Phase II clinical trial of nab-paclitaxel plus cisplatin plus gemcitabine (NABPLAGEM) in patients with untreated advanced pancreatic cancer

被引:0
|
作者
Jameson, Gayle S. [1 ,2 ]
Hosein, Peter J. [3 ]
Pierce, Erin [4 ]
Kamgar, Mandana [5 ]
Gordon, Michael S. [1 ]
Snyder, Courtney [1 ]
Roe, Denise J. [6 ]
Wertheim, Betsy C. [6 ]
Davey, Marina [1 ]
Barrett, Michael T. [7 ]
Von Hoff, Daniel D. [1 ,2 ]
Borazanci, Erkut [1 ,2 ]
机构
[1] HonorHlth Res Inst, 10510 N 92nd St, Scottsdale, AZ 85258 USA
[2] TGen, Translat Genom Res Inst, City Hope, Phoenix, AZ USA
[3] Univ Miami, Miami, FL USA
[4] Ochsner Hlth, New Orleans, LA USA
[5] Med Coll Wisconsin, Milwaukee, WI USA
[6] Univ Arizona, Canc Ctr, Tucson, AZ USA
[7] Mayo Clin, Scottsdale, AZ USA
来源
CANCER MEDICINE | 2024年 / 13卷 / 12期
关键词
clinical trial; nab-paclitaxel plus cisplatin plus gemcitabine; pancreatic adenocarcinoma; phase II; untreated metastatic pancreatic adenocarcinoma; DUCTAL ADENOCARCINOMA;
D O I
10.1002/cam4.7412
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: A previous phase IB/II study of nab-paclitaxel + cisplatin + gemcitabine (NABPLAGEM) in 25 patients with previously untreated metastatic pancreatic ductal adenocarcinoma (PDAC) demonstrated favorable results. This phase II study was conducted to further evaluate the safety, efficacy, and impact on quality of life (QOL) of NABPLAGEM in a multi-center setting. Methods: Participants were >= 18 years; had measurable PDAC; Karnofsky performance status of >= 70%; life expectancy >= 12 weeks; Results: A total of 42 patients were enrolled with a median age of 66.8 years, a majority were male (66.7%) and white (76.2%). Treatment-related adverse events >= grade 3 were: thrombocytopenia (64.3%), anemia (47.6%), and neutropenia (26.1%). OS at 12 months was 38.1%, with 12% of patients alive as of last contact (20-40+ months). In 37 evaluable participants responses included: partial response (40.5%), stable disease (43.2%), and progressive disease (16.2%), with overall response rate of 40.5% and DCR of 88.6%. Statistically significant improvement in QOL was reported during the first three cycles. Conclusion: The primary objective of achieving a 12-month survival comparable to the previous phase Ib/II NABPLAGEM PCRT 12-001 was not achieved in this trial. NABPLAGEM has efficacy in advanced PDAC, demonstrating early disease control noted by improvement in patient symptoms, decrease in tumor volume and tumor markers within the first 9 weeks. The activity and tolerability make this a suitable regimen for further testing in the neoadjuvant setting.
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页数:10
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