High-dose chemotherapy with autologous stem cell support in patients with responding stage IV breast cancer

被引:7
|
作者
Ljungman, P [1 ]
Björkstrand, B
Fornander, T
Höglund, M
Juliusson, G
Lindman, H
Malmström, A
Rotstein, S
Söderberg, M
Wilking, N
Villman, K
Bergh, J
机构
[1] Huddinge Univ Hosp, Dept Hematol, Karolinska Inst, SE-14186 Huddinge, Sweden
[2] Huddinge Univ Hosp, Dept Oncol, Karolinska Inst, SE-14186 Huddinge, Sweden
[3] Univ Uppsala Hosp, Dept Hematol, Uppsala, Sweden
[4] Univ Uppsala Hosp, Dept Oncol, S-75185 Uppsala, Sweden
[5] Linkoping Univ Hosp, Dept Hematol, S-58185 Linkoping, Sweden
[6] Danderyd Hosp, Dept Oncol, S-18288 Danderyd, Sweden
[7] Karlstad Hosp, Dept Oncol, Karlstad, Sweden
[8] Karolinska Hosp, Radiumhemmet, Dept Oncol, S-10401 Stockholm, Sweden
[9] Orebro Hosp, Dept Oncol, Orebro, Sweden
[10] Linkoping Univ Hosp, Dept Oncol, S-58185 Linkoping, Sweden
关键词
breast cancer; stage IV; autologous SCT;
D O I
10.1038/sj.bmt.1701367
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Ninety-four patients underwent high-dose chemotherapy with stem cell support for stage IV breast cancer. The high-dose chemotherapy consisted of the Stamp V regimen in all patients comprising cyclophosphamide, thiotepa and carboplatin (CTCb), Twenty-three patients received sequential high-dose therapies with the first consisting of high-dose melphalan and the second of Stamp V. Two patients died from chemotherapy-related complications resulting in a transplant-related mortality at 100 days of 2.2%, The progression-free survival at 3 years was 36% in patients with no evidence of disease at the first course of high-dose therapy compared with 17% in patients with remaining disease at time of the high-dose therapy (P = 0.03), There was no difference in overall survival between patients with no evidence of disease and other patients. The source of stem cells, single or double courses of high-dose therapy, positive selection of CD34(+) cells, or number of involved sites had no influence on either progression-free survival or overall survival. Further studies of more intensive induction chemotherapy followed by high-dose therapy with stem cell support are indicated.
引用
收藏
页码:445 / 448
页数:4
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