Lanier Claire M, Razavian Niema B, Smith Sydney, D'Agostino Ralph B, Hughes Ryan T
Department of Radiation Oncology, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Department of Biostatistics and Data Science, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Leuk Lymphoma. 2024 Dec;65(14):2199-2206. doi: 10.1080/10428194.2024.2393753. Epub 2024 Sep 5.
The ideal treatment paradigm for bulky diffuse large B-cell lymphoma (DLBCL) remains uncertain. We investigated the impact of tumor bulk in patients treated with systemic therapy alone through Alliance/CALGB 50303. Data from this trial were obtained from the National Cancer Institute's NCTN/NCORP Data Archive. The study assessed the size of nodal sites and estimated progression-free survival (PFS) using Cox proportional hazards models. Stratified analysis factored in International Prognostic Index (IPI) risk scores. Out of 524 patients, 155 had pretreatment scans. Using a 7.5 cm cutoff, 44% were classified as bulky. Bulk did not significantly impact progression-free survival (PFS), whether measured continuously or at thresholds of >5 or >7.5 cm ( = 0.10- = 0.99). Stratified analyses by treatment group and IPI risk group were also non-significant. In this secondary analysis, a significant association between bulk and PFS was not identified.
对于体积较大的弥漫性大B细胞淋巴瘤(DLBCL),理想的治疗模式仍不明确。我们通过Alliance/CALGB 50303研究,调查了单纯接受全身治疗的患者中肿瘤体积的影响。该试验的数据来自美国国立癌症研究所的NCTN/NCORP数据存档库。该研究评估了淋巴结部位的大小,并使用Cox比例风险模型估计无进展生存期(PFS)。分层分析考虑了国际预后指数(IPI)风险评分。在524例患者中,155例进行了治疗前扫描。以7.5厘米为临界值,44%的患者被归类为体积较大。无论连续测量还是以>5或>7.5厘米为临界值测量,肿瘤体积对无进展生存期(PFS)均无显著影响(P=0.10至P=0.99)。按治疗组和IPI风险组进行的分层分析也无显著差异。在这项二次分析中,未发现肿瘤体积与PFS之间存在显著关联。