不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Do Pre-Treatment Biopsy Characteristics Predict Early Tumour Progression in Feline Diffuse Large B Cell Nasal Lymphoma Treated With Radiotherapy?
Do Pre-Treatment Biopsy Characteristics Predict Early Tumour Progression in Feline Diffuse Large B Cell Nasal Lymphoma Treated With Radiotherapy?
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局限性猫鼻淋巴瘤(FeNL)的标准治疗是放射治疗(RT)。在接受RT联合或不联合化疗的猫中,17%-45%会出现早期局部或全身治疗失败。
本研究的目的是确定治疗前活检特征是否能预测FeNL的早期肿瘤进展。纳入标准包括:组织学确诊的FeNL、具有诊断质量的可用石蜡块、RT前分期局限于鼻腔鼻窦、接受IMRT/IGRT(10 × 4.2 Gy)治疗且未接受化疗、至少随访1年。所有RT前活检均经CD3、CD20、CD79a、pan-CK和Ki-67免疫组化复核评估,并确定核分裂活性指数。主要终点为1年无进展生存期(PFS),并计算风险比(HR)及置信区间(CI)。28只猫符合纳入标准,均为弥漫性大B细胞淋巴瘤。17只猫(61%)在1年时无进展。在11只第一年内进展的猫中,2只为局部进展,2只为局部和全身进展,7只为全身进展。核分裂指数(HR:1.03,CI 0.9-1.19,p = 0.645)、Ki-67(HR:1.00,CI 0.98-1.02,p = 0.845)以及肿瘤浸润T细胞> 30%(HR:0.38,CI 0.09-1.56,p = 0.175)与PFS无显著相关性。在这个均一接受RT治疗的FeNL群体中,所评估的RT前组织学参数均不能预测早期治疗失败。
The standard of care treatment for localised feline nasal lymphoma (FeNL) is radiation therapy (RT). Early local or systemic failure occurs in 17%-45% of cats treated with RT with or without chemotherapy. The aim of this study was to determine if pre-treatment biopsy characteristics could predict early tumour progression in FeNL. Inclusion criteria consisted of histologically confirmed FeNL, available paraffin blocks of diagnostic quality, localised to the sinonasal cavity on staging pre-RT, treated with IMRT/IGRT (10 × 4. 2 Gy) without chemotherapy and at least 1 year follow-up. All pre-RT biopsies were reviewed and evaluated with CD3, CD20, CD79a, pan-CK and Ki-67 immunohistochemistry and the mitotic activity index was determined.
The primary endpoint was progression-free survival (PFS) at 1 year and hazard-ratios (HR) with confidence interval (CI) were calculated. Twenty-eight cats fit the inclusion criteria, and all had diffuse large B-cell lymphoma. Seventeen cats (61%) were progression free at 1 year. Of the 11 cats that progressed in the first year, two had local progression, two had both local and systemic progression and seven had systemic progression.
The mitotic index (HR: 1. 03, CI 0. 9-1. 19, p = 0. 645), Ki-67 (HR: 1. 00, CI 0. 98-1. 02, p = 0. 845) and > 30% of tumour-infiltrating T cells (HR: 0. 38, CI 0. 09-1. 56, p = 0. 175) were not significantly associated with PFS. In this uniformly RT treated population of FeNL, none of the evaluated pre-RT histologic parameters could predict early treatment failure.
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