Feasibility of stopping paclitaxel premedication after two doses in patients not experiencing a previous infusion hypersensitivity reaction

被引:27
作者
Berger, Michael J. [1 ,2 ]
Dunlea, Leslie J. [3 ]
Rettig, Amy E.
Lustberg, Maryam B. [3 ]
Phillips, Gary S. [4 ]
Shapiro, Charles L. [3 ]
机构
[1] Ohio State Univ, Dept Pharm, James Comprehens Breast Ctr, Arthur G James Canc Hosp, Columbus, OH 43212 USA
[2] Ohio State Univ, Richard J Solove Res Inst, Columbus, OH 43212 USA
[3] Ohio State Univ, Dept Med Oncol, James Comprehens Breast Ctr, Arthur G James Canc Hosp,Med Ctr, Columbus, OH 43212 USA
[4] Ohio State Univ, Ctr Biostat, Columbus, OH 43212 USA
关键词
Abbreviated; Paclitaxel; Premedication; Prophylaxis; Hypersensitivity; METASTATIC BREAST-CANCER; PHASE-III TRIAL; TRASTUZUMAB; PROPHYLAXIS; MANAGEMENT; CELLS;
D O I
10.1007/s00520-011-1303-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Paclitaxel-based chemotherapy continues to be an integral component in the treatment of many solid tumors. Prolonged use of paclitaxel may result in repeated doses of premedications and potential unwanted side effects. Infusion hypersensitivity reactions occurring beyond the second dose are infrequent and not well characterized. We hypothesized that patients whose paclitaxel premedications were discontinued after two doses were unlikely to experience infusion hypersensitivity reactions with subsequent paclitaxel doses. Patients receiving paclitaxel-based chemotherapy who did not experience an infusion hypersensitivity reaction with their first or second dose had their paclitaxel premedications discontinued. The primary endpoint was to estimate the incidence of rescue medication for the treatment of paclitaxel infusion hypersensitivity during doses 3 to 6 for patients whose paclitaxel premedications had been discontinued. After receiving the first two doses of paclitaxel-based chemotherapy without experiencing an infusion hypersensitivity reaction (any grade), 55 breast cancer patients had their premedications discontinued for all remaining paclitaxel doses. None of these patients required rescue medication to treat an infusion hypersensitivity reaction with subsequent doses. In patients who have not experienced an infusion hypersensitivity reaction with the first two doses of paclitaxel, discontinuation of paclitaxel premedications may be considered an option without an increased risk of infusion hypersensitivity requiring rescue medication.
引用
收藏
页码:1991 / 1997
页数:7
相关论文
共 18 条
[1]  
[Anonymous], 2007, MICROMEDEX DIPHENHYD
[2]  
Bookman MA, 1997, SEMIN ONCOL S19, V24, pS19
[3]   Tapering and discontinuation of glucocorticoid prophylaxis during prolonged weekly to biweekly paclitaxel administration [J].
Braverman, AS ;
Rao, S ;
Salvatti, ME ;
Adamson, B ;
McManus, M ;
Pierre, S .
CHEMOTHERAPY, 2005, 51 (2-3) :116-119
[4]   Phase III trial of nanoparticle albumin-bound paclitaxel compared with polyethylated castor oil-based paclitaxel in women with breast cancer [J].
Gradishar, WJ ;
Tjulandin, S ;
Davidson, N ;
Shaw, H ;
Desai, N ;
Bhar, P ;
Hawkins, M ;
O'Shaughnessy, J .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (31) :7794-7803
[5]   Fatal outcome of a hypersensitivity reaction to paclitaxel: a critical review of premedication regimens [J].
Kloover, JS ;
den Bakker, MA ;
Gelderblom, H ;
van Meerbeeck, JP .
BRITISH JOURNAL OF CANCER, 2004, 90 (02) :304-305
[6]   Dose reduction of steroid premeditation for paclitaxel:: No increase of hypersensitivity reactions [J].
Köppler, H ;
Heymanns, J ;
Weide, R .
ONKOLOGIE, 2001, 24 (03) :283-285
[7]   Management and preparedness for infusion and hypersensitivity reactions [J].
Lenz, Heinz-Josef .
ONCOLOGIST, 2007, 12 (05) :601-609
[8]   Paclitaxel-associated hypersensitivity reactions: Experience of the Gynecologic Oncology Program of the Cleveland Clinic Cancer Center [J].
Markman, M ;
Kennedy, A ;
Webster, K ;
Kulp, B ;
Peterson, G ;
Belinson, J .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (01) :102-105
[9]   An effective and more convenient drug regimen for prophylaxis against paclitaxel-associated hypersensitivity reactions [J].
Markman, M ;
Kennedy, A ;
Webster, K ;
Peterson, G ;
Kulp, B ;
Belinson, J .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1999, 125 (07) :427-429
[10]   Paclitaxel plus bevacizumab versus paclitaxel alone for metastatic breast cancer [J].
Miller, Kathy ;
Wang, Molin ;
Gralow, Julie ;
Dickler, Maura ;
Cobleigh, Melody ;
Perez, Edith A. ;
Shenkier, Tamara ;
Cella, David ;
Davidson, Nancy E. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 357 (26) :2666-2676