Molecular profiling for acromegaly treatment: a validation study

Pharmacologic treatment of acromegaly is currently based upon assay-error strategy, the first-generation somatostatin receptor ligands (SRL) being the first-line treatment. However, about 50% of patients do not respond adequately to SRL. Our objective was to evaluate the potential usefulness of diff...

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Veröffentlicht in:Endocrine-related cancer 2020-06, Vol.27 (6), p.375-389
Hauptverfasser: Puig-Domingo, Manel, Gil, Joan, Sampedro-Nuñez, Miguel, Jordà, Mireia, Webb, Susan M, Serra, Guillermo, Pons, Laura, Salinas, Isabel, Blanco, Alberto, Marques-Pamies, Montserrat, Valassi, Elena, Picó, Antonio, García-Martínez, Araceli, Carrato, Cristina, Buj, Raquel, del Pozo, Carlos, Obiols, Gabriel, Villabona, Carles, Cámara, Rosa, Fajardo-Montañana, Carmen, Alvarez, Clara V, Bernabéu, Ignacio, Marazuela, Mónica
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Sprache:eng
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Zusammenfassung:Pharmacologic treatment of acromegaly is currently based upon assay-error strategy, the first-generation somatostatin receptor ligands (SRL) being the first-line treatment. However, about 50% of patients do not respond adequately to SRL. Our objective was to evaluate the potential usefulness of different molecular markers as predictors of response to SRL. We used somatotropinoma tissue obtained after surgery from a national cohort of 100 acromegalic patients. Seventy-one patients were treated with SRL during at least 6 months under maximal therapeutic doses according to IGF1 values. We analyzed the expression of SSTR2, SSTR5, AIP, CDH1 (E-cadherin), MKI67 (Ki-67), KLK10, DRD2, ARRB1, GHRL, In1-Ghrelin, PLAGL1 and PEBP1 (RKIP) by RT-qPCR and mutations in GNAS gene by Sanger sequencing. The response to SRL was categorized as complete response (CR), partial (PR) or non-response (NR) if IGF1 was normal, between >23 SDS IGF1 at 6 months of follow-up, respectively. From the 71 patients treated, there were 27 CR (38%), 18 PR (25%) and 26 NR (37%). SSTR2, Ki-67 and E-cadherin were associated with SRL response (P 
ISSN:1351-0088
1479-6821
DOI:10.1530/ERC-18-0565