Mariasanta Napolitano1, E. Lucchini2, M.R. De Paolis3, A. Urso4, A. Lucchesi5, N. Vianelli6, F. Zaja7 and C. Santoro8.
1 Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo. Italy.
2 UCO Ematologia - Azienda Sanitaria Universitaria Giuliano-Isontina. Italy.
3 Ospedale 'V. FAZZI' - UO Ematologia, Lecce. Italy.
4 UOC Ematologia, Arcispedale Sant’Anna, Ferrara. Italy.
5 IRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori" - IRST S.r.l. Italy.
6 IRCCS Azienda Ospedaliero-Universitaria di Bologna “Sant’Orsola”, Bologna. Italy.
7 Dipartimento Universitario Clinico di Scienze Mediche Chirurgiche e della Salute, Università degli Studi di Trieste. Italy.
8 UOC Ematologia Azienda Ospedaliera Policlinico Universitario Umberto I. Italy.
Published: May 01, 2025
Received: September 19, 2024
Accepted: April 15, 2025
Mediterr J Hematol Infect Dis 2025, 17(1): e2025041 DOI
10.4084/MJHID.2025.041
This is an Open Access article distributed
under the terms of the Creative Commons Attribution License
(https://creativecommons.org/licenses/by-nc/4.0),
which permits unrestricted use, distribution, and reproduction in any
medium, provided the original work is properly cited.
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To the editor.
Thrombopoietin
receptor agonists (TPO-RAs) are currently part of the second-line
treatment of primary immune thrombocytopenia (ATP). Since their initial
availability, TPO-RAs have been administered earlier in accordance with
the most recent evidence and drug indication.[1-6]
However, the optimal timing of administration, tapering, and
discontinuation of these drugs has not yet been clearly defined. We
have performed a nationwide survey specifically focused on the early
administration of TPO-RAs in the current Italian clinical practice. The
current survey was performed in Italy to evaluate the opinions and
behaviors of expert hematologists in ITP care; it was based on their
experience and not specifically focused on a patient category. Survey
results show that early use of TPO-RAs is frequently adopted in common
clinical practice, also immediately after a first-line therapy with
corticosteroids plus immunoglobulins; the main driver for the early use
is always the clinical condition, in particular, an absent or
unsatisfactory response. The choice of the ideal candidate for early
treatment with TPO-RAs is mainly defined on the basis of comorbidities,
aiming to avoid corticosteroid-related toxicities, while it is
unrelated to age. We have recently published a nationwide survey on the
use of TPO-RA among Italian hematologists,[7] but it
was not merely related to the early use of TPO-RAs. The current work
was developed in the frame of a scientific project (ITP-NET) in
partnership with the National GIMEMA working party on ITP. It was
conceived within the study group and focused on the early use of
TPO-RA. The survey was structured as a 13-item questionnaire, with an
accurate definition of the clarity of questions. Survey items were
structured as close-ended or multiple-choice-style questions. The main
topics of the proposed questions on TPO-RAs referred to: timing and
schedule of administration, ideal candidate profile, perceived risk
factors for their early administration, main factors in favor or
against their early use, the confidence of administration in case of
thrombotic events, pregnancy or other immune-mediated
thrombocytopenias. A full list of the proposed questions is reported in
Table 1.
 |
- Table 1. Full list of questions and proposed answers.
|
The
survey was launched among hematologists from thirty-eight Italian
hematological centers participating in the GIMEMA Foundation between
Jul 3, 2023, and Jul 31, 2023, with a reminder sent to non-respondents
after 2 and 3 weeks. The respondents’ anonymity was guaranteed.
Institutional information was not included. Thus, institutional
permission to participate was not required. Overall, 41 participants
answered the survey. The whole cohort of patients affected by primary
ITP, followed by the Centers participating in the survey, was composed
of 4588 subjects: 20,69% affected by newly diagnosed ITP, 19,53% with
persistent ITP, and 59,78% with chronic ITP.
The main results show
that the choice of the ideal candidate for early treatment with TPO-RAs
is mainly defined on the basis of comorbidities, including
cardiovascular risk factors and corticosteroid-related toxicities,
while it seems unrelated to age. The opinions of the survey
participants were quite heterogeneous regarding some items, such as the
choice of the specific timing of early use and driving reasons in favor
or against early use (Figure 1 and 2).
The most relevant factors against the early administration of TPO-RAs
are diagnostic uncertainty, the risks of over-exposure, and
comorbidities. A front-line treatment with TPO-RAs can be taken into
account in cases of severe bleeding unresponsive to steroids and
immunoglobulins or for a clear need for a “steroids-sparing” approach.
Increased awareness has furthermore emerged among respondents on the
management of thrombotic events requiring the contemporary
administration of anticoagulants or antiplatelet agents. Nowadays,
eltrombopag and romiplostim may be administered to patients affected by
primary ITP, refractory to other treatments (corticosteroids and
immunoglobulins), without consideration of the time from diagnosis. The
Italian Society of Hematology (SIE) recommends their administration
6 months after ITP diagnosis.[8] Early use of TPO-RA
allows, on one side, to reduce exposure to steroids, thus avoiding
serious adverse events, and on the other side, to control the risk of
severe bleeding. The current results have confirmed what was already
perceived among Italian hematologists during the previous evaluation
performed by our group, in particular, to be desirable for an earlier
and much more flexible administration of TPO-RA. Available data suggest
that even if TPO-RAs show overlap efficacy during the different phases
(newly diagnosed, persistent, or chronic) of ITP, the early
administration of eltrombopag and romiplostim may be associated with
improved clinical outcomes,[9-14] particularly referred to as the sustained response off therapy.[15,16]
In a recently published real-world study from the UK, the
administration of TPO-RA early after diagnosis, before other treatment
lines, including rituximab and splenectomy, without concomitant
steroids administration, was predictive of an increased platelet count
of ≥100 × 109/L.[17]
Similar real word evidence, confirming a reduced exposure to
corticosteroids and improved bleeding control after early use of TPO-
RAs were also reported by other groups.[18] Furthermore, TPO-RA administration soon after an unsatisfactory response to steroids resulted in safe and effective.[17,18]
The resultsults of the present survey confirm that Italian
hematologists adopt early therapy with TPO-RAs if necessary. However,
they also support the need to define better the concept of "early use”
of TPO-RAs in up-to-date management of ITP, redefining platelet
response to better evaluate clinical benefits.
 |
Figure 1. Factors supporting an early administration of Tpo-Ra. |
 |
Figure 2. Driving reasons against early use of Tpo-Ra.
|
Moreover,
the concept of refractoriness to TPOra and the management of patients
at high risk for thrombosis that could benefit from this category of
drugs should be reconsidered in light of the results obtained in
real-life experiences and the availability of new drugs.
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