Younger women with estrogen receptor (ER)–positive, HER2-negative breast cancer have significantly worse long-term outcomes, including higher rates of recurrence and metastasis, compared with older women.
Young patients with estrogen receptor (ER)–positive and HER2-negative breast cancers are associated with worse locoregional recurrence-free survival, disease-free survival, and late distant metastasis-free survival, acknowledging the importance of long-term observation and the possibility for personalized treatment approaches based on age, according to a study published in JAMA Network Open.1
Patients diagnosed with breast cancer at a younger age have shown reports of more aggressive pathological features. Additionally, the diagnosis is usually of larger size, greater lymph node involvement, poorly differentiated, and often hormone receptor (HR)–negative disease.
Young patients tend to have more basal-like tumors based on molecular profiling and diagnoses are usually linked to hereditary breast cancer syndromes, often coinciding with poor prognosis in luminal-like disease. Both HR-positive breast cancer and HER2-negative breast cancer are linked to a higher risk of late recurrence compared with alternative subtypes.
In a previous study, younger patients had a worse disease-free survival rate during all time periods compared with older age groups.2 After 5 years, recurrence rates for patients less than 35 years old was 30.4% compared with 18.7% for patients 35 and older. By 10 years, recurrence rates persisted in 40.1% of younger patients and 28.6% of older patients. The overall survival rates for younger women were significantly worse than those for older women.
The current study authors analyzed if younger patients with HR-positive, HER2-negative had a worse prognosis for late distant recurrence even if they were recurrence-free within 5 years after surgery.1
The multicenter retrospective cohort study included data from 3 major institutions in the Republic of Korea: Samsung Medical Center, Gangnam Severance Hospital, and Seoul National University Hospital. The findings were categorized into 3 age groups at diagnosis: 21 to 35 years, 36 to 40 years, and 41 to 45 years.
A total of 2772 patients were enrolled in the study with 13.3% aged 35 or younger, 31.9% aged 36 to 40 years old, and 54.7% aged 41 years or older. The average follow-up duration was 10.8 years. Every patient received adjuvant endocrine therapy for at least 2 years, mostly with tamoxifen (97.5%).
Younger patients had significantly larger proportions of high nuclear grade and histologic grade tumors compared with older patients (21-35 years, 28.9%; 36-40 years, 16.8%; 41-45 years, 18%). There was a greater chance of younger patients receiving adjuvant chemotherapy compared with older patients as well (21-35 years, 83%; 36-40 years, 78.8%; 41-45 years, 73.2%).
The lowest rates for locoregional recurrence-free survival were among the youngest population (21-35 years, 90.1%; 36-40 years, 94.6%; 41-45 years, 97.7%). The disease-free survival rates were also the lowest among the youngest group (21-35 years, 79.3%; 36-40 years, 88.7%; 41-45 years, 94.4%). Additionally, the youngest age group had the lowest rate of distant metastasis-free survival (21-35 years, 89.3%; 36-40 years, 94.2%; 41-45 years, 97.2%).
Study results found the late distant recurrence was linked to the younger age group, higher pathologic T and N stages, higher histologic grade, total mastectomy, and axillary lymph node dissection. While young age was an identifiable independent factor linked to locoregional recurrence-free survival, disease-free survival, and late distant metastasis-free survival, it was not linked to overall survival within the study.
The retrospective design and limited data collection across multiple centers hinder the overall scope of the study. The assessment of impact on oncologic outcomes may be restricted by the absence of BRCA1/2 data, minimal information on ovarian function suppression duration, and a small subset of patients who received adjuvant therapy. The retrospective nature limited the ability to explain differences in younger patients who may have fertility concerns and attempt conception, potentially influencing adherence. Adverse effects of endocrine therapy may have contributed to decreased adherence in this younger population as well.
Age was an independent factor linked with late distant recurrence among young patients with breast cancer diagnosed with HR-positive, HER2-negative subtypes. Study results also align with previous research, including a study that indicated “younger breast cancer patients exhibited more aggressive disease than older patients.”3
“These findings suggest that younger patients, particularly those 35 years or younger, exhibited worse oncologic outcomes compared with older groups, especially in terms of" locoregional recurrence-free survival, disease-free survival, and late distant metastasis-free survival, concluded study authors.1
References
Racial Inequities in Guideline-Adherent Breast Cancer Care and Timely Treatment
November 19th 2024Older non-Hispanic Black adults with early-stage breast cancer are less likely to receive timely treatment and guideline-concordant care, increasing their risk of death compared with non-Hispanic White women.
Read More
Emily Goldberg Shares Insights as a Genetic Counselor for Breast Cancer Risk Screening
October 30th 2023On this episode of Managed Care Cast, Emily Goldberg, MS, CGC, a genetic counselor at JScreen, breaks down how genetic screening for breast cancer works and why it is so important to increase awareness and education around these screening tools available to patients who may be at risk for cancer.
Listen
The Disproportionate Impact of the Pandemic on Health Care Disparities and Cancer
February 22nd 2022On this episode of Managed Care Cast, we discuss how already wide health care inequities in cancer are becoming much worse because of the COVID-19 pandemic, with guest Monica Soni, MD, associate chief medical officer at New Century Health.
Listen
Advancing Breast Cancer Care With HER2-Targeted Therapies
October 10th 2024In this interview from our Institute for Value-Based Medicine® event in Boston, we speak with Michael Hassett, MD, MPH, Dana-Farber Cancer Institute, on the clinical significance and cost implications of HER2 in the breast cancer space.
Read More
Managing Germline Mutations in Hereditary Breast Cancer Risk
October 7th 2024Hereditary breast cancers are caused by germline mutations, which are genetic mutations inherited at conception and so called because they originate in germ cells, those that develop into reproductive cells and become eggs in female individuals and sperm in male individuals.
Read More
Racial Inequities in Guideline-Adherent Breast Cancer Care and Timely Treatment
November 19th 2024Older non-Hispanic Black adults with early-stage breast cancer are less likely to receive timely treatment and guideline-concordant care, increasing their risk of death compared with non-Hispanic White women.
Read More
Emily Goldberg Shares Insights as a Genetic Counselor for Breast Cancer Risk Screening
October 30th 2023On this episode of Managed Care Cast, Emily Goldberg, MS, CGC, a genetic counselor at JScreen, breaks down how genetic screening for breast cancer works and why it is so important to increase awareness and education around these screening tools available to patients who may be at risk for cancer.
Listen
The Disproportionate Impact of the Pandemic on Health Care Disparities and Cancer
February 22nd 2022On this episode of Managed Care Cast, we discuss how already wide health care inequities in cancer are becoming much worse because of the COVID-19 pandemic, with guest Monica Soni, MD, associate chief medical officer at New Century Health.
Listen
Advancing Breast Cancer Care With HER2-Targeted Therapies
October 10th 2024In this interview from our Institute for Value-Based Medicine® event in Boston, we speak with Michael Hassett, MD, MPH, Dana-Farber Cancer Institute, on the clinical significance and cost implications of HER2 in the breast cancer space.
Read More
Managing Germline Mutations in Hereditary Breast Cancer Risk
October 7th 2024Hereditary breast cancers are caused by germline mutations, which are genetic mutations inherited at conception and so called because they originate in germ cells, those that develop into reproductive cells and become eggs in female individuals and sperm in male individuals.
Read More
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