Are There Breast Cancer Patients with Node-Negative Small Tumours, Who Do Not Benefit from Adjuvant Systemic Therapy?

Autor: Maria Blettner, Rolf Kreienberg, Catharina Bartmann, Mathias Krockenberger, Achim Wöckel, J Diessner, Sebastian Häusler, Tanja Stüber, I. Novopashenny, Manfred Wischnewsky, Roland Stein, Wolfgang Janni
Rok vydání: 2017
Předmět:
Adult
0301 basic medicine
Oncology
Cancer Research
medicine.medical_specialty
Receptor
ErbB-2

medicine.medical_treatment
Antineoplastic Agents
Breast Neoplasms
urologic and male genital diseases
Risk Assessment
digestive system
Systemic therapy
Drug Administration Schedule
Young Adult
03 medical and health sciences
0302 clinical medicine
Breast cancer
Germany
Internal medicine
medicine
Carcinoma
Humans
Aged
Neoplasm Staging
Proportional Hazards Models
Retrospective Studies
Aged
80 and over

Chemotherapy
business.industry
General Medicine
Small tumours
Middle Aged
Prognosis
medicine.disease
female genital diseases and pregnancy complications
Node negative
body regions
030104 developmental biology
Chemotherapy
Adjuvant

030220 oncology & carcinogenesis
Practice Guidelines as Topic
Female
business
Adjuvant
Tamoxifen
medicine.drug
Zdroj: Oncology. 92:317-324
ISSN: 1423-0232
0030-2414
Popis: Objective: To identify subgroups of patients with pT1 pN0 breast cancer (BC) who might not profit from adjuvant systemic therapy (AST). Methods: Data of 3,774 pT1 pN0 BC patients from 17 certified BC centres within the BRENDA study group were collected between 1992 and 2008 and retrospectively analysed. Uni- and multivariate analyses were performed using Kaplan-Meier methods and Cox regression models. Results: 279 (7.4%) of the pT1 pN0 BC patients were T1a, 944 (25.0%) were T1b and 2,551 (67.6%) were T1c. There was no significant difference (p > 0.1) in recurrence-free survival (RFS)/overall survival (OAS) between patients with pT1a, pT1b, and T1c. Patients receiving any type of AST had a better outcome compared to women without AST after adjusting for age, tumour size, and intrinsic subtypes (RFS: p < 0.001; OAS: p < 0.001). AST was the most important prognostic parameter for RFS followed by intrinsic subtypes and age. Conclusion: Patients with pT1 pN0 BC profit from AST independently of molecular subtypes, tumour size, age or comorbidity, with 5-year RFS of more than 95%. The correct definition of subgroups of patients who do not need AST is still an open question.
Databáze: OpenAIRE