Use of paclitaxel in patients with pre-existing cardiomyopathy: A review of our experience

被引:26
作者
Gollerkeri, A
Harrold, L
Rose, M
Jain, D
Burtness, BA
机构
[1] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Yale Canc Ctr, New Haven, CT 06520 USA
关键词
cardiomyopathy; paclitaxel; anthracycline; breast cancer; congestive heart failure;
D O I
10.1002/ijc.1295
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cardiac toxicity is frequently the indication for discontinuation of an anthracycline in patients with tumors which remain anthracycline-sensitive. During the 1990s, the most frequently used second-line agents at the Yale Cancer Center (YCC) were the taxanes. The goal of this retrospective analysis was to determine the effect of paclitaxel on cardiac function in patients with cardiomyopathy. YCC outpatient clinic pharmacy order forms were used to identify all patients who had received paclitaxel between December 1995 and November 1997. The clinic records of those patients with a left ventricular ejection fraction (LVEF) of less than or equal to 50% were reviewed to determine the temporal relation between the decreased LVEF and paclitaxel therapy. In addition, clinic records were examined for evidence of prior doxorubicin therapy and history of prior cardiac disease. Between December 1995 and November 1997, 225 patients were treated with paclitaxel in the YCC outpatient clinic. Nine patients had LVEF less than or equal to 50% (mean 37%) prior to initiation of paclitaxel therapy. Six of these patients had equilibrium radionuclide angiocardiographic (ERNA) scans following completion of paclitaxel, In these 6 patients, the mean change in LVEF was +6% (range -3% to +29%). Four patients had improved LVEF following paclitaxel (mean 11%, range 2% to 29%), while 2 patients experienced a decrease in LVEF following paclitaxel treatment (mean 2.5%). The 3 patients who did not have ERNA scans following paclitaxel therapy had no clinical evidence of congestive heart failure. Our experience confirms the results of prior studies that paclitaxel can be safely administered in patients with underlying cardiac dysfunction. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:139 / 141
页数:3
相关论文
共 21 条
[1]   PACLITAXEL ACTIVITY IN HEAVILY PRETREATED BREAST-CANCER - A NATIONAL-CANCER-INSTITUTE TREATMENT REFERRAL CENTER TRIAL [J].
ABRAMS, JS ;
VENA, DA ;
BALTZ, J ;
ADAMS, J ;
MONTELLO, M ;
CHRISTIAN, M ;
ONETTO, N ;
DESMONDHELLMANN, S ;
CANETTA, R ;
FRIEDMAN, MA ;
ARBUCK, SG .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (08) :2056-2065
[2]   Impact of scheduling on toxicity and clinical efficacy of doxorubicin: What do we know in the mid-nineties? [J].
Bielack, SS ;
Erttmann, R ;
KempfBielack, B ;
Winkler, K .
EUROPEAN JOURNAL OF CANCER, 1996, 32A (10) :1652-1660
[3]   CYCLOPHOSPHAMIDE CARDIOTOXICITY IN BONE-MARROW TRANSPLANTATION - A PROSPECTIVE EVALUATION OF NEW DOSING REGIMENS [J].
BRAVERMAN, AC ;
ANTIN, JH ;
PLAPPERT, MT ;
COOK, EF ;
LEE, RT .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (07) :1215-1223
[4]   A phase I study of paclitaxel for mobilization of peripheral blood progenitor cells [J].
Burtness, BA ;
Psyrri, A ;
Rose, M ;
D'Andrea, E ;
Staugaard-Hahn, C ;
Henderson-Bakas, M ;
Clark, MB ;
Mechanic, S ;
Krause, D ;
Snyder, E ;
Cooper, RB ;
Abrantes, J ;
Corringham, R ;
Deisseroth, A ;
Cooper, DL .
BONE MARROW TRANSPLANTATION, 1999, 23 (04) :311-315
[5]   Effect of different chemotherapy regimens on peripheral-blood stem-cell collections in patients with breast cancer receiving granulocyte colony-stimulating factor [J].
Demirer, T ;
Buckner, CD ;
Storer, B ;
Lilleby, K ;
Rowley, S ;
Clift, R ;
Appelbaum, FR ;
Storb, R ;
Bensinger, WI .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (02) :684-690
[6]  
Dombernowsky P, 1996, SEMIN ONCOL, V23, P23
[7]   DOSE-ESCALATION OF PACLITAXEL WITH HIGH-DOSE CYCLOPHOSPHAMIDE, WITH ANALYSIS OF PROGENITOR-CELL MOBILIZATION AND HEMATOLOGIC SUPPORT OF ADVANCED OVARIAN-CANCER PATIENTS RECEIVING RAPIDLY SEQUENCED HIGH-DOSE CARBOPLATIN CYCLOPHOSPHAMIDE COURSES [J].
FENNELLY, D ;
SCHNEIDER, J ;
SPRIGGS, D ;
BENGALA, C ;
HAKES, T ;
REICH, L ;
BARAKAT, R ;
CURTIN, J ;
MOORE, MAS ;
HOSKINS, W ;
NORTON, L ;
CROWN, J .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (05) :1160-1166
[8]   PACLITAXEL IN METASTATIC BREAST-CANCER - A TRIAL OF 2 DOSES BY A 3-HOUR INFUSION IN PATIENTS WITH DISEASE RECURRENCE AFTER PRIOR THERAPY WITH ANTHRACYCLINES [J].
GIANNI, L ;
MUNZONE, E ;
CAPRI, G ;
VILLANI, F ;
SPREAFICO, C ;
TARENZI, E ;
FULFARO, F ;
CARACENI, A ;
MARTINI, C ;
LAFFRANCHI, A ;
VALAGUSSA, P ;
BONADONNA, G .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1995, 87 (15) :1169-1175
[9]   PACLITAXEL BY 3-HOUR INFUSION IN COMBINATION WITH BOLUS DOXORUBICIN IN WOMEN WITH UNTREATED METASTATIC BREAST-CANCER - HIGH ANTITUMOR EFFICACY AND CARDIAC EFFECTS IN A DOSE-FINDING AND SEQUENCE-FINDING STUDY [J].
GIANNI, L ;
MUNZONE, E ;
CAPRI, G ;
FULFARO, F ;
TARENZI, E ;
VILLANI, F ;
SPREAFICO, C ;
LAFFRANCHI, A ;
CARACENI, A ;
MARTINI, C ;
STEFANELLI, M ;
VALAGUSSA, P ;
BONADONNA, G .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (11) :2688-2699
[10]   PHASE-II TRIAL OF TAXOL, AN ACTIVE-DRUG IN THE TREATMENT OF METASTATIC BREAST-CANCER [J].
HOLMES, FA ;
WALTERS, RS ;
THERIAULT, RL ;
FORMAN, AD ;
NEWTON, LK ;
RABER, MN ;
BUZDAR, AU ;
FRYE, DK ;
HORTOBAGYI, GN .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1991, 83 (24) :1797-1805