靶向治疗对原发性淋巴结受累的非霍奇金淋巴瘤的影响

V. Tomacinschii, M. Robu, S. Buruiana, Veronica Finciuc, Ana Grecu, Cristina Dudnic, Dumitrita Urescu, Marina Suschevici
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引用次数: 1

摘要

背景:非霍奇金淋巴瘤是由淋巴组织发展而来的恶性肿瘤。原发性淋巴结(LN)受累是最常见的定位(52-70%)。利妥昔单抗(R)在NHL治疗中的整合代表了一个转折点。本研究的目的是评估R与传统多化疗药物(PChT)联合治疗结节性NHL的治疗效果。材料和方法:对80例诊断为NHL的患者进行描述性队列研究。结果:参与研究的男性39人(48.8%),女性41人(51.2%)。患者的平均年龄为56.09±13.6岁。NHL的发作发生在85.0%的外周淋巴结、7.5%的纵隔淋巴结和7.5%的腹部。I-II期21例(26.2%),III-IV期59例(73.8%)。54例(67.5%)患者诊断出侵袭性NHL,26例(32.5%)患者诊断为惰性NHL。在61例(76.3%)患者中,应用一线R+PChT治疗——第1组(G1),在19例(23.8%)患者中应用常规PChT——第2组(G2)。G1期的总有效率(ORR)为86.8%,G2期为63.1%。G1期63.9%的患者获得完全缓解(CR),G2期47.3%。G1期无进展生存期(PFS)的中位数为20个月,G2期为12个月(p<0.05)。结论:使用利妥昔单抗可提高ORR率(86.8%vs 63.1%)、CR频率(63.9%vs 47.3%)和PFS(20个月vs 12个月,p<0.05)。
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Impact of targeted treatment in non-Hodgkin’s lymphoma with primary lymph node involvement
Background: Non-Hodgkin’s lymphomas (NHL) are malignant tumors that develop from lymphoid tissue. Primary lymph node (LN) involvement is the most common localization (52-70%). The integration of Rituximab (R) in the NHL treatment represented a turning point. The aim of this study was to evaluate the therapeutic impact of the use of R in combination with conventional polychemotherapeutic (PChT) in the treatment of nodal onset NHL. Material and methods: A descriptive cohort study was performed on 80 patients diagnosed with NHL. Results: In the study participated: men – 39(48.8%), women – 41(51.2%). The mean age of the patients was 56.09 ± 13.6 years. The onset of NHL occurred in peripheral l/n in 85.0% of cases, in mediastinal LN – 7.5%, and abdominals in 7.5%. Stages I-II were identified in 21(26.2%) patients, stages III-IV in 59(73.8%) cases. Aggressive NHLs were diagnosed in 54(67.5%) patients, indolent NHLs in 26(32.5%) cases. In 61(76.3%) patients, first-line R+PChT treatment was applied – group 1(G1), and in 19(23.8%) cases conventional PChT was applied – group 2(G2). The overall response rate (ORR) in G1 was 86.8%, in G2 – 63.1%. Complete remissions (CR) were obtained in G1 in 63.9% of patients, in G2 – 47.3% of cases. Progression-free survival (PFS) in G1 had a median of 20 months, and in G2 the median was 12 months (p <0.05). Conclusions: The use of Rituximab increased the ORR rate (86.8% vs 63.1%), the frequency of CR (63.9% vs 47.3%) and PFS (20 months vs 12 months (p <0.05).
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