# Prognosis of Pregnancy-Associated Breast Cancer: A Systematic Review of Contemporary Observational Studies

**Authors:** Dimitrios Zouzoulas, Tilemachos Karalis, Iliana Sofianou, Panagiotis Tzitzis, Themistoklis Mikos, Eleni Timotheadou, Grigoris Grimbizis, Dimitrios Tsolakidis

PMC · DOI: 10.3390/medsci14010120 · Medical Sciences · 2026-03-03

## TL;DR

Breast cancer diagnosed during pregnancy does not worsen outcomes if treated properly, but cancers diagnosed soon after childbirth are more dangerous.

## Contribution

This systematic review clarifies the distinct prognostic differences between pregnancy and postpartum breast cancer.

## Key findings

- Pregnancy-associated breast cancer often presents with more aggressive tumor features.
- Pregnancy itself does not predict worse survival if treatment is not compromised.
- Postpartum diagnosis is linked to higher recurrence and death risks even after adjustment.

## Abstract

Background/Objectives: Pregnancy-associated breast cancer (PABC) is uncommon but increasingly encountered as more women delay childbearing. Its prognostic impact remains controversial, particularly for cancers diagnosed in the early postpartum period. We aimed to synthesize contemporary evidence on the prognosis of breast cancer diagnosed during pregnancy or within 12 months after delivery compared with breast cancer in other young women, with a specific focus on differences between pregnancy time and postpartum disease. Methods: We performed a systematic review of observational studies published from 2005 onwards that reported oncologic outcomes for women with invasive PABC versus non-PABC comparators or PABC-only cohorts with internal timing comparisons. PubMed, Cochrane Library, Scopus and ClinicalTrials.gov were systematically searched using predefined strategies. Two reviewers independently screened records, extracted data and assessed risk of bias using the ROBINS-E tool, treating PABC status as the exposure. Because of substantial heterogeneity in PABC definitions, outcomes and adjustment sets, no meta-analysis was performed. Results: Twenty-one observational studies (single-center, multicenter and population-based) were included. PABC cases more often presented with larger tumors, higher nodal burden, high-grade and hormone receptor-negative/HER2-positive phenotypes and worse survival compared to non-PABC controls. In most contemporary cohorts that delivered guideline-oriented therapy and adjusted for stage and tumor biology, a diagnosis during pregnancy was not an independent predictor of poorer disease-free or overall survival. In contrast, multiple large registry and institutional studies reported significantly higher risks of recurrence and death for cancers diagnosed in the early postpartum period, even after multivariable adjustment. Conclusions: Current evidence suggests that pregnancy itself does not inevitably worsen breast cancer prognosis when treatment is not compromised. However, breast cancers diagnosed soon after childbirth represent a distinct high-risk subgroup. These findings support full-intensity, guideline-based therapy during pregnancy and highlight the need for special attention and further research focused on postpartum breast cancer.

## Linked entities

- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, NODAL (nodal growth differentiation factor) [NCBI Gene 4838] {aka HTX5}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, NR4A1 (nuclear receptor subfamily 4 group A member 1) [NCBI Gene 3164] {aka GFRP1, HMR, N10, NAK-1, NGFIB, NP10}
- **Diseases:** injury to (MESH:D014947), ductal carcinoma in situ (MESH:D002285), death (MESH:D003643), stage I-III disease (MESH:D007676), nodal (MESH:D013611), node (MESH:D012804), hormone receptor-negative disease (MESH:D046150), Cancers (MESH:D009369), aggressive disease (MESH:D010554), male breast cancer (MESH:D018567), Breast Cancer (MESH:D001943), pregnancy (MESH:D011254), inflammatory (MESH:D007249)
- **Chemicals:** anthracycline (MESH:D018943), trastuzumab (MESH:D000068878), taxanes (MESH:D043823)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13028489/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13028489/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028489/full.md

---
Source: https://tomesphere.com/paper/PMC13028489