Literature DB >> 30590584

Recurrence in silent corticotroph adenomas after primary treatment: A systematic review and meta-analysis.

Athanasios Fountas1,2,3, Aikaterini Lavrentaki1,2, Anuradhaa Subramanian4, Konstantinos A Toulis4, Krishnarajah Nirantharakumar4, Niki Karavitaki1,2,3.   

Abstract

CONTEXT: 2017 WHO Classification of Pituitary Tumors grades silent corticotroph adenomas (SCAs) as "high-risk adenomas" due to their aggressive clinical behavior (high probability of recurrence). However, studies comparing recurrence rates of SCAs with other non-functioning pituitary adenoma (NFPAs) subtypes have provided conflicting results.
OBJECTIVE: Estimate recurrence rates of SCAs after primary treatment (surgery±radiotherapy) and recurrence rate ratios (RRR) between SCAs and other NFPA subtypes.
METHODS: Systematic review of published literature reporting on outcomes of SCAs up to October 31, 2017 was conducted. Recurrence rates, RRRs, 95% confidence intervals (CIs) were estimated from each study and pooled using random effects meta-analysis model.
RESULTS: For determination of SCAs recurrence rates, 14 studies (low risk of bias, 297 patients) were selected; recurrence rate was 5.96 (95% CI, 4.3-7.84) per 100 person-years. Based on studies with mean follow-up <5 or ≥5 years, 25% (cumulative incidence 0.25; 95% CI, 0.13-0.38) and 31% (cumulative incidence 0.31; 95% CI, 0.23-0.40) of SCAs had recurrence, respectively. Recurrence rates after surgery or surgery+radiotherapy were 5.41 (95% CI, 3.28-7.96) and 4.88 (95% CI, 0.67-11.54) cases per 100 person-years, respectively. Analysis of 10 eligible studies (moderate risk of bias, 244 SCAs, 1622 NFPAs) showed no significant RRR (1.44; 95% CI, 0.9-2.33, p=0.130) between the groups. Focus on tumors treated solely by surgery also revealed no significant RRR (1.17; 95% CI, 0.79-1.75, p=0.429).
CONCLUSIONS: Based on studies with mean follow-up ≥5 years, 31% of SCAs have recurrence. No evidence supporting higher recurrence risk of SCAs compared with other NFPA subtypes was found.

Entities:  

Year:  2018        PMID: 30590584     DOI: 10.1210/jc.2018-01956

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  14 in total

Review 1.  A standardised diagnostic approach to pituitary neuroendocrine tumours (PitNETs): a European Pituitary Pathology Group (EPPG) proposal.

Authors:  C Villa; A Vasiljevic; M L Jaffrain-Rea; O Ansorge; S Asioli; V Barresi; L Chinezu; M P Gardiman; A Lania; A M Lapshina; L Poliani; L Reiniger; A Righi; W Saeger; J Soukup; M Theodoropoulou; S Uccella; J Trouillas; F Roncaroli
Journal:  Virchows Arch       Date:  2019-10-02       Impact factor: 4.064

2.  Predicting early post-operative remission in pituitary adenomas: evaluation of the modified knosp classification.

Authors:  Marie Buchy; Véronique Lapras; Muriel Rabilloud; Alexandre Vasiljevic; Françoise Borson-Chazot; Emmanuel Jouanneau; Gérald Raverot
Journal:  Pituitary       Date:  2019-10       Impact factor: 4.107

Review 3.  Genetic Basis of ACTH-Secreting Adenomas.

Authors:  Pietro Locantore; Rosa Maria Paragliola; Gianluca Cera; Roberto Novizio; Ettore Maggio; Vittoria Ramunno; Andrea Corsello; Salvatore Maria Corsello
Journal:  Int J Mol Sci       Date:  2022-06-19       Impact factor: 6.208

4.  Impact of histopathological classification of non-functioning adenomas on long term outcomes: comparison of the 2004 and 2017 WHO classifications.

Authors:  Ajay Chatrath; Jacob Kosyakovsky; Parantap Patel; Jungeun Ahn; Mazin Elsarrag; Lena C Young; Angela Wu; Jennifer D Sokolowski; Davis Taylor; John A Jane; M Beatriz S Lopes
Journal:  Pituitary       Date:  2022-10-19       Impact factor: 3.599

5.  DNA damage and growth hormone hypersecretion in pituitary somatotroph adenomas.

Authors:  Anat Ben-Shlomo; Nan Deng; Evelyn Ding; Masaaki Yamamoto; Adam Mamelak; Vera Chesnokova; Artak Labadzhyan; Shlomo Melmed
Journal:  J Clin Invest       Date:  2020-11-02       Impact factor: 14.808

6.  Clinical, Laboratory, and Treatment Profiles of Silent Corticotroph Adenomas That Have Transformed to the Functional Type: A Case Series With a Literature Review.

Authors:  Guangyao Zheng; Lin Lu; Huijuan Zhu; Hui You; Ming Feng; Xiaohai Liu; Congxin Dai; Yong Yao; Renzhi Wang; Huabing Zhang; Xu Sun; Zhaolin Lu
Journal:  Front Endocrinol (Lausanne)       Date:  2020-09-23       Impact factor: 5.555

7.  A clinicoradiological analysis of silent corticotroph adenomas after the introduction of pituitary-specific transcription factors.

Authors:  Abhijit Goyal-Honavar; Sauradeep Sarkar; H S Asha; Nitin Kapoor; Rajesh Balakrishnan; Harshad Vanjare; Geeta Chacko; Ari G Chacko
Journal:  Acta Neurochir (Wien)       Date:  2021-06-28       Impact factor: 2.216

Review 8.  Aggressive Cushing's Disease: Molecular Pathology and Its Therapeutic Approach.

Authors:  Masaaki Yamamoto; Takahiro Nakao; Wataru Ogawa; Hidenori Fukuoka
Journal:  Front Endocrinol (Lausanne)       Date:  2021-06-16       Impact factor: 5.555

Review 9.  Aggressive pituitary neuroendocrine tumors: current practices, controversies, and perspectives, on behalf of the EANS skull base section.

Authors:  Sam Ng; Mahmoud Messerer; Julien Engelhardt; Michaël Bruneau; Jan Frederick Cornelius; Luigi Maria Cavallo; Giulia Cossu; Sebastien Froelich; Torstein R Meling; Dimitrios Paraskevopoulos; Henry W S Schroeder; Marcos Tatagiba; Idoya Zazpe; Moncef Berhouma; Roy T Daniel; Edward R Laws; Engelbert Knosp; Michael Buchfelder; Henri Dufour; Stéphane Gaillard; Timothée Jacquesson; Emmanuel Jouanneau
Journal:  Acta Neurochir (Wien)       Date:  2021-08-08       Impact factor: 2.816

10.  Phosphorylated EGFR (pEGFR T693) as a Novel Predictor of Recurrence in Non-Functioning Pituitary Adenomas.

Authors:  Ashutosh Rai; Liza Das; Kanchan K Mukherjee; Sivashanmugam Dhandapani; Manjul Tripathi; Chirag Kamal Ahuja; Bishan Dass Radotra; Pinaki Dutta
Journal:  Front Endocrinol (Lausanne)       Date:  2021-07-05       Impact factor: 5.555

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