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在接受 CHOP 加利妥昔单抗或 CHOP 加替西莫单抗治疗后,未经治疗的滤泡性淋巴瘤患者继续获得优异的结果:III 期随机研究 SWOG-S0016 的长期随访。

Continued Excellent Outcomes in Previously Untreated Patients With Follicular Lymphoma After Treatment With CHOP Plus Rituximab or CHOP Plus I-Tositumomab: Long-Term Follow-Up of Phase III Randomized Study SWOG-S0016.

机构信息

Mazyar Shadman, Ajay K. Gopal, David G. Maloney, and Oliver W. Press, University of Washington and Fred Hutchinson Cancer Research Center; Hongli Li and Michael LeBlanc, SWOG Statistical Center, Seattle, WA; Lisa Rimsza, Mayo Clinic Arizona, Scottsdale; Catherine M. Spier, University of Arizona, Tucson, AZ; John P. Leonard, Weill Cornell Medical College, New York; Jonathan W. Friedberg, Wilmot Cancer Institute, University of Rochester, Rochester, NY; Mark S. Kaminski, University of Michigan Health System, Ann Arbor, MI; Rita M. Braziel, Oregon Health & Science University, Portland, OR; Bruce D. Cheson, Lombardi Comprehensive Cancer Center, Georgetown University Hospital, Washington, DC; Shaker Dakhil, University of Kansas School of Medicine-Wichita, Wichita, KS; Sonali M. Smith, University of Chicago Medicine, Chicago, IL; and Richard I. Fisher, Fox Chase Cancer Center and Temple University School of Medicine, Philadelphia, PA.

出版信息

J Clin Oncol. 2018 Mar 1;36(7):697-703. doi: 10.1200/JCO.2017.74.5083. Epub 2018 Jan 22.

Abstract

Purpose SWOG S0016 was a phase III randomized study that compared the safety and efficacy of R-CHOP (rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone) with CHOP-RIT (CHOP followed by consolidation with iodine-133-tositumomab radioimmunotherapy) for previously untreated patients with follicular lymphoma. Understanding the long-term outcome of patients provides a benchmark for novel treatment regimens for FL. Patients and Methods Between 2001 and 2008, 531 previously untreated patients with FL were randomly assigned to receive either six cycles of R-CHOP or six cycles of CHOP-RIT. Patients with advanced-stage disease (bulky stage II, III, or IV) of any pathologic grade (1, 2, or 3) were eligible. Results After a median follow-up of 10.3 years, 10-year estimates of progression-free and overall survival were 49% and 78% among all patients, respectively. Patients in the CHOP-RIT arm had significantly better 10-year progression-free survival compared with patients in the R-CHOP arm (56% v 42%; P = .01), but 10-year overall survival was not different between the two arms (75% v 81%; P = .13). There was no significant difference between the CHOP-RIT and R-CHOP arms in regard to incidence of second malignancies (15.1% v 16.1%; P = .81) or myelodysplastic syndrome or acute myeloid leukemia (4.9% v 1.8%; P = .058). The estimated 10-year cumulative incidences of death resulting from second malignancies were not different (7.1% v 3.2%; P = .16), but cumulative incidence of death resulting from myelodysplastic syndrome or acute myeloid leukemia was higher in the CHOP-RIT arm compared with the R-CHOP arm (4% v 0.9%; P = .02). Conclusion Given these outstanding outcomes, immunochemotherapy should remain the standard induction approach for patients with high-risk FL until long-term follow-up of alternative approaches demonstrates superiority.

摘要

SWOG S0016 是一项 III 期随机研究,比较了 R-CHOP(利妥昔单抗联合环磷酰胺、多柔比星、长春新碱和泼尼松)与 CHOP-RIT(CHOP 序贯巩固碘-133 替妥昔单抗放射免疫治疗)在未经治疗的滤泡淋巴瘤患者中的安全性和疗效。了解患者的长期结局为滤泡淋巴瘤的新型治疗方案提供了基准。

患者和方法

在 2001 年至 2008 年间,531 例未经治疗的滤泡淋巴瘤患者被随机分配接受 R-CHOP 或 CHOP-RIT 治疗 6 个周期。所有患者均有晚期疾病(II 期、III 期或 IV 期肿块),任何病理分级(1、2 或 3)。

结果

中位随访 10.3 年后,所有患者的 10 年无进展生存率和总生存率估计值分别为 49%和 78%。CHOP-RIT 组患者的 10 年无进展生存率显著高于 R-CHOP 组(56%比 42%;P=0.01),但两组患者的 10 年总生存率无差异(75%比 81%;P=0.13)。CHOP-RIT 组与 R-CHOP 组的第二恶性肿瘤发生率(15.1%比 16.1%;P=0.81)或骨髓增生异常综合征或急性髓系白血病(4.9%比 1.8%;P=0.058)无显著差异。第二恶性肿瘤导致的死亡累积发生率在两组之间也没有差异(7.1%比 3.2%;P=0.16),但 CHOP-RIT 组骨髓增生异常综合征或急性髓系白血病导致的死亡累积发生率高于 R-CHOP 组(4%比 0.9%;P=0.02)。

结论

鉴于这些出色的结果,免疫化疗应继续成为高危滤泡淋巴瘤患者的标准诱导治疗方法,直到替代方法的长期随访显示出优越性。

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