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Endoscopic endonasal approach for acromegaly: surgical outcomes using 2018 consensus criteria for remission

ABSTRACT

Objective:

The primary aim is to analyze the endoscopic endonasal surgical results in short-term and two-year follow-ups according to the 11th Acromegaly Consensus statement (2018). Indeed, prognostic factors and complications were analyzed.

Subjects and methods:

40 patients who underwent endoscopic endonasal surgery by acromegaly between 2013 to 2020 was analyzed. Patients were considered in remission if an upper limit of normal (ULN) IGF-1 was less than 1.0 at the six-month and two-year follow-ups. Moreover, we assessed the Knosp grade, tumor volumetry, ULN, T2 signal in MRI, reoperation, and complications.

Results:

The mean age of admission was 46.7 years. Thirty-two patients were in remission after six months of surgery (80%), decreasing to 76.32% at the two-year follow-up. All microadenomas presented remission (n = 6). Regarding the complications, three patients had permanent panhypopituitarism (7.5%); postoperative cerebrospinal fluid (CSF) leaks did not occur in this series. The hyperintense signal on the T2 MRI and a higher tumor volumetry were the single predictor's factors of non-emission in a multivariate regression logistic analysis (p < 0.05). Preoperative hormone levels (GH and IGF-1) were not a prognostic factor for remission. The re-operated patients who presented hypersignal already had a high predictor of clinical-operative failure.

Conclusion:

The endoscopic endonasal surgery promotes high short-term and two-year remission rates in acromegaly; the tumor's volumetry and the T2 hypersignal were statistically significant prognostic factors in non-remission – the complications presented at similar rates in comparison to the literature. In invasive GH-secreting tumors, we should offer these patients a multi-disciplinary approach to improve acromegalic patients’ remission rates.

Keywords
Acromegaly; endoscopic endonasal; transsphenoidal surgery; surgical outcomes

INTRODUCTION

Pituitary adenoma accounts for up to 15% of all primary intracranial tumors. Acromegaly is a chronic systemic disease caused by an excessive growth hormone (GH) and insulin-like growth factor 1 (IGF-1) secretion, in a substantial majority due to a GH-secreting pituitary adenoma (11 Cardinal T, Rutkowski MJ, Micko A, Shiroishi M, Jason Liu CS, Wrobel B, et al. Impact of tumor characteristics and pre- and postoperative hormone levels on hormonal remission following endoscopic transsphenoidal surgery in patients with acromegaly. Neurosurg Focus. 2020;48(6):E10.).

Acromegaly has an estimated prevalence and annual incidence of 59 and 3.8 cases per million inhabitants per year, respectively (22 Crisafulli S, Luxi N, Sultana J, Fontana A, Spagnolo F, Giuffrida G, et al. Global epidemiology of acromegaly: a systematic review and meta-analysis. Eur J Endocrinol. 2021;185(2):251-63.). Therefore, the diagnosis is often made during life's 3rd to 4th decade (33 Jallad RS, Bronstein MD. Acromegaly in the elderly patient. Arch Endocrinol Metab. 2019;63(6):638-45.). The key clinical features are acral enlargement, coarse face, headaches, arthropathy, hyperglycemia, cardiomyopathy, and sleep apnea. In addition, the disease increases the standardized mortality ratio (SMR) in 1.7 of these patients compared to the general population (44 Holdaway IM, Bolland MJ, Gamble GD. A meta-analysis of the effect of lowering serum levels of GH and IGF-I on mortality in acromegaly. Eur J Endocrinol. 2008;159(2):89-95.). The diagnosis is confirmed by elevated GH and IGF-1 levels in patients with a specific clinical picture, followed by a pituitary MRI to determine the source of the excess GH (55 Cordido F, Garcia Arnes JA, Marazuela Aspiroz M, Torres Vela E; Grupo de Neuroendocrinologia de la Sociedad Espanola de Endocrinologia y N. [Practical guidelines for diagnosis and treatment of acromegaly. Grupo de Neuroendocrinologia de la Sociedad Espanola de Endocrinologia y Nutricion]. Endocrinol Nutr. 2013;60(8):457e1-e15.). Hormonal control results in the reduction of symptoms and mortality rates; hence, the acromegaly treatment aims to normalize IGF-1 levels, according to the 11th Acromegaly Consensus Conference (66 Melmed S, Bronstein MD, Chanson P, Klibanski A, Casanueva FF, Wass JAH, et al. A Consensus Statement on acromegaly therapeutic outcomes. Nat Rev Endocrinol. 2018;14(9):552-61.).

The treatment options for acromegaly include surgery, medical treatment, and radiosurgery. Surgical resection has been considered the first-line treatment for acromegaly, mainly in pituitary tumor centers of excellence (PTCOE) (77 Casanueva FF, Barkan AL, Buchfelder M, Klibanski A, Laws ER, Loeffler JS, et al. Correction to: Criteria for the definition of Pituitary Tumor Centers of Excellence (PTCOE): A Pituitary Society Statement. Pituitary. 2018;21(6):663.). In this context, the endoscopic endonasal approach has been the best approach for most pituitary tumors. It promotes a broad view, facilitating the resection of tumors in the suprasellar area and the cavernous sinus. The overall biochemical remission rates in endoscopic series vary from 38% to 85% using previous consensus criteria (88 Jane JA Jr, Starke RM, Elzoghby MA, Reames DL, Payne SC, Thorner MO, et al. Endoscopic transsphenoidal surgery for acromegaly: remission using modern criteria, complications, and predictors of outcome. J Clin Endocrinol Metab. 2011;96(9):2732-40.). This study aims to analyze endoscopic endonasal surgical outcomes in short-term and two-year follow-ups, predictors of remission, and complications of acromegalic surgically treated patients from a single tertiary center according to the 11th Acromegaly Consensus Statement (2018) (66 Melmed S, Bronstein MD, Chanson P, Klibanski A, Casanueva FF, Wass JAH, et al. A Consensus Statement on acromegaly therapeutic outcomes. Nat Rev Endocrinol. 2018;14(9):552-61.).

SUBJECTS AND METHODS

All acromegalic patients who underwent surgery between January 2013 and December 2020 had their data retrospectively analyzed. In this sample, of 44 operated patients, four had incomplete data and were excluded.

The diagnosis was defined based on proportionately high growth hormone (GH) and insulin-like growth factor (IGF-1) associated with the contrast enhanced tumors detectable on pituitary resonance imaging (MRI). The IGF-1 upper limit of normal (ULN), calculated by using the patient IGF-1/upper limit of normal IGF-1 for age and sex, was considered high when ≥ 1.00. Several laboratories assessed GH and IGF-1; however, IMMULITE 2000 (Siemens Healthineers, Malvern, PA, USA) chemiluminescent methods are the predominant GH and IGF-1 laboratory kits in the state of Goiás, Brazil, where all patients reside. Moreover, IGF-1 ULN calculation makes IGF-1 assessments comparable among patients.

The contrast T1-weighted and T2-weighted MRI acquisitions were performed. An experienced neuroradiologist (especially regarding modified Knosp and T2 signal – hypointense or hyperintense relative to the adjacent pituitary gland or the grey matter of temporal cortical signal) suggested densely or sparsely granular tumors, respectively (99 Potorac I, Beckers A, Bonneville JF. T2-weighted MRI signal intensity as a predictor of hormonal and tumoral responses to somatostatin receptor ligands in acromegaly: a perspective. Pituitary. 2017;20(1):116-20.). About re-operated patients, the T2-MRI signal was analyzed based on the MRI performed before their first surgery. Tumor volume was calculated using the Di chiro-Nelson formula (V= 1/2 H. W. L); H – the height of hypophysis or craniocaudal size (cm); W – width or lateral size (cm); L – the length of hypophysis or anteroposterior size (cm) (1010 Di Chiro G, Nelson KB. The volume of the sella turcica. Am J Roentgenol Radium Ther Nucl Med. 1962;87:989-1008.). The modified Knosp classification to estimate the cavernous sinus invasion is shown in Table 1. We divided the modified Knosp into two groups: Knosp 0, 1, 2 (non-invasive tumors) and Knosp 3A, 3B e 4 (invasive tumors).

Table 1
Knosp modificated (1111 Micko AS, Wohrer A, Wolfsberger S, Knosp E. Invasion of the cavernous sinus space in pituitary adenomas: endoscopic verification and its correlation with an MRI-based classification. J Neurosurg. 2015;122(4):803-11.)

The primary outcome was defined as biochemical remission according to the 2018 Acromegaly consensus criteria; In this statement, IGF-1 normalization best reflects disease control. IGF-1 levels were evaluated after correcting eventual thyroid and steroidal former postoperative deficits at the six-month and two-year follow-ups. The senior surgeon (RACC) performed all surgical procedures after a careful endocrinological workup. Out of that, nine patients had undergone surgery in another medical facility using the sub-labial transsphenoidal microscopic approach. They were under somatostatin analogs medicine after this approach. The other 31 patients had not been treated with medication for acromegaly. Besides, acromegaly-related comorbidities (such as systemic arterial hypertension, Mellitus Diabetes, and malignant disease) were set down. Normal IGF-1 levels for age and sex and ULN < 1.0, at the six-month and two-year follow-ups, with no somatostatin analogs or cabergoline use, associated with no visible pituitary tumor MRI defined the remission state in a short-term and two-year follow-ups.

Statistical analysis

The Kolmogorov-Smirnov test of normality defined sample distribution. Due to Gaussian distribution, parametric comparisons were made between groups of two by two using paired t-tests. The Wilcoxon test analyzed modified Knosp and the presence of remission. In the unpaired analyzes between different groups, the Mann-Whitney test was used (Wilcoxon rank-sum test). The χ2 test (Chi-square) and corresponding Fisher test were used for risk verification. Pearson's correlation coefficient correlated the different tests for the response pattern taking IGF-1 and the direct measure of the ULN adjusted for sex and age as the standards. The evaluation of remission predictors was analyzed by binomial logistic regression analysis. A p-value < 0.05 was considered statistically significant. All analyzes were performed by R Software, version 4.2 (The R Foundation, USA).

RESULTS

Of 40 patients, 21 patients (52,5%) were female. The mean age at surgery was 46.7 ± 13.1 years (19-73 years). Patients were follow-up with from 6 to 63 months (41.5 ± 21.63 months).

Nine patients (22.5%) underwent a previous surgery in another facility; however, these patients presented a residual lesion at the postoperative pituitary MRI. Thus, they were placed on medical treatment using somatostatin analogs for acromegaly. The remaining 31 patients (77.5%) had not experienced any earlier medical or surgical treatment. Regarding the lesion size, 85% (n = 34) were macroadenomas and 15% (n = 6) were microadenomas. The recorded volume was 1.45 ± 13.64 cm³ (0.034-28.8 cm³). Concerning the modified Knosp score (Table 1), lesions were evaluated at T1 gadolinium-enhanced MRI with the identification of 16 patients in grade 0 (40%), nine patients in grade 1 (22.5%), nine patients in grade 2 (22.5%), three patients in grade 3A (7.5%), one patient in grade 3B (2.5%) and two patients in grade 4 (5%) (1111 Micko AS, Wohrer A, Wolfsberger S, Knosp E. Invasion of the cavernous sinus space in pituitary adenomas: endoscopic verification and its correlation with an MRI-based classification. J Neurosurg. 2015;122(4):803-11.). Hence, 34 (85%) patients harbored non-invasive tumors (Knosp 0, 1, and 2), and six patients (15%) had invasive tumors (Knosp 3A, 3B, and 4). Of the 40 patients, 14 had a hyperintense signal on the T2 MRI (35%), as summarized in Table 2.

Table 2
Demographic characteristics of the series studied in relation to the parameters analyzed

Regarding hormonal assessments obtained through chemiluminescence, the preoperative GH levels were 34.29 ± 125.16 μUI/L (0.4-800 ng/mL), whereas IGF-1 levels had 599.60 ± 244 ng/mL (236-1309 ng/mL). The IGF-1 ULN had a mean of 2.52 ± 1.10 (0.98-5.76). Furthermore, 16 patients (40%) had Mellitus diabetes that impairs the oral glucose tolerance test (OGTT) – GH assessment.

After surgery, GH levels at six months dropped to 1.27 ± 1.71 ng/mL (0.05-10 ng/mL), while IGF-1 levels of 217 ± 136 ng/mL (81-742 ng/mL), (p < 0.05). The calculated ULN was 0.92 ± 0.61 (0.37-3.86). The IGF-1 mean was 203 ± 131 (0.15-545), and the calculated ULN means kept at lower levels of 0.89 ± 0.58 (0.2-3.2), p < 0.001 at two-year follow-up.

Remission data

Eight patients (20%) did not achieve hormonal remission after six months, and 32 were in remission (80%). At two-year follow-up the remission rate decreased to 76.32%. Two patients died one-year after surgery due to COVID-19 and one patient died by non-acromegaly related diseases. One patient relapsed during this period of two-year follow-up after short-term remission. As for the established remission criteria, both GH and IGF-1 were equally effective (p = 0.80).

Two reoperations showed no remission (22.22% of reoperations). Patients who had not undergone previous surgery had a remission rate of 80.64% (25 of 31), against 77.78% of reoperations (7 patients).

Eight macroadenomas (23.52%) do not present remission. Meanwhile, all microadenomas presented remission.

Prognostic factors

Firstly, we performed a univariate logistic regression analysis model considering GH and IGF-1 preoperative levels, tumor volume, reoperation, the signal on T2-weighted MRI, gender, and modified Knosp grade. The p-value was statistically significant if p < 0.2. In the initial model, only signal on T2-weighted MRI, gender, modified Knosp grade, and volume was predictive of remission. In the final logistic regression analysis model, only a higher tumor volume and hyper signal on T2-weighted MRI were predictors for non-remission (Table 3). The hyperintense signal on the T2 MRI was related to a lower remission rate (5 patients, 37.5% in the subgroup) with p < 0.05, as shown in table 3 (p < 0.05). Of the 26 patients with a T2 hypointense signal, only three did not present remission, 11.5% within the subgroup (Figure 1).

Figure 1
Alluvial diagram demonstrating relationship between T2 signal in MRI and remission.
Table 3
Multivariate analysis using by binomial logistic regression of remission with respect to tumor volume and T2 signal

Table 3 summarizes the variables regarding the statistical analysis in the binomial logistic regression based on remission with their respective confidence intervals.

The regression analyzes demonstrate a compelling joint effect of reoperation with hypersignal as factors strongly associated with surgical failure, which cannot be evidenced in the isolated analysis of reoperation. Re-operated patients who presented hypersignal already had a higher prediction of clinical-operative failure.

Additionally, we did not find a significant statistical association between hyposignal on T2 MRI and non-invasive tumors – Knosp (0, 1, 2) (P > 0.05); there was no association found between smaller tumors and hyposignal on T2-MRI using a Chi-square test.

Complications

Three patients developed permanent postoperative panhypopituitarism (7.5%). Epistaxis, transient abducens paresis, cerebrospinal fluid (CSF) leak, meningitis, recurrent rhinosinusitis, and persistent diabetes insipidus occurred once in six isolated patients (2.5% each). There were no procedure-related postoperative deaths during data recording (30 days to 2 years).

Table 3 summarizes the variables regarding the statistical analysis in the binomial logistic regression based on remission with their respective confidence intervals. Figure 2 shows the analysis of covariance.

Figure 2
Signal covariate interaction analysis on T2 in the reoperated and non-reoperated groups based on postoperative ULN level.

The regression analysis demonstrates a compelling joint effect of reoperation with hypersignal as factors strongly associated with surgical failure, which cannot be evidenced in the isolated analysis of reoperation, however, maintained in the isolated analysis of signal on T2 (Figure 2). Re-operated patients who presented hypersignal already had a higher prediction of clinical-operative failure.

DISCUSSION

In recent decades, endoscopic endonasal treatment of sellar lesions has proven to be a viable option for lesions that extend beyond the midline (1212 Hazer DB, Isik S, Berker D, Guler S, Gurlek A, Yucel T, et al. Treatment of acromegaly by endoscopic transsphenoidal surgery: surgical experience in 214 cases and cure rates according to current consensus criteria. J Neurosurg. 2013;119(6):1467-77.). Its importance portrays better exposure, more panoramic and instrument maneuverability, ability to look around anatomical corners using angled lenses, less nasal trauma, greater patient comfort, and better results concerning more extensive tumor resection (1313 Gondim JA, Almeida JP, de Albuquerque LA, Gomes E, Schops M, Ferraz T. Pure endoscopic transsphenoidal surgery for treatment of acromegaly: results of 67 cases treated in a pituitary center. Neurosurg Focus. 2010;29(4):E7.). Thus, the endoscopic technique may be preferred, and it is suggested that more than 90% of pituitary tumors, mainly invasive GH – secreting macroadenomas, should be treated through this approach (1414 Leopoldo C, Leopoldo F, Santos A, Veiga JCE, Lima JVJ, Scalissi NM, et al. Long term follow-up of growth hormone-secreting pituitary adenomas submitted to endoscopic endonasal surgery. Arq Neuropsiquiatr. 2017;75(5):301-6.,1515 Wagenmakers MA, Netea-Maier RT, van Lindert EJ, Pieters GF, Grotenhuis AJ, Hermus AR. Results of endoscopic transsphenoidal pituitary surgery in 40 patients with a growth hormone-secreting macroadenoma. Acta Neurochir (Wien). 2011;153(7):1391-9.).

We found an overall surgical remission of 76% and 100% for macroadenomas and microadenomas, respectively, using the 2018 consensus criteria for remission in acromegaly. This result agrees with other endoscopic series (88 Jane JA Jr, Starke RM, Elzoghby MA, Reames DL, Payne SC, Thorner MO, et al. Endoscopic transsphenoidal surgery for acromegaly: remission using modern criteria, complications, and predictors of outcome. J Clin Endocrinol Metab. 2011;96(9):2732-40.). In these series, the surgical remission rates vary from 67%-100% for microadenomas and 55%-80% for macroadenomas using different consensus criteria (2000 and 2010). We considered six-month follow-up remission patients with normal for age and sex IGF-1 and < 1.0 IGF-1 ULN. When choosing the six-month, the authors tried to avert the delayed decline of IGF-1 levels after surgery, reaching 24% of patients in the final analysis (1616 Fujio S, Tokimura H, Hanaya R, Hirano H, Arita K, Yunoue S, et al. Gradual declination of IGF-1 over a year after transsphenoidal adenomectomy of GH producing pituitary adenomas. Endocr J. 2011;58(12):1087-91.). As the 2018 consensus recommended, a key goal for remission is the normalization of IGF-1 levels. As suggested, we did not consider postoperative GH levels in this analysis for remission due to our practice's lack of ultrasensitive GH assays, pulsatile nature, and multiple GH assay kits. Moreover, 40% of our patients had mellitus diabetes which impairs oral glucose tolerance test (OGTT) – GH evaluation.

Analyzing predictors of remission, we did not find predictions of remission for preoperative GH and IGF-1 levels. On the other hand, the volumetry, and the hyper signal on T2 weighted MRI were predictors for non-remission using binomial logistic regression analysis.

Preoperative GH and IGF-1 levels are considered predictors for remission in some series (1717 Kasuki L, Rocha PDS, Lamback EB, Gadelha MR. Determinants of morbidities and mortality in acromegaly. Arch Endocrinol Metab. 2019;63(6):630-7.,1818 Gadelha MR, Kasuki L, Lim DST, Fleseriu M. Systemic Complications of Acromegaly and the Impact of the Current Treatment Landscape: An Update. Endocr Rev. 2019;40(1):268-332.). However, we did not find this correlation like Antunes and Yildirim (1919 Yildirim AE, Sahinoglu M, Divanlioglu D, Alagoz F, Gurcay AG, Daglioglu E, et al. Endoscopic endonasal transsphenoidal treatment for acromegaly: 2010 consensus criteria for remission and predictors of outcomes. Turk Neurosurg. 2014;24(6):906-12.,2020 Antunes X, Ventura N, Camilo GB, Wildemberg LE, Guasti A, Pereira PJM, et al. Predictors of surgical outcome and early criteria of remission in acromegaly. Endocrine. 2018;60(3):415-22.). Concerning factors associated with non-remission: tumor volumetry is a controversial topic; some series show that higher volume tumors are isolated predictors for remission, in the same way as our study. In other series, they have not observed such a difference. The origin of this controversy is based on a lack of analysis of cavernous sinus tumor invasion in some studies.

As for cavernous sinus invasion, our study demonstrated that tumors with Knosp more than 3B have more propensity to non-remission, like many other studies (11 Cardinal T, Rutkowski MJ, Micko A, Shiroishi M, Jason Liu CS, Wrobel B, et al. Impact of tumor characteristics and pre- and postoperative hormone levels on hormonal remission following endoscopic transsphenoidal surgery in patients with acromegaly. Neurosurg Focus. 2020;48(6):E10.,88 Jane JA Jr, Starke RM, Elzoghby MA, Reames DL, Payne SC, Thorner MO, et al. Endoscopic transsphenoidal surgery for acromegaly: remission using modern criteria, complications, and predictors of outcome. J Clin Endocrinol Metab. 2011;96(9):2732-40.,2121 Albarel F, Castinetti F, Morange I, Conte-Devolx B, Gaudart J, Dufour H, et al. Outcome of multimodal therapy in operated acromegalic patients, a study in 115 patients. Clin Endocrinol (Oxf). 2013;78(2):263-70.). Recently, Mohyeldin and cols. raised questions about the reliability of the Knosp score in predicting an actual invasion of the medial of the cavernous sinus by pituitary adenomas, mainly for acromegalic patients. Their study found invasion in the medial wall in 25%, 67%, and 100% for Knosp 0, 1, 2, 3, and 4, respectively (2222 Mohyeldin A, Katznelson LJ, Hoffman AR, Asmaro K, Ahmadian SS, Eltobgy MM, et al. Prospective intraoperative and histologic evaluation of cavernous sinus medial wall invasion by pituitary adenomas and its implications for acromegaly remission outcomes. Sci Rep. 2022;12(1):9919.). This finding suggests that the medial wall resection should be considered for acromegalic patients once the authors reach remission rates of 92% using this maneuver. This topic is still controversial. Nonetheless, it could explain why we have not achieved remission in four patients with Knosp 1 and 2 despite gross total tumor removal in the intraoperative analysis and postoperative MRI scan.

The hypointense signal on the T2 MRI was highly related to remission: in 23 of 26 patients (88.5% within the subgroup), as seen in the Alluvial Plot (Figure 1). Besides, the hyperintense signal was related to a lower remission rate (5 patients, 37.5% in the subgroup) with p < 0.05. Our study is the first in the literature to report the hyper signal on T2-MRI as a predictor for non-remission. This finding can help us to predict remission using pre-surgical imaging. Potorac and cols. have shown that T2-hypointense tumors are less likely to invade the cavernous sinus and have densely granulated patterns. Those characteristics may implicate a better response to somatostatin ligand therapy and more significant tumor shrinkage (99 Potorac I, Beckers A, Bonneville JF. T2-weighted MRI signal intensity as a predictor of hormonal and tumoral responses to somatostatin receptor ligands in acromegaly: a perspective. Pituitary. 2017;20(1):116-20.,2020 Antunes X, Ventura N, Camilo GB, Wildemberg LE, Guasti A, Pereira PJM, et al. Predictors of surgical outcome and early criteria of remission in acromegaly. Endocrine. 2018;60(3):415-22.,2323 Akkaya E, Akgun MY, Sebnem Durmaz E, Aydin S, Mefkure Ozkaya H, Comunoglu N, et al. T2-weighted magnetic resonance imaging as a novel predictor of surgical remission in newly diagnosed pituitary macroadenomas presenting as acromegaly. J Clin Neurosci. 2021;90:105-11.). On the contrary, analyzing the T2 signal, we found just a single author that evaluated this correlation. Antunes’ article did not find a correlation between the signal on T2 and surgical remission (2020 Antunes X, Ventura N, Camilo GB, Wildemberg LE, Guasti A, Pereira PJM, et al. Predictors of surgical outcome and early criteria of remission in acromegaly. Endocrine. 2018;60(3):415-22.).

Meanwhile, the remission rate on reoperation was 77.78% (7 of 9), and for those who had not undergone previous surgery was 80.64% (25 of 31). It was noted as statistically significant in the covariance analysis (p = 0.0032). Concurring with others studies (2424 Buchfelder M, Schlaffer SM. The surgical treatment of acromegaly. Pituitary. 2017;20(1):76-83.

25 Jahangiri A, Wagner J, Han SW, Zygourakis CC, Han SJ, Tran MT, et al. Morbidity of repeat transsphenoidal surgery assessed in more than 1000 operations. J Neurosurg. 2014;121(1):67-74.

26 Wilson TJ, McKean EL, Barkan AL, Chandler WF, Sullivan SE. Repeat endoscopic transsphenoidal surgery for acromegaly: remission and complications. Pituitary. 2013;16(4):459-64.
-2727 Yamada S, Fukuhara N, Oyama K, Takeshita A, Takeuchi Y. Repeat transsphenoidal surgery for the treatment of remaining or recurring pituitary tumors in acromegaly. Neurosurgery. 2010;67(4):949-56.), surgical results are generally less favorable than in primary operations. Furthermore, some complications increased in reoperations for pituitary tumors because of tissue defects that distort the anatomy and postoperative sequelae, making surgery technically more difficult.

Nevertheless, surgery complications such as epistaxis, transient abducens paresis, meningitis, recurrent rhinosinusitis, and persistent diabetes insipidus (2,5%) were not typical in our series. In addition, one patient had postoperative CSF leaks (2,5%), and three patients had permanent panhypopituitarism (7.5%). The reported incidence of rhinorrhea in the postoperative period of endoscopic pituitary surgery generally varies between 0.7% and 12%, and the risk of permanent diabetes insipidus with endoscopic surgery was 0.7% to 8.5%. Moreover, carotid artery injury is a rare but severe and potentially fatal complication reported at less than 1% (2828 Nishioka H. Recent Evolution of Endoscopic Endonasal Surgery for Treatment of Pituitary Adenomas. Neurol Med Chir (Tokyo). 2017;57(4):151-8.).

On the other hand, Leopoldo and cols. series (23 patients evaluated for GH-secreting adenomas resection) found complications in 56,5% of patients: 8,7% with permanent diabetes insipidus, 17.4% with otorhinolaryngologic complications, 4,3% with meningitis, 21.7% with CSF leaks, and 8.7% developed new panhypopituitarism (1414 Leopoldo C, Leopoldo F, Santos A, Veiga JCE, Lima JVJ, Scalissi NM, et al. Long term follow-up of growth hormone-secreting pituitary adenomas submitted to endoscopic endonasal surgery. Arq Neuropsiquiatr. 2017;75(5):301-6.). Gondim and cols. (67 cases) found epistaxis (6.0%), transitory diabetes insipidus (4.5%), one case of seizure (1.5%) and five cases of permanent thyroid hormone deficiency (7,5%) (1313 Gondim JA, Almeida JP, de Albuquerque LA, Gomes E, Schops M, Ferraz T. Pure endoscopic transsphenoidal surgery for treatment of acromegaly: results of 67 cases treated in a pituitary center. Neurosurg Focus. 2010;29(4):E7.).

As noted, our series had a low complication rate. We can assume that this reflects our objective diagnostic criteria and preoperative imaging, besides optimal and adequate surgical technique. As was also seen in the series by Hazer and cols. in which it was essential for the first surgery to be performed by an experienced senior surgeon, thus contributing to higher cure rates (1212 Hazer DB, Isik S, Berker D, Guler S, Gurlek A, Yucel T, et al. Treatment of acromegaly by endoscopic transsphenoidal surgery: surgical experience in 214 cases and cure rates according to current consensus criteria. J Neurosurg. 2013;119(6):1467-77.).

Although the authors have presented one of the most extensive series in our country of endoscopic endonasal surgery for acromegaly, our study has some limitations due to the sample size and retrospective design.

In conclusion, the endoscopic endonasal surgery promotes high short-term and at two-year remission rates in acromegaly. The tumor's volumetry, and the T2 hypersignal, were statistically significant prognostic factors in non-remission. Complications presented at similar rates in comparison to the literature. In invasive GH secreting tumors, we should offer these patients a multi-disciplinary approach to improve acromegalic patients’ remission rates.

REFERENCES

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Publication Dates

  • Publication in this collection
    03 July 2023
  • Date of issue
    2023

History

  • Received
    03 Nov 2022
  • Accepted
    13 Mar 2023
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