Your browser doesn't support javascript.
loading
CyberKnife robotic radiosurgery in the multimodal management of acromegaly patients with invasive macroadenoma: a single center's experience.
Sala, Elisa; Moore, Justin M; Amorin, Alvaro; Martinez, Hector; Bhowmik, Aprotim C; Lamsam, Layton; Chang, Steven; Soltys, Scott G; Katznelson, Laurence; Harsh, Griffith R.
Afiliação
  • Sala E; Unit of Endocrinology, Department of Clinical Sciences and Community Health, Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
  • Moore JM; Department of Neurological Surgery, Stanford Medical Center, Stanford University, Palo Alto, CA, USA.
  • Amorin A; Department of Neurological Surgery, Stanford Medical Center, Stanford University, Palo Alto, CA, USA.
  • Martinez H; Department of Neurological Surgery, Stanford Medical Center, Stanford University, Palo Alto, CA, USA.
  • Bhowmik AC; Department of Neurological Surgery, Stanford Medical Center, Stanford University, Palo Alto, CA, USA.
  • Lamsam L; Department of Neurological Surgery, Stanford Medical Center, Stanford University, Palo Alto, CA, USA.
  • Chang S; Department of Neurological Surgery, Stanford Medical Center, Stanford University, Palo Alto, CA, USA.
  • Soltys SG; Department of Radiation Oncology, Stanford Medical Center, Stanford University, Palo Alto, CA, USA.
  • Katznelson L; Department of Radiation Oncology, Stanford Medical Center, Stanford University, Palo Alto, CA, USA.
  • Harsh GR; Department of Neurological Surgery, Stanford Medical Center, Stanford University, Palo Alto, CA, USA.
J Neurooncol ; 138(2): 291-298, 2018 Jun.
Article em En | MEDLINE | ID: mdl-29429125
ABSTRACT
Surgery is the primary treatment for acromegaly. However, surgery may not be curative of some tumors, particularly invasive macroadenomas. Adjuvant radiation, specifically robotic stereotactic radiosurgery (rSRS), may improve the endocrine outcome. We retrospectively reviewed hormonal and radiological data of 22 acromegalic patients with invasive macroadenomas treated with rSRS at Stanford University Medical Center between 2000 and 2016. Prior to treatment, the tumor's median maximal diameter was 19 mm (2.5-50 mm). Cavernous sinus invasion occurred in 19 patients (86.3%) and compression of the optic chiasm in 2 (9.0%). At last follow up, with an average follow up of 43.2 months, all patients had a reduction in their IGF-1 levels (median IGF-1% upper limit of normal (ULN) baseline 136% vs last follow up 97%; p = 0.05); 9 patients (40.9%) were cured, and 4 (18.1%) others demonstrated biochemical control of acromegaly. The median time to cure was 50 months and the mean interval to cure or biochemical control was 30.3 months (± 24 months, range 6-84 months). Hypopituitarism was present in 8 patients (36.3%) and new pituitary deficits occurred in 6 patients with a median latency of 31.6 ± 14.5 months. At final radiologic follow-up, 3 tumors (13.6%) were smaller and 19 were stable in size. The mean biologically effective dose (BED) was higher in subjects cured compared to those with persistent disease, 163 Gy3 (± 47) versus 111 Gy3 (± 43), respectively (p = 0.01). No patient suffered visual deterioration. Robotic SRS is a safe and effective treatment for acromegaly radiation-induced visual complications and hypopituitarism is rare.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Hipofisárias / Acromegalia / Adenoma / Radiocirurgia / Procedimentos Cirúrgicos Robóticos Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Hipofisárias / Acromegalia / Adenoma / Radiocirurgia / Procedimentos Cirúrgicos Robóticos Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article