Prognostic Factors of Survival in a Randomized Phase III Trial (MPACT) of Weekly nab-Paclitaxel Plus Gemcitabine Versus Gemcitabine Alone in Patients With Metastatic Pancreatic Cancer

被引:114
|
作者
Tabernero, Josep [1 ,2 ]
Chiorean, E. Gabriela [3 ]
Infante, Jeffrey R. [4 ]
Hingorani, Sunil R. [5 ]
Ganju, Vinod [6 ]
Weekes, Colin [7 ]
Scheithauer, Werner [8 ]
Ramanathan, Ramesh K. [9 ]
Goldstein, David [10 ]
Penenberg, Darryl N. [11 ]
Romano, Alfredo [11 ]
Ferrara, Stefano [11 ]
Von Hoff, Daniel D. [12 ]
机构
[1] Univ Autonoma Barcelona, Vall Hebron Univ Hosp, Med Oncol Dept, Barcelona 08035, Spain
[2] Univ Autonoma Barcelona, Inst Oncol, Med Oncol Dept, Barcelona 08035, Spain
[3] Univ Washington, Div Oncol, Seattle, WA 98195 USA
[4] Sarah Cannon Res Inst, Dept Oncol Hematol, Nashville, TN USA
[5] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
[6] Monash Univ, Peninsula Oncol Ctr, Dept Oncol, Frankston, Vic, Australia
[7] Univ Colorado, Ctr Canc, Div Med Oncol, Aurora, CO USA
[8] Med Univ Wien, Div Clin Oncol, Vienna, Austria
[9] Mayo Clin, Scottsdale, AZ USA
[10] Prince Wales Hosp, Dept Oncol, Randwick, NSW 2031, Australia
[11] Celgene Corp, Summit, NJ USA
[12] Virginia G Piper Canc Ctr Scottsdale Healthcare T, Dept Oncol, Scottsdale, AZ USA
来源
ONCOLOGIST | 2015年 / 20卷 / 02期
关键词
Pancreatic cancer; nab-Paclitaxel; Gemcitabine; Prognostic factors; CARBOHYDRATE ANTIGEN 19-9; SPARC EXPRESSION; TUMOR-MARKER; CHEMOTHERAPY;
D O I
10.1634/theoncologist.2014-0394
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. nab-Paclitaxel in combination with gemcitabine has emerged as a new treatment option for patients with metastatic pancreatic cancer (MPC), based on superiority over gemcitabine demonstrated in the phase III MPACT trial. Previously, Karnofsky performance status (KPS) score and the presence of liver metastases were shown to be predictive of survival with nab-paclitaxel plus gemcitabine treatment. This analysis sought to further explore the relationship between clinical characteristics and survival in the MPACT trial and to identify potential predictors of overall survival and progression-free survival in patients with MPC. Materials and Methods. Cox regression models adjusted for stratification factors and a stepwise multivariate analysis of prespecified baseline prognostic factors were performed. Results. Treatment effect was significantly associated with survival, with a similar magnitude of reduction in risk of death compared with the previously reported primary analysis. Treatment effect consistently favored nab-paclitaxel plus gemcitabine across the majority of the prespecified factors. In addition to KPS score and presence of liver metastases, age and number of metastatic sites were independent prognostic factors of overall and progressionfree survival. Baseline carbohydrate antigen 19-9 was not found to be an independent prognostic factor of survival in this analysis. Conclusion. The results of this analysis confirm broad utility of nab-paclitaxel plus gemcitabine for the treatment of MPC. In addition, these findings suggest that KPS score, presence of liver metastases, age, and number of metastatic sites are important predictors of survival that may be useful when making treatment decisions and designing future clinical trials.
引用
收藏
页码:143 / 150
页数:8
相关论文
共 50 条
  • [21] nab-Paclitaxel Plus Gemcitabine for Metastatic Pancreatic Cancer: Long-Term Survival From a Phase III Trial
    Goldstein, David
    El-Maraghi, Robert Hassan
    Hammel, Pascal
    Heinemann, Volker
    Kunzmann, Volker
    Sastre, Javier
    Scheithauer, Werner
    Siena, Salvatore
    Tabernero, Josep
    Teixeira, Luis
    Tortora, Giampaolo
    Van Laethem, Jean-Luc
    Young, Rosemary
    Penenberg, Darryl Neil
    Lu, Brian
    Romano, Alfredo
    Von Hoff, Daniel D.
    JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2015, 107 (02):
  • [22] CA19-9 decrease at 8 weeks as a predictor of overall survival (OS) in a randomized phase III trial (MPACT) of weekly nab-paclitaxel (nab-P) plus gemcitabine (G) versus G alone in patients with metastatic pancreatic cancer (MPC).
    Chiorean, E. Gabriela
    Von Hoff, Daniel D.
    Ervin, Thomas J.
    Arena, Francis P.
    Infante, Jeffrey R.
    Bathini, Venu Gopal
    Wood, Tina Evans
    Mainwaring, Paul N.
    Muldoon, Robert T.
    Clingan, Philip R.
    Kunzmann, Volker
    Ramanathan, Ramesh K.
    Tabernero, Josep
    Goldstein, David
    Ko, Amy
    Lu, Brian
    JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (15)
  • [23] Performance status dynamics during treatment with nab-paclitaxel plus gemcitabine versus gemcitabine alone for metastatic pancreatic cancer
    Chiorean, E. Gabriela
    Von Hoff, Daniel
    Wan, Yin
    Margunato-Debay, Sandra
    Botteman, Marc
    Goldstein, David
    CANCER MANAGEMENT AND RESEARCH, 2018, 10 : 1389 - 1396
  • [24] Alternating gemcitabine plus nab-paclitaxel and gemcitabine alone versus continuous gemcitabine plus nab-paclitaxel after induction treatment of metastatic pancreatic cancer (ALPACA): a multicentre, randomised, open-label, phase 2 trial
    Dorman, Klara
    Boeck, Stefan
    Caca, Karel
    Reichert, Maximilian
    Ettrich, Thomas J.
    Oettle, Helmut
    Waidmann, Oliver
    Modest, Dominik P.
    Mueller, Lothar
    Michl, Patrick
    Kanzler, Stephan
    Pink, Daniel
    Reinacher-Schick, Anke
    Geissler, Michael
    Pelz, Henning
    Kunzmann, Volker
    Held, Swantje
    Schichtl, Thomas
    Heinemann, Volker
    Kullmann, Frank
    LANCET GASTROENTEROLOGY & HEPATOLOGY, 2024, 9 (10): : 935 - 943
  • [25] RE: nab-Paclitaxel Plus Gemcitabine for Metastatic Pancreatic Cancer: Long-Term Survival From a Phase III Trial
    Velu, Lavanniya K. Palani
    Steele, Colin W.
    Dickson, Euan J.
    Carter, C. Ross
    Mckay, Colin J.
    Horgan, Paul G.
    McMillan, Donald C.
    Jamieson, Nigel B.
    JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2015, 107 (09):
  • [26] SPARC Expression Did Not Predict Efficacy of nab-Paclitaxel plus Gemcitabine or Gemcitabine Alone for Metastatic Pancreatic Cancer in an Exploratory Analysis of the Phase III MPACT Trial (vol 21, pg 4811, 2015)
    Hidalgo, M.
    Plaza, C.
    Musteanu, M.
    Illei, P.
    Brachmann, C. B.
    Heise, C.
    CLINICAL CANCER RESEARCH, 2016, 22 (24) : 6302 - 6302
  • [27] Increased Survival in Pancreatic Cancer with nab-Paclitaxel plus Gemcitabine
    Von Hoff, Daniel D.
    Ervin, Thomas
    Arena, Francis P.
    Chiorean, E. Gabriela
    Infante, Jeffrey
    Moore, Malcolm
    Seay, Thomas
    Tjulandin, Sergei A.
    Ma, Wen Wee
    Saleh, Mansoor N.
    Harris, Marion
    Reni, Michele
    Dowden, Scot
    Laheru, Daniel
    Bahary, Nathan
    Ramanathan, Ramesh K.
    Tabernero, Josep
    Hidalgo, Manuel
    Goldstein, David
    Van Cutsem, Eric
    Wei, Xinyu
    Iglesias, Jose
    Renschler, Markus F.
    NEW ENGLAND JOURNAL OF MEDICINE, 2013, 369 (18): : 1691 - 1703
  • [28] Cost-effectiveness of nab-paclitaxel plus gemcitabine versus erlotinib plus gemcitabine in metastatic pancreatic cancer
    Chiorean, E. Gabriela
    Whiting, Scott
    Binder, Gary
    Dranitsaris, George
    Manax, Victoria
    JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (03)
  • [29] nab-Paclitaxel Plus Gemcitabine Versus Gemcitabine in Patients with Metastatic Pancreatic Adenocarcinoma: Canadian Subgroup Analysis of the Phase 3 MPACT Trial (vol 33, pg 747, 2016)
    Tehfe, Mustapha
    Dowden, Scot
    Kennecke, Hagen
    El-Maraghi, Robert
    Lesperance, Bernard
    Couture, Felix
    Letourneau, Richard
    Liu, Helen
    Romano, Alfredo
    ADVANCES IN THERAPY, 2017, 34 (01) : 277 - 279
  • [30] A randomized trial of pharmacological ascorbate, gemcitabine, and nab-paclitaxel for metastatic pancreatic cancer
    Bodeker, Kellie L.
    Smith, Brian J.
    Berg, Daniel J.
    Chandrasekharan, Chandrikha
    Sharif, Saima
    Fei, Naomi
    Vollstedt, Sandy
    Brown, Heather
    Chandler, Meghan
    Lorack, Amanda
    McMichael, Stacy
    Wulfekuhle, Jared
    Wagner, Brett A.
    Buettner, Garry R.
    Allen, Bryan G.
    Caster, Joseph M.
    Dion, Barbara
    Kamgar, Mandana
    Buatti, John M.
    Cullen, Joseph M.
    REDOX BIOLOGY, 2024, 77