Long-term outcomes of neoadjuvant chemotherapy before chemoradiation for locally advanced pancreatic cancer

被引:48
作者
Arvold, Nils D. [2 ]
Ryan, David P. [3 ]
Niemierko, Andrzej [1 ]
Blaszkowsky, Lawrence S. [3 ]
Kwak, Eunice L. [3 ]
Wo, Jennifer Y. [1 ]
Allen, Jill N. [3 ]
Clark, Jeffrey W. [3 ]
Wadlow, Raymond C. [3 ]
Zhu, Andrew X. [3 ]
Fernandez-del Castillo, Carlos [4 ]
Hong, Theodore S. [1 ]
机构
[1] Massachusetts Gen Hosp, Dept Radiat Oncol, Boston, MA 02114 USA
[2] Harvard Radiat Oncol Program, Boston, MA USA
[3] Massachusetts Gen Hosp, Dept Med, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Dept Surg, Boston, MA 02114 USA
关键词
locally advanced pancreatic cancer; neoadjuvant chemotherapy; chemoradiation; gemcitabine; resection; survival; PHASE-III TRIAL; MAINTENANCE GEMCITABINE; RADIATION-THERAPY; ONCOLOGY-GROUP; MITOMYCIN-C; I TRIAL; CHEMORADIOTHERAPY; ADENOCARCINOMA; RADIOTHERAPY; 5-FLUOROURACIL;
D O I
10.1002/cncr.26633
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Neoadjuvant chemotherapy before chemoradiation therapy (CRT) may improve outcomes for patients with locally advanced pancreatic cancer, but optimal management remains controversial, and prior reports have limited follow-up. METHODS: Seventy consecutive patients with unresectable (n = 46) or borderline resectable (n = 24) locally advanced pancreatic cancer were treated with CRT from 2005 to 2009. Patients typically received 50.4 grays in 28 fractions (91%) with concurrent 5-fluorouracil (84%) or capecitabine (14%). Forty patients received CRT alone, and 30 patients received neoadjuvant chemotherapy before CRT for a median of 4 months, typically gemcitabine (93%). All patients without progression after neoadjuvant chemotherapy were offered CRT. RESULTS: Median follow-up was 14.2 months (range, 3-57 months). Fifty-three percent of patients in the CRT group versus 83% in the neoadjuvant chemotherapy before CRT group had unresectable tumors at diagnosis; after completion of CRT, 20% of patients in both groups underwent resection. Compared with CRT alone, the neoadjuvant chemotherapy before CRT group demonstrated improved median overall survival (OS; 18.7 vs 12.4 months; P = .02) and progression-free survival (11.4 vs 6.7 months; P = .02). On multivariate analysis, receipt of neoadjuvant chemotherapy (adjusted hazard ratio [HR], 0.49; 95% CI, 0.28-0.87; P = .02) and surgical resection (adjusted HR, 0.38; 95% CI, 0.17-0.85; P = .02) were associated with increased OS. CONCLUSIONS: Gemcitabine-based neoadjuvant chemotherapy confers a significant OS advantage by allowing the selection of patients who will derive greatest benefit from CRT. Median survival with this approach was similar to that seen with surgical resection. Cancer 2012;118: 302635. (C) 2011 American Cancer Society.
引用
收藏
页码:3026 / 3035
页数:10
相关论文
共 38 条
[1]  
Anderson S, 2010, J CLIN ONCOL S15, V28
[2]   Neoadjuvant Therapy Is Associated With Improved Survival in Resectable Pancreatic Adenocarcinoma [J].
Artinyan, Avo ;
Anaya, Daniel A. ;
McKenzie, Shaun ;
Ellenhorn, Joshua D. I. ;
Kim, Joseph .
CANCER, 2011, 117 (10) :2044-2049
[3]   PANCREATIC CANCER TUMOR SIZE ON CT SCAN VERSUS PATHOLOGIC SPECIMEN: IMPLICATIONS FOR RADIATION TREATMENT PLANNING [J].
Arvold, Nils D. ;
Niemierko, Andrzej ;
Mamon, Harvey J. ;
Fernandez-del Castillo, Carlos ;
Hong, Theodore S. .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2011, 80 (05) :1383-1390
[4]   Validation of the 6th Edition AJCC Pancreatic Cancer Staging System - Report from the National Cancer Database [J].
Bilimoria, Karl Y. ;
Bentrem, David J. ;
Ko, Clifford Y. ;
Ritchey, Jamie ;
Stewart, Andrew K. ;
Winchester, David P. ;
Talamonti, Mark S. .
CANCER, 2007, 110 (04) :738-744
[5]   Phase I trial of strictly time-scheduled gemcitabine and cisplatin with concurrent radiotherapy in patients with locally advanced pancreatic cancer [J].
Brunner, TB ;
Grabenbauer, GG ;
Klein, P ;
Baum, U ;
Papadopoulos, T ;
Bautz, W ;
Hohenberger, W ;
Sauer, R .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2003, 55 (01) :144-153
[6]   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
[7]   Phase III trial comparing intensive induction chemoradiotherapy (60 Gy, infusional 5-FU and intermittent cisplatin) followed by maintenance gemcitabine with gemcitabine alone for locally advanced unresectable pancreatic cancer.: Definitive results of the 2000-01 FFCD/SFRO study [J].
Chauffert, B. ;
Mornex, F. ;
Bonnetain, F. ;
Rougier, P. ;
Mariette, C. ;
Bouche, O. ;
Bosset, J. F. ;
Aparicio, T. ;
Mineur, L. ;
Azzedine, A. ;
Hammel, P. ;
Butel, J. ;
Stremsdoerfer, N. ;
Maingon, P. ;
Bedenne, L. .
ANNALS OF ONCOLOGY, 2008, 19 (09) :1592-1599
[8]   A randomized Phase III study of radiotherapy alone or with 5-fluorouracil and mitomycin-C in patients with locally advanced adenocarcinoma of the pancreas: Eastern cooperative oncology group study E8282 [J].
Cohen, SJ ;
Dobelbower, R ;
Lipsitz, S ;
Catalano, PJ ;
Sischy, B ;
Smith, TJ ;
Haller, DG .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2005, 62 (05) :1345-1350
[9]   FOLFIRINOX versus Gemcitabine for Metastatic Pancreatic Cancer [J].
Conroy, Thierry ;
Desseigne, Francoise ;
Ychou, Marc ;
Bouche, Olivier ;
Guimbaud, Rosine ;
Becouarn, Yves ;
Adenis, Antoine ;
Raoul, Jean-Luc ;
Gourgou-Bourgade, Sophie ;
de la Fouchardiere, Christelle ;
Bennouna, Jaafar ;
Bachet, Jean-Baptiste ;
Khemissa-Akouz, Faiza ;
Pere-Verge, Denis ;
Delbaldo, Catherine ;
Assenat, Eric ;
Chauffert, Bruno ;
Michel, Pierre ;
Montoto-Grillot, Christine ;
Ducreux, Michel .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 364 (19) :1817-1825
[10]  
COX DR, 1972, J R STAT SOC B, V34, P187