Breast Cancer Recurrence Risk Calculator

Explore how tumor size, grade, lymph nodes, hormone receptors, and HER2 status can affect a five-year recurrence estimate.

Recurrence risk estimate
Use pathology report values. This educational estimate is not a validated treatment decision model.

About breast cancer recurrence risk

Breast cancer recurrence means cancer returns after initial treatment, either near the original breast or regional lymph nodes or at a distant site. Risk is not determined by one measurement. Tumor biology, stage, pathology, treatment response, genomic information, age, other health conditions, and the length of follow-up all contribute. A five-year estimate describes a group probability and cannot predict what will happen to one person. Tumor size and involved lymph nodes reflect anatomic disease burden. Histologic grade describes how different tumor cells appear from normal breast cells and how actively they are likely to behave. Hormone receptor status indicates whether estrogen or progesterone signaling may drive growth and whether endocrine therapy may help. HER2-positive cancers have distinct biology and can respond to HER2-targeted treatments. Modern therapy can substantially change prognosis, which is why untreated historical risk and risk after a recommended treatment plan are not interchangeable. This calculator uses a transparent educational point estimate. It starts with a baseline, adds weight for tumor size, higher grade, positive lymph nodes, hormone receptor negativity, and HER2 positivity, then limits extreme output. It does not implement Oncotype DX, MammaPrint, PREDICT, CTS5, or another validated clinical algorithm. Those tools have specific eligibility criteria, input definitions, treatment assumptions, endpoints, and validation populations that cannot be recreated by a generic score. A pathology report may contain more detail than these fields, including exact receptor percentages, Ki-67, lymphovascular invasion, margins, molecular subtype, nodal burden, and treatment response. Recurrence can also be reported as local, regional, distant, invasive, or disease-free survival, so percentages from different sources may answer different questions. Always compare the time horizon and endpoint before comparing numbers. Use the result to understand the direction in which common factors can influence risk, not as medical advice. An oncologist can integrate pathology, imaging, surgery, radiation, systemic therapy, genetics, menopausal status, and patient priorities. New symptoms or concerns after breast cancer treatment should be discussed with the treating team rather than interpreted through an online calculator.

Recurrence estimate examples

Clinical factorsEstimateInterpretation
1.5 cm, grade 1, 0 nodes, HR positive, HER2 negative8.0%Favorable entered factors keep the educational estimate low.
2.0 cm, grade 2, 1 node, HR positive, HER2 negative17.0%Higher grade and one involved node add to the estimate.
3.0 cm, grade 3, 2 nodes, HR negative, HER2 positive39.0%Several adverse entered factors increase the educational estimate.

How to use the recurrence calculator

  1. Find the invasive tumor size, histologic grade, and positive lymph-node count on the pathology report.
  2. Select the documented hormone receptor and HER2 statuses.
  3. Choose Estimate recurrence risk to view the simplified five-year percentage.
  4. Review the result with an oncology professional who can apply a validated model and treatment context.

Breast cancer recurrence FAQ

Is this the Oncotype DX recurrence score?

No. Oncotype DX is a proprietary genomic assay performed on tumor tissue. This calculator does not use gene expression and cannot reproduce that score.

Does the estimate include treatment benefit?

No specific surgery, radiation, endocrine therapy, chemotherapy, or targeted therapy effect is modeled. Treatment can materially change recurrence risk, so discuss personalized absolute benefit with an oncology team.

What does hormone receptor positive mean?

It generally means tumor cells express estrogen receptors, progesterone receptors, or both. Exact definitions and treatment implications come from the pathology report and clinical team.

Is recurrence risk the same as survival?

No. Recurrence and mortality are different endpoints, and many recurrences can be treated. A recurrence percentage should not be interpreted as a survival percentage.

Can this result guide treatment?

No. Treatment decisions require validated evidence, complete staging, patient health, and informed discussion with specialists.