Combination of irinotecan, oxaliplatin and 5-fluorouracil as a rechallenge regimen for heavily pretreated metastatic colorectal cancer patients

被引:12
|
作者
Fernandes G.D.S. [1 ]
Braghiroli M.I. [2 ,3 ]
Artioli M. [2 ]
Paterlini A.C.C.R. [2 ]
Teixeira M.C. [1 ]
Gumz B.P. [1 ]
Girardi D.M. [1 ]
Braghiroli O.F.M. [4 ]
Costa F.P. [2 ]
Hoff P.M. [2 ,3 ]
机构
[1] Hospital Sírio-Libanês, SGAS 613-conjunto E lote 95-Asa Sul, Brasília, 70200-001, DF
[2] Hospital Sírio-Libanês, São Paulo
[3] Instituto do Câncer do Estado de São Paulo, Universidade de São Paulo, São Paulo
[4] Hospital das Clinicas, Universidade de São Paulo, São Paulo
关键词
Colorectal cancer; Rechallenge; Refractory;
D O I
10.1007/s12029-017-0001-3
中图分类号
学科分类号
摘要
Purpose Our objective was to evaluate the benefit of reexposing patients with refractory metastatic colorectal cancer (mCRC) to a combination of oxaliplatin, irinotecan and 5- fluorouracil treatment. Methods We retrospectively analysed patients with mCRC who received a combination of oxaliplatin, irinotecan and fluorouracil as a rechallenge regimen after progressing on the same drugs. Both FOLFOXIRI and FOLFIRINOX were used. Toxicity was evaluated for each treatment cycle, and survival analysis was performed using the Kaplan-Meier method. Results A total of 21 patients who were treated between January 2011 and December 2013 were selected for this study. Most of the patients (95.2%) had an ECOG status of 0-1. The median age at diagnosis was 52.1 years (range 36-77 years), and 14 (66.6%) patients had wild-type KRAS. Thirteen patients received FOLFIRINOX, and eight received FOLFOXIRI. Most patients had previously received at least three regimens, with 80% receiving anti-VEGF and 66% anti-EGFR antibodies. The response rate was 38%, and 24% patients had stable disease. Themedian time to disease progression was 4.0 months (range 1.0-9.1 months), and the median overall survival duration was 8.6 months (range 6.3-11.5 months). Most patients required dose adjustment and treatment delays. One patient experienced grade 5 neutropenic sepsis. Conclusions Both FOLFIRINOX and FOLFOXIRI are active and potentially feasible rechallenge treatment options for heavily pretreated patients with good performance status. With dose reduction and close monitoring for toxicity, the risk of serious adverse events can be minimised. © Springer Science+Business Media, LLC 2017.
引用
收藏
页码:470 / 475
页数:5
相关论文
共 50 条
  • [21] Oxaliplatin (L-OHP) in combination with leucovorin (LV) and 5-fluorouracil (5FU) in pretreated metastatic colorectal cancer (CRC) patients (PTS).
    Di Stefano, A
    Calandri, C
    Benedetti, G
    Poggi, B
    Mazzoni, F
    Marrocolo, F
    Spagnuolo, P
    Rimondini, S
    Crinò, L
    ANNALS OF ONCOLOGY, 2000, 11 : 68 - 68
  • [22] A phase I/II study of arfolitixorin and 5-fluorouracil in combination with oxaliplatin (plus or minus bevacizumab) or irinotecan in metastatic colorectal cancer
    Carlsson, G.
    Koumarianou, A.
    Guren, T. K.
    Haux, J.
    Katsaounis, P.
    Kentepozidis, N.
    Pfeiffer, P.
    Braendengen, M.
    Mavroudis, D.
    Taffin, H.
    Skintemo, L.
    Tell, R.
    Papadimitriou, C.
    ESMO OPEN, 2022, 7 (05)
  • [23] Oxaliplatin with high-dose leucovorin and infusional 5-fluorouracil in irinotecan-pretreated patients with advanced colorectal cancer (ACC)
    Kouroussis, C
    Souglakos, J
    Mavroudis, D
    Papadouris, S
    Kakolyris, S
    Agelaki, S
    Kalbakis, K
    Panopoulos, C
    Vardakis, N
    Sarra, E
    Georgoulias, V
    AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2002, 25 (06): : 627 - 631
  • [24] Combination of oxaliplatin, fluorouracil, and leucovorin in the treatment of fluoropyrimidine-pretreated patients with metastatic colorectal cancer
    Lee, JH
    Lee, JH
    Kim, TW
    Lee, KH
    Kang, YK
    Lee, JS
    Kim, SH
    Kim, HC
    Yu, CS
    Kim, JC
    Kim, WK
    JOURNAL OF KOREAN MEDICAL SCIENCE, 2001, 16 (01) : 69 - 74
  • [25] Chronomodulated irinotecan, oxaliplatin, and leucovorin-modulated 5-fluorouracil as ambulatory salvage therapy in patients with irinotecan- and oxaliplatin-resistant metastatic colorectal cancer
    Gholam, Dany
    Giacchetti, Sylvie
    Brezault-Bonnet, Catherine
    Bouchahda, Mohamed
    Hauteville, Dominique
    Adam, Rene
    Ducot, Beatrice
    Ghemard, Odile
    Kustlinger, Francis
    Jasmin, Claude
    Levi, Francis
    ONCOLOGIST, 2006, 11 (10): : 1072 - 1080
  • [26] Radiosensitizing Effects of Irinotecan versus Oxaliplatin Alone and in Combination with 5-Fluorouracil on Human Colorectal Cancer Cells
    Frerker, Bernd
    Bock, Felix
    Cappel, Marie-Louise
    Kriesen, Stephan
    Klautke, Gunther
    Hildebrandt, Guido
    Manda, Katrin
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (12)
  • [27] Oxaliplatin reintroduction in patients pretreated with leucovorin, fluorouracil and oxaliplatin for metastatic colorectal cancer (MCRC).
    Maindrault-Goebel, F
    Louvet, C
    André, T
    Carola, E
    Gilles, V
    Garcia, M
    Lotz, JP
    Izrael, V
    Krulik, M
    de Gramont, A
    ANNALS OF ONCOLOGY, 2000, 11 : 50 - 50
  • [28] Combined irinotecan, oxaliplatin and 5-fluorouracil in patients with advanced colorectal cancer -: A feasibility pilot study
    Calvo, E
    Cortés, J
    González-Cao, M
    Rodríguez, J
    Aramendía, JM
    Fernández-Hidalgo, O
    Martín-Algarra, S
    Salgado, JE
    Martínez-Monge, R
    de Irala, J
    Brugarolas, A
    ONCOLOGY, 2002, 63 (03) : 254 - 265
  • [29] A Phase II study of ANGIOZYME® in combination with 5-fluorouracil, leucovorin and irinotecan in the treatment of metastatic colorectal cancer patients
    Usman, N
    Venook, A
    Hurwitz, H
    Cunningham, C
    Fuchs, C
    Burris, H
    Schwartzberg, L
    Pelley, R
    Miller, WH
    Modiano, M
    EUROPEAN JOURNAL OF CANCER, 2002, 38 : S72 - S72
  • [30] Synergistic activity of oxaliplatin and 5-fluorouracil in patients with metastatic colorectal cancer with progressive disease while on or after 5-fluorouracil
    deBraud, F
    Munzone, E
    Nole, F
    De Pas, T
    Biffi, R
    Brienza, S
    Aapro, MS
    AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1998, 21 (03): : 279 - 283