Moving the Target on the Optimal Adjuvant Strategy for Resected Pancreatic Cancers: A Systematic Review with Meta-Analysis

被引:11
作者
Galvano, Antonio [1 ]
Castiglia, Marta [1 ]
Rizzo, Sergio [1 ]
Silvestris, Nicola [2 ]
Brunetti, Oronzo [2 ]
Vaccaro, Giovanni [1 ]
Gristina, Valerio [1 ]
Barraco, Nadia [1 ]
Bono, Marco [3 ]
Guercio, Giovanni [3 ]
Graceffa, Giuseppa [3 ]
Fulfaro, Fabio [1 ]
Gori, Stefania [4 ]
Bazan, Viviana [5 ]
Russo, Antonio [1 ]
机构
[1] Univ Palermo, Dept Surg Oncol & Stomatol Sci, Med Oncol Unit, Via Vespro 129, Palermo 90127, Italy
[2] IRCCS Ist Tumori Giovanni Paolo II Bari, Med Oncol Unit, Viale Orazio Flacco 65, Bari 70124, Italy
[3] Univ Palermo, Dept Surg Oncol & Stomatol Sci, Via Vespro 129, Palermo 90127, Italy
[4] IRCCS Sacro Cuore Don Calabria Hosp, Oncol Dept, Verona 37024, Italy
[5] Univ Palermo, Sch Med, Dept Expt Biomed & Clin Neurosci, Via Vespro 129, Palermo 90127, Italy
关键词
adjuvant; mFOLFIRINOX; pancreatic cancer; systematic review; chemotherapy; meta-analysis; SURGICAL COMPLICATIONS; DUCTAL ADENOCARCINOMA; MODIFIED FOLFIRINOX; OPEN-LABEL; CHEMOTHERAPY; GEMCITABINE; THERAPY; CHEMORADIOTHERAPY; SURGERY; PHASE-3;
D O I
10.3390/cancers12030534
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Combination regimens have shown superiority over single agents in the adjuvant treatment of resected pancreatic cancer (PC), but there are no data supporting definition of the best regimen. This work aimed to compare the efficacy and safety of mFOLFIRINOX, gemcitabine +capecitabine, and gemcitabine +nab/paclitaxel in PC patients. A meta-analysis was performed for direct comparison between trials comparing combination regimens and gemcitabine monotherapy. Subsequently, an indirect comparison was made between trials investigating the efficacy and safety of mFOLFIRINOX, gemcitabine+capecitabine, and gemcitabine+nab/paclitaxel because of the same control arm (gemcitabine). A total of three studies met the selection criteria and were included in our indirect comparison. Indirect comparisons for efficacy outcomes showed a benefit in terms of DFS (disease-free survival)/EFS (event-free survival)/RFS (relapse-free survival) for both mFOLFIRINOX versus gemcitabine+capecitabine (HR 0.69, 95% CI 0.52-0.91) and versus gemcitabine+nab/paclitaxel (HR 0.67, 95% CI 0.50-0.90). No significant advantage was registered for OS (overall survival). Indirect comparisons for safety showed an increase in terms of G3-5 AEs (with the exception of neutropenia) for mFOLFIRINOX versus gemcitabine+capecitabine (RR 1.24, 95% CI 1.03-1.50), while no significant differences were observed versus gemcitabine+nab/paclitaxel. According to our results, mFOLFIRINOX is feasible and manageable and could represent a first option for fit PC resected patients.
引用
收藏
页数:14
相关论文
共 53 条
[1]   Phase II Study of the Triple Combination Chemotherapy of SOXIRI (S-1/Oxaliplatin/Irinotecan) in Patients with Unresectable Pancreatic Ductal Adenocarcinoma [J].
Akahori, Takahiro ;
Sho, Masayuki ;
Yanagimoto, Hiroaki ;
Satoi, Sohei ;
Nagai, Minako ;
Nishiwada, Satoshi ;
Nakagawa, Kenji ;
Nakamura, Kota ;
Yamamoto, Tomohisa ;
Hirooka, Satoshi ;
Yamaki, So ;
Ikeda, Naoya .
ONCOLOGIST, 2019, 24 (06) :749-E224
[2]   Delayed recovery after pancreaticoduodenectomy: A major factor impairing the delivery of adjuvant therapy? [J].
Aloia, Thomas E. ;
Lee, Jeffrey E. ;
Vauthey, Jean-Nicolas ;
Abdalla, Eddie K. ;
Wolff, Robert A. ;
Varadhachary, Gauri R. ;
Abbruzzese, James L. ;
Crane, Christopher H. ;
Evans, Douglas B. ;
Pisters, Peter W. T. .
JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS, 2007, 204 (03) :347-355
[3]   Completion of Adjuvant Chemotherapy After Upfront Surgical Resection for Pancreatic Cancer Is Uncommon Yet Associated With Improved Survival [J].
Altman, Ariella M. ;
Wirth, Keith ;
Marmor, Schelomo ;
Lou, Emil ;
Chang, Katherine ;
Hui, Jane Y. C. ;
Tuttle, Todd M. ;
Jensen, Eric H. ;
Denbo, Jason W. .
ANNALS OF SURGICAL ONCOLOGY, 2019, 26 (12) :4108-4116
[4]  
[Anonymous], 2014, REV MAN REVMAN VERS
[5]   Targeted deep sequencing of circulating tumor DNA in metastatic pancreatic cancer [J].
Berger, Andreas W. ;
Schwerdel, Daniel ;
Ettrich, Thomas J. ;
Hann, Alexander ;
Schmidt, Stefan A. ;
Kleger, Alexander ;
Marienfeld, Ralf ;
Seufferlein, Thomas .
ONCOTARGET, 2018, 9 (02) :2076-2085
[6]   A basic introduction to fixed-effect and random-effects models for meta-analysis [J].
Borenstein, Michael ;
Hedges, Larry V. ;
Higgins, Julian P. T. ;
Rothstein, Hannah R. .
RESEARCH SYNTHESIS METHODS, 2010, 1 (02) :97-111
[7]   The results of direct and indirect treatment comparisons in meta-analysis of randomized controlled trials [J].
Bucher, HC ;
Guyatt, GH ;
Griffith, LE ;
Walter, SD .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1997, 50 (06) :683-691
[8]   Neoadjuvant Chemoradiotherapy and Surgery Versus Surgery Alone in Resectable Pancreatic Cancer: A Single-Center Prospective, Randomized, Controlled Trial Which Failed to Achieve Accrual Targets [J].
Casadei, Riccardo ;
Di Marco, Mariacristina ;
Ricci, Claudio ;
Santini, Donatella ;
Serra, Carla ;
Calculli, Lucia ;
D'Ambra, Marielda ;
Guido, Alessandra ;
Morselli-Labate, Antonio Maria ;
Minni, Francesco .
JOURNAL OF GASTROINTESTINAL SURGERY, 2015, 19 (10) :1802-1812
[9]   FOLFIRINOX for advanced pancreatic cancer: the Princess Margaret Cancer Centre experience [J].
Chllamma, Muralidharan K. ;
Cook, Natalie ;
Dhani, Neesha C. ;
Giby, Kazim ;
Dodd, Anna ;
Wang, Lisa ;
Hedley, David W. ;
Moore, Malcolm J. ;
Knox, Jennifer J. .
BRITISH JOURNAL OF CANCER, 2016, 115 (06) :649-654
[10]   FOLFIRINOX or Gemcitabine as Adjuvant Therapy for Pancreatic Cancer [J].
Conroy, T. ;
Hammel, P. ;
Hebbar, M. ;
Ben Abdelghani, M. ;
Wei, A. C. ;
Raoul, J. -L. ;
Chone, L. ;
Francois, E. ;
Artru, P. ;
Biagi, J. J. ;
Lecomte, T. ;
Assenat, E. ;
Faroux, R. ;
Ychou, M. ;
Volet, J. ;
Sauvanet, A. ;
Breysacher, G. ;
Di Fiore, F. ;
Cripps, C. ;
Kavan, P. ;
Texereau, P. ;
Bouhier-Leporrier, K. ;
Khemissa-Akouz, F. ;
Legoux, J. -L. ;
Juzyna, B. ;
Gourgou, S. ;
O'Callaghan, C. J. ;
Jouffroy-Zeller, C. ;
Rat, P. ;
Malka, D. ;
Castan, F. ;
Bachet, J. -B. .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 379 (25) :2395-2406