5-Fluorouracil/Leucovorin Combined with Irinotecan and Oxaliplatin (FOLFIRINOX) as Second-Line Chemotherapy in Patients with Metastatic Pancreatic Adenocarcinoma

Background: To evaluate the efficacy and toxicity of irinotecan and oxaliplatin plus 5-fluorouracil (FU) and leucovorin (FOLFIRINOX) as second-line therapy in metastatic pancreatic adenocarcinoma (MPA). Patients and Methods: We retrospectively analyzed the medical records of 27 patients with MPA tre...

Full description

Saved in:
Bibliographic Details
Published inOncology Vol. 80; no. 5-6; pp. 301 - 306
Main Authors Assaf, Elias, Verlinde-Carvalho, Muriel, Delbaldo, Catherine, Grenier, Julien, Sellam, Zineb, Pouessel, Damien, Bouaita, Linda, Baumgaertner, Isabelle, Sobhani, Iradj, Tayar, Claude, Paul, Muriel, Culine, Stéphane
Format Journal Article
LanguageEnglish
Published Basel, Switzerland Karger 01.01.2011
S. Karger AG
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Background: To evaluate the efficacy and toxicity of irinotecan and oxaliplatin plus 5-fluorouracil (FU) and leucovorin (FOLFIRINOX) as second-line therapy in metastatic pancreatic adenocarcinoma (MPA). Patients and Methods: We retrospectively analyzed the medical records of 27 patients with MPA treated with FOLFIRINOX as second-line therapy between January 2003 and November 2009 in our hospital. The recommended schedule was oxaliplatin 85 mg/m 2 on day 1 + irinotecan 180 mg/m 2 on day 1 + leucovorin 400 mg/m 2 on day 1 followed by FU 400 mg/m 2 as a bolus on day 1 and 2,400 mg/m 2 as 46-hour continuous infusion biweekly. Results: The median age of the 27 patients (13 males and 14 females) was 63 years (45–83). All patients had progressive disease after first-line chemotherapy by gemcitabine. A total of 167 cycles were administered, with a median number of 6 cycles (1–29) per patient. One toxic death occurred (sepsis). Tolerance of treatment was acceptable, and the relative dose density delivered per patient was 92.8% for oxaliplatin, 89.1% for irinotecan and 96.4% for FU. Grade 3–4 neutropenia occurred in 55.6% of the patients, including 1 febrile neutropenia. The other toxicities were manageable. Regarding efficacy, 22 of the 27 patients were evaluable (WHO and RECIST criteria). Five patients had partial responses and 12 stable disease, resulting in an overall disease control rate of 63%. Median time to progression was 5.4 months (0.7–25.48), and median event-free survival was 3 months (0.5–24.9). Median overall survival was 8.5 months (0–26). A clinical benefit was reported for 55% of the patients. Conclusions: These results confirmed the good safety profile and the efficacy of the FOLFIRINOX regimen as second-line treatment of MPA.
AbstractList Background: To evaluate the efficacy and toxicity of irinotecan and oxaliplatin plus 5-fluorouracil (FU) and leucovorin (FOLFIRINOX) as second-line therapy in metastatic pancreatic adenocarcinoma (MPA). Patients and Methods: We retrospectively analyzed the medical records of 27 patients with MPA treated with FOLFIRINOX as second-line therapy between January 2003 and November 2009 in our hospital. The recommended schedule was oxaliplatin 85 mg/m2 on day 1 + irinotecan 180 mg/m2 on day 1 + leucovorin 400 mg/m2 on day 1 followed by FU 400 mg/m2 as a bolus on day 1 and 2,400 mg/m2 as 46-hour continuous infusion biweekly. Results: The median age of the 27 patients (13 males and 14 females) was 63 years (45–83). All patients had progressive disease after first-line chemotherapy by gemcitabine. A total of 167 cycles were administered, with a median number of 6 cycles (1–29) per patient. One toxic death occurred (sepsis). Tolerance of treatment was acceptable, and the relative dose density delivered per patient was 92.8% for oxaliplatin, 89.1% for irinotecan and 96.4% for FU. Grade 3–4 neutropenia occurred in 55.6% of the patients, including 1 febrile neutropenia. The other toxicities were manageable. Regarding efficacy, 22 of the 27 patients were evaluable (WHO and RECIST criteria). Five patients had partial responses and 12 stable disease, resulting in an overall disease control rate of 63%. Median time to progression was 5.4 months (0.7–25.48), and median event-free survival was 3 months (0.5–24.9). Median overall survival was 8.5 months (0–26). A clinical benefit was reported for 55% of the patients. Conclusions: These results confirmed the good safety profile and the efficacy of the FOLFIRINOX regimen as second-line treatment of MPA.
Background: To evaluate the efficacy and toxicity of irinotecan and oxaliplatin plus 5-fluorouracil (FU) and leucovorin (FOLFIRINOX) as second-line therapy in metastatic pancreatic adenocarcinoma (MPA). Patients and Methods: We retrospectively analyzed the medical records of 27 patients with MPA treated with FOLFIRINOX as second-line therapy between January 2003 and November 2009 in our hospital. The recommended schedule was oxaliplatin 85 mg/m 2 on day 1 + irinotecan 180 mg/m 2 on day 1 + leucovorin 400 mg/m 2 on day 1 followed by FU 400 mg/m 2 as a bolus on day 1 and 2,400 mg/m 2 as 46-hour continuous infusion biweekly. Results: The median age of the 27 patients (13 males and 14 females) was 63 years (45–83). All patients had progressive disease after first-line chemotherapy by gemcitabine. A total of 167 cycles were administered, with a median number of 6 cycles (1–29) per patient. One toxic death occurred (sepsis). Tolerance of treatment was acceptable, and the relative dose density delivered per patient was 92.8% for oxaliplatin, 89.1% for irinotecan and 96.4% for FU. Grade 3–4 neutropenia occurred in 55.6% of the patients, including 1 febrile neutropenia. The other toxicities were manageable. Regarding efficacy, 22 of the 27 patients were evaluable (WHO and RECIST criteria). Five patients had partial responses and 12 stable disease, resulting in an overall disease control rate of 63%. Median time to progression was 5.4 months (0.7–25.48), and median event-free survival was 3 months (0.5–24.9). Median overall survival was 8.5 months (0–26). A clinical benefit was reported for 55% of the patients. Conclusions: These results confirmed the good safety profile and the efficacy of the FOLFIRINOX regimen as second-line treatment of MPA.
Background: To evaluate the efficacy and toxicity of irinotecan and oxaliplatin plus 5-fluorouracil (FU) and leucovorin (FOLFIRINOX) as second-line therapy in metastatic pancreatic adenocarcinoma (MPA). Patients and Methods: We retrospectively analyzed the medical records of 27 patients with MPA treated with FOLFIRINOX as second-line therapy between January 2003 and November 2009 in our hospital. The recommended schedule was oxaliplatin 85 mg/m2 on day 1 + irinotecan 180 mg/m2 on day 1 + leucovorin 400 mg/m2 on day 1 followed by FU 400 mg/m2 as a bolus on day 1 and 2,400 mg/m2 as 46-hour continuous infusion biweekly. Results: The median age of the 27 patients (13 males and 14 females) was 63 years (45-83). All patients had progressive disease after first-line chemotherapy by gemcitabine. A total of 167 cycles were administered, with a median number of 6 cycles (1-29) per patient. One toxic death occurred (sepsis). Tolerance of treatment was acceptable, and the relative dose density delivered per patient was 92.8% for oxaliplatin, 89.1% for irinotecan and 96.4% for FU. Grade 3-4 neutropenia occurred in 55.6% of the patients, including 1 febrile neutropenia. The other toxicities were manageable. Regarding efficacy, 22 of the 27 patients were evaluable (WHO and RECIST criteria). Five patients had partial responses and 12 stable disease, resulting in an overall disease control rate of 63%. Median time to progression was 5.4 months (0.7-25.48), and median event-free survival was 3 months (0.5-24.9). Median overall survival was 8.5 months (0-26). A clinical benefit was reported for 55% of the patients. Conclusions: These results confirmed the good safety profile and the efficacy of the FOLFIRINOX regimen as second-line treatment of MPA. [PUBLICATION ABSTRACT]
BACKGROUNDTo evaluate the efficacy and toxicity of irinotecan and oxaliplatin plus 5-fluorouracil (FU) and leucovorin (FOLFIRINOX) as second-line therapy in metastatic pancreatic adenocarcinoma (MPA).PATIENTS AND METHODSWe retrospectively analyzed the medical records of 27 patients with MPA treated with FOLFIRINOX as second-line therapy between January 2003 and November 2009 in our hospital. The recommended schedule was oxaliplatin 85 mg/m(2) on day 1 + irinotecan 180 mg/m(2) on day 1 + leucovorin 400 mg/m(2) on day 1 followed by FU 400 mg/m(2) as a bolus on day 1 and 2,400 mg/m(2) as 46-hour continuous infusion biweekly.RESULTSThe median age of the 27 patients (13 males and 14 females) was 63 years (45-83). All patients had progressive disease after first-line chemotherapy by gemcitabine. A total of 167 cycles were administered, with a median number of 6 cycles (1-29) per patient. One toxic death occurred (sepsis). Tolerance of treatment was acceptable, and the relative dose density delivered per patient was 92.8% for oxaliplatin, 89.1% for irinotecan and 96.4% for FU. Grade 3-4 neutropenia occurred in 55.6% of the patients, including 1 febrile neutropenia. The other toxicities were manageable. Regarding efficacy, 22 of the 27 patients were evaluable (WHO and RECIST criteria). Five patients had partial responses and 12 stable disease, resulting in an overall disease control rate of 63%. Median time to progression was 5.4 months (0.7-25.48), and median event-free survival was 3 months (0.5-24.9). Median overall survival was 8.5 months (0-26). A clinical benefit was reported for 55% of the patients.CONCLUSIONSThese results confirmed the good safety profile and the efficacy of the FOLFIRINOX regimen as second-line treatment of MPA.
To evaluate the efficacy and toxicity of irinotecan and oxaliplatin plus 5-fluorouracil (FU) and leucovorin (FOLFIRINOX) as second-line therapy in metastatic pancreatic adenocarcinoma (MPA). We retrospectively analyzed the medical records of 27 patients with MPA treated with FOLFIRINOX as second-line therapy between January 2003 and November 2009 in our hospital. The recommended schedule was oxaliplatin 85 mg/m(2) on day 1 + irinotecan 180 mg/m(2) on day 1 + leucovorin 400 mg/m(2) on day 1 followed by FU 400 mg/m(2) as a bolus on day 1 and 2,400 mg/m(2) as 46-hour continuous infusion biweekly. The median age of the 27 patients (13 males and 14 females) was 63 years (45-83). All patients had progressive disease after first-line chemotherapy by gemcitabine. A total of 167 cycles were administered, with a median number of 6 cycles (1-29) per patient. One toxic death occurred (sepsis). Tolerance of treatment was acceptable, and the relative dose density delivered per patient was 92.8% for oxaliplatin, 89.1% for irinotecan and 96.4% for FU. Grade 3-4 neutropenia occurred in 55.6% of the patients, including 1 febrile neutropenia. The other toxicities were manageable. Regarding efficacy, 22 of the 27 patients were evaluable (WHO and RECIST criteria). Five patients had partial responses and 12 stable disease, resulting in an overall disease control rate of 63%. Median time to progression was 5.4 months (0.7-25.48), and median event-free survival was 3 months (0.5-24.9). Median overall survival was 8.5 months (0-26). A clinical benefit was reported for 55% of the patients. These results confirmed the good safety profile and the efficacy of the FOLFIRINOX regimen as second-line treatment of MPA.
Author Sobhani, Iradj
Delbaldo, Catherine
Sellam, Zineb
Baumgaertner, Isabelle
Paul, Muriel
Verlinde-Carvalho, Muriel
Bouaita, Linda
Culine, Stéphane
Pouessel, Damien
Tayar, Claude
Assaf, Elias
Grenier, Julien
Author_xml – sequence: 1
  givenname: Elias
  surname: Assaf
  fullname: Assaf, Elias
  email: elias.assaf@hmn.aphp.fr
– sequence: 2
  givenname: Muriel
  surname: Verlinde-Carvalho
  fullname: Verlinde-Carvalho, Muriel
– sequence: 3
  givenname: Catherine
  surname: Delbaldo
  fullname: Delbaldo, Catherine
– sequence: 4
  givenname: Julien
  surname: Grenier
  fullname: Grenier, Julien
– sequence: 5
  givenname: Zineb
  surname: Sellam
  fullname: Sellam, Zineb
– sequence: 6
  givenname: Damien
  surname: Pouessel
  fullname: Pouessel, Damien
– sequence: 7
  givenname: Linda
  surname: Bouaita
  fullname: Bouaita, Linda
– sequence: 8
  givenname: Isabelle
  surname: Baumgaertner
  fullname: Baumgaertner, Isabelle
– sequence: 9
  givenname: Iradj
  surname: Sobhani
  fullname: Sobhani, Iradj
– sequence: 10
  givenname: Claude
  surname: Tayar
  fullname: Tayar, Claude
– sequence: 11
  givenname: Muriel
  surname: Paul
  fullname: Paul, Muriel
– sequence: 12
  givenname: Stéphane
  surname: Culine
  fullname: Culine, Stéphane
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24497456$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/21778770$$D View this record in MEDLINE/PubMed
BookMark eNpd0UuP0zAQAGALLWK7CwfuCEUrIdhDWL8S28dVRaFSoYiHxC1y7QnNktjFToD9OfxTBlqKxMnW-PPMaOaMnIQYgJCHjD5nrDJXlFLBjabiDpkxyUVJueAnZIZhWnLJ5Ck5y_kGmapkfY-ccqaUVorOyM-qXPRTTHFK1nX91QomF7_F1IViHodNF8AX37txWywxFEdwNhQ2-GL9w_bdrrcjwmeL9WqxfLd8s_50WdhcvAcXgy9X-LmYb2GI4xaS3d0WaN_iDwhj3id9DaPNI4YcPgSX4M_12kOIziaHFQd7n9xtbZ_hweE8Jx8XLz7MX5Wr9cvl_HpVOlHzsazrlgIzlGrlNVRGc8q1NxtujTW-9bVQvFJUCkVrLdu2hpoLAUbyjai8b8U5ebrPu0vx6wR5bIYuO-h7GyBOudFaGaGMkigv_pM3OL6AzTXaaME4oxWiyz1yKeacoG12qRtsum0YbX5vrTluDe3jQ8JpM4A_yr9rQvDkAGx2tm8TDqvL_5yU2FdVo3u0d19s-gzpCA51fgHsCal-
CitedBy_id crossref_primary_10_1177_1756283X17705328
crossref_primary_10_1038_bjc_2015_328
crossref_primary_10_1016_j_suc_2016_07_011
crossref_primary_10_1016_S1674_6384_17_60090_X
crossref_primary_10_1111_imj_13810
crossref_primary_10_2958_suizo_29_885
crossref_primary_10_1159_000356158
crossref_primary_10_1007_s13577_022_00731_3
crossref_primary_10_1177_17588359211018539
crossref_primary_10_3748_wjg_v22_i46_10124
crossref_primary_10_5306_wjco_v7_i1_27
crossref_primary_10_1007_s00761_015_2930_4
crossref_primary_10_1016_j_dld_2018_08_008
crossref_primary_10_1586_14737140_2014_957188
crossref_primary_10_1007_s00280_014_2665_8
crossref_primary_10_1097_MPA_0000000000001833
crossref_primary_10_1053_j_seminoncol_2021_02_002
crossref_primary_10_1186_s12885_021_09069_9
crossref_primary_10_52927_jdcr_2023_11_3_147
crossref_primary_10_1177_1756283X17713879
crossref_primary_10_1016_j_critrevonc_2015_03_008
crossref_primary_10_1097_PPO_0b013e318275896f
crossref_primary_10_5306_wjco_v12_i9_787
crossref_primary_10_1080_02656736_2019_1579371
crossref_primary_10_1007_s11912_012_0290_4
crossref_primary_10_1200_PO_17_00316
crossref_primary_10_1159_000380785
crossref_primary_10_1186_s12885_021_08275_9
crossref_primary_10_3989_redc_2023_3_1981
crossref_primary_10_1089_pancan_2019_0003
crossref_primary_10_1097_MD_0000000000006769
crossref_primary_10_1586_14737140_2015_1081816
crossref_primary_10_4251_wjgo_v10_i12_505
crossref_primary_10_1002_jcp_26183
crossref_primary_10_1093_annonc_mdt200
crossref_primary_10_18027_2224_5057_2023_13_4_60_68
crossref_primary_10_1002_jso_23392
crossref_primary_10_1016_j_pharmthera_2015_08_006
crossref_primary_10_12688_f1000research_2_105_v1
crossref_primary_10_1111_hpb_12119
crossref_primary_10_1200_JCO_2014_56_2728
crossref_primary_10_1007_s12032_016_0753_9
crossref_primary_10_1007_s00432_019_03019_6
crossref_primary_10_1002_jgh3_12555
crossref_primary_10_3748_wjg_v27_i17_1847
crossref_primary_10_1097_PPO_0000000000000294
crossref_primary_10_1016_j_compbiomed_2022_106411
crossref_primary_10_1186_s12885_020_06945_8
crossref_primary_10_1177_1758835919875568
crossref_primary_10_1016_j_clcc_2014_09_005
crossref_primary_10_18632_oncotarget_21939
crossref_primary_10_4166_kjg_2015_66_3_150
crossref_primary_10_1093_annonc_mdx174
crossref_primary_10_1002_jcsm_12307
crossref_primary_10_1007_s00280_012_1981_0
crossref_primary_10_1038_bjc_2013_408
crossref_primary_10_3390_molecules19055611
crossref_primary_10_1016_S0140_6736_15_00986_1
crossref_primary_10_1016_j_esmoop_2021_100049
crossref_primary_10_14694_EdBook_AM_2012_32_173
crossref_primary_10_1080_01635581_2019_1597906
crossref_primary_10_15279_kpba_2020_25_2_72
crossref_primary_10_3390_jcm7010007
crossref_primary_10_1517_13543784_2012_651124
crossref_primary_10_1017_S0007114520003463
crossref_primary_10_17709_2409_2231_2020_7_4_10
crossref_primary_10_2217_fon_15_333
crossref_primary_10_3390_ijms19103219
crossref_primary_10_1016_j_nano_2015_08_007
crossref_primary_10_1159_000493401
crossref_primary_10_3748_wjg_v22_i42_9378
crossref_primary_10_1177_1758835920947970
crossref_primary_10_1007_s12254_012_0001_8
crossref_primary_10_1186_s12885_016_2052_4
Cites_doi 10.1136%2Fgut.2010.216135
10.1097%2F00001813-200009000-00006
10.1007%2Fs00280-008-0839-y
10.1038%2Fsj.bjc.6602966
10.1200%2FJCO.2002.11.149
10.1200%2FJCO.2005.06.050
10.1053%2Fsonc.2002.34269
10.1200%2FJCO.2005.06.023
10.1159%2F000209962
10.1159%2F000080993
10.1002%2Fcncr.10323
10.1634%2Ftheoncologist.6-6-488
10.1200%2FJCO.2005.05.1490
10.1038%2Fsj.bjc.6603026
10.1200%2FJCO.2004.12.082
10.1002%2F1097-0142%2819810101%2947%3A1%3C207%3A%3AAID-CNCR2820470134%3E3.0.CO%3B2-6
10.1007%2Fs10637-005-1446-y
10.1038%2Fsj.bjc.6600883
10.1002%2Fbjs.1800810629
10.1093%2Fannonc%2Fmdg029
10.3322%2Fcanjclin.53.1.5
10.1093%2Fannonc%2Fmdg754
10.1038%2Fsj.bjc.6600446
10.1200%2FJCO.2006.07.0201
10.1097%2FCOC.0b013e31817be5a9
10.1002%2Fcncr.23810
10.1200%2FJCO.2007.11.8521
10.1093%2Fjnci%2F92.3.205
10.1038%2Fsj.bjc.6605374
10.1093%2Foxfordjournals.annonc.a010676
10.1159%2F000197769
ContentType Journal Article
Copyright 2011 S. Karger AG, Basel
2015 INIST-CNRS
Copyright © 2011 S. Karger AG, Basel.
Copyright (c) 2011 S. Karger AG, Basel
Copyright_xml – notice: 2011 S. Karger AG, Basel
– notice: 2015 INIST-CNRS
– notice: Copyright © 2011 S. Karger AG, Basel.
– notice: Copyright (c) 2011 S. Karger AG, Basel
DBID IQODW
CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
3V.
7RV
7T5
7TK
7TO
7X7
7XB
88E
8AO
8C1
8FD
8FI
8FJ
8FK
8G5
ABUWG
AFKRA
AZQEC
BENPR
CCPQU
DWQXO
FR3
FYUFA
GHDGH
GNUQQ
GUQSH
H94
K9-
K9.
KB0
M0R
M0S
M1P
M2O
MBDVC
NAPCQ
P64
PQEST
PQQKQ
PQUKI
PRINS
Q9U
RC3
7X8
DOI 10.1159/000329803
DatabaseName Pascal-Francis
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
CrossRef
ProQuest Central (Corporate)
Nursing & Allied Health Database
Immunology Abstracts
Neurosciences Abstracts
Oncogenes and Growth Factors Abstracts
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
ProQuest Pharma Collection
Public Health Database
Technology Research Database
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
Research Library (Alumni Edition)
ProQuest Central (Alumni Edition)
ProQuest Central UK/Ireland
ProQuest Central Essentials
ProQuest Central
ProQuest One Community College
ProQuest Central Korea
Engineering Research Database
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
Research Library Prep
AIDS and Cancer Research Abstracts
Consumer Health Database (Alumni Edition)
ProQuest Health & Medical Complete (Alumni)
Nursing & Allied Health Database (Alumni Edition)
Consumer Health Database
Health & Medical Collection (Alumni Edition)
Medical Database
Research Library
Research Library (Corporate)
Nursing & Allied Health Premium
Biotechnology and BioEngineering Abstracts
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
ProQuest Central Basic
Genetics Abstracts
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
CrossRef
Research Library Prep
ProQuest Central Student
Oncogenes and Growth Factors Abstracts
Technology Research Database
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
Research Library (Alumni Edition)
ProQuest Pharma Collection
ProQuest Family Health (Alumni Edition)
ProQuest Central China
ProQuest Central
Genetics Abstracts
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
AIDS and Cancer Research Abstracts
ProQuest Research Library
ProQuest Medical Library (Alumni)
ProQuest Public Health
ProQuest Central Basic
ProQuest Family Health
ProQuest One Academic Eastern Edition
ProQuest Nursing & Allied Health Source
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
Neurosciences Abstracts
ProQuest Hospital Collection (Alumni)
Biotechnology and BioEngineering Abstracts
Nursing & Allied Health Premium
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest One Academic UKI Edition
Immunology Abstracts
ProQuest Nursing & Allied Health Source (Alumni)
Engineering Research Database
ProQuest One Academic
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList CrossRef

Research Library Prep
MEDLINE - Academic
MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 3
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1423-0232
EndPage 306
ExternalDocumentID 2484995701
10_1159_000329803
21778770
24497456
329803
Genre Journal Article
GroupedDBID ---
-~X
.GJ
0R~
0~5
0~B
123
29N
30W
328
34G
36B
39C
3O.
3V.
4.4
53G
5RE
7RV
7X7
88E
8AO
8C1
8FI
8FJ
8G5
8UI
AAYIC
ABJNI
ABPAZ
ABUWG
ACGFS
ACPRK
ACPSR
ADAGL
AENEX
AEYAO
AFDXO
AFFNX
AFJJK
AFKRA
AHMBA
ALDHI
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AZPMC
AZQEC
BENPR
BKEYQ
BKNYI
BPHCQ
BVXVI
CAG
CCPQU
COF
CS3
CYUIP
DU5
DWQXO
E0A
EBS
EJD
EMB
EMOBN
EX3
F5P
FB.
FYUFA
GNUQQ
GUQSH
HMCUK
HZ~
IAO
IHR
IHW
IY7
K9-
L7B
M0R
M1P
M2O
N9A
NAPCQ
O1H
O9-
OHT
PQQKQ
PROAC
PSQYO
RIG
RKO
RXVBD
SJN
SV3
UDS
UJ6
UKHRP
WOW
YYQ
ZGI
ZXP
08R
AAKET
ABPTK
ABZSI
ACHQM
IQODW
CGR
CUY
CVF
ECM
EIF
ITC
NPM
AAYXX
CITATION
7T5
7TK
7TO
7XB
8FD
8FK
FR3
H94
K9.
MBDVC
P64
PQEST
PQUKI
PRINS
Q9U
RC3
7X8
ID FETCH-LOGICAL-c362t-66f0e190087d8e5982028d9b2a9a9dfd63725704370684ff6e6233e942b35ddf3
IEDL.DBID BENPR
ISSN 0030-2414
IngestDate Fri Oct 25 09:25:02 EDT 2024
Thu Oct 10 20:01:10 EDT 2024
Wed Sep 18 12:53:54 EDT 2024
Sat Sep 28 07:48:17 EDT 2024
Sun Oct 22 16:06:18 EDT 2023
Thu Aug 29 12:04:44 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 5-6
Keywords Second-line chemotherapy
Irinotecan
FOLFIRINOX
Metastatic pancreatic adenocarcinoma
Oxaliplatin
Fluorouracil
Antineoplastic agent
Calcium folinate
Metastasis
Isomerases
Cancerology
Pancreas cancer
Advanced stage
Second line treatment
Topoisomerase I inhibitor
Pancreatic disease
Platinum II Complexes
Camptothecin derivatives
Human
Enzyme
Fluoropyrimidine derivatives
Transferases
DNA topoisomerase
Enzyme inhibitor
Malignant tumor
Thymidylate synthase
Alkylating agent
Antimetabolic
Methyltransferases
Pyrimidine derivatives
Digestive diseases
Pancreas adenocarcinoma
Cancer
Language English
License Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
CC BY 4.0
Copyright © 2011 S. Karger AG, Basel.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c362t-66f0e190087d8e5982028d9b2a9a9dfd63725704370684ff6e6233e942b35ddf3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PMID 21778770
PQID 898312105
PQPubID 41203
PageCount 6
ParticipantIDs karger_primary_329803
proquest_miscellaneous_887937974
crossref_primary_10_1159_000329803
pascalfrancis_primary_24497456
proquest_journals_898312105
pubmed_primary_21778770
PublicationCentury 2000
PublicationDate 2011-01-01
PublicationDateYYYYMMDD 2011-01-01
PublicationDate_xml – month: 01
  year: 2011
  text: 2011-01-01
  day: 01
PublicationDecade 2010
PublicationPlace Basel, Switzerland
PublicationPlace_xml – name: Basel, Switzerland
– name: Basel
– name: Switzerland
PublicationTitle Oncology
PublicationTitleAlternate Oncology
PublicationYear 2011
Publisher Karger
S. Karger AG
Publisher_xml – name: Karger
– name: S. Karger AG
References Yoo C, Hwang JY, Kim J-E, Kim TW, Lee JS, Park DH, Lee SS, Seo DW, Lee SK, Kim MH, Han DJ, Kim SC, Lee JL: A randomised phase II study of modified FOLFIRI.3 vs. modified FOLFOX as second-line therapy in patients with gemcitabine-refractory advanced pancreatic cancer. Br J Cancer 2009;101:1658–1663.10.1038%2Fsj.bjc.6605374
Miller AB, Hoogstraten B, Staquet M, Winkler A: Reporting results of cancer treatment. Cancer 1981;47:207–214.745981110.1002%2F1097-0142%2819810101%2947%3A1%3C207%3A%3AAID-CNCR2820470134%3E3.0.CO%3B2-6
Novarino A, Satolli MA, Chiappino I, Giacobino A, Bellone G, Rahimi F, Milanesi E, Bertetto O, Ciuffreda L: Oxaliplatin, 5-fluorouracil, and leucovorin as second-line treatment for advanced pancreatic cancer. Am J Clin Oncol 2009;32:44–48.10.1097%2FCOC.0b013e31817be5a9
Oettle H, Arnold D, Esser M, Huhn D, Riess H: Paclitaxel as weekly second-line therapy in patients with advanced pancreatic carcinoma. Anticancer Drugs 2000;11:635–638.1108145510.1097%2F00001813-200009000-00006
Ulrich-Pur H, Raderer M, Verena Kornek G, Schüll B, Schmid K, Haider K, Kwasny W, Depisch D, Schneeweiss B, Lang F, Scheithauer W: Irinotecan plus raltitrexed vs raltitrexed alone in patients with gemcitabine-pretreated advanced pancreatic adenocarcinoma. Br J Cancer 2003;88:1180–1184.1269818110.1038%2Fsj.bjc.6600883
Conroy T, Paillot B, François E, Bugat R, Jacob JH, Stein U, Nasca S, Metges JP, Rixe O, Michel P, Magherini E, Hua A, Deplanque G: Irinotecan plus oxaliplatin and leucovorin-modulated fluorouracil in advanced pancreatic cancer – a Groupe Tumeurs Digestives of the Federation Nationale des Centres de Lutte Contre le Cancer study. J Clin Oncol 2005;23:1228–1236.1571832010.1200%2FJCO.2005.06.050
Therasse P, Arbuck SG, Eisenhauer EA, Wanders J, Kaplan RS, Rubinstein L, Verweij J, Van Glabbeke M, van Oosterom AT, Christian MC, Gwyther SG: New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada. J Natl Cancer Inst 2000;92:205–216.1065543710.1093%2Fjnci%2F92.3.205
Dahan L, Bonnetain F, Ychou M, Mitry E, Gasmi M, Raoul J-L, Cattan S, Phelip J-M, Hammel P, Chauffert B, Michel P, Legoux J-L, Rougier P, Bedenne L, Seitz J-F: Combination 5-fluorouracil, folinic acid and cisplatin (LV5FU2-CDDP) followed by gemcitabine or the reverse sequence in metastatic pancreatic cancer: final results of a randomised strategic phase III trial (FFCD 0301). Gut 2010;59:1527–1534.10.1136%2Fgut.2010.216135
Heinemann V, Quietzsch D, Gieseler F, Gonnermann M, Schönekäs H, Rost A, Neuhaus H, Haag C, Clemens M, Heinrich B, Vehling-Kaiser U, Fuchs M, Fleckenstein D, Gesierich W, Uthgenannt D, Einsele H, Holstege A, Hinke A, Schalhorn A, Wilkowski R: Randomized phase III trial of gemcitabine plus cisplatin compared with gemcitabine alone in advanced pancreatic cancer. J Clin Oncol 2006;24:3946–3952.1692104710.1200%2FJCO.2005.05.1490
Kulke MH, Blaszkowsky LS, Ryan DP, Clark JW, Meyerhardt JA, Zhu AX, Enzinger PC, Kwak EL, Muzikansky A, Lawrence C, Fuchs CS: Capecitabine plus erlotinib in gemcitabine-refractory advanced pancreatic cancer. J Clin Oncol 2007;25:4787–4792.1794772610.1200%2FJCO.2007.11.8521
Scheithauer W, Schüll B, Ulrich-Pur H, Schmid K, Raderer M, Haider K, Kwasny W, Depisch D, Schneeweiss B, Lang F, Kornek GV: Biweekly high-dose gemcitabine alone or in combination with capecitabine in patients with metastatic pancreatic adenocarcinoma: a randomised phase II trial. Ann Oncol 2003;14:97–104.1248830010.1093%2Fannonc%2Fmdg029
Heinemann V: Present and future treatment of pancreatic cancer. Semin Oncol 2002;29(suppl 9):23–31.10.1053%2Fsonc.2002.34269
Glimelius B, Hoffman K, Sjödén PO, Jacobsson G, Sellström H, Enander LK, Linné T, Svensson C: Chemotherapy improves survival and quality of life in advanced pancreatic and biliary cancer. Ann Oncol 1996;7:593–600.887937310.1093%2Foxfordjournals.annonc.a010676
Pelzer U, Stieler J, Roll L, Hilbig A, Dörken B, Riess H, Oettle H: Second-line therapy in refractory pancreatic cancer. Results of a phase II study. Onkologie 2009;32:99–102.1929524710.1159%2F000197769
Yi SY, Park YS, Kim HS, Jun HJ, Kim KH, Chang MH, Park MJ, Uhm JE, Lee J, Park SH, Park JO, Lee JK, Lee KT, Lim HY, Kang WK: Irinotecan monotherapy as second-line treatment in advanced pancreatic cancer. Cancer Chemother Pharmacol 2009;63:1141–1145.10.1007%2Fs00280-008-0839-y
Sant M, Aareleid T, Berrino F, Bielska Lasota M, Carli PM, Faivre J, Grosclaude P, Hédelin G, Matsuda T, Møller H, Möller T, Verdecchia A, Capocaccia R, Gatta G, Micheli A, Santaquilani M, Roazzi P, Lisi D, EUROCARE Working Group: EUROCARE-3: survival of cancer patients diagnosed 1990–94 – results and commentary. Ann Oncol 2003;14(suppl 5):61–118.10.1093%2Fannonc%2Fmdg754
Burris HA 3rd, Moore MJ, Andersen J, Green MR, Rothenberg ML, Modiano MR, Cripps MC, Portenoy RK, Storniolo AM, Tarassoff P, Nelson R, Dorr FA, Stephens CD, Von Hoff DD: Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trial. J Clin Oncol 1997;15:2403–2413.9196156
Jemal A, Murray T, Samuels A, Ghafoor A, Ward E, Thun MJ: Cancer statistics, 2003. CA Cancer J Clin 2003;53:5–26.1256844110.3322%2Fcanjclin.53.1.5
Demols A, Peeters M, Polus M, Marechal R, Gay F, Monsaert E, Hendlisz A, Van Laethem JL: Gemcitabine and oxaliplatin (GEMOX) in gemcitabine refractory advanced pancreatic adenocarcinoma: a phase II study. Br J Cancer 2006;94:481–485.1643498810.1038%2Fsj.bjc.6602966
Abou-Alfa GK, Letourneau R, Harker G, Modiano M, Hurwitz H, Tchekmedyian NS, Feit K, Ackerman J, De Jager RL, Eckhardt SG, O’Reilly EM: Randomized phase III study of exatecan and gemcitabine compared with gemcitabine alone in untreated advanced pancreatic cancer. J Clin Oncol 2006;24:4441–4447.1698311210.1200%2FJCO.2006.07.0201
Haller DG: Future directions in the treatment of pancreatic cancer. Semin Oncol 2002;29(suppl 20):31–39.
Fortune BE, Li X, Kosuri KV, Weatherby LM, Thomas JP, Bekaii-Saab TS: Fixed-dose-rate gemcitabine in combination with oxaliplatin in patients with metastatic pancreatic cancer refractory to standard-dose-rate gemcitabine: a single-institute study. Oncology 2009;76:333–337.1930773910.1159%2F000209962
Conroy T, Desseigne F, Ychou Y, Ducreux M, Bouche O, Gimbaud R, Becouarn Y, Montoto-Grillot C, Gourgou-Bourgade S, Adenis A: Randomized phase III trial comparing FOLFIRINOX (F: 5FU/leucovorin [LV], irinotecan [I], and oxaliplatin [O]) versus gemcitabine (G) as first-line treatment for metastatic pancreatic adenocarcinoma (MPA): preplanned interim analysis results of the PRODIGE 4/ACCORD 11 trial (abstract 4010). J Clin Oncol 2010;28:303s.
Kozuch P, Grossbard ML, Barzdins A, Araneo M, Robin A, Frager D, Homel P, Marino J, DeGregorio P, Bruckner HW: Irinotecan combined with gemcitabine, 5-fluorouracil, leucovorin, and cisplatin (G-FLIP) is an effective and noncrossresistant treatment for chemotherapy refractory metastatic pancreatic cancer. Oncologist 2001;6:488–495.1174321110.1634%2Ftheoncologist.6-6-488
Cantore M, Rabbi C, Fiorentini G, Oliani C, Zamagni D, Iacono C, Mambrini A, Del Freo A, Manni A: Combined irinotecan and oxaliplatin in patients with advanced pre-treated pancreatic cancer. Oncology 2004;67:93–97.1553991110.1159%2F000080993
Pelzer U, Kubica K, Stieler J, Schwaner I, Heil G, Gorner M, Molle M, Hilbig A, Dorken B, Riess H, Oettle H: A randomized trial in patients with gemcitabine-refractory pancreatic cancer. Final results of the CONKO 003 study (abstract). J Clin Oncol 2008;26:215s.
Xiong HQ, Varadhachary GR, Blais JC, Hess KR, Abbruzzese JL, Wolff RA: Phase 2 trial of oxaliplatin plus capecitabine (XELOX) as second-line therapy for patients with advanced pancreatic cancer. Cancer 2008;113:2046–2052.1875653210.1002%2Fcncr.23810
Palmer KR, Kerr M, Knowles G, Cull A, Carter DC, Leonard RC: Chemotherapy prolongs survival in inoperable pancreatic carcinoma. Br J Surg 1994;81:882–885.804461010.1002%2Fbjs.1800810629
Louvet C, Labianca R, Hammel P, Lledo G, Zampino MG, André T, Zaniboni A, Ducreux M, Aitini E, Taïeb J, Faroux R, Lepere C, de Gramont A, GERCOR, GISCAD: Gemcitabine in combination with oxaliplatin compared with gemcitabine alone in locally advanced or metastatic pancreatic cancer: results of a GERCOR and GISCAD phase III trial. J Clin Oncol 2005;23:3509–3516.1590866110.1200%2FJCO.2005.06.023
Gebbia V, Maiello E, Giuliani F, Borsellino N, Caruso M, Di Maggio G, Ferraù F, Bordonaro R, Verderame F, Tralongo P, Di Cristina L, Agueli R, Russo P, Colucci G: Second-line chemotherapy in advanced pancreatic carcinoma: a multicenter survey of the Gruppo Oncologico Italia Meridionale on the activity and safety of the FOLFOX4 regimen in clinical practice. Ann Oncol 2007;18(suppl 6):124–127.
Berlin JD, Catalano P, Thomas JP, Kugler JW, Haller DG, Benson AB 3rd: Phase III study of gemcitabine in combination with fluorouracil versus gemcitabine alone in patients with advanced pancreatic carcinoma: Eastern Cooperative Oncology Group trial E2297. J Clin Oncol 2002;20:3270–3275.1214930110.1200%2FJCO.2002.11.149
Rocha Lima CM, Green MR, Rotche R, Miller WH Jr, Jeffrey GM, Cisar LA, Morganti A, Orlando N, Gruia G, Miller LL: Irinotecan plus gemcitabine results in no survival advantage compared with gemcitabine monotherapy in patients with locally advanced or metastatic pancreatic cancer despite increased tumor response rate. J Clin Oncol 2004;22:3776–3783.1536507410.1200%2FJCO.2004.12.082
Tsavaris N, Kosmas C, Skopelitis H, Gouveris P, Kopterides P, Loukeris D, Sigala F, Zorbala-Sypsa A, Felekouras E, Papalambros E: Second-line treatment with oxaliplatin, leucovorin and 5-fluorouracil in gemcitabine-pretreated advanced pancreatic cancer: a phase II study. Invest New Drugs 2005;23:369–375.1601279710.1007%2Fs10637-005-1446-y
Colucci G, Giuliani F, Gebbia V, Biglietto M, Rabitti P, Uomo G, Cigolari
ref13
ref12
ref15
ref14
ref31
ref30
ref11
ref10
ref2
ref1
ref17
ref16
ref19
ref18
ref24
ref23
ref26
ref25
ref20
ref22
ref21
ref28
ref27
ref29
ref8
ref7
ref9
ref4
ref3
ref6
ref5
References_xml – ident: ref15
  doi: 10.1136%2Fgut.2010.216135
– ident: ref21
  doi: 10.1097%2F00001813-200009000-00006
– ident: ref27
  doi: 10.1007%2Fs00280-008-0839-y
– ident: ref16
  doi: 10.1038%2Fsj.bjc.6602966
– ident: ref6
  doi: 10.1200%2FJCO.2002.11.149
– ident: ref14
  doi: 10.1200%2FJCO.2005.06.050
– ident: ref5
  doi: 10.1053%2Fsonc.2002.34269
– ident: ref10
  doi: 10.1200%2FJCO.2005.06.023
– ident: ref17
  doi: 10.1159%2F000209962
– ident: ref29
  doi: 10.1159%2F000080993
– ident: ref8
  doi: 10.1002%2Fcncr.10323
– ident: ref18
  doi: 10.1634%2Ftheoncologist.6-6-488
– ident: ref9
  doi: 10.1200%2FJCO.2005.05.1490
– ident: ref23
  doi: 10.1038%2Fsj.bjc.6603026
– ident: ref11
  doi: 10.1200%2FJCO.2004.12.082
– ident: ref31
  doi: 10.1002%2F1097-0142%2819810101%2947%3A1%3C207%3A%3AAID-CNCR2820470134%3E3.0.CO%3B2-6
– ident: ref24
  doi: 10.1007%2Fs10637-005-1446-y
– ident: ref25
  doi: 10.1038%2Fsj.bjc.6600883
– ident: ref3
  doi: 10.1002%2Fbjs.1800810629
– ident: ref12
  doi: 10.1093%2Fannonc%2Fmdg029
– ident: ref1
  doi: 10.3322%2Fcanjclin.53.1.5
– ident: ref2
  doi: 10.1093%2Fannonc%2Fmdg754
– ident: ref7
  doi: 10.1038%2Fsj.bjc.6600446
– ident: ref13
  doi: 10.1200%2FJCO.2006.07.0201
– ident: ref20
  doi: 10.1097%2FCOC.0b013e31817be5a9
– ident: ref26
  doi: 10.1002%2Fcncr.23810
– ident: ref19
  doi: 10.1200%2FJCO.2007.11.8521
– ident: ref30
  doi: 10.1093%2Fjnci%2F92.3.205
– ident: ref28
  doi: 10.1038%2Fsj.bjc.6605374
– ident: ref4
  doi: 10.1093%2Foxfordjournals.annonc.a010676
– ident: ref22
  doi: 10.1159%2F000197769
SSID ssj0007546
Score 2.2907648
Snippet Background: To evaluate the efficacy and toxicity of irinotecan and oxaliplatin plus 5-fluorouracil (FU) and leucovorin (FOLFIRINOX) as second-line therapy in...
To evaluate the efficacy and toxicity of irinotecan and oxaliplatin plus 5-fluorouracil (FU) and leucovorin (FOLFIRINOX) as second-line therapy in metastatic...
BACKGROUNDTo evaluate the efficacy and toxicity of irinotecan and oxaliplatin plus 5-fluorouracil (FU) and leucovorin (FOLFIRINOX) as second-line therapy in...
SourceID proquest
crossref
pubmed
pascalfrancis
karger
SourceType Aggregation Database
Index Database
Publisher
StartPage 301
SubjectTerms Adenocarcinoma - drug therapy
Adenocarcinoma - secondary
Adenocarcinoma - surgery
Aged
Aged, 80 and over
Antimetabolites, Antineoplastic - therapeutic use
Antineoplastic Combined Chemotherapy Protocols - adverse effects
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Camptothecin - administration & dosage
Camptothecin - analogs & derivatives
Chemotherapy
Chemotherapy, Adjuvant
Clinical Study
Deoxycytidine - analogs & derivatives
Deoxycytidine - therapeutic use
Disease Progression
Drug Administration Schedule
Female
Fluorouracil - administration & dosage
Gastroenterology. Liver. Pancreas. Abdomen
Humans
Leucovorin - administration & dosage
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Male
Medical Records
Medical sciences
Metastasis
Middle Aged
Neoplasm Staging
Organoplatinum Compounds - administration & dosage
Pancreatic cancer
Pancreatic Neoplasms - drug therapy
Pancreatic Neoplasms - pathology
Pancreatic Neoplasms - surgery
Retrospective Studies
Treatment Failure
Treatment Outcome
Tumors
Title 5-Fluorouracil/Leucovorin Combined with Irinotecan and Oxaliplatin (FOLFIRINOX) as Second-Line Chemotherapy in Patients with Metastatic Pancreatic Adenocarcinoma
URI https://karger.com/doi/10.1159/000329803
https://www.ncbi.nlm.nih.gov/pubmed/21778770
https://www.proquest.com/docview/898312105
https://search.proquest.com/docview/887937974
Volume 80
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lb9QwELboFqFeEI8CobCyEAc4WM0msR2fUKkadVF3typU2lvkV6SKkmw3uwh-Dv-UmY0TxAGkKAfbsqKMPfONZ_wNIW9B408mXhpmVSZY5oxjJlEJCMRwYW2mzS7QPpuL8-vs05IvQ25OG9Iqe524U9SusXhGfpyrPEWyK_5hdcewaBQGV0MFjT2yn4CjkIzI_sez-eXVoIpluKkDK5mBqcoCtRCYcLzBkCYq74tlBYN0_yvmX68xQ1K38JOqrrrFv-HnzgwVj8jDgB_pSSfwx-Ser5-QB7MQIX9KfnFW3G6bNYzT9ub2-MJvbfMds-wobH1wg72jePZKp9CEFA26prp2dPEDAPkKE-Nq-q5YXBTTq-l8sXxPdUs_o9PsGLitniLBQLi09ZPC2MuOl7XtJp35jcYrSjcWOuoOkFp6AroNTOYavrD5pg_JdXH25fSchTIMzIJ12zAhqtgDbohz6XKPhH-ASZwyiVZaucqJVGIpvCyVscizqhIeIFXqVZaYlDtXpc_IqG5q_4JQjKIqzqW1SmQ2dkhWyI0yeayqhDsVkTe9LMpVx7ZR7rwUrspBYBE57KQ0DOnbx38JbegGBANeExcROeqlWIad2pbDuooIHXphi2HcRNe-2cKQHEkEYYqIPO9k_2fqiQSNJ-OX_536iBx0R9H4vCKjzXrrXwOW2Zgx2ZNLCe_8dDIOq_c35BXzoQ
link.rule.ids 315,783,787,12070,12237,21402,27938,27939,31733,31734,33280,33281,33758,33759,43324,43593,43819
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lb9QwELagIOCCeLQQCsVCHOBgNZvETnxCFSLahX0gaKW9RX5FqijJstlF8HP4p8zEThAHkHKKR1aUsWe-8Yy_IeQlWPzJxOWaGZkJllltmU5kAgrRXBiTKd0n2hdLMb3I3q_5OtTmdKGscrCJvaG2rcEz8tNCFimSXfE3m28Mm0ZhcjV00LhObiANF1Ln5-sx3gJn6O_pwDpm4KiyQCwEDhzvL6SJLIZWWcEd3fyC1ddbrI9UHfyi2ve2-Df47J1QeY_cDeiRnnl13yfXXPOA3FqE_PhD8ouz8mrfbkFOmcur07nbm_Y71thR2PgQBDtL8eSVzuAVEjSohqrG0tUPgOMbLItr6KtyNS9nn2bL1fo1VR39jCGzZRC0Oor0AuHK1k8Ksh89K2vnJ124ncILSpcGBhoPRw09A8sGDnMLX9h-VYfkonx3_nbKQhMGZsC37ZgQdewANcRFbguHdH-ASKzUiZJK2tqKNMdGeFmax6LI6lo4AFSpk1miU25tnR6Rg6Zt3GNCMYcqOc-NkSIzsUWqQq6lLmJZJ9zKiLwYdFFtPNdG1ccoXFajwiJy6LU0igzvT_5S2jgM-AViJi4icjxosQr7tKvGVRUROo7CBsOsiWpcuweRAikEYYqIPPK6_zP1JAd7l8dP_jv1c3J7er6YV_PZ8sMxueMPpfF5Sg522717Bqhmp0_6tfsb9bXzeA
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=5-Fluorouracil%2FLeucovorin+Combined+with+Irinotecan+and+Oxaliplatin+%28FOLFIRINOX%29+as+Second-Line+Chemotherapy+in+Patients+with+Metastatic+Pancreatic+Adenocarcinoma&rft.jtitle=Oncology&rft.au=Assaf%2C+Elias&rft.au=Verlinde-Carvalho%2C+Muriel&rft.au=Delbaldo%2C+Catherine&rft.au=Grenier%2C+Julien&rft.date=2011-01-01&rft.issn=0030-2414&rft.eissn=1423-0232&rft.volume=80&rft.issue=5-6&rft.spage=301&rft.epage=306&rft_id=info:doi/10.1159%2F000329803&rft.externalDBID=n%2Fa&rft.externalDocID=10_1159_000329803
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0030-2414&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0030-2414&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0030-2414&client=summon