Peña M, Martinez D F, Paviglianiti A, Balaguer A, Sanz J, Pascual M J, Herruzo B, Solano C, Benzaquén A, Salas M Q, Rovira M, Nieto A, Español I, Huguet M, Bento L, Saéz A J, Mussetti A
Clinical Hematology Department, Institut Català d'Oncologia-Hospitalet, IDIBELL, Barcelona, Spain.
Hematology Department, Hospital de la Santa Creu i Sant Pau, IIB-Sant Pau and José Carreras Leukaemia Research Institutes, Barcelona, Spain.
Bone Marrow Transplant. 2025 Apr 2. doi: 10.1038/s41409-025-02559-5.
The efficacy of thiotepa, busulfan, and fludarabine (TBF) conditioning in lymphoproliferative disorders remains under investigation. We analyzed outcomes in 157 patients with lymphoid malignancies who underwent a first allogeneic hematopoietic stem cell transplantation (alloHCT) following TBF conditioning. Non-relapse mortality (NRM) at 3 years reached 32%, while the cumulative incidence of relapse (CIR) was 19%. At 3 years, progression-free survival (PFS), overall survival (OS), and graft-versus-host disease (GVHD)-free/relapse-free survival (GRFS) were 49.7%, 58.0%, and 44.2%, respectively. The cumulative incidences of grade III-IV acute GVHD at 100 days and moderate-to-severe chronic GVHD at 3 years were 8.3% and 12%, respectively. On multivariate analysis, patients receiving high-dose thiotepa (10 mg/kg) demonstrated a significantly lower CIR than those receiving low-dose thiotepa (5 mg/kg) (HR 2.95 [95% CI, 1.37-6.33], p = 0.006), with no significant effect on NRM. Female donor-to-male recipient transplants were associated with reduced OS (HR 2.0 [95% CI, 1.17-3.44], p = 0.011) and increased NRM (HR 2.43 [95% CI, 1.29-4.35], p = 0.005). TBF conditioning demonstrated a substantial anti-tumor effect, counterbalanced by elevated toxicity. Careful patient selection and effective toxicity mitigation strategies are essential to ensure individuals can tolerate TBF's toxicity while maximizing its benefits in disease control.
噻替派、白消安和氟达拉滨(TBF)预处理方案在淋巴增生性疾病中的疗效仍在研究中。我们分析了157例接受TBF预处理后首次进行异基因造血干细胞移植(alloHCT)的淋巴恶性肿瘤患者的预后情况。3年时的非复发死亡率(NRM)达到32%,而复发累积发生率(CIR)为19%。3年时,无进展生存期(PFS)、总生存期(OS)和无移植物抗宿主病(GVHD)/无复发生存期(GRFS)分别为49.7%、58.0%和44.2%。100天时III-IV级急性GVHD的累积发生率和3年时中重度慢性GVHD的累积发生率分别为8.3%和12%。多因素分析显示,接受高剂量噻替派(10mg/kg)的患者CIR显著低于接受低剂量噻替派(5mg/kg)的患者(风险比[HR] 2.95 [95%置信区间(CI),1.37 - 6.33],p = 0.006),对NRM无显著影响。女性供者至男性受者的移植与OS降低(HR 2.0 [95% CI,1.17 - 3.44],p = 0.011)和NRM增加(HR 2.43 [95% CI,1.29 - 4.35],p = 0.005)相关。TBF预处理显示出显著的抗肿瘤作用,但毒性增加。仔细的患者选择和有效的毒性缓解策略对于确保个体能够耐受TBF的毒性同时最大化其在疾病控制中的益处至关重要。