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. 2024 Jun 28:13:100585.
doi: 10.1016/j.ejro.2024.100585. eCollection 2024 Dec.

The association of magnetic resonance imaging features with five molecular subtypes of breast cancer

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The association of magnetic resonance imaging features with five molecular subtypes of breast cancer

Van Thi Nguyen et al. Eur J Radiol Open. .

Abstract

Objective: To identify the association of magnetic resonance imaging (MRI) features with molecular subtypes of breast cancer (BC).

Materials and methods: A retrospective study was conducted on 112 invasive BC patients with preoperative breast MRI. The confirmed diagnosis and molecular subtypes of BC were based on the postoperative specimens. MRI features were collected by experienced radiologists. The association of MRI features of each subtype was compared to other molecular subtypes in univariate and multivariate logistic regression analyses.

Results: The proportions of luminal A, luminal B HER2-negative, luminal B HER2-positive, HER2-enriched, and triple-negative BC were 14.3 %, 52.7 %, 12.5 %, 10.7 %, and 9.8 %, respectively. Luminal A was associated with hypo-isointensityon T2-weighted images (OR=6.214, 95 % CI: 1.163-33.215) and non-restricted diffusion on DWI-ADC (OR=6.694, 95 % CI: 1.172-38.235). Luminal B HER2-negative was related to the presence of mass (OR=7.245, 95 % CI: 1.760-29.889) and slow/medium initial enhancement pattern (OR=3.654, 95 % CI: 1.588-8.407). There were no associations between MRI features and luminal B HER2-positive. HER2-enriched tended to present as non-mass enhancement lesions (OR=20.498, 95 % CI: 3.145-133.584) with fast uptake in the initial postcontrast phase (OR=9.788, 95 % CI: 1.689-56.740), and distortion (OR=11.471, 95 % CI: 2.250-58.493). Triple-negative were associated with unifocal (OR=7.877, 95 % CI: 1.180-52.589), hyperintensityon T2-weighted images (OR=14.496, 95 % CI: 1.303-161.328), rim-enhanced lesions (OR=18.706, 95 % CI: 1.915-182.764), and surrounding tissue edema (OR=5.768, 95 % CI: 1.040-31.987).

Conclusion: Each molecular subtype of BC has distinct features on breast MRI. These characteristics can serve as an adjunct to immunohistochemistry in diagnosing molecular subtypes, particularly in cases, where traditional methods yield equivocal results.

Keywords: Breast cancer; MRI features; Molecular subtypes.

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Conflict of interest statement

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Figures

Fig. 1
Fig. 1
Flowchart.
Fig. 2
Fig. 2
Luminal A subtype breast cancer.
Fig. 3
Fig. 3
Luminal B HER2-negative breast cancer.
Fig. 4
Fig. 4
HER2-enriched-like breast cancer.
Fig. 5
Fig. 5
Triple-negative breast cancer.
Fig. 6
Fig. 6
Luminal B HER2-positive breast cancer characterized by both mass-like and non-mass-like lesions on MRI.

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References

    1. Sung H., Ferlay J., Siegel R.L., et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J. Clin. 2021;71(3):209–249. doi: 10.3322/caac.21660. - DOI - PubMed
    1. Guo L., Kong D., Liu J., et al. Breast cancer heterogeneity and its implication in personalized precision therapy. Exp. Hematol. Oncol. 2023;12(1):3. doi: 10.1186/s40164-022-00363-1. - DOI - PMC - PubMed
    1. Coates A.S., Winer E.P., Goldhirsch A., et al. Tailoring therapies--improving the management of early breast cancer: St Gallen international expert consensus on the primary therapy of early breast cancer 2015. Ann. Oncol. 2015;26(8):1533–1546. doi: 10.1093/annonc/mdv221. - DOI - PMC - PubMed
    1. Goldhirsch A., Wood W.C., Coates A.S., et al. Strategies for subtypes--dealing with the diversity of breast cancer: highlights of the St. Gallen international expert consensus on the primary therapy of early breast cancer 2011. Ann. Oncol. 2011;22(8):1736–1747. doi: 10.1093/annonc/mdr304. - DOI - PMC - PubMed
    1. Loibl S., Andre F., Bachelot T., et al. Early breast cancer: ESMO clinical practice guideline for diagnosis, treatment and follow-up. Ann. Oncol. 2024;35(2):159–182. doi: 10.1016/j.annonc.2023.11.016. - DOI - PubMed

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