Prediction Models and Decision Aids for Women with Ductal Carcinoma In Situ: A Systematic Literature Review

Autor: Renée Schmitz, Erica Wilthagen, Frederieke van Duijnhoven, Marja van Oirsouw, Ellen Verschuur, Thomas Lynch, Rinaa Punglia, E. Hwang, Jelle Wesseling, Marjanka Schmidt, Eveline Bleiker, Ellen Engelhardt, null Grand Challenge PRECISION Consortium

Publikováno v: Cancers. 14(13)

Even though Ductal Carcinoma in Situ (DCIS) can potentially be an invasive breast cancer (IBC) precursor, most DCIS lesions never will progress to IBC if left untreated. Because we cannot predict yet which DCIS lesions will and which will not progres

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5971b23e54d0a81b0630d1d597a217c0
https://pubmed.ncbi.nlm.nih.gov/35805030

Oncologist-led

Autor: Sook-Yee, Yoon, Siu Wan, Wong, Joanna, Lim, Syuhada, Ahmad, Shivaani, Mariapun, Heamanthaa, Padmanabhan, Nur Tiara, Hassan, Shao Yan, Lau, Gaik-Siew, Ch'ng, Muzhirah, Haniffa, Winnie P, Ong, Kavitha, Rethanavelu, Lip Hen, Moey, Wee Teik, Keng, Jamil, Omar, Mohd Norazam, Mohd Abas, Chee Meng, Yong, Vickneswaren, Ramasamy, Mohd Rushdan, Md Noor, Ismail, Aliyas, Michael C K, Lim, Anuradha, Suberamaniam, Noor Azmi, Mat Adenan, Zatul Akmar, Ahmad, Gwo Fuang, Ho, Rozita, Abdul Malik, Suguna, Subramaniam, Boom Ping, Khoo, Arivendran, Raja, Yeung Sing, Chin, Wee Wee, Sim, Beng Hock, Teh, Swee Kiong, Kho, Eunice S E, Ong, Pei Jye, Voon, Ghazali, Ismail, Chui Ling, Lee, Badrul Zaman, Abdullah, Kwong Sheng, Loo, Chun Sen, Lim, Saw Joo, Lee, Keng Joo Lim, Lim, Mohamad Nasir, Shafiee, Fuad, Ismail, Zarina Abdul, Latiff, Mohd Pazudin, Ismail, Mohamad Faiz, Mohamed Jamli, Suresh, Kumarasamy, Kin Wah, Leong, John, Low, Mastura, Md Yusof, Ahmad Muzamir, Ahmad Mustafa, Nor Huda, Mat Ali, Mary, Makanjang, Shahila, Tayib, Nellie, Cheah, Boon Kiong, Lim, Chee Kin, Fong, Yoke Ching, Foo, Matin, Mellor Abdullah, Teck Sin, Tan, Doris S Y, Chow, Kean Fatt, Ho, Rakesh, Raman, Ahmad, Radzi, Azura, Deniel, Daren C Y, Teoh, Soo Fan, Ang, Joseph K, Joseph, Paul Hock Oon, Ng, Lye-Mun, Tho, Azura Rozila, Ahmad, Ileena, Muin, Eveline, Bleiker, Angela, George, Meow-Keong, Thong, Yin Ling, Woo, Soo Hwang, Teo

Publikováno v: Journal of medical genetics. 59(3)

Identifying patients withThe Mainstreaming Genetic Counselling for Ovarian Cancer Patients (MaGiC) study is a prospective, two-arm observational study comparing oncologist-led and genetics-led counselling. This study included 790 multiethnic patients

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cc9e0d1015c77c242547fdc540725442
https://pubmed.ncbi.nlm.nih.gov/33526602

Pancreatic cyst survey imposes low psychological burden: preliminary results of the Pacyfic study

Autor: Kasper Over Beek, Anne Kamps, Priscilla Van Riet, Di Marco Mariacristina, Giulia Zerboni, Jeanine Van Hoft, Silvia Carrara, Claudio Ricci, Tamas Gonna, Eric Schoon, Marcin Polkowsky, George Beyer, Pieter Honkoop, Laurens Van der Waaij, Riccardo Casadei, Gabriele Capurso, Marco Bruno, Eveline Bleiker, Djuna Cahen

Objectives: to evaluate the perception and psychological burden of pancreatic cyst surveillance from a participant's perspective. Methods: The present patient survey is part of an international cohort study (PACYFIC study, www.pacyfic.net) which pros

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______4094::157e374e4c01fc14407db41eb69f9663
http://hdl.handle.net/11585/680906

Familial gastric cancer: guidelines for diagnosis, treatment and periodic surveillance

Autor: Irma, Kluijt, Rolf H, Sijmons, Nicoline, Hoogerbrugge, John T, Plukker, Daphne, de Jong, J Han, van Krieken, Richard, van Hillegersberg, Marjolijn, Ligtenberg, Eveline, Bleiker, Anemieke, Cats, E, Bleiker

Publikováno v: Familial Cancer, 11, 363-9
Familial Cancer, 11, 3, pp. 363-9
Familial cancer, 11(3), 363-369. Springer Netherlands
Familial Cancer, 11(3), 363-369. SPRINGER

Contains fulltext : 107891.pdf (Publisher’s version ) (Closed access) Hereditary diffuse gastric cancer (HDGC) is a relatively rare disorder, with a mutated CDH1 gene as the only known cause. Carriers of a germline mutation in CDH1 have a lifetime

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e83878b8765096f0fa579342a48f1341
https://doi.org/10.1007/s10689-012-9521-y