Optimising the use of cetuximab in the continuum of care for patients with metastatic colorectal cancer

被引:46
作者
Goldberg, Richard M. [1 ]
Montagut, Clara [2 ]
Wainberg, Zev A. [3 ]
Ronga, Philippe [4 ]
Audhuy, Francois [4 ]
Taieb, Julien [5 ]
Stintzing, Sebastian [6 ]
Siena, Salvatore [7 ]
Santini, Daniele [8 ]
机构
[1] West Virginia Univ, Canc Signature Program, Canc Inst, Morgantown, WV 26506 USA
[2] Hosp Mar IMIM, Dept Med Oncol, Gastrointestinal Canc, Barcelona, Spain
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Div Hematol Oncol, Los Angeles, CA 90095 USA
[4] Merck KGaA, Global Med Affairs, Darmstadt, Germany
[5] Paris Descartes Univ, Hop Europeen Georges Pompidou, AP HP, Sorbonne Paris Cite,Dept GI Oncol, Paris, France
[6] Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Med 3, Munich, Germany
[7] Univ Milan, Niguarda Canc Ctr, Grande Osped Metropolitano Niguarda, Dept Hematol & Oncol, Milan, Italy
[8] Univ Campus Biomed, Unit Med Oncol, Rome, Italy
关键词
ANTI-EGFR THERAPY; FACTOR RECEPTOR INHIBITORS; SINGLE-AGENT PANITUMUMAB; PRIMARY TUMOR LOCATION; PLUS IRINOTECAN; 2ND-LINE TREATMENT; PHASE-III; RAS MUTATIONS; CONTAINING CHEMOTHERAPY; MONOCLONAL-ANTIBODIES;
D O I
10.1136/esmoopen-2018-000353
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The anti-epidermal growth factor receptor (EGFR) monoclonal antibody cetuximab in combination with chemotherapy is a standard of care in the first-line treatment of RAS wild-type (wt) metastatic colorectal cancer (mCRC) and has demonstrated efficacy in later lines. Progressive disease (PD) occurs when tumours develop resistance to a therapy, although controversy remains about whether PD on a combination of chemotherapy and targeted agents implies resistance to both components. Here, we propose that some patients may gain additional clinical benefit from the reuse of cetuximab after having PD on regimens including cetuximab in an earlier treatment line. We conducted a non-systematic literature search in PubMed and reviewed published and ongoing clinical trials, focusing on laterline cetuximab reuse in patients with mCRC. Evidence from multiple studies suggests that cetuximab can be an efficacious and tolerable treatment when continued or when fit patients with mCRC are retreated with it after a break from anti-EGFR therapy. Furthermore, on the basis of available preclinical and clinical evidence, we propose that longitudinal monitoring of RAS status may identify patients suitable for such a strategy. Patients who experience progression on cetuximab plus chemotherapy but have maintained RAS wt tumour status may benefit from continuation of cetuximab with a chemotherapy backbone switch because they have probably developed resistance to the chemotherapeutic agents rather than the biologic component of the regimen. Conversely, patients whose disease progresses on cetuximab-based therapy due to drug-selected clonal expansion of RAS-mutant tumour cells may regain sensitivity to cetuximab following a defined break from anti-EGFR therapy. Looking to the future, we propose that RAS status determination at disease progression by liquid, needle or excisional biopsy may identify patients eligible for cetuximab continuation and rechallenge. With this approach, treatment benefit can be extended, adding to established continuum-of-care strategies in patients with mCRC.
引用
收藏
页数:10
相关论文
共 114 条
[1]  
[Anonymous], J CLIN ONCOL S
[2]  
[Anonymous], 2012, Estimated Cancer Incidence, Mortality and Prevalence Worldwide in 2012
[3]   Trastuzumab Rechallenge After Lapatinib- and Trastuzumab-Resistant Disease Progression in HER2-Positive Breast Cancer [J].
Araki, Kazuhiro ;
Fukada, Ippei ;
Horii, Rie ;
Takahashi, Shunji ;
Akiyama, Futoshi ;
Iwase, Takuji ;
Ito, Yoshinori .
CLINICAL BREAST CANCER, 2015, 15 (06) :432-439
[4]   Emergence of Multiple EGFR Extracellular Mutations during Cetuximab Treatment in Colorectal Cancer [J].
Arena, Sabrina ;
Bellosillo, Beatriz ;
Siravegna, Giulia ;
Martinez, Alejandro ;
Canadas, Israel ;
Lazzari, Luca ;
Ferruz, Noelia ;
Russo, Mariangela ;
Misale, Sandra ;
Gonzalez, Iria ;
Iglesias, Mar ;
Gavilan, Elena ;
Corti, Giorgio ;
Hobor, Sebastijan ;
Crisafulli, Giovanni ;
Salido, Marta ;
Sanchez, Juan ;
Dalmases, Alba ;
Bellmunt, Joaquim ;
De Fabritiis, Gianni ;
Rovira, Ana ;
Di Nicolantonio, Federica ;
Albanell, Joan ;
Bardelli, Alberto ;
Montagut, Clara .
CLINICAL CANCER RESEARCH, 2015, 21 (09) :2157-2166
[5]   Prognostic and predictive value of primary tumour side in patients with RAS wild-type metastatic colorectal cancer treated with chemotherapy and EGFR directed antibodies in six randomized trials [J].
Arnold, D. ;
Lueza, B. ;
Douillard, J. -Y. ;
Peeters, M. ;
Lenz, H. -J. ;
Venook, A. ;
Heinemann, V. ;
Van Cutsem, E. ;
Pignon, J. -P. ;
Tabernero, J. ;
Cervantes, A. ;
Ciardiello, F. .
ANNALS OF ONCOLOGY, 2017, 28 (08) :1713-1729
[6]   RAS mutations concordance in circulating tumor DNA (ctDNA) and tissue in metastatic colorectal cancer (mCRC): RASANC, an AGEO prospective multicenter Study. [J].
Bachet, Jean-Baptiste ;
Bouche, Olivier ;
Taieb, Julien ;
Dubreuil, Olivier ;
Garcia, Marie-Line ;
Meurisse, Aurelia ;
Gornet, Jean-Marc ;
Artru, Pascal ;
Louafi, Samy ;
Soularue, Emilie ;
Baumgaertner, Isabelle ;
Coriat, Romain ;
Tougeron, David ;
Lecomte, Thierry ;
Mary, Florence ;
Marthey, Lysiane ;
Blons, Helene ;
Taly, Valerie ;
Bonnetain, Franck ;
Laurent-Puig, Pierre .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35
[7]   Eribulin long-term response and rechallenge: report of two clinical cases [J].
Barbieri, Elena ;
Rubino, Daniela ;
Hakim, Rossella ;
Fini, Angela ;
Lenzi, Manuela ;
Zamagni, Claudio .
FUTURE ONCOLOGY, 2017, 13 (11) :35-43
[8]  
Bennouna J, 2017, ANN ONCOL, V28, P158
[9]   Observational Cohort Study of Patients With Metastatic Colorectal Cancer Initiating Chemotherapy in Combination With Bevacizumab (CONCERT) [J].
Bennouna, Jaafar ;
Phelip, Jean-Marc ;
Andre, Thierry ;
Asselain, Bernard ;
Kone, Sebastien ;
Ducreux, Michel .
CLINICAL COLORECTAL CANCER, 2017, 16 (02) :129-+
[10]   Detection of Circulating Tumor DNA in Early- and Late-Stage Human Malignancies [J].
Bettegowda, Chetan ;
Sausen, Mark ;
Leary, Rebecca J. ;
Kinde, Isaac ;
Wang, Yuxuan ;
Agrawal, Nishant ;
Bartlett, Bjarne R. ;
Wang, Hao ;
Luber, Brandon ;
Alani, Rhoda M. ;
Antonarakis, Emmanuel S. ;
Azad, Nilofer S. ;
Bardelli, Alberto ;
Brem, Henry ;
Cameron, John L. ;
Lee, Clarence C. ;
Fecher, Leslie A. ;
Gallia, Gary L. ;
Gibbs, Peter ;
Le, Dung ;
Giuntoli, Robert L. ;
Goggins, Michael ;
Hogarty, Michael D. ;
Holdhoff, Matthias ;
Hong, Seung-Mo ;
Jiao, Yuchen ;
Juhl, Hartmut H. ;
Kim, Jenny J. ;
Siravegna, Giulia ;
Laheru, Daniel A. ;
Lauricella, Calogero ;
Lim, Michael ;
Lipson, Evan J. ;
Marie, Suely Kazue Nagahashi ;
Netto, George J. ;
Oliner, Kelly S. ;
Olivi, Alessandro ;
Olsson, Louise ;
Riggins, Gregory J. ;
Sartore-Bianchi, Andrea ;
Schmidt, Kerstin ;
Shih, Ie-Ming ;
Oba-Shinjo, Sueli Mieko ;
Siena, Salvatore ;
Theodorescu, Dan ;
Tie, Jeanne ;
Harkins, Timothy T. ;
Veronese, Silvio ;
Wang, Tian-Li ;
Weingart, Jon D. .
SCIENCE TRANSLATIONAL MEDICINE, 2014, 6 (224)