Bridging Clinical Trials and Reality: Care and Outcomes of PTCLs Patients as retrieved by the National Ukraine Lymphoma Registry

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Abstract Summary

Introduction:

Peripheral T-cell lymphomas (PTCLs) are rare, heterogeneous hematological disorders with poor outcomes under standard therapies. In 2019, Ukraine launched a prospective national lymphoma registry to collect real-world data on subtypes to better understand clinical features, treatment effectiveness, and management disparities.

Methods:

Between 2019 and 2025, 1,763 patients were registered; 100 with nodal PTCLs were available for analysis. Data on histology, clinical characteristics, treatment approaches, responses, and survival outcomes were recorded.

Objectives:

To identify common PTCL subtypes, describe clinical features, patterns of care, and outcomes, and highlight the importance of real-world data.

Results:

A total of 100 patients with PTCLs and NKTCL were registered by 15 centers. Median age at diagnosis was 54 years (range 18–83), with a male:female ratio of 49:51. The most common histologic subtypes were PTCL-NOS (35), AITL (25), ALK-negative ALCL (11), ATLL (9), and ALK-positive ALCL (7). Most frequent first-line regimens were CHOEP, CHOP/CHOP-like, and BV-CHP (41.0%, 29.5%, and 10.3%), with transplantation in 5 cases (6%). First-line therapy data were available in 78 patients. Mean follow-up was 16 months (0.3–64). Twenty-nine patients were refractory or relapsed; mean time to event was 5.5 months (0.07–23). One- and two-year OS were 81% and 68.4%, while PFS rates were 48% and 42.3%, respectively. In univariate analysis, only the presence of B-symptoms showed significant association with relapse (p=0.02).(Figure1)

Conclusion:

The Ukraine Lymphoma Registry describes the unfavorable outcomes of patients with PTCL treated in a real-world setting, in an area with frequent limitations in access to medication and diagnostics. These findings remain preliminary, and additional analyses are needed to improve characterization of care patterns, risk prediction, and optimal treatment strategies.

Submission ID :
TCLF18
head of bone marrow transplantation department
,
Ukrainian cancer institute
Jules Bordet Institute
Ukrainian National Cancer Institute
Research Centre for Radiation Medicine, Academy of Medical Sciences of Ukraine, Kyiv
Ukrainian National Cancer Institute
CE “Poltava Regional Clinical Hospital n.a. M.V.Sklifosovsky PRC"
Kyiv City Hospital №9
Ukrainian National Cancer Institute
Ukrainian National Cancer Institute
Kyiv City Hospital №9
STATE INSTITUTION «INSTITUTE OF BLOOD PATHOLOGY AND TRANSFUSION MEDICINE OF NATIONAL ACADEMY OF MEDICAL SCIENCES OF UKRAINE
Department of Physics and Chemistry, University of Palermo
Communal Non-Profit Enterprise "Podilsky Regional Oncology Center" of the Vinnytsia Regional Council
MUNICIPAL NON-PROFIT ENTERPRISE «MEDICAL CENTER OF KYIV»
MUNICIPAL NON-PROFIT ENTERPRISE «MEDICAL CENTER OF KYIV»
Volyn regional clinical hospital
Khmelnytskyi Regional Clinical Hospital
Ukrainian National Cancer Institute
Feofaniya Clinical Hospital
non-profit municipal enterprise "city clinical hospital #4" dnipro city council
Feofaniya Clinical Hospital
Non-profit municipal enterprise "city clinical hospital #4" dnipro city council
Non-profit municipal enterprise "city clinical hospital #4" dnipro city council
Odessa Regional Hospital
Ukrainian National Cancer Institute
Ukrainian National Cancer Institute
Ukrainian National Cancer Institute
Ukrainian National Cancer Institute
Research Centre for Radiation Medicine, Academy of Medical Sciences of Ukraine, Kyiv
Ukrainian National Cancer Institute
National Research Center for Radiation Medicine, Hematology and Oncology of The National Academy of Medical Sciences of Ukraine
National Research Center for Radiation Medicine, Hematology and Oncology of The National Academy of Medical Sciences of Ukraine
Ukrainian National Cancer Institute
University of Modena and Reggio Emilia, Modena, Italy
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