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Platinum chemotherapy for early triple-negative breast cancer.
Mason, Sofia Re; Willson, Melina L; Egger, Sam J; Beith, Jane; Dear, Rachel F; Goodwin, Annabel.
Afiliação
  • Mason SR; Garvan Institute of Medical Research, Darlinghurst, Australia; St Vincent's Clinical School, UNSW, Sydney, Australia; Chris O'Brien Lifehouse, Camperdown, Australia; Concord Cancer Centre, Concord Repatriation General Hospital, Concord, Australia. Electronic address: sofia.mason@unsw.edu.au.
  • Willson ML; Evidence Integration, NHMRC Clinical Trials Centre, The University of Sydney, Sydney, Australia.
  • Egger SJ; Cancer Research Division, Cancer Council NSW, Sydney, Australia; The Daffodil Centre, The University of Sydney, Sydney, Australia.
  • Beith J; Chris O'Brien Lifehouse, Camperdown, Australia.
  • Dear RF; Sydney Medical School, The University of Sydney, Sydney, Australia; The Kinghorn Cancer Centre, Darlinghurst, Australia.
  • Goodwin A; Chris O'Brien Lifehouse, Camperdown, Australia; Concord Cancer Centre, Concord Repatriation General Hospital, Concord, Australia; Sydney Medical School, The University of Sydney, Sydney, Australia.
Breast ; 75: 103712, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38492276
ABSTRACT

BACKGROUND:

Triple-negative breast cancer (TNBC) is an aggressive subtype of breast cancer associated with shorter survival and a higher likelihood of recurrence. In early TNBC, platinum chemotherapy has been shown to improve pathological complete response (pCR); however, its effect on long-term survival outcomes has not been fully elucidated.

METHODS:

Randomised controlled trials examining neoadjuvant or adjuvant platinum chemotherapy for early TNBC were included. Primary outcomes were disease-free survival (DFS) and overall survival (OS). Secondary outcomes were pCR, treatment adherence, grade III or IV toxicity related to chemotherapy, and quality of life.

RESULTS:

From 3972 records, we included 20 published studies. All studies reporting DFS and OS used carboplatin. Inclusion of platinum chemotherapy improved DFS (neoadjuvant hazard ratio (HR) 0.63, 95% confidence interval (CI) 0.53 to 0.75; adjuvant HR 0.69, 95% CI 0.54 to 0.88) and OS (neoadjuvant HR 0.69, 95% CI 0.55 to 0.86; adjuvant 0.70, 95% CI 0.50 to 0.96). Our analysis confirmed platinum chemotherapy increased pCR rates (risk ratio (RR) 1.44, 95% CI 1.31 to 1.59). There were no differences seen in examined subgroups. Platinum chemotherapy was associated with reduced dose intensity and increased haematological toxicity.

CONCLUSIONS:

Platinum-based chemotherapy using carboplatin in the adjuvant or neoadjuvant setting improves long-term outcomes of DFS and OS in early TNBC, with no evidence of differences by subgroup. This was at the cost of more frequent chemotherapy delays and dose reductions, and greater haematological toxicity. These findings support the use of platinum-based chemotherapy for people with early TNBC.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ensaios Clínicos Controlados Aleatórios como Assunto / Carboplatina / Terapia Neoadjuvante / Neoplasias de Mama Triplo Negativas Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Breast Assunto da revista: ENDOCRINOLOGIA / NEOPLASIAS Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ensaios Clínicos Controlados Aleatórios como Assunto / Carboplatina / Terapia Neoadjuvante / Neoplasias de Mama Triplo Negativas Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Breast Assunto da revista: ENDOCRINOLOGIA / NEOPLASIAS Ano de publicação: 2024 Tipo de documento: Article