Breast Cancer Multifocality and Multicentricity and Locoregional Recurrence

Author:

Lynch Siobhan P.12,Lei Xiudong32,Hsu Limin42,Meric-Bernstam Funda52,Buchholz Thomas A.52,Zhang Hong62,Hortobágyi Gabriel N.42,Gonzalez-Angulo Ana M.472,Valero Vicente42

Affiliation:

1. Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA

2. Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA

3. Departments of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA

4. Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA

5. Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA

6. Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA

7. Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA

Abstract

Abstract Background. The impact of multifocal (MF) or multicentric (MC) breast cancer on locoregional (LR) control rates is unknown. Methods. MF was defined as two or more separate invasive tumors in the same quadrant of the breast. MC was defined as two or more separate invasive tumors occupying more than one quadrant of the same breast. Patients were categorized by LR treatment: breast conservation therapy (BCT; n = 256), mastectomy (n = 466), or mastectomy plus postmastectomy radiation therapy (PMRT; n = 184). All patients with MC disease had mastectomy (10 patients treated with BCT for MC disease were excluded). The Kaplan-Meier product limit method was used to calculate 5-year LR control rate. Cox proportional hazards models were used to determine independent associations of multifocality or multicentricity with LR control. Results. A total of 906 patients had either MF disease (n = 673) or MC disease (n = 233). With median follow-up of 52 months, the 5-year LR control rate was 99% for MF, 96% for MC, and 98% for unifocal tumors (p = .44). Subset analysis revealed no difference in LR control regardless of the LR treatment (p = .67 for BCT, p = .37 for mastectomy, p = .29 for mastectomy plus PMRT). There were five in-breast recurrences after BCT in the MF group. MF and MC did not have an independent impact on LR control rate on multivariate analysis. Conclusion. MF and MC disease are not independent risk factors for LR recurrence. Patients with MF and MC breast cancer had rates of LR control similar to those of their unifocal counterparts. These data suggest that BCT is a safe option for patients with MF tumors and that MF or MC disease alone is not an indication for PMRT.

Funder

National Cancer Institute

National Cancer Institute Breast Specialized Program for Research Excellence

University of Texas MD Anderson's Cancer Center

MD Anderson Breast Cancer Management System

Breast Tumor Bank

Nelly B. Connally Breast Cancer Research Fund

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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