Complete response with fluorouracil and irinotecan with a BRAFV600E and EGFR inhibitor in BRAF-mutated metastatic colorectal cancer: a case report

被引:9
作者
Wang, Zhan [1 ]
Dai, Wei-Ping [1 ]
Zang, Yuan-Sheng [1 ]
机构
[1] Second Mil Med Univ, Changzheng Hosp, Dept Med Oncol, 415 Fengyang Rd, Shanghai 200003, Peoples R China
关键词
mCRC; BRAF(V600E) mutation; fluorouracil; vemurafenib; irinotecan; cetuximab; CHEMOTHERAPY; VEMURAFENIB; THERAPY; KRAS;
D O I
10.2147/OTT.S180845
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
Background: Patients with BRAF (v-Raf murine sarcoma viral oncogene homolog B) V600E-mutated metastatic colorectal cancer (mCRC) have a poor prognosis. The Southwest Oncology Group (SWOG) 1406 study evaluated the efficacy of vemurafenib in combination with irinotecan and cetuximab for simultaneous inhibition of epidermal growth factor receptor (EGFR) and BRAF in patients with BRAF(V600E)-mutated mCRC. Although the combination achieved higher progression-free survival (PFS) and disease control rates (DCRs), there was no complete response (CR) for the drug combination. In this case report, we report the complete recession of metastasis in a patient treated with irinotecan, cetuximab, vemurafenib, and 5-fluorouracil. Case presentation: A 44-year-old male patient with hepatitis B was diagnosed with rightsided colon adenocarcinoma. He was treated with capecitabine plus oxaliplatin as postoperative adjuvant chemotherapy for eight cycles with a disease-free survival (DFS) of 1 year before the emergence of peritoneal and pelvic metastases. BRAF(V600E) mutation was positive and chemotherapy included 12 courses of 5-fluorouracil, vemurafenib, irinotecan, and cetuximab. Complete response with recession of metastases was observed. Conclusion: The combination of fluorouracil and irinotecan with a BRAF(V600E) and EGFR inhibitor may have synergistic action, leading to recession of secondary metastases in patients with BRAF(V600E)-mutated colorectal cancer.
引用
收藏
页码:443 / 447
页数:5
相关论文
共 30 条
[1]   American Society of Clinical Oncology Provisional Clinical Opinion: Testing for KRAS Gene Mutations in Patients With Metastatic Colorectal Carcinoma to Predict Response to Anti-Epidermal Growth Factor Receptor Monoclonal Antibody Therapy [J].
Allegra, Carmen J. ;
Jessup, J. Milburn ;
Somerfield, Mark R. ;
Hamilton, Stanley R. ;
Hammond, Elizabeth H. ;
Hayes, Daniel F. ;
McAllister, Pamela K. ;
Morton, Roscoe F. ;
Schilsky, Richard L. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (12) :2091-2096
[2]  
[Anonymous], 2018, J CLIN ONCOL S
[3]   The therapeutic potential of targeting the BRAF mutation in patients with colorectal cancer [J].
Bahrami, Afsane ;
Hesari, AmirReza ;
Khazaei, Majid ;
Hassanian, Seyed Mahdi ;
Ferns, Gordon A. ;
Avan, Amir .
JOURNAL OF CELLULAR PHYSIOLOGY, 2018, 233 (03) :2162-2169
[4]   BRAFV600E: Implications for Carcinogenesis and Molecular Therapy [J].
Cantwell-Dorris, Emma R. ;
O'Leary, John J. ;
Sheils, Orla M. .
MOLECULAR CANCER THERAPEUTICS, 2011, 10 (03) :385-394
[5]   Improved Survival with Vemurafenib in Melanoma with BRAF V600E Mutation [J].
Chapman, Paul B. ;
Hauschild, Axel ;
Robert, Caroline ;
Haanen, John B. ;
Ascierto, Paolo ;
Larkin, James ;
Dummer, Reinhard ;
Garbe, Claus ;
Testori, Alessandro ;
Maio, Michele ;
Hogg, David ;
Lorigan, Paul ;
Lebbe, Celeste ;
Jouary, Thomas ;
Schadendorf, Dirk ;
Ribas, Antoni ;
O'Day, Steven J. ;
Sosman, Jeffrey A. ;
Kirkwood, John M. ;
Eggermont, Alexander M. M. ;
Dreno, Brigitte ;
Nolop, Keith ;
Li, Jiang ;
Nelson, Betty ;
Hou, Jeannie ;
Lee, Richard J. ;
Flaherty, Keith T. ;
McArthur, Grant A. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 364 (26) :2507-2516
[6]   BRAF-Mutated Colorectal Cancer: What Is the Optimal Strategy for Treatment? [J].
Cohen, Romain ;
Cervera, Pascale ;
Svrcek, Magali ;
Pellat, Anna ;
Dreyer, Chantal ;
de Gramont, Aimery ;
Andre, Thierry .
CURRENT TREATMENT OPTIONS IN ONCOLOGY, 2017, 18 (02)
[7]   Irinotecan combined with fluorouracil compared with fluorouracil alone as first-line treatment for metastatic colorectal cancer: a multicentre randomised trial [J].
Douillard, JY ;
Cunningham, D ;
Roth, AD ;
Navarro, M ;
James, RD ;
Karasek, P ;
Jandik, P ;
Iveson, T ;
Carmichael, J ;
Alakl, M ;
Gruia, G ;
Awad, L ;
Rougier, P .
LANCET, 2000, 355 (9209) :1041-1047
[8]   Attributable causes of colorectal cancer in China [J].
Gu, Meng-Jia ;
Huang, Qiu-Chi ;
Bao, Cheng-Zhen ;
Li, Ying-Jun ;
Li, Xiao-Qin ;
Ye, Ding ;
Ye, Zhen-Hua ;
Chen, Kun ;
Wang, Jian-Bing .
BMC CANCER, 2018, 18
[9]   A Review of the Evolution of Systemic Chemotherapy in the Management of Colorectal Cancer [J].
Gustavsson, Bengt ;
Carlsson, Goran ;
Machover, David ;
Petrelli, Nicholas ;
Roth, Arnaud ;
Schmoll, Hans-Joachim ;
Tveit, Kjell-Magne ;
Gibson, Fernando .
CLINICAL COLORECTAL CANCER, 2015, 14 (01) :1-10
[10]   Phase IB Study of Vemurafenib in Combination with Irinotecan and Cetuximab in Patients with Metastatic Colorectal Cancer with BRAFV600E Mutation [J].
Hong, David S. ;
Morris, Van K. ;
El Osta, Badi ;
Sorokin, Alexey V. ;
Janku, Filip ;
Fu, Siqing ;
Overman, Michael J. ;
Piha-Paul, Sarina ;
Subbiah, Vivek ;
Kee, Bryan ;
Tsimberidou, Apostolia M. ;
Fogelman, David ;
Bellido, Jorge ;
Shureiqi, Imad ;
Huang, Helen ;
Atkins, Johnique ;
Tarcic, Gabi ;
Sommer, Nicolas ;
Lanman, Richard ;
Meric-Bernstam, Funda ;
Kopetz, Scott .
CANCER DISCOVERY, 2016, 6 (12) :1352-1365