Stereotactic radiosurgery for secretory pituitary adenomas: systematic review and International Stereotactic Radiosurgery Society practice recommendations

Author:

Mathieu David1,Kotecha Rupesh2,Sahgal Arjun3,De Salles Antonio4,Fariselli Laura5,Pollock Bruce E.6,Levivier Marc7,Ma Lijun8,Paddick Ian9,Regis Jean1011,Yomo Shoji12,Suh John H.13,Rubens Muni2,Sheehan Jason P.14

Affiliation:

1. Division of Neurosurgery, Université de Sherbrooke, Centre de recherche du Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Quebec, Canada;

2. Department of Radiation Oncology, Miami Cancer Institute, Baptist Health South Florida, Miami, Florida;

3. Department of Radiation Oncology, Sunnybrook Health Sciences Centre, University of Toronto, Ontario, Canada;

4. Department of Neurosurgery, University of California, Los Angeles, California;

5. Radiotherapy Unit–Neurosurgery Department, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy;

6. Department of Neurologic Surgery, Mayo Clinic, Rochester, Minnesota;

7. Department of Neurosurgery and Gamma Knife Center, Lausanne University Hospital, Lausanne, Switzerland;

8. Department of Radiation Oncology, University of California, San Francisco, California;

9. Medical Physics Ltd., Reading, United Kingdom;

10. Cromwell Hospital, London, United Kingdom;

11. Functional and Stereotaxic Neurosurgery Department, Clinical Neuroscience Federation, La Timone Hospital, Aix-Marseille University, Marseille, France;

12. Division of Radiation Oncology, Aizawa Comprehensive Cancer Center, Aizawa Hospital, Matsumoto, Japan

13. Department of Radiation Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio; and

14. Department of Neurological Surgery, University of Virginia, Charlottesville, Virginia

Abstract

OBJECTIVE A systematic review was performed to provide objective evidence on the use of stereotactic radiosurgery (SRS) in the management of secretory pituitary adenomas and develop consensus recommendations. METHODS The authors performed a systematic review of the English-language literature up until June 2018 using the PRISMA guidelines. The PubMed (Medline), Embase, and Cochrane databases were searched. A total of 45 articles reporting single-institution outcomes of SRS for acromegaly, Cushing’s disease, and prolactinomas were selected and included in the analysis. RESULTS For acromegaly, random effects meta-analysis estimates for crude tumor control rate, crude endocrine remission rate, and any new hypopituitarism rates were 97.0% (95% CI 96.0%–98.0%), 44.0% (95% CI 35.0%–53.0%), and 17.0% (95% CI 13.0%–23.0%), respectively. For Cushing’s disease, random effects estimates for crude tumor control rate, crude endocrine remission rate, and any new hypopituitarism rate were 92.0% (95% CI 87.0%–95.0%), 48.0% (95% CI 35.0%–61.0%), and 21.0% (95% CI 13.0%–31.0%), respectively. For prolactinomas, random effects estimates for crude tumor control rate, crude endocrine remission rate, and any new hypopituitarism rate were 93.0% (95% CI 90.0%–95.0%), 28.0% (95% CI 19.0%–39.0%), and 12.0% (95% CI 6.0%–24.0%), respectively. Meta-regression analysis did not show a statistically significant association between mean margin dose with crude endocrine remission rate or mean margin dose with development of any new hypopituitarism rate for any of the secretory subtypes. CONCLUSIONS SRS offers effective tumor control of hormone-producing pituitary adenomas in the majority of patients but a lower rate of endocrine improvement or remission.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

Genetics,Animal Science and Zoology

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