FOLFIRI and regorafenib combination therapy with dose escalation of irinotecan as fourth-line treatment for patients with metastatic colon cancer according to UGT1A1 genotyping

被引:16
作者
Lu, Chien-Yu [1 ,2 ]
Yeh, Yung-Sung [3 ,4 ,5 ]
Huang, Ching-Wen [5 ,6 ]
Ma, Cheng-Jen [4 ,5 ]
Yu, Fang-Jung [1 ,2 ]
Wang, Jaw-Yuan [4 ,5 ,6 ,7 ,8 ,9 ,10 ]
机构
[1] Kaohsiung Med Univ, Fac Med, Coll Med, Dept Internal Med,Div Gastroenterol, Kaohsiung 807, Taiwan
[2] Kaohsiung Med Univ, Fac Med, Coll Med, Dept Internal Med, Kaohsiung 807, Taiwan
[3] Kaohsiung Med Univ, Kaohsiung Municipal Hsiao Kang Hosp, Dept Emergency Med, Kaohsiung 807, Taiwan
[4] Kaohsiung Med Univ, Coll Med, Grad Inst Clin Med, Kaohsiung 807, Taiwan
[5] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Dept Surg, Div Gastroenterol & Gen Surg, Kaohsiung 807, Taiwan
[6] Kaohsiung Med Univ, Coll Med, Grad Inst Med, Kaohsiung 807, Taiwan
[7] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Ctr Canc, Kaohsiung 807, Taiwan
[8] Kaohsiung Med Univ, Coll Med, Dept Genom Med, Kaohsiung 807, Taiwan
[9] Kaohsiung Med Univ, Coll Med, Dept Surg, Kaohsiung 807, Taiwan
[10] Kaohsiung Med Univ, Ctr Biomarkers & Biotech Drugs, Kaohsiung 807, Taiwan
关键词
UGT1A1; irinotecan; dose escalation; metastatic colon cancer; regorafenib; ADVANCED COLORECTAL-CANCER; 1ST-LINE TREATMENT; 2ND-LINE TREATMENT; BEVACIZUMAB; MULTICENTER; METABOLISM; CPT-11; TRIAL; 1A1;
D O I
10.2147/OTT.S69774
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Here we report a case of metastatic colon cancer treated with 5-fluorouracil, leucovorin, and escalated doses of irinotecan (FOLFIRI) combined with regorafenib in the fourth-line setting after uridine diphosphate glucuronosyltransferase (UGT)1A1 genotyping analysis. A 66-year-old male was initially diagnosed with Union Internationale Contre le Cancer stage III descending colon cancer and underwent curative surgery. He received postoperative adjuvant chemotherapy; however, liver metastasis developed and a partial hepatectomy was performed thereafter. Unfortunately, pulmonary metastases and recurrent liver tumors were found despite a series of systemic treatments with multiple combinations of cytotoxic and biologic agents. Recently, a novel multikinase inhibitor, regorafenib, was approved for the treatment of metastatic colorectal cancer refractory to other therapeutic modalities. As further treatment, we combined regorafenib with FOLFIRI, which included dose escalations of irinotecan, after UGT1A1 genotyping analysis. The therapeutic results were promising, with the improvement in liver and pulmonary metastases being classified as stable disease and partial response, respectively. Moreover, the progression-free survival was over 6 months. FOLFIRI, with dose escalation of irinotecan according to UGT1A1 genotyping plus regorafenib appears to be a promising salvage therapy for patients with refractory metastatic colorectal cancer.
引用
收藏
页码:2143 / 2146
页数:4
相关论文
共 17 条
[1]   New Developments in the Second-Line Treatment of Metastatic Colorectal Cancer: Potential Place in Therapy [J].
Arnold, Dirk ;
Stein, Alexander .
DRUGS, 2013, 73 (09) :883-891
[2]   Regorafenib: A Novel Multitargeted Tyrosine Kinase Inhibitor for Colorectal Cancer and Gastrointestinal Stromal Tumors [J].
Crona, Daniel J. ;
Keisler, Meredith D. ;
Walko, Christine M. .
ANNALS OF PHARMACOTHERAPY, 2013, 47 (12) :1685-1696
[3]   Prevention and management of adverse events related to regorafenib [J].
De Wit, Mieke ;
Boers-Doets, Christine B. ;
Saettini, Alessandra ;
Vermeersch, Kristina ;
Roncero de Juan, Carmen ;
Ouwerkerk, Jan ;
Raynard, See-See ;
Bazin, Ashley ;
Cremolini, Chiara .
SUPPORTIVE CARE IN CANCER, 2014, 22 (03) :837-846
[4]   Regorafenib monotherapy for previously treated metastatic colorectal cancer (CORRECT): an international, multicentre, randomised, placebo-controlled, phase 3 trial [J].
Grothey, Axel ;
Van Cutsem, Eric ;
Sobrero, Alberto ;
Siena, Salvatore ;
Falcone, Alfredo ;
Ychou, Marc ;
Humblet, Yves ;
Bouche, Olivier ;
Mineur, Laurent ;
Barone, Carlo ;
Adenis, Antoine ;
Tabernero, Josep ;
Yoshino, Takayuki ;
Lenz, Heinz-Josef ;
Goldberg, Richard M. ;
Sargent, Daniel J. ;
Cihon, Frank ;
Cupit, Lisa ;
Wagner, Andrea ;
Laurent, Dirk .
LANCET, 2013, 381 (9863) :303-312
[5]   Current place of high-dose irinotecan chemotherapy in patients with metastatic colorectal cancer [J].
Hebbar, Mohamed ;
Ychou, Marc ;
Ducreux, Michel .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2009, 135 (06) :749-752
[6]   Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer [J].
Hurwitz, H ;
Fehrenbacher, L ;
Novotny, W ;
Cartwright, T ;
Hainsworth, J ;
Heim, W ;
Berlin, J ;
Baron, A ;
Griffing, S ;
Holmgren, E ;
Ferrara, N ;
Fyfe, G ;
Rogers, B ;
Ross, R ;
Kabbinavar, F .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (23) :2335-2342
[7]   Genetic predisposition to the metabolism of irinotecan (CPT-11) - Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes [J].
Iyer, L ;
King, CD ;
Whitington, PF ;
Green, MD ;
Roy, SK ;
Tephly, TR ;
Coffman, BL ;
Ratain, MJ .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (04) :847-854
[8]   Prognostic advantage of irinotecan dose escalation according to uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) genotyping in patients with metastatic colorectal cancer treated with bevacizumab combined with 5-fluorouracil/leucovorin with irinotecan in a first-line setting [J].
Lu, Chien-Yu ;
Huang, Ching-Wen ;
Hu, Huang-Ming ;
Tsai, Hsiang-Lin ;
Huang, Chun-Ming ;
Yu, Fang-Jung ;
Huang, Ming-Yii ;
Chang, Se-Fen ;
Huang, Meng-Lin ;
Wang, Jaw-Yuan .
TRANSLATIONAL RESEARCH, 2014, 164 (02) :169-176
[9]   A genotype-directed phase I-IV dose-finding study of irinotecan in combination with fluorouracil/leucovorin as first-line treatment in advanced colorectal cancer [J].
Marcuello, E. ;
Paez, D. ;
Pare, L. ;
Salazar, J. ;
Sebio, A. ;
del Rio, E. ;
Baiget, M. .
BRITISH JOURNAL OF CANCER, 2011, 105 (01) :53-57
[10]  
Mathijssen RHJ, 2001, CLIN CANCER RES, V7, P2182