Re Alessandro, Cattaneo Chiara, Michieli Mariagrazia, Casari Salvatore, Spina Michele, Rupolo Maurizio, Allione Bernardino, Nosari Annamaria, Schiantarelli Clara, Vigano Mariagrazia, Izzi Immacolata, Ferremi Piero, Lanfranchi Arnalda, Mazzuccato Mauro, Carosi Gianpiero, Tirelli Umberto, Rossi Giuseppe
Divisione di Ematologia, Spedali Civili, p.le Spedali Civili, 1, 25123 Brescia, Italy.
J Clin Oncol. 2003 Dec 1;21(23):4423-7. doi: 10.1200/JCO.2003.06.039. Epub 2003 Oct 27.
High-dose therapy (HDT) and peripheral-blood stem-cell transplantation (PBSCT) in HIV-associated lymphoma (HIV-Ly) has been recently reported in selected patients. We describe the results of a multi-institutional program of HDT and PBSCT as salvage therapy in HIV-Ly responsive to highly active antiretroviral therapy (HAART) in unselected patients.
Patients with resistant or relapsed HIV-Ly after first-line chemotherapy (CT) underwent PBSC collection after a course of second-line CT or cyclophosphamide and granulocyte colony-stimulating factor. Patients with chemotherapy-sensitive disease received carmustine, etoposide, cytarabine, and melphalan (BEAM regimen) and PBSC reinfusion. Effective HAART was maintained during the entire program.
Sixteen consecutive patients entered the program. Adequate collection of PBSC was obtained in 80% of patients (median CD34+ cells 6.8 x 106/kg). Three patients had early progression. Ten patients (62%) received PBSCT with prompt engraftment in all patients (neutrophils and platelet engraftment after a median of 10 days [range, 8 to 10 days] and 13 days [range, 8 to 18 days], respectively). No patients died as a result of opportunistic or other infections or treatment-related complications. Eight of nine assessable patients achieved complete remission (one patient after radiotherapy for residual disease) and one patient achieved partial remission. Two patients experienced relapse and died at +10 and +14 months. Six patients are alive and disease free at a median of 8 months after transplantation.
Our data confirm that HDT plus PBSCT is feasible and active as salvage therapy in HIV-Ly on a multi-institutional basis and in unselected HAART-responding patients. HIV infection should no longer preclude the opportunity of HDT in patients with lymphoma.
近期有报道称,部分患者接受了高剂量疗法(HDT)及外周血干细胞移植(PBSCT)用于治疗HIV相关淋巴瘤(HIV-Ly)。我们描述了一项多机构项目的结果,该项目采用HDT及PBSCT作为挽救疗法,用于未经选择的、对高效抗逆转录病毒疗法(HAART)有反应的HIV-Ly患者。
一线化疗(CT)后出现耐药或复发的HIV-Ly患者,在接受二线CT疗程或环磷酰胺及粒细胞集落刺激因子治疗后进行外周血干细胞采集。化疗敏感疾病患者接受卡莫司汀、依托泊苷、阿糖胞苷及美法仑(BEAM方案)治疗并回输外周血干细胞。在整个项目期间维持有效的HAART。
16例连续患者进入该项目。80%的患者获得了足够的外周血干细胞采集量(中位CD34+细胞数为6.8×10⁶/kg)。3例患者出现早期进展。10例患者(62%)接受了PBSCT,所有患者均迅速植入(中性粒细胞和血小板植入的中位时间分别为10天[范围8至10天]和13天[范围8至18天])。没有患者因机会性感染或其他感染或治疗相关并发症死亡。9例可评估患者中有8例实现完全缓解(1例患者在对残留疾病进行放疗后),1例患者实现部分缓解。2例患者复发并分别在+10个月和+14个月时死亡。6例患者存活且无疾病,移植后中位时间为8个月。
我们的数据证实,在多机构基础上以及未经选择的对HAART有反应的患者中,HDT加PBSCT作为HIV-Ly的挽救疗法是可行且有效的。HIV感染不应再成为淋巴瘤患者接受HDT的障碍。