Treatment of Metastatic Colorectal Cancer: Standard of Care and Future Perspectives

被引:32
作者
Holch, Julian [1 ,2 ]
Stintzing, Sebastian [1 ]
Heinemann, Volker [1 ,2 ]
机构
[1] Ludwig Maximilians Univ LMU, Klinikum Univ Munchen, Dept Internal Med 3, Munich, Germany
[2] Ludwig Maximilians Univ LMU, Klinikum Univ Munchen, Comprehens Canc Ctr Munich, Munich, Germany
关键词
Metastatic colorectal cancer; Palliative chemotherapy; RAS mutation; BRAF mutation; BEVACIZUMAB PLUS CAPECITABINE; RANDOMIZED CONTROLLED-TRIAL; PHASE-III TRIAL; 1ST-LINE TREATMENT; OPEN-LABEL; PANITUMUMAB PLUS; 1ST PROGRESSION; BRAF MUTATION; COLON-CANCER; KRAS G13D;
D O I
10.1159/000446052
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Palliative chemotherapy for metastatic colorectal cancer has undergone substantial changes in recent years. The implementation of modern biologicals in the treatment has substantially improved overall survival up to 30 months. With the increasing number of therapeutic options, the question of optimal treatment sequence arises, which is addressed in current studies like FIRE 4 or STRATEGIC-1. Furthermore, clinical and molecular biomarkers to predict efficacy and tolerability are urgently needed. Today, the detection of activating RAS mutations is the only validated biomarker which precludes patients from anti-EGFR treatment. The detection of BRAF mutation V600E is associated with a very poor prognosis corresponding to a survival of 9-12 months. Prospective trials evaluating an optimal approach to this subgroup are still missing. First results from strategies targeting the aberrant signal transduction are promising and require further validation. Despite the advances so far, life expectancy unfortunately continues to be limited in the majority of patients with metastatic colorectal cancer. New strategies are needed to improve the prognosis. To this end, the identification of Her2/neu as a potential target and first experiences with checkpoint inhibition in patients with mismatch repair-deficient tumors are promising and also require further validation. (C) 2016 S. Karger GmbH, Freiburg
引用
收藏
页码:178 / 183
页数:6
相关论文
共 48 条
[1]
[Anonymous], J CLIN ONCOL S
[2]
[Anonymous], J CLIN ONCOL S3
[3]
[Anonymous], ANN ONCOL S4
[4]
Maintenance strategy with fluoropyrimidines (FP) plus Bevacizumab (Bev), Bev alone, or no treatment, following a standard combination of FP, oxaliplatin (Ox), and Bev as first-line treatment for patients with metastatic colorectal cancer (mCRC): A phase III non-inferiority trial (AIO KRK 0207). [J].
Arnold, Dirk ;
Graeven, Ullrich ;
Lerchenmuller, Christian A. ;
Killing, Brigitta ;
Depenbusch, Reinhard ;
Steffens, Claus-Christoph ;
Al-Batran, Salah-Eddin ;
Lange, Thoralf ;
Dietrich, Georg ;
Stoehimacher, Jan ;
Tannapfel, Andrea ;
Schmoll, Hans-Joachim ;
Reinacher-Schick, Anke ;
Hegewisch-Becker, Susanna .
JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (15)
[5]
Continuation of bevacizumab after first progression in metastatic colorectal cancer (ML18147): a randomised phase 3 trial [J].
Bennouna, Jaafar ;
Sastre, Javier ;
Arnold, Dirk ;
Osterlund, Pia ;
Greil, Richard ;
Van Cutsem, Eric ;
von Moos, Roger ;
Maria Vieitez, Jose ;
Bouche, Olivier ;
Borg, Christophe ;
Steffens, Claus-Christoph ;
Alonso-Orduna, Vicente ;
Schlichting, Christoph ;
Reyes-Rivera, Irmarie ;
Bendahmane, Belguendouz ;
Andre, Thierry ;
Kubicka, Stefan .
LANCET ONCOLOGY, 2013, 14 (01) :29-37
[6]
Efficacy according to biomarker status of cetuximab plus FOLFOX-4 as first-line treatment for metastatic colorectal cancer: the OPUS study [J].
Bokemeyer, C. ;
Bondarenko, I. ;
Hartmann, J. T. ;
de Braud, F. ;
Schuch, G. ;
Zubel, A. ;
Celik, I. ;
Schlichting, M. ;
Koralewski, P. .
ANNALS OF ONCOLOGY, 2011, 22 (07) :1535-1546
[7]
BRUCKNER HW, 1991, SEMIN ONCOL, V18, P443
[8]
STRATEGIC-1: A multiple-lines, randomized, open-label GERCOR phase III study in patients with unresectable wild-type RAS metastatic colorectal cancer [J].
Chibaudel, Benoist ;
Bonnetain, Franck ;
Tournigand, Christophe ;
de Larauze, Marine Hug ;
de Gramont, Armand ;
Laurent-Puig, Pierre ;
Paget, Jerome ;
Hadengue, Alexandra ;
Notelet, Dominique ;
Benetkiewicz, Magdalena ;
Andre, Thierry ;
de Gramont, Aimery .
BMC CANCER, 2015, 15
[9]
FOLFOXIRI plus bevacizumab versus FOLFIRI plus bevacizumab as first-line treatment of patients with metastatic colorectal cancer: updated overall survival and molecular subgroup analyses of the open-label, phase 3 TRIBE study [J].
Cremolini, Chiara ;
Loupakis, Fotios ;
Antoniotti, Carlotta ;
Lupi, Cristiana ;
Sensi, Elisa ;
Lonardi, Sara ;
Mezi, Silvia ;
Tomasello, Gianluca ;
Ronzoni, Monica ;
Zaniboni, Alberto ;
Tonini, Giuseppe ;
Carlomagno, Chiara ;
Allegrini, Giacomo ;
Chiara, Silvana ;
D'Amico, Mauro ;
Granetto, Cristina ;
Cazzaniga, Marina ;
Boni, Luca ;
Fontanini, Gabriella ;
Falcone, Alfredo .
LANCET ONCOLOGY, 2015, 16 (13) :1306-1315
[10]
Bevacizumab plus capecitabine versus capecitabine alone in elderly patients with previously untreated metastatic colorectal cancer (AVEX): an open-label, randomised phase 3 trial [J].
Cunningham, David ;
Lang, Istvan ;
Marcuello, Eugenio ;
Lorusso, Vito ;
Ocvirk, Janja ;
Shin, Dong Bok ;
Jonker, Derek ;
Osborne, Stuart ;
Andre, Niko ;
Waterkamp, Daniel ;
Saunders, Mark P. .
LANCET ONCOLOGY, 2013, 14 (11) :1077-1085