Experimental Hematology
Volume 35, Issue 4 , Pages 534-540, April 2007

Yttrium-90–ibritumomab tiuxetan (Zevalin) combined with high-dose BEAM chemotherapy and autologous stem cell transplantation for chemo-refractory aggressive non-Hodgkin's lymphoma

  • Avichai Shimoni

      Affiliations

    • Division of Hematology and Bone Marrow Transplantation, Chaim Sheba Medical Center, Tel-Hashomer, Israel
    • Corresponding Author InformationOffprint requests to: Avichai Shimoni, M.D., Department of Bone Marrow Transplantation, Chaim Sheba Medical Center, Tel-Hashomer, Israel
  • ,
  • S. Tzila Zwas

      Affiliations

    • Department of Nuclear Medicine, Chaim Sheba Medical Center, Tel-Hashomer, Israel
  • ,
  • Yakov Oksman

      Affiliations

    • Department of Nuclear Medicine, Chaim Sheba Medical Center, Tel-Hashomer, Israel
  • ,
  • Izhar Hardan

      Affiliations

    • Division of Hematology and Bone Marrow Transplantation, Chaim Sheba Medical Center, Tel-Hashomer, Israel
  • ,
  • Noga Shem-Tov

      Affiliations

    • Division of Hematology and Bone Marrow Transplantation, Chaim Sheba Medical Center, Tel-Hashomer, Israel
  • ,
  • Ronit Yerushalmi

      Affiliations

    • Division of Hematology and Bone Marrow Transplantation, Chaim Sheba Medical Center, Tel-Hashomer, Israel
  • ,
  • Abraham Avigdor

      Affiliations

    • Division of Hematology and Bone Marrow Transplantation, Chaim Sheba Medical Center, Tel-Hashomer, Israel
  • ,
  • Isaac Ben-Bassat

      Affiliations

    • Division of Hematology and Bone Marrow Transplantation, Chaim Sheba Medical Center, Tel-Hashomer, Israel
  • ,
  • Arnon Nagler

      Affiliations

    • Division of Hematology and Bone Marrow Transplantation, Chaim Sheba Medical Center, Tel-Hashomer, Israel

Received 29 October 2006; received in revised form 19 December 2006; accepted 18 January 2007.

Objective

To determine the safety and outcome following standard-dose ibritumomab tiuxetan followed by BEAM high-dose chemotherapy and autologous stem cell transplantation (ASCT) in patients with chemo-refractory aggressive non-Hodgkin's lymphoma.

Patients and Methods

The study included 23 patients, median age 55 years (range, 35–66) with chemo-refractory lymphoma, either primary refractory (n = 11) or in refractory relapse (n = 12). Rituximab 250 mg/m2 followed by ibritumomab tiuxetan 0.4 mCi/kg were given on day −14 and high-dose BEAM chemotherapy started on day −6.

Results

All patients engrafted. Twenty-one patients are evaluable for response; 11 achieved CR, 9 achieved PR, 5 of whom converted to CR with additional radiation therapy (overall CR rate 76%). With a median follow-up of 17 months (range, 4–27) 16 patients are alive and 12 are progression-free. The estimated 2-year overall and progression-free survival are 67% (95% CI, 46–87%) and 52% (95% CI, 31–72%), respectively. The day-100 rate of treatment-related mortality was 9% (95% CI, 2–33%) and the 2-year cumulative incidence of relapse was 31% (95% CI, 17–57%). Extensive prior therapy (>3 lines), high LDH and IPI score at ASCT, bulky disease, and progression during last chemotherapy were risk factors for reduced survival.

Conclusion

Ibritumomab tiuxetan–BEAM and ASCT is relatively safe and may improve outcome in patients with refractory lymphoma. Although excess nonrelapse mortality can not be ruled out, relapse rate was relatively low, resulting in improved outcome. Standard-risk patients with chemo-sensitive disease may also benefit from ibritumomab tiuxetan–BEAM and ASCT. This hypothesis merits further study in larger-scale prospective randomized studies.

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PII: S0301-472X(07)00050-1

doi:10.1016/j.exphem.2007.01.043

Experimental Hematology
Volume 35, Issue 4 , Pages 534-540, April 2007