Optimizing Patient Selection for Irreversible Electroporation of Locally Advanced Pancreatic Cancer: Analyses of Survival

被引:10
作者
Woeste, Matthew R. [1 ]
Wilson, Khaleel D. [1 ]
Kruse, Edward J. [2 ]
Weiss, Matthew J. [3 ]
Christein, John D. [4 ]
White, Rebekah R. [5 ]
Martin, Robert C. G. [1 ]
机构
[1] Univ Louisville, Sch Med, Dept Surg, Div Surg Oncol, Louisville, KY 40292 USA
[2] Augusta Univ, Med Ctr, Sect Surg Oncol, Dept Surg, Augusta, GA USA
[3] Johns Hopkins Univ, Dept Surg, Div Surg Oncol, Baltimore, MD USA
[4] Univ Alabama Birmingham, Div Gastrointestinal Surg, Dept Surg, Birmingham, AL USA
[5] Univ Calif San Diego, Moores Canc Ctr, Gastrointestinal Canc Unit, San Diego, CA 92103 USA
关键词
locally advanced pancreatic cancer; irreversible electroporation (IRE); overall survival; patient selection; recurrence; progression free survival; LONG-TERM SURVIVAL; DIABETES-MELLITUS; PLUS RADIOTHERAPY; TUMOR ABLATION; ADENOCARCINOMA; BORDERLINE; THERAPY; CHEMOTHERAPY; GEMCITABINE; FOLFIRINOX;
D O I
10.3389/fonc.2021.817220
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundIrreversible electroporation (IRE) has emerged as a viable consolidative therapy after induction chemotherapy, in which this combination has improved overall survival of locally advanced pancreatic cancer (LAPC). Optimal timing and patient selection for irreversible electroporation remains a clinically unmet need. The aim of this study was to investigate preoperative factors that may assist in predicting progression-free and overall survival following IRE. MethodsA multi-institutional, prospectively maintained database was reviewed for patients with LAPC treated with induction chemotherapy followed by open-technique irreversible electroporation from 7/2015-5/2019. RECIST 1.1 criteria were used to assess tumor response and radiological progression. Overall survival (OS) and progression-free survival (PFS) were recorded. Survival analyses were performed using Kaplan Meier and Cox multivariable regression analyses. Results187 LAPC patients (median age 62 years range, 21 - 91, 65% men, 35% women) were treated with IRE. Median PFS was 21.7 months and median OS from diagnosis was 25.5 months. On multivariable analysis, age <= 61 (HR 0.41, 95%CI 0.21-0.78, p<0.008) and no prior radiation (HR 0.49, 95%CI 0.26-0.94, p=0.03) were positive predictors of OS after IRE. Age <= 61(HR 0.53, 95%CI, 0.28-.99, p=0.046) and FOLFIRINOX followed by gemcitabine/abraxane induction chemotherapy (HR 0.37,95%CI 0.15-0.89, p=0.027) predicted prolonged PFS after IRE. Abnormal CA19-9 values at the time of surgery negatively impacted both OS (HR 2.46, 95%CI 1.28-4.72, p<0.007) and PFS (HR 2.192, 95%CI 1.143-4.201, p=0.018) following IRE. ConclusionsAge, CA 19-9 response, avoidance of pre-IRE radiation, and FOLFIRINOX plus gemcitabine/abraxane induction chemotherapy are prominent factors to consider when referring or selecting LAPC patients to undergo IRE.
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页数:12
相关论文
共 76 条
[1]   CT Findings of Patients Treated with Irreversible Electroporation for Locally Advanced Pancreatic Cancer [J].
Akinwande, Olaguoke ;
Ahmad, Shakeeb S. ;
Van Meter, Tracy ;
Schulz, Brittany ;
Martin, Robert C. G. .
JOURNAL OF ONCOLOGY, 2015, 2015
[2]   Frailty predicts risk of life-threatening complications and mortality after pancreatic resections [J].
Augustin, Toms ;
Burstein, Matthew D. ;
Schneider, Eric B. ;
Morris-Stiff, Gareth ;
Wey, Jane ;
Chalikonda, Sticharan ;
Walsh, R. Matthew .
SURGERY, 2016, 160 (04) :987-995
[3]   Concurrent chemotherapy alone versus irreversible electroporation followed by chemotherapy on survival in patients with locally advanced pancreatic cancer [J].
Belfiore, Giuseppe ;
Belfiore, Maria Paola ;
Reginelli, Alfonso ;
Capasso, Raffaella ;
Romano, Francesco ;
Ianniello, Giovanni Pietro ;
Cappabianca, Salvatore ;
Brunese, Luca .
MEDICAL ONCOLOGY, 2017, 34 (03)
[4]   Electrochemotherapy with Irreversible Electroporation and FOLFIRINOX Improves Survival in Murine Models of Pancreatic Adenocarcinoma [J].
Bhutiani, Neal ;
Li, Yan ;
Zheng, Qianqian ;
Pandit, Harshul ;
Shi, Xiaoju ;
Chen, Yujia ;
Yu, Youxi ;
Pulliam, Zachary R. ;
Tan, Min ;
Martin, Robert C. G., II .
ANNALS OF SURGICAL ONCOLOGY, 2020, 27 (11) :4348-4359
[5]   Irreversible Electroporation Enhances Delivery of Gemcitabine to Pancreatic Adenocarcinoma [J].
Bhutiani, Neal ;
Agle, Steven ;
Li, Yan ;
Li, Suping ;
Martin, Robert C. G., II .
JOURNAL OF SURGICAL ONCOLOGY, 2016, 114 (02) :181-186
[6]   Neoadjuvant Modified (m) FOLFIRINOX for Locally Advanced Unresectable (LAPC) and Borderline Resectable (BRPC) Adenocarcinoma of the Pancreas [J].
Blazer, Marlo ;
Wu, Christina ;
Goldberg, Richard M. ;
Phillips, Gary ;
Schmidt, Carl ;
Muscarella, Peter ;
Wuthrick, Evan ;
Williams, Terrence M. ;
Reardon, Joshua ;
Ellison, E. Christopher ;
Bloomston, Mark ;
Bekaii-Saab, Tanios .
ANNALS OF SURGICAL ONCOLOGY, 2015, 22 (04) :1153-1159
[7]   Serum CA 19-9 Response to Neoadjuvant Therapy is Associated with Outcome in Pancreatic Adenocarcinoma [J].
Boone, Brian A. ;
Steve, Jennifer ;
Zenati, Mazen S. ;
Hogg, Melissa E. ;
Singhi, Aatur D. ;
Bartlett, David L. ;
Zureikat, Amer H. ;
Bahary, Nathan ;
Zeh, Herbert J., III .
ANNALS OF SURGICAL ONCOLOGY, 2014, 21 (13) :4351-4358
[8]   Irreversible Electroporation of the Pancreas: Definitive Local Therapy Without Systemic Effects [J].
Bower, Matthew ;
Sherwood, Leslie ;
Li, Yan ;
Martin, Robert .
JOURNAL OF SURGICAL ONCOLOGY, 2011, 104 (01) :22-28
[9]   Human pancreatic cancer-associated stellate cells remain activated after in vivo chemoradiation [J].
Cabrera, M. Carla ;
Tilahun, Estifanos ;
Nakles, Rebecca ;
Diaz-Cruz, Edgar S. ;
Charabaty, Aline ;
Suy, Simeng ;
Jackson, Patrick ;
Ley, Lisa ;
Slack, Rebecca ;
Jha, Reena ;
Collins, Sean P. ;
Haddad, Nadim ;
Kallakury, Bhaskar V. S. ;
Schroeder, Timm ;
Pishvaian, Michael J. ;
Furth, Priscilla A. .
FRONTIERS IN ONCOLOGY, 2014, 4
[10]   Pretreatment Assessment of Resectable and Borderline Resectable Pancreatic Cancer: Expert Consensus Statement [J].
Callery, Mark P. ;
Chang, Kenneth J. ;
Fishman, Elliot K. ;
Talamonti, Mark S. ;
Traverso, L. William ;
Linehan, David C. .
ANNALS OF SURGICAL ONCOLOGY, 2009, 16 (07) :1727-1733