Characterization of Oligometastatic Disease in a Real-World Nationwide Cohort of 3447 Patients With de Novo Metastatic Breast Cancer

Author:

Steenbruggen Tessa G1ORCID,Schaapveld Michael2ORCID,Horlings Hugo M3ORCID,Sanders Joyce3ORCID,Hogewoning Sander J4ORCID,Lips Esther H5ORCID,Vrancken Peeters Marie-Jeanne T6,Kok Niels F6,Wiersma Terry7ORCID,Esserman Laura8ORCID,van ‘t Veer Laura J9,Linn Sabine C110ORCID,Siesling Sabine411ORCID,Sonke Gabe S112ORCID

Affiliation:

1. Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands

2. Department of Epidemiology, The Netherlands Cancer Institute, Amsterdam, the Netherlands

3. Department of Pathology, The Netherlands Cancer Institute, Amsterdam, the Netherlands

4. Department of Research and Development, Netherlands Comprehensive Cancer Organisation, Utrecht, the Netherlands

5. Department of Molecular Pathology, The Netherlands Cancer Institute, Amsterdam, the Netherlands

6. Department of Surgical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands

7. Department of Radiation Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands

8. Department of Surgical Oncology, University of California San Francisco, San Francisco, CA, USA

9. Department of Laboratory Medicine, University of California San Francisco, San Francisco, CA, USA

10. Department of Molecular Pathology, University Medical Center Utrecht, Utrecht, the Netherlands

11. Department of Health Technology and Services Research, Technical Medical Centre, University of Twente, Enschede, the Netherlands

12. Department of Clinical Oncology, University of Amsterdam, Amsterdam, the Netherlands

Abstract

Abstract Background Observational studies in metastatic breast cancer (MBC) show that long-term overall survival (OS) is associated with limited tumor burden, or oligo-MBC (OMBC). However, a uniform definition of OMBC is lacking. In this real-world nationwide cohort, we aimed to define the optimal OMBC threshold and factors associated with survival in patients with OMBC. Methods 3535 patients aged younger than 80 years at diagnosis of de novo MBC in the Netherlands between January 2000 and December 2007 were included. Detailed clinical, therapy, and outcome data were collected from medical records of a sample of the patients. Using inverse-sampling-probability weighting, the analysis cohort (n = 3447) was constructed. We assessed OS according to number of metastases at diagnosis to determine the optimal OMBC threshold. Next, we applied Cox regression models with inverse-sampling-probability weighting to study associations with OS and progression-free survival in OMBC. All statistical tests were 2-sided. Results Compared with more than 5 distant metastases, adjusted hazard ratios for OS (with 95% confidence interval [CI] based on robust standard errors) for 1, 2-3, and 4-5 metastases were 0.70 (95% CI = 0.52 to 0.96), 0.63 (95% CI = 0.45 to 0.89), and 0.91 (95% CI = 0.61 to 1.37), respectively. Ten-year OS estimates for patients with no more than 3 vs more than 3 metastases were 14.9% and 3.4% (P < .001). In multivariable analyses, premenopausal andperimenopausal status, absence of lung metastases, and local therapy of metastases (surgery and/or radiotherapy) added to systemic therapy were statistically significantly associated with better OS and progression-free survival in OMBC, independent of local therapy of the primary tumor. Conclusion OMBC defined as MBC limited to 1-3 metastases was associated with favorable OS. In OMBC, local therapy of metastases was associated with better OS, particularly if patients were premenopausal or perimenopausal without lung metastases.

Funder

Dutch Cancer Society/Pink Ribbon

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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