Van Besien Koen, Mehra Rakesh, Wadehra Navin, Stock Wendy, Khouri Issa, Giralt Sergio, Devine Steve, Wickrema Amittha, Peace David, Sosman Jeff, Gajewski Jim, Champlin Richard
Section of Hematology/Oncology, University of Illinois Chicago, 60637, USA.
Biol Blood Marrow Transplant. 2004 Jun;10(6):386-94. doi: 10.1016/j.bbmt.2004.01.004.
Previous work suggested that interleukin (IL)-2 can be used for eradicating residual disease in autologous grafts and for preventing recurrence. We report a phase II study of autologous peripheral blood stem cell transplantation with in vitro IL-2 incubation of peripheral blood stem cells and posttransplantation IL-2 in patients with recurrent or refractory non-Hodgkin lymphoma. Salvage chemotherapy consisted of ifosfamide and etoposide. Responding patients underwent autologous peripheral blood stem cell transplantation. IL-2-incubated stem cells were infused on day 0. IL-2 1 mIU/m2 was given from day 1 until day 28. Four monthly maintenance cycles of IL-2 4 mIU/m2 subcutaneously twice daily days 1 to 5 and days 8 to 11 were administered thereafter. Eighty-four evaluable patients were enrolled, and 60 proceeded to transplantation, of which 56 received IL-2-incubated stem cells. The average received dose of posttransplantation IL-2 was 30% to 50% of planned. Only 42 patients received maintenance IL-2. The average received maintenance dose of IL-2 was also approximately 30% of planned. Most dose reductions were due to toxicity or patient refusal. Three-year survival and progression-free survival for all registered patients were 43% (95% confidence interval [CI], 33%-53%) and 31% (95% CI, 21%-41%), respectively. For the 60 patients undergoing transplantation, they were 59% (95% CI, 46%-72%) and 44% (95% CI, 31%-57%), respectively. There was no relation between the dose of IL-2 received and outcome. Survival and disease-free survival of the study group were similar to those of a previous study cohort that received unmanipulated stem cells and no systemic IL-2. Administration of IL-2-incubated peripheral blood stem cells and intensive posttransplantation IL-2 was associated with considerable but rapidly reversible toxicity. No effect on long-term outcome was observed.
先前的研究表明,白细胞介素(IL)-2可用于清除自体移植物中的残留疾病并预防复发。我们报告了一项针对复发或难治性非霍奇金淋巴瘤患者的II期研究,该研究采用体外IL-2孵育外周血干细胞并在移植后使用IL-2进行自体外周血干细胞移植。挽救性化疗方案为异环磷酰胺和依托泊苷。有反应的患者接受自体外周血干细胞移植。在第0天输注经IL-2孵育的干细胞。从第1天至第28天给予IL-2 1 mIU/m²。此后,每月进行4个周期的维持治疗,在第1至5天和第8至11天每天皮下注射2次IL-2 4 mIU/m²。共有84例可评估患者入组,其中60例进行了移植,其中56例接受了经IL-2孵育的干细胞。移植后IL-2的平均接受剂量为计划剂量的30%至50%。只有42例患者接受了维持性IL-2治疗。IL-2的平均接受维持剂量也约为计划剂量的30%。大多数剂量减少是由于毒性或患者拒绝。所有登记患者的3年生存率和无进展生存率分别为43%(95%置信区间[CI],33%-53%)和31%(95%CI,21%-41%)。对于60例接受移植的患者,3年生存率和无进展生存率分别为59%(95%CI,46%-72%)和44%(95%CI,31%-57%)。接受的IL-2剂量与治疗结果之间无关联。研究组的生存率和无病生存率与先前接受未处理干细胞且未使用全身性IL-2的研究队列相似。给予经IL-2孵育的外周血干细胞和强化的移植后IL-2治疗会导致相当大但迅速可逆的毒性。未观察到对长期治疗结果的影响。