Risk factors for development of pneumonitis after high-dose chemotherapy with cyclophosphamide, BCNU and etoposide followed by autologous stem cell transplant

被引:26
作者
Lane, Andrew A. [2 ]
Armand, Philippe [2 ]
Feng, Yang [3 ]
Neuberg, Donna S. [3 ]
Abramson, Jeremy S.
Brown, Jennifer R. [2 ]
Fisher, David C. [2 ]
LaCasce, Ann S. [2 ]
Jacobsen, Eric D. [2 ]
McAfee, Steven L.
Spitzer, Thomas R.
Freedman, Arnold S. [2 ]
Chen, Yi-Bin [1 ,2 ]
机构
[1] Massachusetts Gen Hosp, Dept Hematol Oncol, Div Bone Marrow Transplantat, Ctr Canc, Boston, MA 02114 USA
[2] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA 02115 USA
关键词
Transplant toxicity; clinical results; lymphoma and Hodgkin disease; BONE-MARROW-TRANSPLANTATION; REFRACTORY HODGKINS-DISEASE; LYMPHOID MALIGNANCIES; PREPARATIVE REGIMENS; CARMUSTINE; TOXICITY; EFFICACY; THERAPY;
D O I
10.3109/10428194.2011.645208
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pneumonitis is a complication of high-dose chemotherapy and autologous stem cell transplant (HDC-ASCT) regimens containing BCNU. Our goal was to define the incidence and risk factors for pneumonitis in patients with lymphoma receiving a uniform conditioning regimen in the modern era. We studied 222 patients who received HDC-ASCT using cyclophosphamide, BCNU and VP-16 (CBV). Pneumonitis incidence was 22%, with 19% receiving systemic corticosteroid treatment and 8% requiring inpatient hospitalization for pneumonitis. Three patients died secondary to pneumonitis-related complications. The following variables were independently associated with pneumonitis: prior mediastinal radiation (odds ratio [OR] 6.5, 95% confi dence interval [CI] 2.3 -18.9, p = 0.0005), total BCNU dose above 1000 mg (OR 3.4, 95% CI 1.3-8.7, p = 0.012) and age less than 54 (OR 3.0, 95% CI 1.4-6.5, p = 0.0037). Increased vigilance for symptoms of pneumonitis is warranted for patients with prior mediastinal radiation and for younger patients, and dose reduction may be considered for patients who would receive greater than 1000 mg of BCNU.
引用
收藏
页码:1130 / 1136
页数:7
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