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口服低剂量氟达拉滨、环磷酰胺和利妥昔单抗(旧-FCR)联合化疗免疫治疗老年慢性淋巴细胞白血病患者。

Chemoimmunotherapy with oral low-dose fludarabine, cyclophosphamide and rituximab (old-FCR) as treatment for elderly patients with chronic lymphocytic leukaemia.

机构信息

Hematology, Azienda Ospedaliera Universitaria, Siena, Italy.

Hematology, Azienda Ospedaliera Universitaria, Siena, Italy.

出版信息

Leuk Res. 2014 Aug;38(8):891-5. doi: 10.1016/j.leukres.2014.05.016. Epub 2014 Jun 2.

DOI:10.1016/j.leukres.2014.05.016
PMID:24934847
Abstract

Median age at diagnosis for chronic lymphocytic leukaemia (CLL) patients is now 72 years, thus a consistent number of patients may not tolerate standard doses i.v. of fludarabine, cyclophosphamide and rituximab (FCR), the best available therapy, due to unacceptable myelotoxicity and risk of severe infections. We studied safety and efficacy of the addition of rituximab to the oral low-dose FC regimen (old-FCR) in a selected population of 30 elderly (median age 75, 15 untreated, 15 treated with 1 prior therapy) CLL patients. Complete remission (CR) rate was 80% in the untreated patients (overall response rate, ORR 93%), and 30% in pretreated patients (ORR 74%). Progression free survivals (PFS) were 45 months and 30 months in the untreated and treated patients, respectively. In patients achieving CR, old-FCR led to PFS of 67 months. Moreover, haematological toxicity was mild (grade 3-4: 15%) and patients were treated mostly in outpatient clinic. Old-FCR could be a good therapy option for elderly CLL patients outside clinical trials, larger studies are needed to confirm our findings.

摘要

目前慢性淋巴细胞白血病(CLL)患者的诊断中位年龄为 72 岁,因此相当数量的患者可能因无法耐受标准剂量静脉注射氟达拉滨、环磷酰胺和利妥昔单抗(FCR)——这一最佳可用疗法,而出现无法耐受的骨髓毒性和严重感染风险。我们在 30 名年龄较大的(中位年龄 75 岁,15 名未经治疗,15 名接受过 1 次治疗)CLL 患者中选择了一个亚组,研究了利妥昔单抗联合口服低剂量 FC 方案(旧-FCR)的安全性和疗效。未经治疗的患者的完全缓解(CR)率为 80%(总缓解率,ORR 为 93%),而经治患者的 ORR 为 74%。无进展生存期(PFS)分别为未治疗患者的 45 个月和治疗患者的 30 个月。在达到 CR 的患者中,旧-FCR 导致 PFS 为 67 个月。此外,血液学毒性较轻(3-4 级:15%),且大多数患者在门诊治疗。对于临床试验以外的老年 CLL 患者,旧-FCR 可能是一种较好的治疗选择,需要更大规模的研究来证实我们的发现。

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