Early Primary Gastric Lymphoma with Adverse Prognosis Factors. Is it Benefit Adding Rituximab to CHOP-14?

A. Avilés, S. Cleto
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Abstract

Objective: Assess if the addition of rituximab to a dose-dense chemotherapy regimen in patients with primary gastric diffuse large B-cell lymphoma (PGL) in early stage, but, associated with worse prognostic factors. Patients and Methods: Patients with pathological diagnosis of PGL and early stages, but, with elevated levels of beta 2 microglobulin and lactic dehydrogenase, age > 18 years age without upper limit, no gender differences, previously untreated, were recruit in an open label clinical trial, to received CHOP-14 (cyclophosphamide, vincristine, doxorubicin and prednisone, dose dense, every 14 days) and compare with patients that received R-CHOP14 (rituximab + CHOP-14). Results: Between March 2011 to December 2016, 141 patients were taken entry to the study: no statistical differences were observed in clinical and laboratory characteristics. Complete response (CR) was observed in 68 out of 72 (94.4%) patients in the CHOP-R14, and 67 out of 69 (95.1%) patients in the CHOP14 regimen. Actuarial curves at 5-years show that progression-free survival (PFS) was 89% (95%Confidence Interval (CI) in the CHOP-R14, that did not have statistical differences in the CHOP-14 arm: 92% (95%CI: 83% -97%) (p 0.887); the overall survival were: 90% (95% CI:86%-97%) and 93.4% (95% CI: 86% to 97%) (p 0,665). Toxicities were severe granulocytopenia and infection-related, but no dead were observed. Until now, late toxicities as acute leukemia, second neoplasms and cardiac damage has not been observed. Conclusion: The use of dose dense regimen (CHOP-14) confirm that is useful in the treatment of PGL associated to worse prognosis factors, the addition of rituximab did not show any benefit.
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具有不良预后因素的早期原发性胃淋巴瘤。利妥昔单抗加入CHOP-14是否有益?
目的:评估早期原发性胃弥漫性大b细胞淋巴瘤(PGL)患者在大剂量化疗方案中加入利妥昔单抗是否与预后不良因素相关。患者和方法:病理诊断为PGL及早期,但β 2微球蛋白和乳酸脱氢酶水平升高,年龄> 18岁,年龄无上限,无性别差异,既往未接受治疗的患者,在一项开放标签临床试验中招募,接受CHOP-14(环磷酰胺、新碱、阿霉素和泼尼松,剂量大,每14天一次),并与接受R-CHOP14(美罗华单抗+ CHOP-14)的患者进行比较。结果:2011年3月至2016年12月,141例患者入组,临床及实验室特征无统计学差异。在CHOP14 - r14方案中,72例患者中有68例(94.4%)观察到完全缓解(CR),而在CHOP14方案中,69例患者中有67例(95.1%)观察到完全缓解(CR)。5年的精算曲线显示,CHOP-R14组的无进展生存期(PFS)为89%(95%置信区间(CI),在CHOP-14组中无统计学差异:92% (95%CI: 83% -97%) (p 0.887);总生存率分别为:90% (95% CI:86% ~ 97%)和93.4% (95% CI:86% ~ 97%) (p = 0.665)。毒性为严重的粒细胞减少和感染相关,但未观察到死亡。到目前为止,晚期毒性如急性白血病、二次肿瘤和心脏损伤尚未观察到。结论:剂量密集方案(CHOP-14)的使用证实对PGL相关预后较差因素的治疗是有用的,利妥昔单抗的加入没有显示出任何益处。
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