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Blood, 15 December 2004, Vol. 104, No. 13, pp. 3865-3871.
Prepublished online as a Blood First Edition Paper on August 10, 2004; DOI 10.1182/blood-2004-03-1105.


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Submitted March 30, 2004
Accepted July 24, 2004

Outcome Following Alemtuzumab (CAMPATH-1H) -Containing Reduced Intensity Allogeneic Transplant Regimen for Relapsed and Refractory Non-Hodgkin's Lymphoma (NHL)

Emma Morris*, Kirsty Thomson, Charles Craddock, Prem Mahendra, Donald Milligan, Gordon Cook, Graeme Murray Smith, Anne Parker, Steve Schey, Rajesh Chopra, Christopher Hatton, Jane Tighe, Anne Hunter, Karl Peggs, David Linch, Anthony Goldstone, and Stephen Mackinnon

Department of Haematology, University College London Hospitals, London, United Kingdom; Department of Immunology, Imperial College, London, United Kingdom
Department of Haematology, University College London Hospitals, London, United Kingdom
UK Collaborative Group, London, United Kingdom

* Corresponding author; email: emma.morris{at}ic.ac.uk.

We report the outcome following RIT for NHL in 88 patients (LG-NHL n=41, HG-NHL n=37, MCL n=10). 37 had received prior autografts and 21 were in CR at transplant. Conditioning was with alemtuzumab, fludarabine and melphalan. Sixty-five patients received PBSC from HLA-identical siblings and 23 received BM from matched unrelated donors. GVHD prophylaxis was with cyclosporin A. Grade III-IV acute GVHD developed in 4 patients and chronic GVHD in 6 patients. With a median follow-up of 36 months (range 18-60), the actuarial overall survival (OS) at 3 years was 34% for HG-NHL, 60% for MCL and 73% for LG-NHL (p=<0.001). The 100-day and 3-year TRM for patients with LG-NHL were 2% and 11% respectively, and were better (p=0.01) than for patients with HG-NHL (27% and 38% respectively). The actuarial current progression free survival (PFS) at 3 years, including those who achieved remission following DLI for progression, was 65% for LG-NHL 50% for MCL and 34% for HG-NHL (p=0.002). 21 patients received DLI for MRD, persistent disease or relapse and 15 received DLI for mixed hematopoietic chimerism. Patients with relapsed LG-NHL and CLL achieve excellent PFS with extremely low TRM and GVHD, even when matched family donors are unavailable.


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