TY - JOUR
T1 - The clinical use of circulating tumor cells (CTCs) enumeration for staging of metastatic breast cancer (MBC)
T2 - International expert consensus paper
AU - Cristofanilli, Massimo
AU - Pierga, Jean Yves
AU - Reuben, James
AU - Rademaker, Alfred
AU - Davis, Andrew A.
AU - Peeters, Dieter J.
AU - Fehm, Tanja
AU - Nolé, Franco
AU - Gisbert-Criado, Rafael
AU - Mavroudis, Dimitrios
AU - Grisanti, Salvatore
AU - Giuliano, Mario
AU - Garcia-Saenz, Jose A.
AU - Stebbing, Justin
AU - Caldas, Carlos
AU - Gazzaniga, Paola
AU - Manso, Luis
AU - Zamarchi, Rita
AU - de Lascoiti, Angela Fernandez
AU - De Mattos-Arruda, Leticia
AU - Ignatiadis, Michail
AU - Cabel, Luc
AU - van Laere, Steven J.
AU - Meier-Stiegen, Franziska
AU - Sandri, Maria Teresa
AU - Vidal-Martinez, Jose
AU - Politaki, Eleni
AU - Consoli, Francesca
AU - Generali, Daniele
AU - Cappelletti, Maria Rosa
AU - Diaz-Rubio, Eduardo
AU - Krell, Jonathan
AU - Dawson, Sarah Jane
AU - Raimondi, Cristina
AU - Rutten, Annemie
AU - Janni, Wolfgang
AU - Munzone, Elisabetta
AU - Carañana, Vicente
AU - Agelaki, Sofia
AU - Almici, Camillo
AU - Dirix, Luc
AU - Solomayer, Erich Franz
AU - Zorzino, Laura
AU - Darrigues, Lauren
AU - Reis-Filho, Jorge S.
AU - Gerratana, Lorenzo
AU - Michiels, Stefan
AU - Bidard, François Clément
AU - Pantel, Klaus
N1 - Publisher Copyright:
© 2018
PY - 2019/2/1
Y1 - 2019/2/1
N2 - Background: The heterogeneity of metastatic breast cancer (MBC) necessitates novel biomarkers allowing stratification of patients for treatment selection and drug development. We propose to use the prognostic utility of circulating tumor cells (CTCs) for stratification of patients with stage IV disease. Methods: In a retrospective, pooled analysis of individual patient data from 18 cohorts, including 2436 MBC patients, a CTC threshold of 5 cells per 7.5 ml was used for stratification based on molecular subtypes, disease location, and prior treatments. Patients with ≥ 5 CTCs were classified as Stage IV aggressive , those with < 5 CTCs as Stage IV indolent. Survival was analyzed using Kaplan-Meier curves and the log rank test. Results: For all patients, Stage IV indolent patients had longer median overall survival than those with Stage IV aggressive (36.3 months vs. 16.0 months, P < 0.0001) and similarly for de novo MBC patients (41.4 months Stage IV indolent vs. 18.7 months Stage IV aggressive , p < 0.0001). Moreover, patients with Stage IV indolent disease had significantly longer overall survival across all disease subtypes compared to the aggressive cohort: hormone receptor-positive (44 months vs. 17.3 months, P < 0.0001), HER2-positive (36.7 months vs. 20.4 months, P < 0.0001), and triple negative (23.8 months vs. 9.0 months, P < 0.0001). Similar results were obtained regardless of prior treatment or disease location. Conclusions: We confirm the identification of two subgroups of MBC, Stage IV indolent and Stage IV aggressive , independent of clinical and molecular variables. Thus, CTC count should be considered an important tool for staging of advanced disease and for disease stratification in prospective clinical trials.
AB - Background: The heterogeneity of metastatic breast cancer (MBC) necessitates novel biomarkers allowing stratification of patients for treatment selection and drug development. We propose to use the prognostic utility of circulating tumor cells (CTCs) for stratification of patients with stage IV disease. Methods: In a retrospective, pooled analysis of individual patient data from 18 cohorts, including 2436 MBC patients, a CTC threshold of 5 cells per 7.5 ml was used for stratification based on molecular subtypes, disease location, and prior treatments. Patients with ≥ 5 CTCs were classified as Stage IV aggressive , those with < 5 CTCs as Stage IV indolent. Survival was analyzed using Kaplan-Meier curves and the log rank test. Results: For all patients, Stage IV indolent patients had longer median overall survival than those with Stage IV aggressive (36.3 months vs. 16.0 months, P < 0.0001) and similarly for de novo MBC patients (41.4 months Stage IV indolent vs. 18.7 months Stage IV aggressive , p < 0.0001). Moreover, patients with Stage IV indolent disease had significantly longer overall survival across all disease subtypes compared to the aggressive cohort: hormone receptor-positive (44 months vs. 17.3 months, P < 0.0001), HER2-positive (36.7 months vs. 20.4 months, P < 0.0001), and triple negative (23.8 months vs. 9.0 months, P < 0.0001). Similar results were obtained regardless of prior treatment or disease location. Conclusions: We confirm the identification of two subgroups of MBC, Stage IV indolent and Stage IV aggressive , independent of clinical and molecular variables. Thus, CTC count should be considered an important tool for staging of advanced disease and for disease stratification in prospective clinical trials.
KW - Biomarker
KW - CTCs
KW - Circulating tumor cells
KW - MBC
KW - Metastatic breast cancer
KW - Survival
UR - http://www.scopus.com/inward/record.url?scp=85059001216&partnerID=8YFLogxK
U2 - 10.1016/j.critrevonc.2018.12.004
DO - 10.1016/j.critrevonc.2018.12.004
M3 - Review article
C2 - 30771872
AN - SCOPUS:85059001216
SN - 1040-8428
VL - 134
SP - 39
EP - 45
JO - Critical Reviews in Oncology/Hematology
JF - Critical Reviews in Oncology/Hematology
ER -