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Featured researches published by Ana Opinião.


Ecancermedicalscience | 2018

Men seeking counselling in a Breast Cancer Risk Evaluation Clinic

Ana Catarina Freitas; Ana Opinião; Sofia Fragoso; Hugo Nunes; Madalena Santos; Ana Clara; ra Bento; Ana Luis; Jorge Silva; Cecília Moura; Bruno Felipe; Patricia Machado; Sidonia Santos; Saudade André; Paula Rodrigues; Joana Parreira; Fátima Vaz

Background Hereditary breast and ovary cancer syndrome affects both genders but little is known about the uptake of genetic services by men. The objective of this study is to characterise the male population counselled through a multidisciplinary breast/ovarian program. Methods Descriptive analysis of male patients counselled from January 2000 to December 2015. Data in this analysis include new cancer diagnoses during prospective follow up. Results From 4,320 families registered, 362 male patients were identified: 236 (65.2%) from hereditary cancer families (HCF) and 126 (34.8%) from non-HCF. In HCF, 121 patients (51.3%) were mutation carriers (MC): BRCA2 – 102 (84.3%), BRCA1 – 16 (13.2%), CHEK2 – 1 (0.8%) and TP53 – 2 (1.7%). Non-HCF included 126 patients: 85 (67.5%) belonged to families without pathogenic mutations or with variants of unknown clinical significance; 22 (17.5%) refused testing after counselling and 19 (15.0%) did not meet criteria for testing. Both HCF and non-HCF included patients with previous cancer diagnoses: HCF- Breast Cancer (BC) - 18; prostate cancer (PC) - 13; melanoma - 1; others - 7) and non-HCF (BC - 77; PC - 20; gastric cancer (GC) - 1; melanoma - 8; bladder cancer - 1; others - 22). From the 121 MC identified (including the TP53 and CHEK2 carriers), 97 patients (80.2%) adhered to prospective surveillance. With a median follow-up of 36.9 months, 17 cancers were diagnosed in 14 patients, PC being the most frequently diagnosed neoplasia (5 cases). Eleven patients (78.6%) are alive and three patients died of advanced cancer (2 with GC, 1 with disseminated adenocarcinoma). Conclusion We observed a high adherence to counselling, genetic testing and active surveillance by men belonging to hereditary BC families. Male carriers of pathogenic DNA variants are at risk for several cancers and should be included in prospective follow-up studies.


Annals of Oncology | 2014

898PPRIMARY CYTOREDUCTIVE SURGERY (PCS) VS NEOADJUVANT CHEMOTHERAPY (NACT) FOR ADVANCED OVARIAN CARCINOMA (AOC): DECISION CRITERIA AND EFFICACY OUTCOMES

H. Nunes; Fátima Vaz; A. Mayer; A.F. Jorge; T. Margarida; Ana Opinião; A. Guimarães; António Moreira

ABSTRACT Aim: PCS is the standard of care for aOC but NACT and interval debulking surgery (IDS) are acceptable treatment options for patients (pts) with stages IIIC and IV OC. Our aims are to characterize OC pts treated with PCS or NACT in our centre and to analyse decision criteria and efficacy outcomes of both strategies. Methods: All pts with ovarian tumours registered at the Southern Portuguese Cancer Registry (ROR-Sul) between 2006-2011 were reviewed for age at diagnosis, histology, FIGO stage, treatment (none, surgery and/or CT), progression free survival (PFS), overall survival (OS), criteria for NACT, number of platinum based CT cycles and residual macroscopic disease. Results: From 345 pts registered with ovarian tumours, 258 were epithelial ovarian cancers (EOC) (75%). EOC pts had a median age of 62 yrs (10-90); 64 (25%) were treated with surgery alone, 53 (21%) with NACT (stages IIIB-3, IIIC-15, IV-29) and 94 (37%) with PCS (25% stages IA-IC; 23% IIA-IIIA; 51% IIIB-IV).Other pts (17%) were not treated at our centre (only pathology review, multidisciplinary decision or death before treatment). For similar stages (IIIB-IV), median age was higher for NACT pts (64 yrs, 36-90) vs 59 yrs (33-82); median number of CT cycles was 8 (NACT) and 6 (PCS). Nine pts in the NACT group progressed and died before IDS. Complete resection of macroscopic disease was achieved in 24 (55%) of NACT pts and in 17 (36%) of PCS pts. Median OS and PFS were 29,2 and 8,1 months (NACT) and 38,1 months and 10,6 months (PCS). Bad prognosis pathology (mucinous/clear cell) was observed in 10 pts (3 NACT, 7 PCS). NACT decision was based on radiological criteria (74% of cases) such as implants >2cm outside the pelvis, lymphadenopathies above renal hilum, pre-sacred retroperitoneal disease or liver metastasis. In 14 pts (26%), comorbidities contraindicated upfront surgery. Conclusions: NACT was mostly decided for older pts with contraindications for upfront surgery and/or with radiologically determined unresectable disease. Observed OS was similar to that observed in trials with more fit pts. OS for the PDS group is in line with previous reports of single centre studies with experience in OC treatment. Disclosure: All authors have declared no conflicts of interest.


Archive | 2018

Treatment Decisions and Survival in Ovarian Cancer

Hugo de Seabra Martins Nunes; Alexandra Mayer; Ana FranciscaJorge; Teresa Margarida Cunha; Ana Opinião; António Guimarães; Fátima Vaz


Journal of Clinical Oncology | 2018

Beyond BRCA1 and BRCA2: Implementation of a multigene panel for the upfront testing of germline mutations in ovarian cancer.

Maria Beatriz Mira; I Miguel; Sofia Fragoso; Ana Luis; Ana Clara; Sandra Bento; Ana Opinião; Patricia Machado; Sidonia Santos; Paula Rodrigues; Joana Parreira; Ana Francisca; Fátima Vaz


Annals of Oncology | 2018

237PIndex BRCA1/2 testing under a multidisciplinary program

D H R Machado; Sofia Fragoso; Ana Opinião; Ana Clara; S. Bento; A C Luís; I Miguel; Sidonia Santos; Patricia Machado; Paula Rodrigues; Joana Parreira; Fátima Vaz


Annals of Oncology | 2018

993PIndividual and familial phenotype in hereditary ovarian cancer

M B D O Mira; I Miguel; Sofia Fragoso; Ana Opinião; A C Luís; Ana Clara; S. Bento; Patricia Machado; Sidonia Santos; Paula Rodrigues; Joana Parreira; Fátima Vaz


Journal of Clinical Oncology | 2017

Somatic versus germline BRCA mutations screening in ovarian cancer.

Hugo Nunes; Patricia Machado; Sofia Fragoso; Sidonia Santos; Fernanda Silva; Ana Félix; Ana Luis; Ana Opinião; Ana Clara; Sandra Bento; Ana Miranda; Ana Francisca; Fátima Vaz


Annals of Oncology | 2017

1236PDoes melanoma or other skin cancers belong to the BRCA2 phenotype

R. Vitorino; Fátima Vaz; A.L. Carvalho; S. Bento; Ana Luis; Ana Opinião; Ana Clara; J. Dupont; Sidonia Santos; Patricia Machado; Sofia Fragoso; Paula Rodrigues; Joana Parreira; C. Moura


Archive | 2016

Cancro ginecológico – consensos nacionais 2016

Abilio Lacerda; Alcides Pereira; Alexandra Rico Sofia; Almerinda Petiz; Ana Félix; Ana Francisco Jorge; Ana Palha; Ana Marta Costa; Ana Opinião; Ana Rodrigues


Journal of Clinical Oncology | 2016

Men seeking counselling in a Breast Cancer Evaluation Clinic: fifteen years experience of a multidisciplinary program.

Ana Catarina Freitas; Ana Opinião; Hugo Nunes; Ana Clara; Sandra Bento; Ana Luis; Jorge Silva; Cecília Moura; Bruno Filipe; Sofia Fragoso; Patricia Machado; Sidonia Santos; Paula Rodrigues; Joana Parreira; Fátima Vaz

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Dive into the Ana Opinião's collaboration.

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Fátima Vaz

Instituto Português de Oncologia Francisco Gentil

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Patricia Machado

Instituto Português de Oncologia Francisco Gentil

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Sidonia Santos

Instituto Português de Oncologia Francisco Gentil

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Ana Clara

Instituto Português de Oncologia Francisco Gentil

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Sofia Fragoso

Instituto Português de Oncologia Francisco Gentil

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Joana Parreira

Instituto Português de Oncologia Francisco Gentil

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Paula Rodrigues

Instituto Português de Oncologia Francisco Gentil

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Ana Luis

Instituto Português de Oncologia Francisco Gentil

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Hugo Nunes

Instituto Português de Oncologia Francisco Gentil

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I Miguel

Instituto Português de Oncologia Francisco Gentil

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