| Literature DB >> 17988993 |
Sakurako Izaki1, Hiroaki Goto, Kumiko Okuda, Motoi Matsuda, Yuka Watanabe, Kenichirou Fujioka, Noriyuki Hanzawa, Hiroko Sumita, Hiroyuki Takahashi, Shoko Goto, Sumio Kai, Haruyuki Sekiguchi, Tetsunori Funabiki, Hideki Sasaki, Koichiro Ikuta, Shumpei Yokota.
Abstract
We retrospectively evaluated early and long-term complications of an intensified conditioning regimen consisting of busulfan and etoposide in combination with either nimustine hydrochloride (ACNU) (BVA regimen, n = 18) or melphalan (BVL regimen, n = 34) in 52 children with acute leukemia or non-Hodgkin's lymphoma. With a median follow-up of 13.2 years after the BVA regimen and 8.1 years after the BVL regimen, 61% and 76% of patients, respectively, are in continuous complete remission. Transplantation-related mortality was 17% and 6% after the BVA and BVL regimens, respectively, and the corresponding relapse rates were 17% and 15%. The most common and severe toxicity was pulmonary complication in the BVA regimen, which was seen in 67% of patients and was life-threatening in 20%. Thirty-three percent of patients after the BVA regimen and 24% after BVL died of relapse or disease progression (n = 9), interstitial pneumonia (n = 2), fungal pneumonia (n = 1), or chronic graft-versus-host disease (n = 2). One of the long-term survivors developed secondary leukemia. A significant decrease in the height standard deviation score of more than 2 SD from diagnosis to the last follow-up was seen in 17% of the patients, with hypothyroidism in 15%, and alopecia in 42%. Because our experience is limited to a small heterogeneous population of patients who mainly underwent transplantation in the first remission, we cannot draw conclusions on the treatment's effectiveness. The BVL regimen is tolerable, however, because no regimen-related death was observed, whereas the BVA regimen is not recommended because of the high incidence of pulmonary complications. The effectiveness of the BVL regimen requires further study.Entities:
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Year: 2007 PMID: 17988993 DOI: 10.1532/IJH97.06231
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490