Highly durable response to capecitabine in patient with metastatic estrogen receptor positive breast cancer: A case report.


Journal

Medicine
ISSN: 1536-5964
Titre abrégé: Medicine (Baltimore)
Pays: United States
ID NLM: 2985248R

Informations de publication

Date de publication:
Sep 2019
Historique:
entrez: 14 9 2019
pubmed: 14 9 2019
medline: 1 10 2019
Statut: ppublish

Résumé

In estrogen receptor-positive HER2-negative (ER+HER2-) metastatic breast cancer, chemotherapy should be offered only to patients who develop endocrine resistance or have a rapid disease progression. However, the correct sequence of chemotherapy administration is still debated. We report the case of a 49-year-old woman with ER+ HER2- metastatic breast cancer who experienced an exceptionally long response to capecitabine administered as second-line therapy following a first-line anthracycline-based chemotherapy. The patient was diagnosed with ER+ HER2- metastatic breast cancer with massive liver involvement and mediastinal lymph nodes metastasis. This patient was treated with capecitabine 1000 mg/mq bid given intermittently for 14 days within a 21-day cycle as a second-line therapy following a rapid progression on letrozole treatment given as a maintenance therapy. Our patient experienced a progression-free survival (PFS) >3 years with an exceptionally good quality of life (QoL). In ER+HER2- metastatic breast cancer patients, capecitabine monochemotherapy in second line may be associated with a particularly satisfactory PFS and no impact in terms of QoL. Future studies focused on biomarkers with predictive ability may help select patients who represent the best candidates to this treatment.

Identifiants

pubmed: 31517852
doi: 10.1097/MD.0000000000017135
pii: 00005792-201909130-00043
pmc: PMC6750334
doi:

Substances chimiques

Antimetabolites, Antineoplastic 0
Receptors, Estrogen 0
Capecitabine 6804DJ8Z9U

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e17135

Références

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Auteurs

Giacomo Barchiesi (G)

IRCCS - Regina Elena Cancer Institute, Division of Medical Oncology 2.

Eriseld Krasniqi (E)

IRCCS - Regina Elena Cancer Institute, Division of Medical Oncology 2.

Maddalena Barba (M)

IRCCS - Regina Elena Cancer Institute, Division of Medical Oncology 2.

Marina Della Giulia (MD)

IRCCS - Regina Elena Cancer Institute, Division of Medical Oncology 2.

Laura Pizzuti (L)

IRCCS - Regina Elena Cancer Institute, Division of Medical Oncology 2.

Gioia Massimiani (G)

IRCCS - Regina Elena Cancer Institute, Division of Medical Oncology 2.

Gennaro Ciliberto (G)

IRCCS - Regina Elena Cancer Institute, Scientific Direction, Rome, Italy.

Patrizia Vici (P)

IRCCS - Regina Elena Cancer Institute, Division of Medical Oncology 2.

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Classifications MeSH