Literature DB >> 35076871

Breast cancer recurrence: factors impacting occurrence and survival.

Donald Courtney1, Matthew G Davey2, Brian M Moloney1, Michael K Barry1, Karl Sweeney1, Ray P McLaughlin1, Carmel M Malone1, Aoife J Lowery1, Michael J Kerin1.   

Abstract

BACKGROUND: Breast cancer mortality has decreased due to improved screening and treatment options. Nevertheless, 25-30% of patients develop disease recurrence and die from the disease dissemination. Patients who develop metastatic disease represent a heterogeneous group and management plans are dependent on molecular subtype, disease burden and metastatic site. AIM: To determine predictive clinicopathological factors of disease recurrence and their impact on survival in the molecular era.
METHODS: Consecutive patients who breast cancer developed recurrence at our tertiary referral centre between 2000 and 2015 were included. Clinicopathological and treatment data were assessed using descriptive statistics. Oncological outcome was assessed using Cox regression and Kaplan Meier analyses.
RESULTS: Two hundred sixty-five consecutive patients who developed breast cancer recurrence were included; median age at metastasis was 59.3 years (range 27-87 years), and median time to recurrence (TTR) was 47.7 ± 38.5 months (range 3.0-194.3 months). Survival was 24.2% (64/265) 53.2% were luminal A (LABC) (141/265), 18.5% were luminal B (LBBC) (49/265), 18.5% were triple negative (TNBC) (49/265), and 9.8% were human epidermal growth factor receptor-2 overexpressing (HER2 +) (26/265). TTR for patients with LABC was 56.0 ± 41.3 months, LBBC was 48.4 ± 41.1 months, TNBC was 26.9 ± 28.5 months and HER2 + was 34.3 ± 21.8 months. Increased grade (P < 0.001), Nottingham Prognostic Indices (P < 0.001), TNBC (P < 0.001), HER2 + subtype (P < 0.001) and receiving targeted therapy (P = 0.006) predicted shorted TTR. Estrogen receptor positivity (P < 0.001), progesterone receptor positivity (P = 0.010), invasive lobular carcinoma (P = 0.009) and receiving endocrine therapy (P = 0.001) predicted longer TTR.
CONCLUSION: Readily available clinicopathological factors predict risk of metastatic dissemination. Developing a tailored program to identify patients at risk of recurrence is crucial in controlling metastatic dissemination of breast cancer.
© 2022. The Author(s).

Entities:  

Keywords:  Breast cancer; Metastasis; Personalized medicine; Recurrence

Year:  2022        PMID: 35076871     DOI: 10.1007/s11845-022-02926-x

Source DB:  PubMed          Journal:  Ir J Med Sci        ISSN: 0021-1265            Impact factor:   1.568


  45 in total

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Authors:  Kimberly D Miller; Rebecca L Siegel; Chun Chieh Lin; Angela B Mariotto; Joan L Kramer; Julia H Rowland; Kevin D Stein; Rick Alteri; Ahmedin Jemal
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9.  Somatic mutations, clinicopathologic characteristics, and survival in patients with untreated breast cancer with bone-only and non-bone sites of first metastasis.

Authors:  Miho Kono; Takeo Fujii; Naoko Matsuda; Kenichi Harano; Huiqin Chen; Chetna Wathoo; Aron Y Joon; Debu Tripathy; Funda Meric-Bernstam; Naoto T Ueno
Journal:  J Cancer       Date:  2018-09-08       Impact factor: 4.207

10.  Receptor conversion in metastatic breast cancer: a prognosticator of survival.

Authors:  Xiangying Meng; Santai Song; Ze-fei Jiang; Bing Sun; Tao Wang; Shaohua Zhang; Shikai Wu
Journal:  Oncotarget       Date:  2016-11-01
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