Metronomic Chemo-Endocrine Therapy (FulVEC) as a Salvage Treatment for Patients with Advanced, Treatment-Refractory ER+/HER2-Breast Cancer-A Retrospective Analysis of Consecutive Patients Data.

FulVEC breast cancer chemo-endocrine therapy metronomic chemotherapy

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
08 Feb 2023
Historique:
received: 23 12 2022
revised: 16 01 2023
accepted: 06 02 2023
entrez: 25 2 2023
pubmed: 26 2 2023
medline: 26 2 2023
Statut: epublish

Résumé

Breast cancer, with 2.3 million new cases and 0.7 million deaths every year, represents a great medical challenge worldwide. These numbers confirm that approx. 30% of BC patients will develop an incurable disease requiring life-long, palliative systemic treatment. Endocrine treatment and chemotherapy administered in a sequential fashion are the basic treatment options in advanced ER+/HER2- BC, which is the most common BC type. The palliative, long-term treatment of advanced BC should not only be highly active but also minimally toxic to allow long-term survival with the optimal quality of life. A combination of metronomic chemotherapy (MC) with endocrine treatment (ET) in patients who failed earlier lines of ET represents an interesting and promising option. The methodology includes retrospective data analyses of pretreated, metastatic ER+/HER2- BC (mBC) patients who were treated with the FulVEC regimen combining fulvestrant and MC (cyclophosphamide, vinorelbine, and capecitabine). Thirty-nine previously treated (median 2 lines 1-9) mBC patients received FulVEC. The median PFS and OS were 8.4 and 21.5 months, respectively. Biochemical responses (CA-15.3 serum marker decline ≥50%) were observed in 48.7%, and any increase in CA-15.3 was observed in 23.1% of patients. The activity of FulVEC was independent of previous treatments with fulvestrant of cytotoxic components of the FulVEC regimen. The treatment was safe and well tolerated. Metronomic chemo-endocrine therapy with FulVEC regimen represents an interesting option and compares favorably with other approaches in patients' refractory to endocrine treatments. A phase II randomized trial is warranted.

Sections du résumé

BACKGROUND BACKGROUND
Breast cancer, with 2.3 million new cases and 0.7 million deaths every year, represents a great medical challenge worldwide. These numbers confirm that approx. 30% of BC patients will develop an incurable disease requiring life-long, palliative systemic treatment. Endocrine treatment and chemotherapy administered in a sequential fashion are the basic treatment options in advanced ER+/HER2- BC, which is the most common BC type. The palliative, long-term treatment of advanced BC should not only be highly active but also minimally toxic to allow long-term survival with the optimal quality of life. A combination of metronomic chemotherapy (MC) with endocrine treatment (ET) in patients who failed earlier lines of ET represents an interesting and promising option.
METHODS METHODS
The methodology includes retrospective data analyses of pretreated, metastatic ER+/HER2- BC (mBC) patients who were treated with the FulVEC regimen combining fulvestrant and MC (cyclophosphamide, vinorelbine, and capecitabine).
RESULTS RESULTS
Thirty-nine previously treated (median 2 lines 1-9) mBC patients received FulVEC. The median PFS and OS were 8.4 and 21.5 months, respectively. Biochemical responses (CA-15.3 serum marker decline ≥50%) were observed in 48.7%, and any increase in CA-15.3 was observed in 23.1% of patients. The activity of FulVEC was independent of previous treatments with fulvestrant of cytotoxic components of the FulVEC regimen. The treatment was safe and well tolerated.
CONCLUSIONS CONCLUSIONS
Metronomic chemo-endocrine therapy with FulVEC regimen represents an interesting option and compares favorably with other approaches in patients' refractory to endocrine treatments. A phase II randomized trial is warranted.

Identifiants

pubmed: 36835886
pii: jcm12041350
doi: 10.3390/jcm12041350
pmc: PMC9958758
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Jagiellonian University - Medical College
ID : N41/DBS/000706

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Auteurs

Anna Buda-Nowak (A)

Department of Oncology, Jagiellonian University Medical College, University Hospital, 30-501 Krakow, Poland.

Łukasz Kwinta (Ł)

Department of Oncology, Jagiellonian University Medical College, University Hospital, 30-501 Krakow, Poland.
Department of Oncology, Jagiellonian University Medical College, 31-008 Krakow, Poland.

Paweł Potocki (P)

Department of Oncology, Jagiellonian University Medical College, University Hospital, 30-501 Krakow, Poland.
Department of Oncology, Jagiellonian University Medical College, 31-008 Krakow, Poland.

Anna Michałowska-Kaczmarczyk (A)

Department of Oncology, Jagiellonian University Medical College, University Hospital, 30-501 Krakow, Poland.
Department of Oncology, Jagiellonian University Medical College, 31-008 Krakow, Poland.

Agnieszka Słowik (A)

Department of Oncology, Jagiellonian University Medical College, University Hospital, 30-501 Krakow, Poland.

Kamil Konopka (K)

Department of Oncology, Jagiellonian University Medical College, University Hospital, 30-501 Krakow, Poland.
Department of Oncology, Jagiellonian University Medical College, 31-008 Krakow, Poland.

Joanna Streb (J)

Department of Oncology, Jagiellonian University Medical College, University Hospital, 30-501 Krakow, Poland.
Department of Oncology, Jagiellonian University Medical College, 31-008 Krakow, Poland.

Maciej Koniewski (M)

Institute of Sociology, Jagiellonian University, 30-962 Krakow, Poland.

Piotr J Wysocki (PJ)

Department of Oncology, Jagiellonian University Medical College, University Hospital, 30-501 Krakow, Poland.
Department of Oncology, Jagiellonian University Medical College, 31-008 Krakow, Poland.

Classifications MeSH