CC BY-NC-ND 4.0 · Avicenna J Med 2020; 10(04): 227-231
DOI: 10.4103/ajm.ajm_59_19
Original Article

R-IDARAM treatment in central nervous system lymphomas: a single-center experience and review of the literature

Senem Maral
Department of Hematology, Dıskapı Research and Training Hospital, Ankara, Turkey
,
Murat Albayrak
Department of Hematology, Dıskapı Research and Training Hospital, Ankara, Turkey
,
Cigdem Pala
Department of Hematology, Dıskapı Research and Training Hospital, Ankara, Turkey
,
Abdulkerim Yıldız
Department of Hematology, Dıskapı Research and Training Hospital, Ankara, Turkey
,
Hacer B Ozturk
Department of Hematology, Dıskapı Research and Training Hospital, Ankara, Turkey
,
Osman Sahin
Department of Hematology, Dıskapı Research and Training Hospital, Ankara, Turkey
› Author Affiliations

Subject Editor: Financial support and sponsorship Nil.

Abstract

Introduction: Central nervous system lymphomas (CNSLs) require effective treatment strategies due to aggressive nature of disease. Despite therapeutic approaches having improved in the last decades, there is no standard treatment for these patients. As a CNSL targeted-therapy IDARAM protocol was developed, the outcomes were reported with a few studies. We observed the R-IDARAM protocol in our CNSL cases, and we discuss the effectiveness, tolerability, and toxicity with a review of the literature in this article. Subjects and Methods: We retrospectively analyzed response rates, progression-free survival, adverse events, and long-term side effects in patients who were treated by modified R-IDARAM as standard clinical care of CNSL in our hematology department. Results: Response was achieved in five of nine patients. Three patients (two primary CNSL and one secondary CNSL) are still being followed up without disease progression with a median duration of follow-up of 79 months (88, 79, and 17 months, respectively). Manageable hematological side effects including thrombocytopenia and neutropenia were experienced by all patients. Conclusion: R-IDARAM protocol may be an option with high early response rates and manageable toxicity. Hematological side effects are the main problem, and long-term neurological toxicity is not common. Eligible patients must continue with autologous stem cell transplantation due to poor long-term survival outcomes.



Publication History

Article published online:
04 August 2021

© 2020. Syrian American Medical Society. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

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