Jose M Baena-Canada

Dr. Jose M Baena-Canada

orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2014 in The Lancet Oncology
Verified
Journal Article
Closed access
SAStefan Aebi
Stefan Aebi
SGShari Gelber
Shari Gelber
SAStewart J Anderson
Stewart J Anderson
ILIstván Láng
István Láng
ARAndré Robidoux
André Robidoux
IWIrene L Wapnir
Irene L Wapnir

1 November 2006 in Clinical and Translational Oncology
Verified
Journal Article
Closed access
PDF file
MFMaría J. Huertas Fernández
María J. Huertas Fernández
JBJose M Baena-Canada
Jose M Baena-Canada
MBMaría J. Martínez Bautista
María J. Martínez Bautista
EAEsperanza Arriola Arellano
Esperanza Arriola Arellano
MPMaría Victoria García Palacios
María Victoria García Palacios

6 September 2021 in British Journal of Cancer
Verified
Journal Article
Open access
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Carolina DonatCarolina Donat
Carolina Donat
ÁGÁngel Guerrero-Zotano
Ángel Guerrero-Zotano
ACAna Casas
Ana Casas
JBJose M Baena-Canada
Jose M Baena-Canada
VLVirginia Lope
Virginia Lope
MPMarina Pollán
Marina Pollán
Background: Whether there are lifetime points of greater sensitivity to the deleterious effects of alcohol intake on the breasts remains inconclusive. Objective: To compare the influence of distinctive trajectories of alcohol consumption throughout a woman’s life on development of breast cancer (BC). Methods: 1278 confirmed invasive BC cases and matched (by age and residence) controls from the Epi-GEICAM study (Spain) were used. The novel group-based trajectory modelling was used to identify different alcohol consumption trajectories throughout women’s lifetime. Results: Four alcohol trajectories were identified. The first comprised women (45%) with low alcohol consumption (<5 g/day) throughout their life. The second included those (33%) who gradually moved from a low alcohol consumption in adolescence to a moderate in adulthood (5 to <15 g/day), never having a high consumption; and oppositely, women in the third trajectory (16%) moved from moderate consumption in adolescence, to a lower consumption in adulthood. Women in the fourth (6%) moved from a moderate alcohol consumption in adolescence to the highest consumption in adulthood (≥15 g/day), never having a low alcohol consumption. Comparing with the first trajectory, the fourth doubled BC risk (OR 2.19; 95% CI 1.27, 3.77), followed by the third (OR 1.44; 0.96, 2.16) and ultimately by the second trajectory (OR 1.17; 0.86, 1.58). The magnitude of BC risk was greater in postmenopausal women, especially in those with underweight or normal weight. When alcohol consumption was independently examined at each life stage, ≥15 g/day of alcohol consumption in adolescence was strongly associated with BC risk followed by consumption in adulthood. Conclusions: The greater the alcohol consumption accumulated throughout life, the greater the risk of BC, especially in postmenopausal women. Alcohol consumption during adolescence may particularly influence BC risk.

26 June 2013 in Family Practice
Verified
Journal Article
Open access
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JBJose M Baena-Canada
Jose M Baena-Canada
PRPatricia Ramírez-Daffós
Patricia Ramírez-Daffós
CCCristina Cortés-Carmona
Cristina Cortés-Carmona
PRPetra Rosado-Varela
Petra Rosado-Varela
JNJuan Nieto-Vera
Juan Nieto-Vera
EBEncarnación Benítez-Rodríguez
Encarnación Benítez-Rodríguez
Hospitals have traditionally been the place where the follow-up of breast cancer patients occurs in Spain. To describe the evolution of long-term survivors of breast cancer according to type of follow-up received (in primary or specialist/hospital care), measuring impact of care type on health, cost, health-related quality of life (HRQL) and satisfaction results. Retrospective study of cohorts with disease-free patients followed up for at least 5 years in Oncology. Using personal questionnaires, the type and cost of the follow-up, events, HRQL and satisfaction were analysed. Ninety-eight women were surveyed, 60 in primary and 38 in specialist care. There were no differences between groups in diagnosis of metastasis or new primary tumours. The number of annual visits per patient was 0.98 (0.48) in primary and 1.11 (0.38) in specialist care (P = 0.19). In primary, 44.6% were programmed and 55.4% on demand; in specialist, 94.6% were programmed and 5.4% on demand (P = 0.0001). The costs of follow-up in primary care were lower—€112.86 (77.54) versus €184.61 (85.87) per patient and year (P = 0.0001). No differences were reported in HRQL. Preference for specialist care was expressed by 80%, versus 10% for primary, with 10% indifferent. Patients showed greater satisfaction with specialist care in all questionnaire dimensions. Compliance with follow-up protocol was high in both groups. In specialist care nearly all the visits were programmed and in primary almost half were on demand. In our locality, primary is more cost-effective than specialist care, but patients express greater satisfaction with specialist follow-up and hence prefer it.

1 December 2014 in The Breast
Verified
Journal Article
Closed access
JBJose M Baena-Canada
Jose M Baena-Canada
PRPetra Rosado-Varela
Petra Rosado-Varela
IEInmaculada Expósito-Álvarez
Inmaculada Expósito-Álvarez
MGMacarena González-Guerrero
Macarena González-Guerrero
JNJuan Nieto-Vera
Juan Nieto-Vera
EBEncarnación Benítez-Rodríguez
Encarnación Benítez-Rodríguez

1 December 2012 in European Journal of Cancer
Verified
Journal Article
Closed access
JBJose M Baena-Canada
Jose M Baena-Canada
SESara Estalella-Mendoza
Sara Estalella-Mendoza
PRPetra Rosado-Varela
Petra Rosado-Varela
IEInmaculada Expósito-Álvarez
Inmaculada Expósito-Álvarez
MGMacarena González-Guerrero
Macarena González-Guerrero
EBEncarnación Benítez-Rodríguez
Encarnación Benítez-Rodríguez