Early administration of donor lymphocyte infusions upon molecular relapse after allogeneic hematopoietic stem cell transplantation for chronic myeloid leukemia: a study by the Chronic Malignancies Working Party of the EBMT
Yves Chalandon,
Jakob R. Passweg,
Cesare Guglielmi,
Simona Iacobelli,
Jane Apperley,
Nicolaas P.M. Schaap,
Jürgen Finke,
Marie Robin,
Roberta Fedele,
Dominique Bron,
Ibrahim Yakoub-Agha,
Anja van Biezen,
Theo de Witte,
Nicolaus Kröger,
Eduardo Olavarria
Affiliations
Yves Chalandon
Division of Hematology, Department of Medical Specialties, University Hospital, Geneva, Switzerland
Jakob R. Passweg
Hematology Division, University Hospital, Basel, Switzerland
Cesare Guglielmi
Universita La Sapienza, II Facolta di Medicina, U.O.C Ematologia A.O.S. Andrea, Rome, Italy
Simona Iacobelli
Centro di Biostatistica e Bioinformatica, Università “Tor Vergata”, Rome, Italy
Jane Apperley
Imperial College, Department of Haematology, Hammersmith Hospital, London, UK
Nicolaas P.M. Schaap
Radboud University - Nijmegen Medical Center, Department of Hematology, Nijmegen, The Netherlands
Jürgen Finke
Dept. of Medicine-Hematology, Oncology, University of Freiburg, Freiburg, Germany
Marie Robin
Dept. of Hematology-BMT, Hopital St. Louis, Paris, France
Roberta Fedele
Centro Unico Regionale Trapianti, Azienda Ospedaliera, Reggio Calabria, Italy
Patients with chronic myeloid leukemia relapsing after allogeneic hematopoietic stem cell transplantation may be treated by tyrosine kinase inhibitors and/or by donor lymphocyte infusions. The best strategies and timing of administration of lymphocytes are unclear. We analyzed 155 patients who relapsed after allogeneic stem cell transplantation with disease detectable only by molecular methods and who subsequently received lymphocytes. Transplants were performed in first chronic phase (n=125) or in advanced disease (n=29) from identical siblings (n=84) or unrelated donors (n=71) between 1986 and 2003. They received lymphocytes either during molecular relapse (n=85) or upon progression to more advanced disease (1993 to 2004). The median interval from relapse to lymphocyte infusion was 210 (0–1673) days. The median follow up after it was 46 (3–135) months. Overall survival was 76±4% at five years after lymphocyte infusions (89±8% with sibling donors and 63±13% with unrelated donors (P=0.003)). Survival was 69±14% when lymphocytes were given within six months of the detection of molecular relapse and 81±10% (P=0.061) when given later; 81±11% if given at molecular relapse versus 71±12% (P=0.26) with more advanced disease. In multivariate analysis survival was worse if the donor was unrelated (HR 2.54 (95% CI: 1.15–5.53), P=0.021) and better with lymphocyte infusions beyond six months from molecular relapse (HR 0.4 (95%CI: 0.19–0.84), P=0.018). These data confirm the remarkable efficacy of lymphocyte infusions for this disease. There appears to be no advantage from administering it early upon detection of molecular relapse in patients who received allogeneic stem cell transplantation for chronic myeloid leukemia.