Validation of Residual Cancer Burden as Prognostic Factor for Breast Cancer Patients After Neoadjuvant Therapy.


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
Dec 2019
Historique:
received: 01 06 2019
pubmed: 28 8 2019
medline: 18 4 2020
entrez: 28 8 2019
Statut: ppublish

Résumé

Assessing the residual cancer burden (RCB) predictive performance, the potential subgroup effects, and time-dependent impact on breast cancer patients who underwent neoadjuvant therapy in a developer's independent cohort is essential for its usage in clinical routine. Between 2011 and 2016, the RCB scores of 184 female breast cancer patients were prospectively collected, and subsequent clinicopathological and follow-up data were obtained retrospectively. Recurrence-free survival (RFS), overall survival (OS), as well as subgroup analysis, and time-dependent variables were calculated with multivariate, complex, or linear statistical models. A total of 184 patients (HER2 33%, TNBC 27%), with a mean follow-up time of 4 years, treated with neoadjuvant systemic therapy (92% anthracycline-taxane based) were analyzed revealing 43 events (38 recurrences, 28 deaths). High RCB scores were associated with recurrence (median index: 2.34 vs. 1.39 points, rank-sum p < 0.0001), decreased RFS (hazard ratio [HR] = 1.80, 95% confidence interval [CI] 1.44-2.24, p < 0.0001) and reduced OS (HR 1.96, 95% CI 1.49-2.59, p < 0.0001). The RCB score showed proportionality of hazards (interaction HR with linear follow-up time = 1.00, p = 0.896) and good discriminating power (Harrell's c index 0.7). Our results confirm the RCB score as externally valid prognostic marker and being independent of molecular subtype for RFS and OS in a clinical setting.

Sections du résumé

BACKGROUND BACKGROUND
Assessing the residual cancer burden (RCB) predictive performance, the potential subgroup effects, and time-dependent impact on breast cancer patients who underwent neoadjuvant therapy in a developer's independent cohort is essential for its usage in clinical routine.
METHODS METHODS
Between 2011 and 2016, the RCB scores of 184 female breast cancer patients were prospectively collected, and subsequent clinicopathological and follow-up data were obtained retrospectively. Recurrence-free survival (RFS), overall survival (OS), as well as subgroup analysis, and time-dependent variables were calculated with multivariate, complex, or linear statistical models.
RESULTS RESULTS
A total of 184 patients (HER2 33%, TNBC 27%), with a mean follow-up time of 4 years, treated with neoadjuvant systemic therapy (92% anthracycline-taxane based) were analyzed revealing 43 events (38 recurrences, 28 deaths). High RCB scores were associated with recurrence (median index: 2.34 vs. 1.39 points, rank-sum p < 0.0001), decreased RFS (hazard ratio [HR] = 1.80, 95% confidence interval [CI] 1.44-2.24, p < 0.0001) and reduced OS (HR 1.96, 95% CI 1.49-2.59, p < 0.0001). The RCB score showed proportionality of hazards (interaction HR with linear follow-up time = 1.00, p = 0.896) and good discriminating power (Harrell's c index 0.7).
CONCLUSIONS CONCLUSIONS
Our results confirm the RCB score as externally valid prognostic marker and being independent of molecular subtype for RFS and OS in a clinical setting.

Identifiants

pubmed: 31452052
doi: 10.1245/s10434-019-07741-w
pii: 10.1245/s10434-019-07741-w
pmc: PMC6864028
doi:

Types de publication

Journal Article Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

4274-4283

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Auteurs

Hannah Deborah Müller (HD)

Division of Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.

Florian Posch (F)

Division of Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.

Christoph Suppan (C)

Division of Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.

Ute Bargfrieder (U)

Department of Pathology, Hospital Graz South-West, Graz, Austria.

Melanie Gumpoldsberger (M)

Division of Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.

Robert Hammer (R)

Department of Surgery, Hospital Graz South-West, Graz, Austria.

Hubert Hauser (H)

Department of Surgery, Hospital Graz South-West, Graz, Austria.

Nadia Dandachi (N)

Division of Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.

Kurt Prein (K)

Department of Pathology, Hospital Graz South-West, Graz, Austria.

Herbert Stoeger (H)

Division of Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.

Sigurd Lax (S)

Department of Pathology, Hospital Graz South-West, Graz, Austria.
Institute of Pathology, Medical University of Graz, Graz, Austria.
Department of Pathology, Johannes Keppler Univeristy Linz, Linz, Austria.

Marija Balic (M)

Division of Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria. marija.balic@medunigraz.at.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria. marija.balic@medunigraz.at.

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