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临床实践指南:滤泡性淋巴瘤——诊断、治疗及随访

Clinical Practice Guideline: Follicular Lymphoma—Diagnosis, Treatment, and Follow-up.

作者信息

Zoellner Anna, Herfarth Klaus, Herold Michael, Klapper Wolfram, Skoetz Nicole, Hiddemann Wolfgang

出版信息

Dtsch Arztebl Int. 2021 Apr 30;118(Forthcoming):320-5. doi: 10.3238/arztebl.m2021.0022.

Abstract

BACKGROUND

Follicular lymphoma (FL) occurs predominantly at advanced age, with an annual incidence of 3-5 cases per 100 000 inhabitants in Western countries. The clinical course is heterogeneous.

METHODS

For this new guideline, systematic literature searches were conducted in medical databases (MEDLINE, PubMed Central) (up to November 2017) and in the Guidelines International Network (G-I-N), and recent publications were added.

RESULTS

The results of 21 systematic reviews with meta-analyses, 75 randomized controlled trials, and 58 prospective and retrospective studies were evaluated. Lymph-node biopsy is necessary for initial diagnosis of FL. CT scanning of the neck, thorax, and abdomen should be performed to assess how far the disease has spread, together with bone marrow biopsy and, if required, PET/CT. In early FL (stages I and II; 10-15 %), potentially curative radiotherapy combined with an anti-CD 20 antibody is recommended. In advanced disease (stages III and IV), watchful waiting is indicated for patients who have no clinical symptoms and a low tumor burden. Patients with clinical symptoms and/or high tumor burden should receive chemotherapy in combination with an anti-CD 20 antibody, followed by 2 years' maintenance treatment with an anti-CD 20 antibody.

CONCLUSION

Given the good long-term prognosis of FL, the treatment must be chosen with care and thorough follow-up is necessary to ensure detection of late sequelae such as second malignancies or organ damage.

摘要

背景

滤泡性淋巴瘤(FL)主要发生于老年人群,在西方国家,其年发病率为每10万居民中有3 - 5例。临床病程具有异质性。

方法

为制定本新指南,我们在医学数据库(MEDLINE、PubMed Central)(截至2017年11月)以及指南国际网络(G - I - N)中进行了系统的文献检索,并纳入了近期发表的文献。

结果

对21项带有荟萃分析的系统评价、75项随机对照试验以及58项前瞻性和回顾性研究的结果进行了评估。FL的初始诊断需要进行淋巴结活检。应进行颈部、胸部和腹部的CT扫描,以评估疾病的扩散程度,同时进行骨髓活检,必要时进行PET/CT检查。对于早期FL(Ⅰ期和Ⅱ期;10 - 15%),推荐采用可能治愈性的放疗联合抗CD20抗体。对于晚期疾病(Ⅲ期和Ⅳ期),对于没有临床症状且肿瘤负荷低的患者,建议密切观察等待。有临床症状和/或肿瘤负荷高的患者应接受化疗联合抗CD20抗体治疗,随后用抗CD20抗体进行2年的维持治疗。

结论

鉴于FL良好的长期预后,治疗必须谨慎选择,并且需要进行全面的随访以确保发现晚期后遗症,如第二原发性恶性肿瘤或器官损害。

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本文引用的文献

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