Authors' Affiliations: Clinical Research Division; SWOG Statistical Center, Fred Hutchinson Cancer Research Center; Medical Oncology, University of Washington Medical Center, Seattle, Washington; Department of Pathology; Arizona Cancer Center, University of Arizona, Tucson, Arizona; James P. Wilmot Cancer Center, University of Rochester Medical Center, Rochester; Roswell Park Cancer Institute, Buffalo, New York; Cancer and Leukemia Group B; University of Michigan, Ann Arbor, Michigan; Department of Pathology, Oregon Health and Science University, Portland, Oregon; Georgetown University Hospital, Washington; Wichita Community Clinical Oncology Program, Wichita, Kansas; and Fox Chase Cancer Center-Temple Health, Temple University, Philadelphia PA.
Clin Cancer Res. 2013 Dec 1;19(23):6624-32. doi: 10.1158/1078-0432.CCR-13-1120. Epub 2013 Oct 15.
There is currently no consensus on optimal frontline therapy for patients with follicular lymphoma. We analyzed a phase III randomized intergroup trial comparing six cycles of CHOP-R (cyclophosphamide-Adriamycin-vincristine-prednisone (Oncovin)-rituximab) with six cycles of CHOP followed by iodine-131 tositumomab radioimmunotherapy (RIT) to assess whether any subsets benefited more from one treatment or the other, and to compare three prognostic models.
We conducted univariate and multivariate Cox regression analyses of 532 patients enrolled on this trial and compared the prognostic value of the FLIPI (follicular lymphoma international prognostic index), FLIPI2, and LDH + β2M (lactate dehydrogenase + β2-microglobulin) models.
Outcomes were excellent, but not statistically different between the two study arms [5-year progression-free survival (PFS) of 60% with CHOP-R and 66% with CHOP-RIT (P = 0.11); 5-year overall survival (OS) of 92% with CHOP-R and 86% with CHOP-RIT (P = 0.08); overall response rate of 84% for both arms]. The only factor found to potentially predict the impact of treatment was serum β2M; among patients with normal β2M, CHOP-RIT patients had better PFS compared with CHOP-R patients, whereas among patients with high serum β2M, PFS by arm was similar (interaction P value = 0.02).
All three prognostic models (FLIPI, FLIPI2, and LDH + β2M) predicted both PFS and OS well, though the LDH + β2M model is easiest to apply and identified an especially poor risk subset. In an exploratory analysis using the latter model, there was a statistically significant trend suggesting that low-risk patients had superior observed PFS if treated with CHOP-RIT, whereas high-risk patients had a better PFS with CHOP-R.
目前对于滤泡性淋巴瘤患者的一线治疗还没有达成共识。我们分析了一项比较 6 个周期 CHOP-R(环磷酰胺-阿霉素-长春新碱-泼尼松(Oncovin)-利妥昔单抗)与 6 个周期 CHOP 序贯碘-131 托西莫单抗放射免疫疗法(RIT)的 III 期随机分组临床试验,以评估是否某些亚组从一种治疗中获益更多,以及比较三种预后模型。
我们对该试验入组的 532 例患者进行了单变量和多变量 Cox 回归分析,并比较了滤泡性淋巴瘤国际预后指数(FLIPI)、FLIPI2 和 LDH+β2M(乳酸脱氢酶+β2-微球蛋白)模型的预后价值。
结果非常好,但两组之间无统计学差异[CHOP-R 组和 CHOP-RIT 组的 5 年无进展生存率(PFS)分别为 60%和 66%(P=0.11);CHOP-R 组和 CHOP-RIT 组的 5 年总生存率(OS)分别为 92%和 86%(P=0.08);两组的总缓解率均为 84%]。唯一发现可能预测治疗效果的因素是血清β2M;在β2M 正常的患者中,与 CHOP-R 组相比,CHOP-RIT 组的 PFS 更好,而在血清β2M 高的患者中,两组的 PFS 相似(交互 P 值=0.02)。
所有三种预后模型(FLIPI、FLIPI2 和 LDH+β2M)均能很好地预测 PFS 和 OS,但 LDH+β2M 模型最容易应用,并确定了一个预后特别差的亚组。在使用后一种模型进行的探索性分析中,有一个统计学上显著的趋势表明,如果接受 CHOP-RIT 治疗,低危患者的观察到的 PFS 更好,而高危患者的 PFS 更好。