Neratinib and Capecitabine for the Treatment of Leptomeningeal Metastases from HER2-Positive Breast Cancer: A Series in the Setting of a Compassionate Program.

breast cancer human epidermal growth factor receptor leptomeningeal metastases neratinib

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
25 Feb 2022
Historique:
received: 15 01 2022
revised: 15 02 2022
accepted: 24 02 2022
entrez: 10 3 2022
pubmed: 11 3 2022
medline: 11 3 2022
Statut: epublish

Résumé

Leptomeningeal metastasis is a neurological complication from HER2-positive breast cancer with a poor prognosis and limited treatment options. This study has evaluated the activity of neratinib in association with capecitabine in 10 patients with LM from HER2-positive BC after the failure of multiple lines of treatment, including trastuzumab-based therapy, within a compassionate program, and a comparison was made with a historical control group of 10 patients. Patients aged ≥ 18 years with histological diagnosis of primary HER2-positive BC, either amplified or mutated, and newly-diagnosed LM were enrolled. Coexistence of BM that has or has not received radiotherapy, as well as prior chemotherapy, hormone therapy, or monoclonal HER2-targeting antibodies or antibody-drug conjugates, were allowed, with the exclusion of lapatinib. Six-months OS was 60% with a median OS of 10 months (95% CI: 2.00-17.0). Three-month intracranial PFS was 60% with a median intracranial PFS of 4.0 months (95% CI: 2.00-6.0). The neurological benefit was observed in 70% of patients with a median duration of neurological response of 6.5 months. The best radiological response was stable disease in 60% of patients. This small series shows that the combination of neratinib and capecitabine is a safe treatment in LM from heavily pretreated HER2-positive BC with clinical efficacy in some patients and is worth investigating in a larger study.

Sections du résumé

BACKGROUND BACKGROUND
Leptomeningeal metastasis is a neurological complication from HER2-positive breast cancer with a poor prognosis and limited treatment options. This study has evaluated the activity of neratinib in association with capecitabine in 10 patients with LM from HER2-positive BC after the failure of multiple lines of treatment, including trastuzumab-based therapy, within a compassionate program, and a comparison was made with a historical control group of 10 patients.
METHODS METHODS
Patients aged ≥ 18 years with histological diagnosis of primary HER2-positive BC, either amplified or mutated, and newly-diagnosed LM were enrolled. Coexistence of BM that has or has not received radiotherapy, as well as prior chemotherapy, hormone therapy, or monoclonal HER2-targeting antibodies or antibody-drug conjugates, were allowed, with the exclusion of lapatinib.
RESULTS RESULTS
Six-months OS was 60% with a median OS of 10 months (95% CI: 2.00-17.0). Three-month intracranial PFS was 60% with a median intracranial PFS of 4.0 months (95% CI: 2.00-6.0). The neurological benefit was observed in 70% of patients with a median duration of neurological response of 6.5 months. The best radiological response was stable disease in 60% of patients.
CONCLUSIONS CONCLUSIONS
This small series shows that the combination of neratinib and capecitabine is a safe treatment in LM from heavily pretreated HER2-positive BC with clinical efficacy in some patients and is worth investigating in a larger study.

Identifiants

pubmed: 35267501
pii: cancers14051192
doi: 10.3390/cancers14051192
pmc: PMC8909342
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Alessia Pellerino (A)

Division of Neuro-Oncology, Department of Neuroscience, University and City of Health and Science Hospital, 10126 Turin, Italy.

Riccardo Soffietti (R)

Division of Neuro-Oncology, Department of Neuroscience, University and City of Health and Science Hospital, 10126 Turin, Italy.

Francesco Bruno (F)

Division of Neuro-Oncology, Department of Neuroscience, University and City of Health and Science Hospital, 10126 Turin, Italy.

Roberta Manna (R)

Department of Medical, Surgical Sciences and Advanced Technologies GF Ingrassia, University of Catania, 95131 Catania, Italy.

Erminia Muscolino (E)

Division of Neuro-Oncology, Department of Neuroscience, University and City of Health and Science Hospital, 10126 Turin, Italy.

Pierangela Botta (P)

Division of Neuro-Oncology, Department of Neuroscience, University and City of Health and Science Hospital, 10126 Turin, Italy.

Rosa Palmiero (R)

Division of Neuro-Oncology, Department of Neuroscience, University and City of Health and Science Hospital, 10126 Turin, Italy.

Roberta Rudà (R)

Department of Neurology, Castelfranco Veneto and Treviso Hospital, 31100 Treviso, Italy.

Classifications MeSH