弥漫性大B细胞淋巴瘤
医学
美罗华
长春新碱
放射治疗
肿瘤科
人口
临床试验
淋巴瘤
内科学
阶段(地层学)
环磷酰胺
化疗
生物
环境卫生
古生物学
作者
Eliza A Hawkes,Allison Barraclough,Laurie H. Sehn
出处
期刊:Blood
[Elsevier BV]
日期:2022-02-10
卷期号:139 (6): 822-834
被引量:12
标识
DOI:10.1182/blood.2021013998
摘要
Diffuse large B-cell lymphoma (DLBCL), the most common lymphoma subtype, is localized in 25% to 30% of patients. Prognosis in patients with limited-stage DLBCL (LS-DLBCL) is excellent with 10-year overall survival of at least 70% to 80%. Improved insights into the disease biology, the availability of positron-emission tomography (PET) scans, and recent dedicated clinical trials within this unique population have led to evolving treatment paradigms. However, no standard definition of LS-DLBCL exists, and although generally defined as Ann Arbor stages I to II disease with largest mass size <10 cm in diameter, variations across studies cause challenges in interpretation. Similar to advanced-stage disease, rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP) immunochemotherapy forms the basis of treatment, with combined modality therapy including 3 cycles of systemic treatment and involved-site radiation therapy being a predominant historical standard. Yet the well-described continuous risk of relapse beyond 5 years and established late complications of radiotherapy have challenged previous strategies. More rigorous baseline staging and response assessment with PET may improve decision making. Recent clinical studies have focused on minimizing toxicities while maximizing disease outcomes using strategies such as abbreviated immunochemotherapy alone and PET-adapted radiotherapy delivery. This comprehensive review provides an update of recent literature with recommendations for integration into clinical practice for LS-DLBCL patients.
科研通智能强力驱动
Strongly Powered by AbleSci AI