Cardiac and pulmonary toxicity in patients undergoing high-dose chemotherapy for lymphoma and breast cancer: prognostic factors

被引:57
作者
Brockstein, BE
Smiley, C
Al-Sadir, J
Williams, SF
机构
[1] Univ Chicago, Dept Internal Med, Hematol Oncol Sect, Chicago, IL 60637 USA
[2] Univ Chicago, Cardiol Sect, Chicago, IL 60637 USA
关键词
cardiac toxicity; pulmonary toxicity; stem cell transplant; ejection fraction; breast cancer; lymphoma;
D O I
10.1038/sj.bmt.1702234
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We sought to define risk factors predisposing breast cancer and lymphoma patients to cardiac and pulmonary toxicity when undergoing high-dose chemotherapy (HDC) and autologous stem cell rescue (ASCR), Additionally, we evaluated in depth the predictive value of the ejection fraction measured prior to HDC in determining cardiac toxicity. In this retrospective analysis, 24 variables were examined in 138 patients undergoing HDC and ASCR from 1990 until 1995, Logistic regression models were used to model the probability of experiencing cardiac and pulmonary toxicity as a function of the 24 prognostic covariates. Cardiac toxicity occurred in 12% of patients and pulmonary toxicity in 24% of patients, Bivariate analyses showed that patients with lymphoma las opposed to breast cancer) and those with a higher cardiac risk factor score were more likely to experience cardiac toxicity, Multivariate logistic regression models predicted lymphoma and older age to be risk factors for cardiac toxicity, History of an abnormal ejection fraction and higher doses of anthracyclines prior to HDC may also contribute to cardiac toxicity. Pulmonary toxicity occurred more commonly in lymphoma than breast cancer patients, likely due to the busulfan used in the HDC regimen. No other risk factors for pulmonary toxicity were identified. We conclude that older patients with lymphoma should be carefully evaluated prior to being accepted for HDC programs. Older patients with breast cancer may tolerate this procedure well, There is a trend towards cardiac toxicity in patients with a past history of low ejection fraction, although seemingly poor cardiac risk patients may fare well with HDC if carefully selected with the aid of a thorough cardiac evaluation.
引用
收藏
页码:885 / 894
页数:10
相关论文
共 45 条
  • [1] BEARMAN SI, 1990, BONE MARROW TRANSPL, V5, P173
  • [2] Behar S, 1997, EUR HEART J, V18, P52, DOI 10.1093/oxfordjournals.eurheartj.a015117
  • [3] RADIATION THERAPY-INDUCED CARDIAC INJURY
    BENOFF, LJ
    SCHWEITZER, P
    [J]. AMERICAN HEART JOURNAL, 1995, 129 (06) : 1193 - 1196
  • [4] BLUM RH, 1973, CANCER, V31, P903, DOI 10.1002/1097-0142(197304)31:4<903::AID-CNCR2820310422>3.0.CO
  • [5] 2-N
  • [6] Evaluation of long-term toxicity after chemotherapy for testicular cancer
    Bokemeyer, C
    Berger, CC
    Kuczyk, MA
    Schmoll, HJ
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (11) : 2923 - 2932
  • [7] CYCLOPHOSPHAMIDE CARDIOTOXICITY IN BONE-MARROW TRANSPLANTATION - A PROSPECTIVE EVALUATION OF NEW DOSING REGIMENS
    BRAVERMAN, AC
    ANTIN, JH
    PLAPPERT, MT
    COOK, EF
    LEE, RT
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (07) : 1215 - 1223
  • [8] EARLY ANTHRACYCLINE CARDIOTOXICITY
    BRISTOW, MR
    THOMPSON, PD
    MARTIN, RP
    MASON, JW
    BILLINGHAM, ME
    HARRISON, DC
    [J]. AMERICAN JOURNAL OF MEDICINE, 1978, 65 (05) : 823 - 832
  • [9] High-dose chemotherapy with autologous stem cell rescue for breast cancer: Yesterday, today and tomorrow
    Brockstein, BE
    Williams, SF
    [J]. STEM CELLS, 1996, 14 (01) : 79 - 89
  • [10] Early identification of anthracycline cardiomyopathy: Possibilities and implications
    BuLock, FA
    Mott, MG
    Oakhill, A
    Martin, RP
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1996, 75 (05) : 416 - 422