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Rummel and colleagues' study comes at an important time in the treatment of indolent non-Hodgkin's lymphoma, when the addition of rituximab as first-line maintenance treatment is known to improve progression-free survival. In the PRIMA study,10 patients with untreated follicular lymphoma received one of three chemoimmunotherapy induction regimens, including R-CHOP, which was given to about 75% of patients. Those who responded to chemoimmunotherapy were randomly assigned to either observation or maintenance rituximab (375 mg/m2 every 8 weeks for 2 years). 3-year progression-free survival was 75% in the rituximab maintanence group versus 58% in the observation group. Similar findings have been shown after CVP and single-agent rituximab.1112 Results of the PRIMA study are in line with those for patients with follicular lymphoma in Rummel and colleagues' study, showing a 3-year progression-free survival of 70% after bendamustine plus rituximab versus only 50% after R-CHOP alone (table). In.the PRIMA study, patients in the rituximab maintenance group had more toxic effects than did those in the observation group; however, in both groups, grade 2-4 infections were the most common adverse event (39% and 24%, respectively). This result draws attention to several unresolved questions: how does bendamustine plus rituximab compare with R-CHOP, with rituximab for the first-line maintenance treatment of indolent non-Hodgkin's lymphoma? Does rituximab maintenance have a role after bendamustine plus rituximab, and could that use, or the addition of other drugs, further improve outcomes with this combination treatment? Finally, how do the two treatment options, if equally effective, compare in cost?
机译:Rummel及其同事的研究是在治疗惰性非霍奇金淋巴瘤的重要时刻,当时已知将利妥昔单抗作为一线维持治疗可改善无进展生存期。在PRIMA研究中,有10位未经治疗的滤泡性淋巴瘤患者接受了三种化学免疫疗法诱导方案中的一种,其中包括R-CHOP,约有75%的患者接受了该方案。对化学免疫治疗有反应的患者被随机分配至观察或维持利妥昔单抗治疗(每8周375 mg / m2,持续2年)。利妥昔单抗维持组的3年无进展生存率为75%,而观察组为58%。 CVP和单药利妥昔单抗后也显示出相似的结果。1112PRIMA研究的结果与Rummel及其同事的研究中的滤泡性淋巴瘤患者的研究结果一致,显示苯达莫司汀治疗后3年无进展生存率为70%。加利妥昔单抗,而仅进行R-CHOP治疗后仅为50%(表)。在PRIMA研究中,利妥昔单抗维持组的患者比观察组具有更大的毒性作用。但是,在两组中,最常见的不良事件均为2-4级感染(分别为39%和24%)。该结果引起人们对几个尚未解决的问题的关注:苯达莫司汀加利妥昔单抗与R-CHOP和利妥昔单抗用于惰性非霍奇金淋巴瘤的一线维持治疗的效果如何?苯达莫司汀加利妥昔单抗后,利妥昔单抗的维持是否有作用?使用或联合使用其他药物能否通过这种联合治疗进一步改善预后?最后,如果同等有效,这两种治疗方案的成本如何比较?

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