The Future of Somatostatin Receptor Ligands in Acromegaly

被引:52
作者
Gadelha, Monica R. [1 ,2 ,3 ,4 ,5 ]
Wildemberg, Luiz Eduardo [1 ,2 ,3 ,4 ]
Kasuki, Leandro [1 ,2 ,3 ,4 ]
机构
[1] Univ Fed Rio de Janeiro, Med Sch, Endocrine Unit, BR-21941913 Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Med Sch, Neuroendocrinol Res Ctr, BR-21941913 Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro, Hosp Univ Clementino Fraga Filho, BR-21941913 Rio De Janeiro, Brazil
[4] Inst Estadual Cerebro Paulo Niemeyer, Neuroendocrine Unit, Secretaria Estadual Saude, BR-20231092 Rio De Janeiro, Brazil
[5] Inst Estadual Cerebro Paulo Niemeyer, Neuropathol & Mol Genet Lab, Secretaria Estadual Saude, BR-20231092 Rio De Janeiro, Brazil
关键词
acromegaly; biomarker; precision medicine; somatostatin receptor; somatostatin receptor ligands; GENE-EXPRESSION LEVELS; PITUITARY-ADENOMAS; OCTREOTIDE LAR; GROWTH-HORMONE; QUANTITATIVE-ANALYSIS; BIOCHEMICAL RESPONSE; CLINICAL-RESPONSE; POTENT INHIBITOR; ORAL OCTREOTIDE; PRIMARY THERAPY;
D O I
10.1210/clinem/dgab726
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Currently, the first-generation somatostatin receptor ligands (fg-SRLs), octreotide LAR and lanreotide autogel, are the mainstays of acromegaly treatment and achieve biochemical control in approximately 40% of patients and tumor shrinkage in over 60% of patients. Pasireotide, a second-generation SRL, shows higher efficacy with respect to both biochemical control and tumor shrinkage but has a worse safety profile. In this review, we discuss the future perspectives of currently available SRLs, focusing on the use of biomarkers of response and precision medicine, new formulations of these SRLs and new drugs, which are under development. Precision medicine, which is based on biomarkers of response to treatment, will help guide the decision-making process by allowing physicians to choose the appropriate drug for each patient and improving response rates. New formulations of available SRLs, such as oral, subcutaneous depot, and nasal octreotide, may improve patients' adherence to treatment and quality of life since there will be more options available that better suit each patient. Finally, new drugs, such as paltusotine, somatropin, ONO-5788, and ONO-ST-468, may improve treatment adherence and present higher efficacy than currently available drugs.
引用
收藏
页码:297 / 308
页数:12
相关论文
共 100 条
[1]   Novel long-acting somatostatin analog with endocrine selectivity: Potent suppression of growth hormone but not of insulin [J].
Afargan, M ;
Janson, ET ;
Gelerman, G ;
Rosenfeld, R ;
Ziv, O ;
Karpov, O ;
Wolf, A ;
Bracha, M ;
Shohat, D ;
Liapakis, G ;
Gilon, C ;
Hoffman, A ;
Stephensky, D ;
Oberg, K .
ENDOCRINOLOGY, 2001, 142 (01) :477-486
[2]   New and emerging pharmacological treatment options for acromegaly [J].
Antunes, Ximene ;
Kasuki, Leandro ;
Gadelha, Monica R. .
EXPERT OPINION ON PHARMACOTHERAPY, 2021, 22 (12) :1615-1623
[3]  
BAUER W, 1982, LIFE SCI, V31, P1133, DOI 10.1016/0024-3205(82)90087-X
[4]  
Boguslawska A, J CLIN MED, V29, P1377
[5]   Brazilian multicenter study on pegvisomant treatment in acromegaly [J].
Boguszewski, Cesar L. ;
Huayllas, Martha Katherine P. ;
Vilar, Lucio ;
Naves, Luciana Ansaneli ;
Ribeiro-Oliveira Junior, Antonio ;
Soares, Beatriz Santana ;
Czepielewski, Mauro Antonio ;
Abucham, Julio ;
Correa-Silva, Silvia Regina ;
Bronstein, Marcello Delano ;
Jallad, Raquel Soares ;
Duarte, Felipe Gaia ;
Musolino, Nina Rosa ;
Kasuki, Leandro ;
Gadelha, Monica Roberto .
ARCHIVES OF ENDOCRINOLOGY METABOLISM, 2019, 63 (04) :328-336
[6]   Long-term treatment with pegvisomant: observations from 2090 acromegaly patients in ACROSTUDY [J].
Buchfelder, Michael ;
van der Lely, Aart-Jan ;
Biller, Beverly M. K. ;
Webb, Susan M. ;
Brue, Thierry ;
Strasburger, Christian J. ;
Ghigo, Ezio ;
Camacho-Hubners, Cecilia ;
Pang, Kaijie ;
Lavenbergt, Joanne ;
Jonsson, Peter ;
Hey-Hadavi, Juliana H. .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2018, 179 (06) :419-427
[7]   Tumor Shrinkage With Lanreotide Autogel 120 mg as Primary Therapy in Acromegaly: Results of a Prospective Multicenter Clinical Trial [J].
Caron, Philippe J. ;
Bevan, John S. ;
Petersenn, Stephan ;
Flanagan, Daniel ;
Tabarin, Antoine ;
Prevost, Gaetan ;
Maisonobe, Pascal ;
Clermont, Antoine .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2014, 99 (04) :1282-1290
[8]   Long-Term Remission of Acromegaly after Octreotide Withdrawal Is an Uncommon and Frequently Unsustainable Event [J].
Casagrande, Alessandra ;
Bronstein, Marcello D. ;
Jallad, Raquel S. ;
Moraes, Aline B. ;
Elias, Paula C. L. ;
Castro, Margaret ;
Czepielewski, Mauro A. ;
Boschi, Artur ;
Ribeiro-Oliveira, Antonio, Jr. ;
Schweizer, Junia R. O. L. ;
Vilar, Lucio ;
Nazato, Debora M. ;
Gadelha, Monica R. ;
Abucham, Julio .
NEUROENDOCRINOLOGY, 2017, 104 (03) :273-279
[9]   Acromegaly: correlation between expression of somatostatin receptor subtypes and response to octreotide-lar treatment [J].
Casarini, Ana Paula M. ;
Jallad, Raquel S. ;
Pinto, Emilia M. ;
Soares, Ibere C. ;
Nonogaki, Suely ;
Giannella-Neto, Daniel ;
Musolino, Nina R. ;
Alves, Venancio A. F. ;
Bronstein, Marcello D. .
PITUITARY, 2009, 12 (04) :297-303
[10]   Somatostatin Analogs Modulate AIP in Somatotroph Adenomas: The Role of the ZAC1 Pathway [J].
Chahal, Harvinder S. ;
Trivellin, Giampaolo ;
Leontiou, Chrysanthia A. ;
Alband, Neda ;
Fowkes, Robert C. ;
Tahir, Asil ;
Igreja, Susana C. ;
Chapple, J. Paul ;
Jordan, Susan ;
Lupp, Amelie ;
Schulz, Stefan ;
Ansorge, Olaf ;
Karavitaki, Niki ;
Carlsen, Eivind ;
Wass, John A. H. ;
Grossman, Ashley B. ;
Korbonits, Marta .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2012, 97 (08) :E1411-E1420