International Journal of Hematology

, Volume 99, Issue 1, pp 69–78 | Cite as

High-dose therapy and autologous stem cell transplantation in peripheral T-cell lymphoma: treatment outcome and prognostic factor analysis

  • Lin Gui
  • Yuan-kai Shi
  • Xiao-hui He
  • Ying-heng Lei
  • Hong-zhi Zhang
  • Xiao-hong Han
  • Sheng-yu Zhou
  • Peng Liu
  • Jiang-liang Yang
  • Mei Dong
  • Chang-gong Zhang
  • Sheng Yang
  • Yan Qin
Original Article

Abstract

Peripheral T-cell lymphoma (PTCL) carries a poor prognosis with conventional treatment. We retrospectively analyzed data from 45 patients with PTCL who received high-dose therapy and autologous stem cell transplantation (HDT/ASCT) from 1990 to 2008 in our center. Eighteen patients underwent HDT/ASCT in complete remission to induction chemotherapy (CR1), and 27 patients underwent HDT/ASCT in other disease statuses. The median follow-up was 113.5 months (range 52.6–261.0) for surviving patients. The 5-year overall survival (OS) and progression-free survival (PFS) were 64 and 60 %, respectively. The 5-year OS for patients in CR1 and in other disease statuses was 89 and 47 %, respectively (P = 0.002), and 5-year PFS was 83 and 43 % (P = 0.007). In the subgroup excluding anaplastic large cell lymphoma, patients transplanted in CR1 also had significantly better 5-year OS (82 vs. 37 %, P = 0.009) and PFS (82 vs. 33 %, P = 0.008) than those transplanted in other disease statuses. Multivariate analysis showed that CR1 status was the only significant prognostic factor for OS (P = 0.040) and PFS (P = 0.040). These results support the use of HDT/ASCT consolidation in CR1 for PTCL patients. Prospective randomized trials are necessary to confirm the efficacy of this approach.

Keywords

High-dose therapy Autologous stem cell transplantation Peripheral T-cell lymphoma 

Notes

Acknowledgements

This work was supported in part by Grants from the National Key Technologies Research and Development Program of China during the 9th Five-Year Plan Period [A201996103 96-906-01-12], the Ministry of Education Doctor Foundation of China [20010023018, 20050023045 and 200800230019], the Ying Dong Fok Foundation for Young College Teacher [B231996001], and the General Program of the National Natural Science Foundation of China [30873012]. And we thank Ke-huan Luo, Feng Pan, Shi-kai Wu and Yin-yu Liu for their selfless and hard work in the study.

Conflict of interest

The authors declare that they have no conflict of interest.

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Copyright information

© The Japanese Society of Hematology 2013

Authors and Affiliations

  • Lin Gui
    • 1
  • Yuan-kai Shi
    • 1
  • Xiao-hui He
    • 1
  • Ying-heng Lei
    • 1
  • Hong-zhi Zhang
    • 1
  • Xiao-hong Han
    • 1
  • Sheng-yu Zhou
    • 1
  • Peng Liu
    • 1
  • Jiang-liang Yang
    • 1
  • Mei Dong
    • 1
  • Chang-gong Zhang
    • 1
  • Sheng Yang
    • 1
  • Yan Qin
    • 1
  1. 1.Department of Medical Oncology, Cancer Institute/HospitalChinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing Key Laboratory of Clinical Study on Anticancer Molecular Targeted DrugsBeijingChina

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