資料載入中.....
|
請使用永久網址來引用或連結此文件:
http://ir.nhri.org.tw/handle/3990099045/9635
|
| 題名: | Expanded analyses of NAPOLI-1: Phase 3 study of nal-IRI (MM-398), with or without 5-fluorouracil (5FU) and leucovorin (LV), versus 5-fluorouracil and leucovorin (5FU/LV), in metastatic pancreatic cancer (mPAC) previously treated with gemcitabine-based therapy |
| 作者: | Siveke, JT;Chen, LT;Von Hoff, DD;Li, CP;Wang-Gillam, A;Bodoky, G;Dean, A;Shan, YS;Jameson, G;Macarulla, T;Lee, KH;Cunningham, D;Blanc, JF;Hubner, RA;Chiu, CF;Schwartsmann, G;Braiteh, F;Moyo, V;Belanger, B;Bayever, E |
| 貢獻者: | National Institute of Cancer Research |
| 摘要: | Question: Nal-IRI is a nanoliposomal encapsulated formulation of irinotecan. OS in the ITT population was significantly longer with nal-IRI+5FU/LV (n = 117) vs 5FU/LV (n = 119) (median OS was 6.1 m vs 4.2 m; unstratified HR = 0.67, log-rank test p = 0.012). Most frequent grade 3+ AEs included neutropenia, fatigue and GI-effects. Thes e expanded, pre-specified analyses have been presented. Methods: Patients with mPAC (n = 417) previously treated with gemcitabine-based therapy, were randomized 1:1:1 to receive: Nal-IRI (120 mg/m 2 ; IV 90 min) q3w; 5FU (2,000 mg/m 2 ; 24 h) + LV (200 mg/m 2 ; 30 min) ×4w followed by 2w rest; or combination of nal-IRI (80 mg/m 2 ; IV 90 min) prior to 5FU (2,400 mg/m 2 ; 46h) + LV (400 mg/m 2 ; 30min) q2w. Primary endpoint was OS. The ITT population included all randomized patients; the Per Protocol (PP) population included patients who received ≥80% of the target dose in the first 6 weeks and did not violate any in/ exclusion criteria. Results: Analysis of the PP populations confirmed the favorable OS of the combination nal-IRI+5FU/LV, which was also reflected by the PFS, ORR and CA19-9 levels. Median OS in the PP population for nal-IRI+5FU/ LV-arm was 8.9 m (n = 66) vs 5.1 m (n = 71) for 5FU/LV (unstratified HR = 0.57, log-rank test p = 0.011). The nal-IRI monotherapy arm did not show a statistically significant OS improvement over 5FU/LV. Analysis of subgroups, based on pretreatment characteristics including stage at diagnosis, time since initial histological diagnosis, prior lines of therapy, time since last prior therapy, and CA19-9, favored OS for the nal-IRI+5FU/ LV arm. Conclusions: Expanded analysis of the PP population and sensitivity analyses support the favorability of nal-IRI+5FU/LV over 5FU/LV, with amanageable safety profile. |
| 日期: | 2016-02 |
| 關聯: | Oncology Research and Treatment. 2016 Feb;39(Suppl. 1):170. |
| Link to: | http://dx.doi.org/10.1159/000444354 |
| JIF/Ranking 2023: | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=2296-5270&DestApp=IC2JCR |
| Cited Times(WOS): | https://www.webofscience.com/wos/woscc/full-record/WOS:000371353700553 |
| 顯示於類別: | [陳立宗] 會議論文/會議摘要
|
文件中的檔案:
| 檔案 |
描述 |
大小 | 格式 | 瀏覽次數 |
|---|
| ISI000371353700553.pdf | | 73Kb | Adobe PDF | 286 | 檢視/開啟 |
|
在NHRI中所有的資料項目都受到原著作權保護.
|
