Coiffier Bertrand
Hospices Civils de Lyon, Lyon, France.
Semin Oncol. 2004 Feb;31 Suppl 2:7-11. doi: 10.1053/j.seminoncol.2003.12.003.
In the past, CHOP chemotherapy (cyclophosphamide, doxorubicin, vincristine, prednisone) was considered the gold standard treatment for aggressive non-Hodgkin's lymphoma (NHL). CHOP is only curative in approximately 40% of patients, and numerous clinical trials have been carried out to find a treatment that can increase the cure rate. For some patients with aggressive NHL, it is possible to improve survival by intensification of chemotherapy compared with standard CHOP. This approach is not appropriate for all patients, and careful patient selection is necessary to achieve benefit. Early high-dose treatment/autologous stem cell transplantation may be beneficial for some patients, but not in patients with low-risk disease or those over 60 years of age who are not eligible for autologous stem cell transplantation. The most striking and consistent improvement over CHOP chemotherapy in the treatment of aggressive NHL is the addition of rituximab. A phase III randomized study Groupe d'Etudes des Lymphomes de l'Adulte (GELA LNH 98.5) compared rituximab plus CHOP with CHOP alone in treatment of 399 patients aged 60 to 80 years of age with aggressive NHL. The addition of rituximab resulted in higher overall and complete response rates, and at a median follow-up of 3 years, event-free and overall survival were significantly higher in patients treated with rituximab plus CHOP compared with CHOP alone. The benefits of adding rituximab to CHOP were not restricted to a subgroup of patients, but were evident in patients with high- and low-risk disease. The addition of rituximab to CHOP also overcame bcl-2-associated resistance to chemotherapy. There is no standard chemotherapy regimen for relapsed patients, but results from several single-arm studies suggest the addition of rituximab will increase the complete response rate to many different salvage regimens. The development of newer treatment strategies incorporating rituximab may improve the cure rate further.
过去,CHOP化疗方案(环磷酰胺、阿霉素、长春新碱、泼尼松)被认为是侵袭性非霍奇金淋巴瘤(NHL)的金标准治疗方案。CHOP方案仅能治愈约40%的患者,因此开展了大量临床试验以寻找能提高治愈率的治疗方法。对于一些侵袭性NHL患者,与标准CHOP方案相比,强化化疗有可能提高生存率。但这种方法并不适用于所有患者,必须谨慎选择患者才能获益。早期大剂量治疗/自体干细胞移植可能对部分患者有益,但不适用于低风险疾病患者或年龄超过60岁且不符合自体干细胞移植条件的患者。在侵袭性NHL治疗中,相对于CHOP化疗最显著且一致的改善是加入了利妥昔单抗。一项成人淋巴瘤研究组(GELA LNH 98.5)的III期随机研究比较了利妥昔单抗联合CHOP与单纯CHOP治疗399例年龄在60至80岁的侵袭性NHL患者的疗效。加入利妥昔单抗后总体缓解率和完全缓解率更高,在中位随访3年时,利妥昔单抗联合CHOP治疗的患者无事件生存期和总生存期显著高于单纯CHOP治疗的患者。将利妥昔单抗加入CHOP的益处并不局限于某一亚组患者,在高风险和低风险疾病患者中均有体现。将利妥昔单抗加入CHOP还克服了bcl - 2相关的化疗耐药性。对于复发患者尚无标准化疗方案,但多项单臂研究结果表明,加入利妥昔单抗可提高许多不同挽救方案的完全缓解率。纳入利妥昔单抗的更新治疗策略的发展可能会进一步提高治愈率。