients relapsed and 16 received another line of treatment after R-HDMP, with median time to next treatment of 13.5 months. Thirteen out of the 24 patients improved performance status and were subsequently considered fit for chemo-immunotherapy. R-HDMP is a valuable option for elderly and frail patients, with low risk of severe myelotoxicity and other severe adverse events. It was shown to work as a bridge to other lines of treatment, including chemo-immunotherapy.
大剂量甲基泼尼松龙联合利妥昔单抗(R-HDMP)是不适合化疗免疫治疗的慢性淋巴细胞白血病/小淋巴细胞淋巴瘤(CLL/SLL)患者的有效治疗方法,并且已被证明可有效治疗伴有自身免疫性血细胞减少症的 CLL/SLL。我们对 9 年来接受 R-HDMP 治疗的 CLL/SLL 患者进行了回顾性单中心研究。共纳入 39 例患者,治疗时的中位年龄为 77 岁。大多数患者处于 Rai III/IV 期和 Binet C 期。28 例患者在治疗时存在复发/难治性疾病,其中中位数为 1 线既往治疗;53.8%有氟达拉滨暴露史,25%有利妥昔单抗暴露史。分别有 10.2%和 17.9%的患者出现 3-4 级中性粒细胞减少和血小板减少。治疗期间,51.3%有记录的感染并发症,但未发现其他 3-4 级非血液学毒性。总缓解率为 64%。中位总生存期和无进展生存期分别为 24 个月和 13 个月。24 例患者复发,16 例患者在接受 R-HDMP 治疗后接受了另一线治疗,下一治疗的中位时间为 13.5 个月。24 例患者中有 13 例的体能状态得到改善,随后被认为适合化疗免疫治疗。R-HDMP 是老年和体弱患者的有价值选择,具有低严重骨髓毒性和其他严重不良事件风险。它已被证明可作为与其他治疗线(包括化疗免疫治疗)桥接的治疗方法。