Efficacy of adjuvant trastuzumab in women with HER2-positive T1a or bN0M0 breast cancer: a population-based cohort study.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
20 01 2022
Historique:
received: 04 06 2021
accepted: 03 01 2022
entrez: 21 1 2022
pubmed: 22 1 2022
medline: 3 3 2022
Statut: epublish

Résumé

Adjuvant trastuzumab has been associated with superior survival in women with ≥ T1c or node-positive HER2-positive early-stage breast cancer; however, there is a lack of phase III trials in women with T1a/bN0 disease. Our study aimed to assess the outcomes of women with HER2-positive T1a/bN0 breast cancer who received adjuvant trastuzumab in Saskatchewan, Canada. We evaluated all women diagnosed with HER2-positive T1a/bN0 breast cancer in Saskatchewan between 2008 and 2017. We performed Cox proportional multivariable analysis to determine factors correlated with survival. In addition, inverse probability treatment weighting (IPTW) using propensity score was performed to assess benefit of adjuvant trastuzumab. Ninety-one eligible women with a median age of 61 years (range 30-89) were identified. Thirty-nine (43%) women received adjuvant trastuzumab. Women who received trastuzumab were younger and had a higher rate of T1b disease. Overall, 3% of women who received trastuzumab compared to 12% of women who did not receive trastuzumab developed breast cancer recurrence (p = 0.23). Five-year disease-free survival (DFS) of women who received adjuvant trastuzumab was 94.8% compared to 82.7% of women who did not receive trastuzumab (p = 0.22). Five-year overall survival was 100% of women who received trastuzumab compared to 90.4% of women who did not receive adjuvant trastuzumab (p = 0.038). In the multivariable analysis, grade III tumors were correlated with inferior DFS (hazard ratio [HR] 5.5, 95% CI [1.7-17.7]). The propensity score using the inverse probability of treatment weighting showed that lack of adjuvant trastuzumab was correlated inferior DFS, with an HR of 4 (95% CI 1.05-15.5). Women with HER2-positive T1a/bN0 breast cancer had overall low recurrence of breast cancer. However, the results of this exploratory analysis indicate that women who received adjuvant trastuzumab had better survival.

Identifiants

pubmed: 35058536
doi: 10.1038/s41598-022-05209-8
pii: 10.1038/s41598-022-05209-8
pmc: PMC8776836
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1
Trastuzumab P188ANX8CK

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1068

Informations de copyright

© 2022. The Author(s).

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Auteurs

Sanji Ali (S)

College of Medicine, University of Saskatchewan, Saskatoon, Canada.

Jace Hendry (J)

College of Medicine, University of Saskatchewan, Saskatoon, Canada.

Duc Le (D)

College of Medicine, University of Saskatchewan, Saskatoon, Canada.
Saskatoon Cancer Center, Saskatchewan Cancer Agency, University of Saskatchewan, 20 Campus Drive, Saskatoon, SK, S7N4H4, Canada.

Prosanta K Mondal (PK)

Clinical Research Support Unit, University of Saskatchewan, Saskatoon, Canada.

Amer Sami (A)

College of Medicine, University of Saskatchewan, Saskatoon, Canada.
Saskatoon Cancer Center, Saskatchewan Cancer Agency, University of Saskatchewan, 20 Campus Drive, Saskatoon, SK, S7N4H4, Canada.

Haji Chalchal (H)

College of Medicine, University of Saskatchewan, Saskatoon, Canada.
Allan Blair Cancer Center, Saskatchewan Cancer Agency, Saskatoon, Canada.

Kamal Haider (K)

College of Medicine, University of Saskatchewan, Saskatoon, Canada.
Saskatoon Cancer Center, Saskatchewan Cancer Agency, University of Saskatchewan, 20 Campus Drive, Saskatoon, SK, S7N4H4, Canada.

Osama Ahmed (O)

College of Medicine, University of Saskatchewan, Saskatoon, Canada.
Saskatoon Cancer Center, Saskatchewan Cancer Agency, University of Saskatchewan, 20 Campus Drive, Saskatoon, SK, S7N4H4, Canada.

Ali El-Gayed (A)

College of Medicine, University of Saskatchewan, Saskatoon, Canada.
Saskatoon Cancer Center, Saskatchewan Cancer Agency, University of Saskatchewan, 20 Campus Drive, Saskatoon, SK, S7N4H4, Canada.

Philip Wright (P)

College of Medicine, University of Saskatchewan, Saskatoon, Canada.
Saskatoon Cancer Center, Saskatchewan Cancer Agency, University of Saskatchewan, 20 Campus Drive, Saskatoon, SK, S7N4H4, Canada.

Mehrnoosh Pauls (M)

College of Medicine, University of Saskatchewan, Saskatoon, Canada.
Saskatoon Cancer Center, Saskatchewan Cancer Agency, University of Saskatchewan, 20 Campus Drive, Saskatoon, SK, S7N4H4, Canada.

Kate Johnson (K)

College of Medicine, University of Saskatchewan, Saskatoon, Canada.
Saskatoon Cancer Center, Saskatchewan Cancer Agency, University of Saskatchewan, 20 Campus Drive, Saskatoon, SK, S7N4H4, Canada.

Shahid Ahmed (S)

College of Medicine, University of Saskatchewan, Saskatoon, Canada. shahid.ahmed@saskcancer.ca.
Saskatoon Cancer Center, Saskatchewan Cancer Agency, University of Saskatchewan, 20 Campus Drive, Saskatoon, SK, S7N4H4, Canada. shahid.ahmed@saskcancer.ca.

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