CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Combined Aerobic and Resistance Training Improves Body Composition, Alters Cardiometabolic Risk, and Ameliorates Cancer-Related Indicators in Breast Cancer Patients and Survivors with Overweight/Obesity: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.
Combined Aerobic and Resistance Training Improves Body Composition, Alters Cardiometabolic Risk, and Ameliorates Cancer-Related Indicators in Breast Cancer Patients and Survivors with Overweight/Obesity: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.
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肥胖的乳腺癌幸存者面临癌症复发、合并症和死亡的高风险。本综述旨在系统评价有氧与抗阻联合训练(CAR-T)对超重/肥胖乳腺癌患者及幸存者体成分、脂质稳态、炎症、脂肪因子、癌因性疲乏、睡眠和生活质量的影响。在 PubMed、Web of Science、Scopus、Science Direct、Cochrane 和 Google Scholar 数据库中进行了电子检索,检索时间自建库至 2024 年 1 月 8 日。选择符合纳入标准的随机对照试验(RCT)进行分析。采用 Cochrane 偏倚风险工具评估符合条件的研究,并采用 GRADE 方法评价证据质量。使用随机效应模型,连续变量数据以均数差(MD)和标准化均数差(SMD)及 95% 置信区间(CI)进行分析。
我们评估了数据的偏倚风险、异质性、敏感性、报告偏倚和证据质量。本系统综述共纳入 17 项随机对照试验,涉及 1,148 名女性患者和幸存者(平均年龄:54.0 ± 3.4 岁)。主要结局显示体重指数(SMD -0.57 kg/m 2,p = 0.04)、体脂率(SMD -0.50%,p = 0.02)、脂肪量(SMD -0.63 kg,p = 0.04)、臀围(MD -3.14 cm,p = 0.02)和去脂体重(SMD 1.03 kg,p < 0.001)均有显著改善。次要结局表明高密度脂蛋白胆固醇(MD -0.05 mmol/L,p = 0.008)、NK 细胞(SMD 0.42%,p = 0.04)显著增加,甘油三酯(MD -81.90 mg/dL,p < 0.01)、总胆固醇(SMD -0.95 mmol/L,p < 0.01)、肿瘤坏死因子 α(SMD -0.89 pg/mL,p = 0.03)和瘦素(SMD -0.63 ng/mL,p = 0.03)。
此外,在癌症相关性疲劳(SMD -0.98,p = 0.03)、睡眠(SMD -1.17,p < 0.001)和生活质量(SMD 2.94,p = 0.02)评分方面也发现了有益的改善。大多数结局的估计效应置信度极低至低。目前的研究结果表明,CAR-T 可被视为一种辅助疗法,用于支持运动后观察到的常规临床方法。
然而,需要进一步的高质量研究来评估 CAR-T 是否是一种有价值的干预措施,以减少超重/肥胖乳腺癌患者的积极药物使用。
Breast cancer survivors with obesity are at a high risk of cancer recurrence, comorbidity, and mortality. This review aims to systematically evaluate the effects of combined aerobic and resistance training (CART) on body composition, lipid homeostasis, inflammation, adipokines, cancer-related fatigue, sleep, and quality of life in breast cancer patients and survivors with overweight/obesity. An electronic search was conducted in PubMed, Web of Science, Scopus, Science Direct, Cochrane, and Google Scholar databases from inception up to January 8, 2024.
Randomized controlled trials (RCTs) meeting the inclusion criteria were selected for the analysis. The Cochrane risk of bias tool was used to assess eligible studies, and the GRADE method to evaluate the quality of evidence. A random-effects model was used, and data were analyzed using mean (MD) and standardized mean differences (SMD) for continuous variables with 95% confidence intervals (CI).
We assessed the data for risk of bias, heterogeneity, sensitivity, reporting bias, and quality of evidence. A total of 17 randomized controlled trials were included in the systematic review involving 1,148 female patients and survivors (mean age: 54. 0 ± 3. 4 years). The primary outcomes showed significant improvements in body mass index (SMD -0. 57 kg/m 2 , p = 0. 04), body fat (SMD -0. 50%, p = 0. 02), fat mass (SMD -0. 63 kg, p = 0. 04), hip circumference (MD -3. 14 cm, p = 0. 02), and fat-free mass (SMD 1. 03 kg, p < 0. 001). The secondary outcomes indicated significant increases in high-density lipoprotein cholesterol (MD -0. 05 mmol/L, p = 0.
008), natural killer cells (SMD 0. 42%, p = 0. 04), reductions in triglycerides (MD -81. 90 mg/dL, p < 0. 01), total cholesterol (SMD -0. 95 mmol/L, p < 0. 01), tumor necrosis factor α (SMD -0. 89 pg/mL, p = 0. 03), and leptin (SMD -0. 63 ng/mL, p = 0. 03). Also, beneficial alterations were found in cancer-related fatigue (SMD -0.
98, p = 0. 03), sleep (SMD -1. 17, p < 0. 001), and quality of life (SMD 2. 94, p = 0. 02) scores. There was very low to low confidence in the estimated effect of most of the outcomes. The present findings reveal that CART could be considered an adjunct therapy in supporting the conventional clinical approach observed following exercise.
However, further high-quality research is needed to evaluate whether CART would be a valuable intervention to lower aggressive pharmacologic use in breast cancer patients with overweight/obesity.
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