Chemotherapy for prostate cancer

被引:92
作者
Gilligan, T [1 ]
Kantoff, PW [1 ]
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Lank Ctr Genitourinary Oncol, Boston, MA 02115 USA
关键词
D O I
10.1016/S0090-4295(02)01583-2
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Androgen deprivation therapy remains the mainstay of therapy for patients with advanced prostate cancer and for selected patients with localized prostate cancer. Androgen deprivation therapy is the model of target-based therapies in this disease. Although it is clear that other target-based therapies need to be developed, cytotoxic chemotherapy is emerging as an effective form of treatment for men with prostate cancer. The early studies combining mitoxantrone plus a corticosteroid demonstrated that chemotherapy could be given to men with symptomatic hormone-refractory prostate cancer with minimal toxicity, and significant palliation could be provided. Since then, it has been recognized that estramustine, when combined with a variety of microtubular inhibitors, is very active in hormone-refractory prostate cancer. Doublets combining estramustine plus a taxane seem to be the most active. Although it appears that estramustine may add some activity to taxanes, the mechanism of its activity is uncertain, and its overall value is similarly questioned, particularly in light of its significant toxicity. Regimens that omit estramustine are being explored (ie, either taxane alone or taxane plus biologic agents). In addition, triplet therapy (combining estramustine plus a taxane plus a third drug, such as carboplatin or etoposide) is being explored. Finally, the utility of chemotherapy is beginning to be explored in the context of earlier disease in the neoadjuvant, adjuvant, or serologically relapsing group of patients. Data from these studies are just beginning to be gathered.
引用
收藏
页码:94 / 100
页数:7
相关论文
共 47 条
[21]   Paclitaxel, estramustine phosphate, and carboplatin in patients with advanced prostate cancer [J].
Kelly, WK ;
Curley, T ;
Slovin, S ;
Heller, G ;
McCaffrey, J ;
Bajorin, D ;
Ciolino, A ;
Regan, K ;
Schwartz, M ;
Kantoff, P ;
George, D ;
Oh, W ;
Smith, M ;
Kaufman, D ;
Small, EJ ;
Schwartz, L ;
Larson, S ;
Tong, W ;
Scher, H .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (01) :44-53
[22]  
KOSTY MP, 2001, P AN M AM SOC CLIN, V20, pB152
[23]   Unique synergism or antagonism of combinations of chemotherapeutic and hormonal agents in human prostate cancer cell lines [J].
Kreis, W ;
Budman, DR ;
Calabro, A .
BRITISH JOURNAL OF UROLOGY, 1997, 79 (02) :196-202
[24]  
MAREEL MM, 1988, CANCER RES, V48, P1842
[25]   Neoadjuvant docetaxel followed by radical prostatectomy in patients with high-risk localized prostate cancer: A preliminary report [J].
Oh, WK ;
George, DJ ;
Kaufman, DS ;
Moss, K ;
Smith, MR ;
Richie, JP ;
Kantoff, PW .
SEMINARS IN ONCOLOGY, 2001, 28 (04) :40-44
[26]   Management of hormone refractory prostate cancer: Current standards and future prospects [J].
Oh, WK ;
Kantoff, PW .
JOURNAL OF UROLOGY, 1998, 160 (04) :1220-1229
[27]   Health-related quality of life in men with metastatic prostate cancer treated with prednisone alone or mitoxantrone and prednisone [J].
Osoba, D ;
Tannock, IF ;
Ernst, DS ;
Neville, AJ .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (06) :1654-1663
[28]  
Petrylak DP, 1999, SEMIN ONCOL, V26, P28
[29]  
PETRYLAK DP, 2000, P AN M AM SOC CLIN, V19, pA334
[30]   Neoadjuvant chemotherapy and hormonal therapy followed by radical prostatectomy: Feasibility and preliminary results [J].
Pettaway, CA ;
Pisters, LL ;
Troncoso, P ;
Slaton, J ;
Finn, L ;
Kamoi, K ;
Logothetis, CJ .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (05) :1050-1057