Radioimmunotherapy of heavily pre-treated, non-Hodgkin's lymphoma patients: efficacy and safety in a routine setting

Anticancer Res. 2009 Nov;29(11):4771-7.

Abstract

The aim of the present study waw to assess efficacy and safety of radio-immunotherapy with Zevalin (RIT-Z) in heavily pre-treated, rituximab-refractory patients.

Patients and methods: We studied 12 patients with indolent lymphoma and 7 with aggressive lymphoma. The median number of prior rituximab-containing treatments was 2; overall, 3 therapies had been previously given. Ten patients received RIT-Z as salvage therapy, 9 at high risk of relapse received RIT-Z as consolidation. Staging and follow-up were obtained by positron-emission tomography. Outcomes assessed were failure-free survival (FFS) and time to next treatment (TTNT).

Results: Overall FFS and TTNT were 5 and 11 months, respectively; median follow-up 13 months. Major findings were i) no long-term remissions observed in 7 patients who had not responded to their most recent therapy and ii) lack of association between any pre-therapy variables analysed and outcomes. Different subgroups showed no difference in terms of toxicity.

Conclusion: We encourage the use of RIT-Z as a consolidation for pre-treated patients with both indolent and aggressive lymphoma.

MeSH terms

  • Adult
  • Aged
  • Antibodies, Monoclonal / administration & dosage*
  • Antibodies, Monoclonal, Murine-Derived
  • Drug Resistance, Neoplasm
  • Female
  • Humans
  • Lymphoma, Follicular / radiotherapy*
  • Lymphoma, Large B-Cell, Diffuse / radiotherapy*
  • Male
  • Middle Aged
  • Radioimmunotherapy / adverse effects
  • Radioimmunotherapy / methods*
  • Retrospective Studies
  • Rituximab
  • Yttrium Radioisotopes / administration & dosage*

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Murine-Derived
  • Yttrium Radioisotopes
  • Rituximab
  • ibritumomab tiuxetan