TY - JOUR
T1 - Real-world clinical and survival outcomes of patients with early relapsed triple-negative breast cancer from the ESME national cohort
AU - Grinda, Thomas
AU - Antoine, Alison
AU - Jacot, William
AU - Cottu, Paul Henri
AU - de la Motte Rouge, Thibault
AU - Frenel, Jean Sébastien
AU - Mailliez, Audrey
AU - Dalenc, Florence
AU - Goncalves, Anthony
AU - Clatot, Florian
AU - Mouret Reynier, Marie Ange
AU - Levy, Christelle
AU - Ferrero, Jean Marc
AU - Desmoulins, Isabelle
AU - Uwer, Lionel
AU - Petit, Thierry
AU - Jouannaud, Christelle
AU - Arnedos, Monica
AU - Chevrot, Michaël
AU - Courtinard, Coralie
AU - Tredan, Olivier
AU - Brain, Etienne
AU - Pérol, David
AU - Pistilli, Barbara
AU - Delaloge, Suzette
N1 - Publisher Copyright:
© 2023 Elsevier Ltd
PY - 2023/8/1
Y1 - 2023/8/1
N2 - Background: Early metastatic relapse of triple-negative breast cancer (mTNBC) after anthracyclins and/or taxanes based (A/T) primary treatment represents a highly aggressive cancer situation requiring urgent characterisation and handling. Epidemio-Strategy-Medico-Economical-Metastatic Breast Cancer (ESME-MBC) database, a multicenter, national, observational cohort (NCT03275311) provides recent data on this entity. Methods: All ESME patients diagnosed between 2008 and 2020 with mTNBC occurring as a relapse after a systemic neoadjuvant/adjuvant taxane and/or anthracycline-based chemotherapy were included. Early relapses were defined by a metastatic diagnosis up to 12 months of the end of neo/adjuvant A/T chemotherapy. We assessed overall survival (OS) and progression-free-survival under first-line treatment (PFS1) by early versus late relapse (≥12 months). Results: Patients with early relapse (N = 881, 46%) were younger and had a larger tumour burden at primary diagnosis than those with late relapses (N = 1045). Early relapse rates appeared stable over time. Median OS was 10.1 months (95% CI 9.3–10.9) in patients with early relapse versus 17.1 months (95% CI 15.7–18.2) in those with late relapse (adjusted hazard-ratio (aHR): 1.92 (95% CI 1.73–2.13); p < 0.001). The median PFS1 was respectively 3.1 months (95% CI 2.9–3.4) and 5.3 months (95% CI 5.1–5.8); (aHR: 1.66; [95% CI 1.50–1.83]; p < 0.001). Among early relapsed patients, a higher number of metastatic sites, visceral disease but not treatment types, were independently associated with a poorer OS. Conclusion: These real-world data provide strong evidence on the dismal prognosis, higher treatment resistance and major unmet medical need associated with early relapsed mTNBC. Database registration: clinicaltrials.gov
AB - Background: Early metastatic relapse of triple-negative breast cancer (mTNBC) after anthracyclins and/or taxanes based (A/T) primary treatment represents a highly aggressive cancer situation requiring urgent characterisation and handling. Epidemio-Strategy-Medico-Economical-Metastatic Breast Cancer (ESME-MBC) database, a multicenter, national, observational cohort (NCT03275311) provides recent data on this entity. Methods: All ESME patients diagnosed between 2008 and 2020 with mTNBC occurring as a relapse after a systemic neoadjuvant/adjuvant taxane and/or anthracycline-based chemotherapy were included. Early relapses were defined by a metastatic diagnosis up to 12 months of the end of neo/adjuvant A/T chemotherapy. We assessed overall survival (OS) and progression-free-survival under first-line treatment (PFS1) by early versus late relapse (≥12 months). Results: Patients with early relapse (N = 881, 46%) were younger and had a larger tumour burden at primary diagnosis than those with late relapses (N = 1045). Early relapse rates appeared stable over time. Median OS was 10.1 months (95% CI 9.3–10.9) in patients with early relapse versus 17.1 months (95% CI 15.7–18.2) in those with late relapse (adjusted hazard-ratio (aHR): 1.92 (95% CI 1.73–2.13); p < 0.001). The median PFS1 was respectively 3.1 months (95% CI 2.9–3.4) and 5.3 months (95% CI 5.1–5.8); (aHR: 1.66; [95% CI 1.50–1.83]; p < 0.001). Among early relapsed patients, a higher number of metastatic sites, visceral disease but not treatment types, were independently associated with a poorer OS. Conclusion: These real-world data provide strong evidence on the dismal prognosis, higher treatment resistance and major unmet medical need associated with early relapsed mTNBC. Database registration: clinicaltrials.gov
KW - Breast cancer
KW - ESME cohort
KW - Overall survival
KW - Real-world data
KW - Triple-negative breast cancer
UR - http://www.scopus.com/inward/record.url?scp=85162758963&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2023.05.023
DO - 10.1016/j.ejca.2023.05.023
M3 - Article
AN - SCOPUS:85162758963
SN - 0959-8049
VL - 189
JO - European Journal of Cancer
JF - European Journal of Cancer
M1 - 112935
ER -