Blood Reviews
Volume 21, Issue 5 , Pages 233-243, September 2007

Therapy of Relapsed Hodgkin Lymphoma

  • Amanda F. Cashen

      Affiliations

    • 660 S. Euclid Ave., Box 8007, St. Louis, MO 63110, Tel.: +1 314 454 8306; fax: +1 314 454 7551.
  • ,
  • Nancy L. Bartlett

      Affiliations

    • Corresponding Author InformationCorresponding author. Tel.: +1 314 362 5654; fax: +1 314 747 5123.
    • 660 S. Euclid Ave., Box 8056, St. Louis, MO 63110.

Division of Oncology, Washington University School of Medicine, 660 S. Euclid Ave., St. Louis, MO 63110, USA

Summary 

The majority of patients who are diagnosed with Hodgkin lymphoma (HL) will be cured with primary chemotherapy. For those who relapse, autologous stem cell transplantation (ASCT) has become the standard of care. Randomized clinical trials have demonstrated that approximately 50% of patients with chemosensitive relapsed HL can achieve long term disease free survival with ASCT. However, optimal therapy of those who have chemorefractory disease or who relapse after an ASCT has not been established. Reduced intensity allogeneic stem cell transplantation may benefit these patients, although a definite graft versus HL effect has not been demonstrated and treatment-related mortality remains relatively high. New salvage regimens that incorporate gemcitabine, vinorelbine, rituximab, and/or monoclonal antibodies against CD30 are being investigated.

Keywords: Hodgkin lymphoma, Autologous stem cell transplantation, Allogeneic stem cell transplantation, Salvage therapy

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0268-960X(07)00033-1

doi:10.1016/j.blre.2007.06.001

Blood Reviews
Volume 21, Issue 5 , Pages 233-243, September 2007