PET-guided repeat transsphenoidal surgery for previously deemed unresectable lateral disease in acromegaly

Author:

Bashari Waiel A.12,Senanayake Russell12,Koulouri Olympia12,Gillett Daniel13,MacFarlane James12,Powlson Andrew S.12,Fernandez-Pombo Antia12,Bano Gul4,Martin Andrew J.5,Scoffings Daniel16,Cheow Heok136,Mendichovszky Iosif136,Tysome James17,Donnelly Neil17,Santarius Thomas18,Kolias Angelos18,Mannion Richard18,Gurnell Mark12

Affiliation:

1. Cambridge Endocrine Molecular Imaging Group,

2. Metabolic Research Laboratories, Wellcome Trust-MRC Institute of Metabolic Science; Departments of

3. Nuclear Medicine,

4. Endocrinology and

5. Neurosurgery, St George’s University Hospital, London, United Kingdom

6. Radiology,

7. Otolaryngology, and

8. Neurosurgery, University of Cambridge and National Institute for Health Research Cambridge Biomedical Research Centre, Addenbrooke’s Hospital, Hills Road, Cambridge; and Departments of

Abstract

OBJECTIVEThe object of this study was to determine if revision transsphenoidal surgery (TSS), guided by 11C-methionine PET/CT coregistered with volumetric MRI (Met-PET/MRCR), can lead to remission in patients with persistent acromegaly due to a postoperative lateral disease remnant.METHODSThe authors identified 9 patients with persistent acromegaly following primary intervention (TSS ± medical therapy ± radiotherapy) in whom further surgery had initially been discounted because of equivocal MRI findings with suspected lateral sellar and/or parasellar disease (cases with clear Knosp grade 4 disease were excluded). All patients underwent Met-PET/MRCR. Scan findings were used by the pituitary multidisciplinary team to inform decision-making regarding repeat surgery. Revision TSS was performed with wide lateral exploration as guided by the PET findings. Endocrine reassessment was performed at 6–10 weeks after surgery, with longitudinal follow-up thereafter.RESULTSMet-PET/MRCR revealed focal tracer uptake in the lateral sellar and/or parasellar region(s) in all 9 patients, which correlated with sites of suspected residual tumor on volumetric MRI. At surgery, tumor was identified and resected in 5 patients, although histological analysis confirmed somatotroph tumor in only 4 cases. In the other 4 patients, no definite tumor was seen, but equivocal tissue was removed. Despite the uncertainty at surgery, all patients showed immediate significant improvements in clinical and biochemical parameters. In the 8 patients for whom long-term follow-up data were available, insulin-like growth factor 1 (IGF-1) was ≤ 1.2 times the upper limit of normal (ULN) in all subjects and ≤ 1 times the ULN in 6 subjects, and these findings have been maintained for up to 28 months (median 8 months, mean 13 months) with no requirement for adjunctive medical therapy or radiotherapy. No patient suffered any additional pituitary deficit or other complication of surgery.CONCLUSIONSThis study provides proof of concept that Met-PET/MRCR can be helpful in the evaluation of residual lateral sellar/parasellar disease in persistent acromegaly and facilitate targeted revision TSS in a subgroup of patients.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

Neurology (clinical),General Medicine,Surgery

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