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76篇 您的检索式:作者名="CHAPMAN PB"
    题名 作者 年代 出处 被引量
1Vemurafenib改善伴BRAF V600E突变的黑色素瘤患者的生存率显示文摘背景 BRAF激酶抑制剂vemurafenib(PLX4032)的1期和2期临床试验已证实其对伴BRAFV600E突变的转移性黑色素瘤患者的反应率超过50%。方法我们在675例既往未经治疗、伴BRAFV600E突变的转移性黑色素瘤患者中,实施了一项Ⅲ期随机化临床试验以比较vemurafenib和Dacarbazine(氮烯唑胺)。患者通过随机分配,分别接受vemurafenib(每次口服960mg,每天两次)或氮烯唑胺(每3周静脉注射1000mg·m-2体表面积)。本研究主要终点是比较总体生存率及无进展期生存率。次要终点包括反应率、反应持续时间以及安全性。计划在死亡98例患者时进行中期分析、死亡196例时进行最终分析。结果在治疗6个月后,vemurafenib组总体生存率为84%(95%置信区间[CI],78-89),而氮烯唑胺组为64%(95%CI,56-73)。在对总体生存率的中期分析及无进展期生存率的最终分析中,与氮烯唑胺相比,vemurafenib能相对减低63%的死亡风险,以及减低74%的死亡或者疾病进展风险(两种比较P<0.001)。通过数据及安全监督委员会进行独立中期分析审查后,建议氮烯唑胺组患者也转而服用vemurafenib。对Vemurafenib反应率是48%而氮烯唑胺只有5%。伴Vemurafenib常见不良反应为关节痛、皮疹、疲劳、脱发、角化棘皮瘤或鳞状细胞癌、光过敏、恶心和腹泻;38%的患者因为毒副作用要求调整剂量。结论 Vemurafenib能改善既往未经治疗、伴有BRAFV600E突变的黑色素瘤患者的总体及无进展期生存率。(本研究由瑞士罗氏制药有限公司资助;BRIM-3临床试验编号:NCT01006980)涂超 Chapman PB Hauschild A Robert C 2011肿瘤药学2011,1,5:2
2Improved survival with vemurafenib in melanoma with BRAF V600E mutation 显示文摘Chapman PB Hauschild A Robert C 2011N Engl J Med2011,364,:1
3Phase Ⅲ multicenter randomized trial of the Dartmouth regimen versus daearbazine in patients with metastatic melanoma 显示文摘Chapman PB Einhorn LH Meyers ML 1999Clin Cancer Res1999,5,6:1
4Consistent antibody response against ganglio-side GD2 induced in patients with melanoma by a GD2 lactonekeyhole limpet hemoeyanin conjugate vaccine plus immunological adjuvant QS-21 显示文摘Ragupathi G Livingston PO Hood C Gathuru J Krown SE Chapman PB 2003Clin Cancer Res2003,9,14:1
5Improved survival with vemurafenib in melanoma with BRAF V600E mutation 显示文摘Chapman PB Hauschild A Robert C 2011N Engl J Med2011,364,26:1
6Improved sur-viral with vemurafenib in melanoma with BRAF V600E muta- tion 显示文摘Chapman PB Hauschild A Robert C 2011N Engl j Med2011,364,26:1
7Improved survival with vemurafenib in melanoma with BRAF V600E mutation显示文摘Chapman PB Hauschild A Robert C 2011N Engl J Med2011,364,26:1
8The history and future of chemotherapy for melanoma显示文摘YANG AS CHAPMAN PB 2009Hematol Oneal Clin North Am2009,23,3:1
9A phase Ⅱ study of imatinib mesylate (IM) for patients with advanced melanoma harboring somatic alterations of KIT显示文摘Carvajal RD Chapman PB Wolchok JD 0,,15:1
10Front-line approach to metastatic BRAF-mutant melanoma diagnosis,molecular evaluation, and treatment choice 显示文摘CHAPMAN PB HAUSCHILD A SONDAK VK 2014Am Soc Clin On-col Educ Book2014,,:1
11Improved survival with vemurafenib in melanoma with BRAF V600E mutation显示文摘Chapman PB Hauschild A Robert C 2011N Engl J Med2011,364,26:1
12Improved survival with vemurafenib in melanoma with BRAF V600E rnutation显示文摘CHAPMAN PB HAUSCHILD A ROBERT C 2011N EnglJ Med2011,364,26:1
13The history and future of chemotherapy for melanoma显示文摘Yang AS Chapman PB 2009Hematol Oncol Clin North Am2009,23,3:1
14Phase Ⅲ multi-center randomized trial of the Dartmouth regimen versus dacarbazine in patient with metastatic melanoma 显示文摘Chapman PB Einhorn LH Meyers ML 1999J Clin Oncol1999,17,9:1
15Improved survival with vemurafenib in melanoma with BRAF V600E mutation显示文摘Chapman PB Hauschild A Robert C 2011N Engl J Med Jun2011,364,26:1
16Improved survival with vemurafenib in melanoma with BRAF V6OOE mutation显示文摘Chapman PB Hauschild A Robert C 2011N Engl J Med2011,364,26:1
17Phase Ⅲ randomized,open-label,multicenter trial (BRIM3) comparing BRAF inhibitor vemurafenib with dacarbazine (DTIC) in patients with V600EBRAF-mutated melanoma显示文摘Chapman PB Hauschild A Robert C 0,,:1
18Safety and efficacy of vemurafenib in BRAF(V6OOE) and BRAF(V600K) mutation-posi- tive melanoma ( BRIM - 3 ) : extended follow-up of a phase 3, ran- domised, open-label study 显示文摘Mc-Arthur GA Chapman PB Robert C 2014Lancet Oncol2014,15,3:1
19The history and future of chemotherapy for melanoma显示文摘Yang AS Chapman PB 2009Hematol Oncol Clin North Am2009,23,3:1
20Improved sur- vival with vemurafenib in melanoma with BRAF V600E mutation显示文摘Chapman PB Hauschild A Robert C 2011N Engl J Med2011,364,26:1
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