Long-term outcome in young women with breast cancer: a population-based study

被引:93
作者
Fredholm, Hanna [1 ,2 ]
Magnusson, Kristina [3 ]
Lindstrom, Linda S. [4 ]
Garmo, Hans [5 ,6 ]
Falt, Sonja Eaker [5 ]
Lindman, Henrik [7 ]
Bergh, Jonas [8 ]
Holmberg, Lars [5 ,6 ]
Ponten, Fredrik [3 ]
Frisell, Jan [1 ,2 ]
Fredriksson, Irma [1 ,2 ]
机构
[1] Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden
[2] Karolinska Univ Hosp, Dept Breast & Endocrine Surg, S-17176 Stockholm, Sweden
[3] Uppsala Univ, Dept Immunol Genet & Pathol, Sci Life Lab, Uppsala, Sweden
[4] Karolinska Inst, Dept Biosci & Nutr, Stockholm, Sweden
[5] Uppsala Univ, Univ Uppsala Hosp, Dept Surg Sci, Reg Canc Ctr, Uppsala, Sweden
[6] Kings Coll London, Fac Life Sci & Med, Div Canc Studies, London, England
[7] Uppsala Univ, Univ Uppsala Hosp, Dept Radiol Oncol & Radiat Sci, Uppsala, Sweden
[8] Karolinska Inst, Karolinska Univ Hosp, Dept Pathol & Oncol, Canc Ctr Karolinska & Karolinska Oncol,Radiumhemm, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Breast cancer; Young age; Subtype; Luminal B; Early stage; Prognosis; Population-based; SINGLE INSTITUTIONAL EXPERIENCE; GENE-EXPRESSION; NEOADJUVANT CHEMOTHERAPY; LESS-THAN-35; YEARS; WORSE PROGNOSIS; AGE; SUBTYPES; THERAPY; DIAGNOSIS; SURVIVAL;
D O I
10.1007/s10549-016-3983-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Whether young age at diagnosis of breast cancer is an independent risk factor for death remains controversial, and the question whether young age should be considered in treatment decisions is still to be answered. From a population-based cohort of 22,017 women with breast cancer, all women < 35 years (n = 471) were compared to a random sample of 700 women aged 35-69 years from the same cohort. Information on patient and tumor characteristics, treatment, and follow-up was collected from the medical records. Tissue microarrays were produced for analysis of classical biomarkers. Breast cancer-specific survival (BCSS), distant disease-free survival (DDFS), and locoregional recurrence-free survival (LRFS) by age were compared using women 50-69 years as reference. At 10 years follow-up, women < 35 years and 35-39 years had a worse BCSS [age < 35 years 69 % (HR 2.75, 95 % CI 1.93-3.94), age 35-39 years 76 % (HR 2.33, 95 % CI 1.54-3.52), age 40-49 years 84 % (HR 1.53, 95 % CI 0.97-2.39), and age 50-69 years 89 % (reference)]. The worse BCSS was statistically significant in stages I-IIa and Luminal B tumors. At multivariate analysis age < 35 years and 35-39 years confined a risk in LRFS (HR 2.13, 95 % CI 1.21-3.76 and HR 1.97, 95 % CI 1.06-3.68) but not in DDFS and BCSS. In the subgroup of women < 40 years with luminal tumors stage I-IIa, low age remained an independent risk factor also in DDFS (HR 1.87, 95 % CI 1.03-3.44). Young women have a high risk of systemic disease even when diagnosed in an early stage. The excess risk of relapse is most pronounced in Luminal B tumors, where low age is an independent prognostic factor of DDFS and LRFS.
引用
收藏
页码:131 / 143
页数:13
相关论文
共 53 条
[41]   Nonadherence to adjuvant tamoxifen therapy in women with primary breast cancer [J].
Partridge, AH ;
Wang, PS ;
Winer, EP ;
Avorn, J .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (04) :602-606
[42]   The Effect of Age on Delay in Diagnosis and Stage of Breast Cancer [J].
Partridge, Ann H. ;
Hughes, Melissa E. ;
Ottesen, Rebecca A. ;
Wong, Yu-Ning ;
Edge, Stephen B. ;
Theriault, Richard L. ;
Blayney, Douglas W. ;
Niland, Joyce C. ;
Winer, Eric P. ;
Weeks, Jane C. ;
Tamimi, Rulla M. .
ONCOLOGIST, 2012, 17 (06) :775-782
[43]   The Human Protein Atlas as a proteomic resource for biomarker discovery [J].
Ponten, F. ;
Schwenk, J. M. ;
Asplund, A. ;
Edqvist, P. -H. D. .
JOURNAL OF INTERNAL MEDICINE, 2011, 270 (05) :428-446
[44]   Breast cancer in young women: have the prognostic implications of breast cancer subtypes changed over time? [J].
Sheridan, Wilson ;
Scott, Tyldesley ;
Caroline, Speers ;
Yvonne, Zheng ;
Vanessa, Bernstein ;
David, Voduc ;
Karen, Gelmon ;
Stephen, Chia .
BREAST CANCER RESEARCH AND TREATMENT, 2014, 147 (03) :617-629
[45]   Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications [J].
Sorlie, T ;
Perou, CM ;
Tibshirani, R ;
Aas, T ;
Geisler, S ;
Johnsen, H ;
Hastie, T ;
Eisen, MB ;
van de Rijn, M ;
Jeffrey, SS ;
Thorsen, T ;
Quist, H ;
Matese, JC ;
Brown, PO ;
Botstein, D ;
Lonning, PE ;
Borresen-Dale, AL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (19) :10869-10874
[46]   Luminal B subtype: A key factor for the worse prognosis of young breast cancer patients in China [J].
Tang, Li-Chen ;
Jin, Xi ;
Yang, Hai-Yuan ;
He, Min ;
Chang, Helena ;
Shao, Zhi-Ming ;
Di, Gen-Hong .
BMC CANCER, 2015, 15
[47]   Chromogenic in situ hybridization -: A practical alternative for fluorescence in situ hybridization to detect HER-2/neu oncogene amplification in archival breast cancer samples [J].
Tanner, M ;
Gancberg, D ;
Di Leo, A ;
Larsimont, D ;
Rouas, G ;
Piccart, MJ ;
Isola, J .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (05) :1467-1472
[48]   Towards a knowledge-based Human Protein Atlas [J].
Uhlen, Mathias ;
Oksvold, Per ;
Fagerberg, Linn ;
Lundberg, Emma ;
Jonasson, Kalle ;
Forsberg, Mattias ;
Zwahlen, Martin ;
Kampf, Caroline ;
Wester, Kenneth ;
Hober, Sophia ;
Wernerus, Henrik ;
Bjorling, Lisa ;
Ponten, Fredrik .
NATURE BIOTECHNOLOGY, 2010, 28 (12) :1248-1250
[49]   Chromogenic in situ hybridisation for the assessment of HER2 status in breast cancer:: an international validation ring study [J].
van de Vijver, Marc ;
Bilous, Michael ;
Hanna, Wedad ;
Hofmann, Manfred ;
Kristel, Petra ;
Penault-Llorca, Fredrique ;
Rueschoff, Josef .
BREAST CANCER RESEARCH, 2007, 9 (05) :R68
[50]   The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies [J].
von Elm, Erik ;
Altman, Douglas G. ;
Egger, Matthias ;
Pocock, Stuart J. ;
Gotzsche, Peter C. ;
Vandenbroucke, Jan P. .
LANCET, 2007, 370 (9596) :1453-1457