在现实临床实践中,治疗典型霍奇金淋巴瘤患者的遥远结果:新西伯利亚血液学分支的经验

Q4 Medicine
Мария Сергеевна Войтко, Т. И. Поспелова, И. Н. Нечунаева, Я. Ю. Шебуняева
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 Materials & Methods. The study enrolled 408 cHL patients treated and followed-up at the hematological unit of the Novosibirsk Municipal Clinical Hospital No. 2 from January 2008 to December 2021. The median age of patients was 33 years (range 26–44 years). Among them 223 (54.7 %) female and 185 (45.3 %) male patients. There were more patients with cHL stages III (n = 103; 25.2 %) and IV (n = 120; 29.4 %) than with stage II, which was identified in 185 (45.4 %) patients. ABVD regimen was administered to 132 (32.3 %) patients, 47 (11.5 %) patients received ABVD escalated to BEACOPP. BEACOPP therapy was performed in 229 (56.2 %) patients. Subsequent radiotherapy was assigned to 202 (49.5 %) patients. Second-line therapy was required by 89 (21.8 %) patients with relapsed and resistant cHL.
 Results. The 10-year overall survival (OS) was 81 %, and the 5-year OS was 91 %. Similar progression-free survival (PFS) rates were 86 % and 77 %, respectively. The 10-year PFS in patients with stage II was 87 %, while in patients with stages II (mediastinal bulky mass), III and IV, it was only 69 % (p = 0.002). The 10-year OS in patients with localized stages was 91 %, and in patients with generalized stages it was 79 % (p = 0.0006). The 10-year OS in patients less than 45 years of age was 88 %, and in patients more than 45 years of age it was 69 %. The 10-year PFS in patients less than 45 years of age was 84 %, and in the older age group it was 60 % (p = 0.001).
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引用次数: 0

摘要

的目标。在现实世界的临床实践中评估新西伯利亚经典霍奇金淋巴瘤(cHL)治疗的长期效果。 材料,方法。该研究纳入了2008年1月至2021年12月期间在新西伯利亚市第二临床医院血液科接受治疗和随访的408名cHL患者。患者的中位年龄为33岁(范围26-44岁)。其中女性223例(54.7%),男性185例(45.3%)。cHL III期患者较多(n = 103;25.2%)和IV (n = 120;29.4%),而在185例(45.4%)患者中发现了II期。132例(32.3%)患者接受ABVD方案,47例(11.5%)患者接受ABVD升级至BEACOPP方案。229例(56.2%)患者接受了BEACOPP治疗。202例(49.5%)患者接受后续放疗。89例(21.8%)复发和耐药cHL患者需要二线治疗。结果。10年总生存率为81%,5年总生存率为91%。相似的无进展生存(PFS)率分别为86%和77%。II期患者的10年PFS为87%,而II期(纵隔块状肿块)、III期和IV期患者的10年PFS仅为69% (p = 0.002)。局限性分期患者的10年OS为91%,广泛性分期患者的10年OS为79% (p = 0.0006)。45岁以下患者的10年OS为88%,45岁以上患者的10年OS为69%。45岁以下患者的10年PFS为84%,老年组为60% (p = 0.001)。 结论。研究结果表明,cHL患者的长期生存率很高,与其他研究组的数据具有很好的可比性。尽管如此,科学研究仍应继续,以制定适合风险的最佳cHL化疗方案,并进一步确定改善这种恶性肿瘤治疗结果的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Отдаленные результаты лечения пациентов с классической лимфомой Ходжкина в реальной клинической практике: опыт гематологического отделения Новосибирска
Aim. To assess the long-term results of classical Hodgkin’s lymphoma (cHL) treatment in Novosibirsk in real-world clinical practice. Materials & Methods. The study enrolled 408 cHL patients treated and followed-up at the hematological unit of the Novosibirsk Municipal Clinical Hospital No. 2 from January 2008 to December 2021. The median age of patients was 33 years (range 26–44 years). Among them 223 (54.7 %) female and 185 (45.3 %) male patients. There were more patients with cHL stages III (n = 103; 25.2 %) and IV (n = 120; 29.4 %) than with stage II, which was identified in 185 (45.4 %) patients. ABVD regimen was administered to 132 (32.3 %) patients, 47 (11.5 %) patients received ABVD escalated to BEACOPP. BEACOPP therapy was performed in 229 (56.2 %) patients. Subsequent radiotherapy was assigned to 202 (49.5 %) patients. Second-line therapy was required by 89 (21.8 %) patients with relapsed and resistant cHL. Results. The 10-year overall survival (OS) was 81 %, and the 5-year OS was 91 %. Similar progression-free survival (PFS) rates were 86 % and 77 %, respectively. The 10-year PFS in patients with stage II was 87 %, while in patients with stages II (mediastinal bulky mass), III and IV, it was only 69 % (p = 0.002). The 10-year OS in patients with localized stages was 91 %, and in patients with generalized stages it was 79 % (p = 0.0006). The 10-year OS in patients less than 45 years of age was 88 %, and in patients more than 45 years of age it was 69 %. The 10-year PFS in patients less than 45 years of age was 84 %, and in the older age group it was 60 % (p = 0.001). Conclusion. The study results demonstrate high rates of long-term survival of cHL patients and are well comparable with the data of other study groups. Nevertheless, scientific research should be continued to develop optimal risk-adapted programs of cHL chemotherapy and to define further prospects for improving the treatment outcomes of this malignant tumor.
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