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https://doi.org/10.1530/EJE-19-0753
European Journal of Endocrinology
182:2 177–183 D Kim and others PRL cut-ofs and tumor size
reduction
Prolactin ≤1 ng/mL predicts
macroprolactinoma reduction after
cabergoline therapy
Daham Kim, Cheol Ryong Ku, Kyungwon Kim, Hyein Jung and Eun Jig Lee
Department of Internal Medicine, Institute of Endocrine Research, Yonsei University College of Medicine,
Seoul, Korea
Abstract
Objective: The association between prolactin level variation and prolactinoma size reduction remains unclear. This
study aimed to determine the prolactin level cut-of predictive of a tumor size reduction.
Design: Retrospective cohort study.
Methods: We reviewed medical records of patients with prolactinoma who received primary cabergoline therapy and
for whom complete data on pituitary hormone assays and sellar MRI at baseline and 3 months post treatment were
available. We tested whether the certain prolactin level after 3 months post treatment predicted better response.
Results: Prolactin levels normalized in 109 (88.6%) of 123 included macroprolactinoma patients. The mean tumor
size reduction was 22.9%, and patients in the lowest prolactin tertile (≤0.7) had the highest frequency of tumor size
reductions of ≥20% (73.7 vs 52.9% and 45.9% in tertiles 2 (>0.7 to 2.6) and 3 (>2.6 to 20), P = 0.015). Patients with
prolactin levels ≤1 ng/mL exhibited larger tumor size reductions vs those with prolactin levels of 1–20 (27.2 ± 18.3% vs
19.5 ± 13.9%, P = 0.014), 1–10 (19.3 ± 13.7%, P = 0.017) and 1–5 ng/mL (19.2 ± 14.3%, P = 0.039). A multivariable logistic
regression analysis revealed that a prolactin level ≤1 ng/mL at 3 months and high-dose cabergoline therapy were
signifcantly associated with tumor size reductions of ≥20% (odds ratio (OR): 2.8, 95% confdence interval (CI): 1.2–6.7,
P = 0.017; OR: 2.0, 95% CI: 1.0–3.9, P = 0.043).
Conclusions: A prolactin level ≤1 ng/mL at 3 months after cabergoline treatment was correlated with a signifcant
tumor size reduction in patients with macroprolactinoma. This fnding may help clinical decision making when treating
macroprolactinoma patients.
Introduction
Prolactinomas are the most commonly occurring pituitary
adenomas, accounting for approximately 40% of all
pituitary tumors and 50–60% of all functional pituitary
tumors (1). These tumors cause headaches, visual
dysfunction, hypopituitarism, and hyperprolactinemia
(2). Patients with prolactinoma typically exhibit the
clinical features of hyperprolactinemia, including gonadal
dysfunction, amenorrhea, and galactorrhea.
Serum prolactin level normalization and tumor
shrinkage are the major goals of prolactinoma treatment.
The frst line of therapy involves medical management
with dopamine agonists such as bromocriptine and
cabergoline. Surgical resection is generally reserved for
patients who are unresponsive or intolerant to medical
therapy. Cabergoline, a specifc D2 receptor agonist, is the
frst choice of treatment because of its superior effcacy
and better tolerability (3). The recommended cabergoline
dosage for initiation is 0.25–0.5 mg twice a week, whereas
the usual weekly maintenance doses range from 0.25 to
3.0 mg (4).
Correspondence
should be addressed
to C R Ku
Email
CR079@yuhs.ac
European Journal of
Endocrinology
(2020) 182, 177–183
Clinical Study
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