| Literature DB >> 30454872 |
Camille E Puronen1, Ryan D Cassaday2, Philip A Stevenson3, Brenda M Sandmaier4, Mary E Flowers4, Damian J Green4, David G Maloney4, Rainer F Storb4, Oliver W Press4, Ajay K Gopal5.
Abstract
Nonmyeloablative allogeneic hematopoietic cell transplantation (HCT) can provide prolonged remissions in patients with advanced B cell lymphoma (B-NHL) via the graft-versus-lymphoma effect, although inferior results are seen in patients with chemoresistant, bulky, or aggressive disease. Radioimmunotherapy can safely induce responses in B-NHL with minimal nonhematologic toxicity. Initial results of 90Y-ibritumomab tiuxetan-based allografting demonstrated early safety and disease control in nonremission patients but with short follow-up. Here we report the long-term outcomes of patients treated on this study with specific emphasis on patients achieving early remissions. Eleven of 40 patients were alive at a median follow-up of 9 years (range, 5.3 to 10.2). Fourteen (35%) deaths were due to disease progression and 14 (35%) deaths to complications from HCT. One patient died of a Merkel cell carcinoma. The 5-year overall and progression-free survival for patients with indolent B-NHL was 40% and 27.5%, respectively. None of the patients with diffuse large B cell lymphoma was a long-term disease-free survivor regardless of early remission status. 90Y-ibritumomab tiuxetan-based allografting represents a viable option in patients with indolent histologies. Improved strategies are needed for aggressive B-NHL. The original trial was registered at www.clinicaltrials.gov as NCT00119392.Entities:
Keywords: (90)Y-ibritumomab tiuxetan; Allogeneic transplant; B cell lymphoma; Long-term follow-up; Radioimmunotherapy; Zevalin
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Year: 2018 PMID: 30454872 PMCID: PMC6251312 DOI: 10.1016/j.bbmt.2018.06.033
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742