期刊文献+
共找到3篇文章
< 1 >
每页显示 20 50 100
Prognostic significance of the pre-chemotherapy lymphocyte-to-monocyte ratio in patients with previously untreated metastatic colorectal cancer receiving FOLFOX chemotherapy 被引量:10
1
作者 Gui-Nan Lin Pan-Pan Liu +3 位作者 Dong-Ying Liu jie-wen peng Jian-Jun Xiao Zhong-Jun Xia 《Chinese Journal of Cancer》 SCIE CAS CSCD 2016年第3期142-150,共9页
Background:As a surrogate marker of systemic inflammation,the lymphocyte-to-monocyte ratio(LMR) is an independent prognostic factor for various malignancies.This study investigated the prognostic significance of the p... Background:As a surrogate marker of systemic inflammation,the lymphocyte-to-monocyte ratio(LMR) is an independent prognostic factor for various malignancies.This study investigated the prognostic significance of the pre-chemotherapy LMR in patients with previously untreated metastatic colorectal cancer(mCRC) receiving chemotherapy.Methods:The present study included newly diagnosed mCRC patients treated between January 2005 and December 2013 with FOLFOX chemotherapy,specifically oxaliplatin 180 mg/m^2 on day 1,with leucovorin 400 mg/m^2administered as a 2-hour infusion before the administration of 5-fluorouracil 400 mg/m^2 as an intravenous bolus injection,and 5-fluorouracil 2400 mg/m^2 as a 46-h infusion immediately after 5-fluorouracil bolus injection.The LMR was calculated as the absolute count of lymphocytes divided by the absolute count of monocytes.COX proportional hazards analysis was performed to evaluate the association of LMR with survival outcomes.Results:A total of 488 patients were included.Patients with high pre-chemotherapy LMR experienced significant improvements in progression-free survival(PFS,9.2 vs.7.6 months,P < 0.001) and overall survival(OS,19.4 vs.16.6 months,P < 0.001) compared with patients with low pre-chemotherapy LMR.Subsequent COX multivariate analysis showed that high pre-chemotherapy LMR(>3.11) was an independent favorable prognostic factor for PFS and OS.Additionally,patients whose LMR remained high(high-high subgroup),increased(low-high subgroup),or decreased(high-low subgroup) following chemotherapy showed better results in terms of PFS and OS than patients whose LMR remained low(low-low subgroup) after chemotherapy.Conclusions:For patients with previously untreated mCRC receiving FOLFOX chemotherapy,an elevated pre-chemotherapy LMR is an independent favorable prognostic factor for PFS and OS,and changes in the LMR before and after chemotherapy seem to predict the benefit of chemotherapy. 展开更多
关键词 METASTATIC colorectal cancer Inflammation Lymphocyte Monocyte Prognosis
下载PDF
阿瑞匹坦用于预防女性胃肠道肿瘤患者化疗所致恶心呕吐的疗效研究
2
作者 De-Shen Wang Ming-Tao Hu +12 位作者 Zhi-Qiang Wang Chao Ren Miao-Zhen Qiu Hui-Yan Luo Ying Jin William Pat Fong Shu-Bin Wang jie-wen peng Qing-Feng Zou Qiong Tan Feng-Hua Wang Yu-Hong Li 梁军(翻译/校对) 《癌症》 CAS 2022年第2期87-96,共10页
背景与目的 预防化疗所致恶心呕吐在肿瘤治疗的全程管理中是十分重要的一环。本研究评价了在高危女性胃肠道肿瘤患者中,在帕洛诺司琼、地塞米松基础上联用阿瑞匹坦能否进一步预防或减轻FOLFIRI方案(氟尿嘧啶、亚叶酸和伊立替康)或FOLFO... 背景与目的 预防化疗所致恶心呕吐在肿瘤治疗的全程管理中是十分重要的一环。本研究评价了在高危女性胃肠道肿瘤患者中,在帕洛诺司琼、地塞米松基础上联用阿瑞匹坦能否进一步预防或减轻FOLFIRI方案(氟尿嘧啶、亚叶酸和伊立替康)或FOLFOX方案(氟尿嘧啶、亚叶酸和奥沙利铂)化疗所致恶心呕吐的发生率和严重程度。方法 本研究为随机、双盲、安慰剂对照、Ⅲ期临床研究。纳入患者为年龄≤50岁的年轻女性,既往饮酒较少或无饮酒史,确诊为胃肠道肿瘤且正在接受FOLFOX或FOLFIRI方案化疗。2015年8月4日至2020年3月31日期间共有248例女性患者入组,按1∶1比率随机分配至干预组和对照组。采用意向性分析评价患者的基线特征和疗效。分析日期为2020年10月30日。患者随机分配至阿瑞匹坦组(阿瑞匹坦:化疗第1天125 mg,化疗开始前60 min口服;第2、3天80 mg,每天早上口服;帕洛诺司琼0.25 mg静脉注射;地塞米松:化疗第1天6 mg,化疗开始前30 min口服)或安慰剂组(安慰剂:化疗第1天125 mg,化疗开始前60 min口服;第2、3天80 mg,每天早上口服;帕洛诺司琼0.25 mg静脉注射;地塞米松:化疗第1天12 mg,化疗开始前30 min口服)。主要研究终点为完全缓解(complete response,CR)率,定义为第1周期化疗后全程(overall phase)无呕吐发作或未使用解救性治疗药物的患者的比例。其他疗效指标,如无恶心、无呕吐的患者比例等,作为次要研究终点和探索性研究终点。结果 共有来自中国4个临床研究中心的248例患者入组,其中243例[阿瑞匹坦组125(51.4%)例、对照组118(48.5%)例]患者可进行疗效和安全性分析。所有患者的平均[mean(SD)]年龄为40.1(7.3)岁。阿瑞匹坦组的CR率显著高于对照组,包括全程[107(87.0%)vs. 80(66.7%),P<0.001]、急性期[114(92.7%)vs. 91(75.8%),P=0.001]和延迟期[109(88.6%)vs. 84 (70.0%),P=0.001]。两组不良事件的发生率[100(80.0%)vs. 96(81.3%),P=0.79]相似,未观察到与阿瑞匹坦治疗相关的3或4级不良事件。多因素分析显示阿瑞匹坦的应用是唯一与全程CR相关的独立因素。结论 在较年轻的、少量饮酒或无饮酒史的胃肠道肿瘤的女性患者中,帕洛诺司琼和地塞米松基础上联用阿瑞匹坦可增强FOLFOX或FOLFIRI方案化疗时的止吐疗效,耐受性良好。 展开更多
关键词 阿瑞匹坦 胃肠道肿瘤 化疗所致恶心呕吐
下载PDF
Three-year Follow-up on the Safety and Effectiveness of Rituximab Plus Chemotherapy as First-Line Treatment of Diffuse Large B-Cell Lymphoma and Follicular Lymphoma in Real-World Clinical Settings in China: A Prospective, Multicenter, Noninterventional Study 被引量:3
3
作者 Jian-Qiu WU Yong-Ping Song +22 位作者 Li-Ping Su Ming-Zhi Zhang Wei Li Yu Hu Xiao-Hong Zhang Yu-Huan Gao Zuo-Xing Niu Ru Feng Wei Wang jie-wen peng Xiao-Lin Li Xue-Nong Ouyang Chang-Ping Wu Wei-Jing Zhang Yun Zeng Zhen Xiao Ying-Min Liang Yong-Zhi Zhuang Ji-Shi Wang Zi-Min Sun Hai Bai Tong-Jian Cui Ji-Feng Feng 《Chinese Medical Journal》 SCIE CAS CSCD 2018年第15期1767-1775,共9页
Background: Prospective real-life data on the safety and effectiveness of rituximab in Chinese patients with diffuse large B-cell lymphoma (DLBCL) or follicular lymphoma (FL) are limited. This real-world study ai... Background: Prospective real-life data on the safety and effectiveness of rituximab in Chinese patients with diffuse large B-cell lymphoma (DLBCL) or follicular lymphoma (FL) are limited. This real-world study aimed to evaluate long-term safety and effectiveness outcomes ofrituximab plus chemotherapy (R-chemo) as first-line treatment in Chinese patients with DLBCL or FL. Hepatitis B virus (HBV) reactivation management was also investigated. Methods: A prospective, multicenter, single-arm, noninterventional study of previously untreated CD20-positive DLBCL or FL patients receiving first-line R-chemo treatment at 24 centers in China was conducted between January 17, 2011 and October 31, 2016. Enrolled patients underwent safety and effectiveness assessments after the last rituximab dose and were followed up for 3 years. Effectiveness endpoints included progression-free survival (PFS) and overall survival (OS). Safety endpoints were adverse events (AEs), serious AEs, drug-related AEs, and AEs of special interest. We also reported data on the incidence of HBV reactivation. Results: In total, 283 previously untreated CD20-positive DLBCL and 31 FL patients from 24 centers were enrolled. Three-year PFS was 59% (95% confidence interval [CI]: 50-67%) for DLBCL patients and 46% (95% CI: 20-69%) for FL patients. For DLBCL patients, multivariate analyses showed that PFS was not associated with international prognostic index, tumor maximum diameter, HBV infection status, or number ofrituximab treatment cycles, and OS was only associated with age 〉60 years (P 〈 0.05). R-chemo was well tolerated. The incidence of HBV reactivation in hepatitis B surface antigen (HBsAg)-positive and HBsAg-negative/hepatitis B core antibody-positive patients was 13% (3/24) and 4% (3/69), respectively. Conclusions: R-chemo is effective and safe in real-world clinical practice as first-line treatment for DLBCL and FL in China, and that HBV reactivation during R-chemo is manageable with preventive measures and treatment. 展开更多
关键词 Asian Hematopoietic Malignancy Hepatitis B Virus Observational Study RITUXIMAB
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部