Loss of PTEN Expression, PIK3CA Mutations, and Breast Cancer Survival in the Nurses’ Health Studies

Author:

Wang Tengteng12ORCID,Heng Yujing J.3ORCID,Baker Gabrielle M.3ORCID,Bret-Mounet Vanessa C.3ORCID,Quintana Liza M.3ORCID,Frueh Lisa1ORCID,Hankinson Susan E.4ORCID,Holmes Michelle D.12ORCID,Chen Wendy Y.15ORCID,Willett Walter C.26ORCID,Rosner Bernard17ORCID,Tamimi Rulla M.8ORCID,Eliassen A. Heather126ORCID

Affiliation:

1. 1Channing Division of Network Medicine, Department of Medicine, Brigham & Women's Hospital, and Harvard Medical School, Boston, Massachusetts.

2. 2Department of Epidemiology, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.

3. 3Department of Pathology, Beth Israel Deaconess Medical Center, Boston, Massachusetts.

4. 4Department of Biostatistics and Epidemiology, University of Massachusetts School of Public Health and Health Sciences, Amherst, Massachusetts.

5. 5Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.

6. 6Department of Nutrition, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.

7. 7Department of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.

8. 8Department of Population Health Sciences, Weill Cornell Medicine, New York, New York.

Abstract

Abstract Background: The relationships between PTEN loss and/or PIK3CA mutation and breast cancer prognosis remain controversial. We aim to examine the associations in large epidemiologic cohorts. Methods: We followed women with invasive breast cancer from the Nurses’ Health Studies with available data on tumor PTEN expression (n = 4,111) and PIK3CA mutation (n = 2,930). PTEN expression was evaluated by IHC and digitally scored (0%–100%). Pyrosequencing of six hotspot mutations of PIK3CA was performed. Results: We found loss of PTEN expression (≤10%) occurred in 17% of cases, and PIK3CA mutations were detected in 11% of cases. After adjusting for clinical and lifestyle factors, PTEN loss was not associated with worse breast cancer-specific mortality among all samples [HR, 0.85; 95% confidence intervals (CI), 0.71–1.03] or among estrogen receptor (ER)-positive tumors (HR, 0.99; 95% CI, 0.79–1.24). However, among ER-negative tumors, PTEN loss was associated with lower breast cancer-specific mortality (HR, 0.68; 95% CI, 0.48–0.95). PIK3CA mutation was not strongly associated with breast cancer-specific mortality (HR, 0.89; 95% CI, 0.67–1.17). Compared with tumors without PTEN loss and without PIK3CA mutation, those with alterations (n = 540) were not at higher risk (HR, 1.07; 95% CI, 0.86–1.34). However, women with both PTEN loss and PIK3CA mutation (n = 38) were at an increased risk of breast cancer-specific mortality (HR, 1.65; 95% CI, 0.83–3.26). Conclusions: In this large epidemiologic study, the PTEN-mortality association was more pronounced for ER-negative tumors, and the joint PTEN loss and PIK3CA mutation may be associated with worse prognosis. Impact: Further studies with a larger sample of ER-negative tumors are needed to replicate our findings and elucidate underlying mechanisms.

Funder

National Cancer Institute

Publisher

American Association for Cancer Research (AACR)

Subject

Oncology,Epidemiology

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