决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Risk of non-Hodgkin lymphoma in breast cancer survivors: a nationwide cohort study.
我们选取了2002年1月1日至2016年12月31日期间所有新诊断乳腺癌并接受根治性治疗的女性(N = 84,969),以及按年龄匹配的1:10非乳腺癌对照样本(N = 1,057,674)。
多项研究提示雌激素对淋巴瘤发生具有保护作用。乳腺癌的治疗由亚型分类驱动,激素受体状态的评估对治疗选择很重要。因此,我们评估了乳腺癌与NHL发病率之间的关联。我们利用韩国基于人群的全国性登记数据库开展了一项回顾性队列研究。我们选取了2002年1月1日至2016年12月31日期间所有新诊断乳腺癌并接受根治性治疗的女性(N = 84,969)以及按年龄匹配的1:10非乳腺癌对照样本(N = 1,057,674)。新发乳腺癌(时变暴露)为暴露因素,任何类型NHL的发生为结局,包括弥漫大B细胞淋巴瘤(DLBCL)、滤泡性淋巴瘤(FL)、成熟T/NK细胞淋巴瘤、间变性大细胞淋巴瘤(ALCL)以及未特指类型的NHL。随访期间,共发生1564例新发NHL病例。在调整体重指数、酒精摄入、体力活动、吸烟、收入和合并症后,与乳腺癌发生相关的NHL完全调整风险比(HR)为1.64(95% CI = 1.34-2.00)。与50岁及以上或未接受激素治疗者相比,年龄<50岁和接受激素治疗(他莫昔芬或芳香化酶抑制剂)的参与者中NHL的调整HR分别高得多。乳腺癌的发生与NHL风险显著增加相关,尤其是滤泡性淋巴瘤和成熟T/NK细胞淋巴瘤。特别是,接受激素治疗的患者和较年轻患者的NHL风险更高。
Several studies have suggested that estrogens have a protective function against lymphomagenesis. The treatment of breast cancer is driven by subtype classification, and the assessment of hormone receptor status is important for treatment selection. Thus, we evaluated the association between breast cancer and the incidence of NHL. We conducted a retrospective cohort study using a population-based nationwide registry in South Korea. We selected all women with newly diagnosed breast cancer between January 1st, 2002 and December 31st, 2016 who received curative treatment (N = 84,969) and a 1:10 sample of age-matched non-breast cancer controls (N = 1,057,674). Incident breast cancer (time-varying exposure) was the exposure and development of any type of NHL, including diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL), mature T/NK-cell lymphomas, anaplastic large cell lymphoma (ALCL), and unspecified types of NHL, was the outcome. During follow-up, 1564 incident cases of NHL occurred. The fully adjusted Hazard Ratio (HR) for NHL associated with the development of breast cancer was 1.64 (95% CI = 1.34-2.00) after adjusting for body mass index, alcohol intake, physical activity, smoking, income, and comorbidity. The adjusted HR for NHL was much higher in participants who were aged <50 years and who received hormone therapy (either tamoxifen or aromatase inhibitors) than in those 50 years or who did not receive hormone therapy, respectively. The development of breast cancer was associated with a significantly increased risk of NHL, particularly follicular lymphoma and mature T/NK-cell lymphoma. In particular, the risk of NHL was higher in patients receiving hormone therapy and in younger patients.
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