Treatment Strategies for Dopamine Agonist-Resistant and Aggressive Prolactinomas: A Comprehensive Analysis of the Literature

Author:

Sari Ramazan12,Altinoz Meric A.3ORCID,Ozlu Eylem Burcu Kahraman1,Sav Aydin4,Danyeli Ayca Ersen5,Baskan Ozdil6,Er Ozlem7,Elmaci Ilhan18

Affiliation:

1. Department of Neurosurgery, Acibadem Hospital, Maslak, Istanbul, Turkey

2. Avrasya University, Health Sciences Faculty, Trabzon, Turkey

3. Department of Biochemistry, Acibadem University, Istanbul, Turkey

4. Department of Pathology, Yeditepe University, Istanbul, Turkey

5. Department of Pathology, Acibadem Mehmet Ali Aydinlar University, School of Medicine, Istanbul, Turkey

6. Department of Radiology, Memorial Hospital, Istanbul, Turkey

7. Department of Medical Oncology, Acibadem Mehmet Ali Aydinlar University, School of Medicine, Istanbul, Turkey

8. Department of Neurosurgery, Acibadem Mehmet Ali Aydinlar University, School of Medicine, Istanbul, Turkey

Abstract

AbstractDespite most of the prolactinomas can be treated with endocrine therapy and/or surgery, a significant percentage of these tumors can be resistant to endocrine treatments and/or recur with prominent invasion into the surrounding anatomical structures. Hence, clinical, pathological, and molecular definitions of aggressive prolactinomas are important to guide for classical and novel treatment modalities. In this review, we aimed to define molecular endocrinological features of dopamine agonist-resistant and aggressive prolactinomas for designing future multimodality treatments. Besides surgery, temozolomide chemotherapy and radiotherapy, peptide receptor radionuclide therapy, estrogen pathway modulators, progesterone antagonists or agonists, mTOR/akt inhibitors, pasireotide, gefitinib/lapatinib, everolimus, and metformin are tested in preclinical models, anecdotal cases, and in small case series. Moreover, chorionic gonadotropin, gonadotropin releasing hormone, TGFβ and PRDM2 may seem like possible future targets for managing aggressive prolactinomas. Lastly, we discussed our management of a unique prolactinoma case by asking which tumors’ proliferative index (Ki67) increased from 5–6% to 26% in two subsequent surgeries performed in a 2-year period, exerted massive invasive growth, and secreted huge levels of prolactin leading up to levels of 1 605 671 ng/dl in blood.

Publisher

Georg Thieme Verlag KG

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,General Medicine,Endocrinology, Diabetes and Metabolism

Reference47 articles.

1. Temozolomide retreatment in a recurrent prolactin-secreting pituitary adenoma: Hormonal and radiographic response;R E Strowd;J Oncol Pharm Pract,2016

2. Identification of human prolactinoma related genes by DNA microarray;L Zhao;J Cancer Res Ther,2014

3. Clinical management of difficult to treat macroprolactinomas;N Sahakian;Expert Rev Endocrinol Metab,2019

4. Clinical, Pathological, and Molecular Factors of Aggressiveness in Lactotroph Tumours;J Trouillas;Neuroendocrinology,2019

5. What causes a prolactinoma to be aggressive or to become a pituitary carcinoma?;J Phillips;Hormones (Athens),2012

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