Literature DB >> 28255411

Structured assessment and followup for patients with hereditary kidney tumour syndromes.

Jean-Baptiste Lattouf1, Stephen E Pautler2, M Neil Reaume3, Raymond H Kim4, Melanie Care5, Jane Green6, Alan So7, Philippe D Violette8, Issam Saliba9, Philippe Major10, Shane Silver11, Richard Leicht12, Joan Basiuk13, Simon Tanguay14, Michael A S Jewett15, Darrel Drachenberg16.   

Abstract

INTRODUCTION: Optimal clinical assessment and subsequent followup of patients with or suspected of having a hereditary renal cell carcinoma syndrome (hRCC) is not standardized and practice varies widely. We propose protocols to optimize these processes in patients with hRCC to encourage a more uniform approach to management that can then be evaluated.
METHODS: A review of the literature, including existing guidelines, was carried out for the years 1985-2015. Expert consensus was used to define recommendations for initial assessment and followup.
RESULTS: Recommendations for newly diagnosed patients' assessment and optimal ages to initiate followup protocols for von Hippel Lindau disease (VHL), hereditary papillary renal cancer (HPRC), hereditary leiomyomatosis with renal cell carcinoma (HLRCC), Birt-Hogg-Dubé syndrome (BHD), familial paraganglioma-pheochromocytoma syndromes (PGL-PCC), and tuberous sclerosis (TSC) are proposed.
CONCLUSIONS: Our proposed consensus for structured assessment and followup is intended as a roadmap for the care of patients with hRCC to guide healthcare providers. Although the list of syndromes included is not exhaustive, the document serves as a starting point for future updates.

Entities:  

Year:  2016        PMID: 28255411      PMCID: PMC5325749          DOI: 10.5489/cuaj.3798

Source DB:  PubMed          Journal:  Can Urol Assoc J        ISSN: 1911-6470            Impact factor:   1.862


  47 in total

1.  Familial non-VHL non-papillary clear-cell renal cancer.

Authors:  B T Teh; S Giraud; N F Sari; S I Hii; J P Bergerat; C Larsson; J M Limacher; D Nicol
Journal:  Lancet       Date:  1997-03-22       Impact factor: 79.321

2.  Two North American families with hereditary papillary renal carcinoma and identical novel mutations in the MET proto-oncogene.

Authors:  L Schmidt; K Junker; G Weirich; G Glenn; P Choyke; I Lubensky; Z Zhuang; M Jeffers; G Vande Woude; H Neumann; M Walther; W M Linehan; B Zbar
Journal:  Cancer Res       Date:  1998-04-15       Impact factor: 12.701

3.  Imaging features of hereditary papillary renal cancers.

Authors:  P L Choyke; M M Walther; G M Glenn; J R Wagner; D J Venzon; I A Lubensky; B Zbar; W M Linehan
Journal:  J Comput Assist Tomogr       Date:  1997 Sep-Oct       Impact factor: 1.826

4.  Metastatic pheochromocytoma/paraganglioma related to primary tumor development in childhood or adolescence: significant link to SDHB mutations.

Authors:  Kathryn S King; Tamara Prodanov; Vitaly Kantorovich; Tito Fojo; Jacqueline K Hewitt; Margaret Zacharin; Robert Wesley; Maya Lodish; Margarita Raygada; Anne-Paule Gimenez-Roqueplo; Shana McCormack; Graeme Eisenhofer; Dragana Milosevic; Electron Kebebew; Constantine A Stratakis; Karel Pacak
Journal:  J Clin Oncol       Date:  2011-10-03       Impact factor: 44.544

Review 5.  Birt-Hogg-Dubé syndrome: diagnosis and management.

Authors:  Fred H Menko; Maurice A M van Steensel; Sophie Giraud; Lennart Friis-Hansen; Stéphane Richard; Silvana Ungari; Magnus Nordenskjöld; Thomas Vo Hansen; John Solly; Eamonn R Maher
Journal:  Lancet Oncol       Date:  2009-12       Impact factor: 41.316

Review 6.  von Hippel-Lindau disease.

Authors:  Russell R Lonser; Gladys M Glenn; McClellan Walther; Emily Y Chew; Steven K Libutti; W Marston Linehan; Edward H Oldfield
Journal:  Lancet       Date:  2003-06-14       Impact factor: 79.321

7.  Genetic/familial high-risk assessment: breast and ovarian, version 1.2014.

Authors:  Mary B Daly; Robert Pilarski; Jennifer E Axilbund; Saundra S Buys; Beth Crawford; Susan Friedman; Judy E Garber; Carolyn Horton; Virginia Kaklamani; Catherine Klein; Wendy Kohlmann; Allison Kurian; Jennifer Litton; Lisa Madlensky; P Kelly Marcom; Sofia D Merajver; Kenneth Offit; Tuya Pal; Boris Pasche; Gwen Reiser; Kristen Mahoney Shannon; Elizabeth Swisher; Nicoleta C Voian; Jeffrey N Weitzel; Alison Whelan; Georgia L Wiesner; Mary A Dwyer; Rashmi Kumar
Journal:  J Natl Compr Canc Netw       Date:  2014-09       Impact factor: 11.908

8.  Succinate dehydrogenase kidney cancer: an aggressive example of the Warburg effect in cancer.

Authors:  Christopher J Ricketts; Brian Shuch; Cathy D Vocke; Adam R Metwalli; Gennady Bratslavsky; Lindsay Middelton; Youfeng Yang; Ming-Hui Wei; Stephen E Pautler; James Peterson; Catherine A Stolle; Berton Zbar; Maria J Merino; Laura S Schmidt; Peter A Pinto; Ramaprasad Srinivasan; Karel Pacak; W Marston Linehan
Journal:  J Urol       Date:  2012-10-18       Impact factor: 7.450

9.  Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.

Authors:  E R Maher; A R Webster; F M Richards; J S Green; P A Crossey; S J Payne; A T Moore
Journal:  J Med Genet       Date:  1996-04       Impact factor: 6.318

10.  Tuberous sclerosis complex surveillance and management: recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference.

Authors:  Darcy A Krueger; Hope Northrup
Journal:  Pediatr Neurol       Date:  2013-10       Impact factor: 3.372

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  5 in total

1.  Correction of data.

Authors: 
Journal:  Can Urol Assoc J       Date:  2017-08-15       Impact factor: 1.862

2.  Canadian Urological Association guideline: Management of small renal masses - Full-text.

Authors:  Patrick O Richard; Philippe D Violette; Bimal Bhindi; Rodney H Breau; Wassim Kassouf; Luke T Lavallée; Michael Jewett; John R Kachura; Anil Kapoor; Maxine Noel-Lamy; Michael Ordon; Stephen E Pautler; Frédéric Pouliot; Alan I So; Ricardo A Rendon; Simon Tanguay; Christine Collins; Maryam Kandi; Bobby Shayegan; Andrew Weller; Antonio Finelli; Andrea Kokorovic; Jay Nayak
Journal:  Can Urol Assoc J       Date:  2022-02       Impact factor: 1.862

3.  Early-onset renal cell carcinoma in PTEN harmatoma tumour syndrome.

Authors:  Raymond H Kim; Xiangling Wang; Andrew J Evans; Steven C Campbell; Jane K Nguyen; Kirsten M Farncombe; Charis Eng
Journal:  NPJ Genom Med       Date:  2020-09-29       Impact factor: 8.617

4.  Bevacizumab Plus Erlotinib Combination Therapy for Advanced Hereditary Leiomyomatosis and Renal Cell Carcinoma-Associated Renal Cell Carcinoma: A Multicenter Retrospective Analysis in Korean Patients.

Authors:  Yeonjoo Choi; Bhumsuk Keam; Miso Kim; Shinkyo Yoon; Dalyong Kim; Jong Gwon Choi; Ja Young Seo; Inkeun Park; Jae Lyun Lee
Journal:  Cancer Res Treat       Date:  2019-03-25       Impact factor: 4.679

5.  Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome in Spain: Clinical and Genetic Characterization.

Authors:  A Beatriz Sánchez-Heras; Adela Castillejo; Juan D García-Díaz; Mercedes Robledo; Alexandre Teulé; Rosario Sánchez; Ángel Zúñiga; Enrique Lastra; Mercedes Durán; Gemma Llort; Carmen Yagüe; Teresa Ramon Y Cajal; Consol López San Martin; Adrià López-Fernández; Judith Balmaña; Luis Robles; José M Mesa-Latorre; Isabel Chirivella; María Fonfria; Raquel Perea Ibañez; M Isabel Castillejo; Inés Escandell; Luis Gomez; Pere Berbel; Jose Luis Soto
Journal:  Cancers (Basel)       Date:  2020-11-05       Impact factor: 6.639

  5 in total

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