Clinical features and treatment outcomes of angioimmunoblastic T-cell lymphona

  • Byeong Bae Park
  • , Baek Yeol Ryoo
  • , Jae H. Lee
  • , Hyuck C. Kwon
  • , Sung H. Yang
  • , Hye J. Kang
  • , Hyo J. Kim
  • , Sung Y. Oh
  • , Young H. Ko
  • , Joo R. Huh
  • , Seung S. Lee
  • , Eun M. Nam
  • , Keon W. Park
  • , Jung H. Kim
  • , Jung H. Kang
  • , Soo M. Bang
  • , Sarah Park
  • , Kihyun Kim
  • , Keunchil Park
  • , Cheolwon Suh
  • Won S. Kim

Research output: Contribution to journalArticlepeer-review

33 Scopus citations

Abstract

The objective of this retrospective study was to investigate clinical features and treatment outcomes in patients with angioimmunoblastic T-cell lymphoma (AITL), data of which were collected over a 15-year period. Sixty-five patients diagnosed with AITL were included in the study. About half of the patients (46.2%) presented with poor performance status (ECOG ≥2); 72.3% of patients belonged to high intermediate or high-risk of IPI and same proportion belonged to Class 2 of PIT (Prognostic index for PTCL-U), and most patients (95.4%) were diagnosed at an advanced stage. At diagnosis, 27 patients (41.5%) presented with malignant pleural effusion, and 22 patients (33.8%) had skin involvement. Most of the initial chemotherapy regimens were anthracycline-based (88.2%). Overall response rate to initial chemotherapy was 86.2% (64.7% of complete response, 21.5% of partial response). The median progression-free survival and overall survival of all patients was 7.1 months (95% CI, 2.8-11.4) and 15.1 months (95% CI, 6.7-23.5), respectively. Age, performance status, and PIT scores were predictive prognostic factors for survival. In conclusion, although AITLs showed a good response to the initial chemotherapy, their response durations were short; therefore, chemotherapy for AITL should be modified or intensified as in high-dose chemotherapy.

Original languageEnglish
Pages (from-to)716-722
Number of pages7
JournalLeukemia and Lymphoma
Volume48
Issue number4
DOIs
StatePublished - Apr 2007

Keywords

  • Angioimmunoblastic T-cell lymphoma
  • Clinical features
  • Treatment outcomes

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