Lee Jung-Hee, Lee Je-Hwan, Kim Dae-Young, Seol Miee, Lee Young-Shin, Kang Young-Ah, Jeon Mijin, Lee Kyoo-Hyung
Department of Hematology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Department of Hematology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Clin Lymphoma Myeloma Leuk. 2015 Nov;15(11):655-63. doi: 10.1016/j.clml.2015.08.087. Epub 2015 Sep 3.
Conditioning therapy with fludarabine and melphalan 140 mg/m(2) has been widely used before allogeneic hematopoietic cell transplantation (HCT) for lymphoma. A lower dose of melphalan might result in lower mortality and morbidity without compromising engraftment.
In our phase II trial, we investigated a conditioning regimen of fludarabine (30 mg/m(2)/day for 5 days on days -6 to -2) and melphalan (100 mg/m(2) on day -2). Antithymocyte globulin was added to fludarabine and melphalan for unrelated or mismatched familial donor HCT. The present study included 26 patients with lymphoma (B-cell in 10, T-cell in 11, and natural killer/T-cell lymphoma in 2).
An objective tumor response after HCT was observed in 18 patients (75.0%; complete in 14 and partial in 4). Acute and chronic graft-versus-host disease (GVHD) occurred in 23.1% and 55.0% of the assessable patients, respectively. The 5-year overall survival, nonrelapse mortality, progression-free survival, and event-free survival rate was 40.4%, 21.6%, 39.2%, and 30.8%, respectively. Donor lymphocyte infusions were given to 3 patients who had developed a relapse or progression after HCT, and 2 of whom had a showed partial response. Patients with severe chronic GVHD had greater overall survival than those with no, mild, or moderate chronic GVHD.
Conditioning therapy with a lower dose of melphalan, combined with fludarabine, appears to be promising in allogeneic HCT for lymphoma. The Clinicaltrials.gov identification number for the present study is NCT00772811.
氟达拉滨联合140mg/m²美法仑的预处理方案已在淋巴瘤异基因造血细胞移植(HCT)前广泛应用。较低剂量的美法仑可能在不影响植入的情况下降低死亡率和发病率。
在我们的II期试验中,我们研究了一种预处理方案,即氟达拉滨(在第-6至-2天,30mg/m²/天,共5天)和美法仑(在第-2天,100mg/m²)。对于无关或不匹配的家族供体HCT,在氟达拉滨和美法仑中加入抗胸腺细胞球蛋白。本研究纳入了26例淋巴瘤患者(10例B细胞淋巴瘤、11例T细胞淋巴瘤和2例自然杀伤/T细胞淋巴瘤)。
18例患者(75.0%)在HCT后观察到客观肿瘤反应(14例完全缓解,4例部分缓解)。可评估患者中分别有23.1%和55.0%发生了急性和慢性移植物抗宿主病(GVHD)。5年总生存率、无复发生存率、无进展生存率和无事件生存率分别为40.4%、21.6%、39.2%和30.8%。3例HCT后复发或进展的患者接受了供体淋巴细胞输注,其中2例显示部分缓解。重度慢性GVHD患者的总生存率高于无、轻度或中度慢性GVHD患者。
较低剂量美法仑联合氟达拉滨的预处理方案在淋巴瘤异基因HCT中似乎很有前景。本研究在Clinicaltrials.gov的识别号为NCT00772811。