Treatment outcomes of T and natural-killer/T-cell lymphoma with ifosfamide, carboplatin and etoposide chemotherapy
- PMID: 35481622
- PMCID: PMC9458502
- DOI: 10.1002/cnr2.1552
Treatment outcomes of T and natural-killer/T-cell lymphoma with ifosfamide, carboplatin and etoposide chemotherapy
Abstract
Background: Contemporary data of peripheral T-cell lymphoma (PTCL) and natural-killer/T-cell lymphoma (NKTL) patients treated with ifosfamide, carboplatin and etoposide (ICE) are limited.
Aims: We performed a retrospective analysis to estimate outcomes of ICE-treated PTCL and NKTL patients at three tertiary cancer centres in Singapore.
Methods and results: Patients were identified through lymphoma databases from National Cancer Centre Singapore (NCCS), National University Hospital, Singapore (NUHS), and Singapore General Hospital (SGH). Responses and survival outcomes were determined from electronic medical records. A total of 75 patients with a median age of 50 were included. ICE was used as first-line treatment in 14 patients (19%) and as subsequent lines of treatment in 61 patients (81%). The overall response rates (ORR) for all patients was 63% (40% complete response [CR]). The ORR and CR in the first line were 86% and 64% respectively. At a median follow-up duration of 71.0 months, the median progression-free (PFS) and overall survival (OS) for all patients were 4.4 months (95%CI, 2.7-6.0) and 16 months (95%CI, 8.3-45.4) respectively.
Conclusion: In summary, ICE showed high ORR but poor PFS in relapsed/refractory PTCL and NKTL. ORR of ICE in the first line setting appears better than real-world CHOP data and warrants further study.
Keywords: Asia; T-cell lymphoma; chemotherapy; haematology-oncology; natural-killer/T-cell lymphoma.
© 2022 The Authors. Cancer Reports published by Wiley Periodicals LLC.
Conflict of interest statement
The authors have stated explicitly that there are no conflicts of interest in connection with this article.
References
-
- Gisselbrecht C, Gaulard P, Lepage E, et al. Prognostic significance of T‐cell phenotype in aggressive non‐Hodgkin's lymphomas. Groupe d'Etudes des Lymphomes de l'Adulte (GELA). Blood. 1998;92(1):76‐82. - PubMed
-
- Melnyk A, Rodriguez A, Pugh WC, Cabannillas F. Evaluation of the revised European‐American Lymphoma Classification confirms the clinical relevance of immunophenotype in 560 cases of aggressive non‐Hodgkin's lymphoma ‐ PubMed. Blood. 1997;89(12):4514‐4520. - PubMed
-
- Vose JM, Neumann M, Harris ME, Armitage J, Weisenburger D. Interantional T‐cell lymphoma project. International peripheral T‐cell and natural killer/T‐cell lymphoma study: pathology findings and clinical outcomes international T‐cell lymphoma project. J Clin Oncol. 2008;26(25):4124‐4130. - PubMed
-
- Yamaguchi M, Kwong YL, Kim WS, et al. Phase II study of SMILE chemotherapy for newly diagnosed stage IV, relapsed, or refractory extranodal natural killer (NK)/T‐cell lymphoma, nasal type: the NK‐cell tumor study group study. J Clin Oncol. 2011;29(33):4410‐4416. - PubMed
-
- Kwong YL, Kim WS, Lim ST, et al. SMILE for natural killer/T‐cell lymphoma: analysis of safety and efficacy from the Asia lymphoma study group. Blood. 2012;120(15):2973‐2980. - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
