High-dose ifosfamide and etoposide with filgrastim for stem cell mobilization in patients with advanced ovarian cancer

被引:0
作者
ML Donato
D Gershenson
C Ippoliti
JT Wharton
RC Bast
A Aleman
P Anderlini
JG Gajewski
S Giralt
J Molldrem
N Ueno
J Lauppe
M Korbling
J Boyer
D Bodurka-Bevers
M Bevers
T Burke
R Freedman
C Levenback
J Wolf
RE Champlin
机构
[1] The University of Texas MD Anderson Cancer Center,Department of Blood and Marrow Transplantation
[2] The University of Texas MD Anderson Cancer Center,Department of Gynecologic Oncology
[3] The University of Texas MD Anderson Cancer Center,Division of Pharmacy
[4] The University of Texas MD Anderson Cancer Center,Department of Clinical Investigation
来源
Bone Marrow Transplantation | 2000年 / 25卷
关键词
ovarian cancer; stem cell collection; ifosfamide; etoposide;
D O I
暂无
中图分类号
学科分类号
摘要
High-dose chemotherapy combined with autologous peripheral blood stem cell transplantation has shown promise as treatment for recurrent or persistent epithelial ovarian cancer. We evaluated the stem cell mobilization regimen of high-dose ifosfamide plus etoposide in 32 patients with epithelial ovarian cancer, who had a positive second-look laparatomy or recurrent disease. Ifosfamide was given at 10 g/m2 by continuous i.v. from days 1 to 3. Etoposide was given at 150 mg/m2 every 12 h for six doses on days 1–3. Filgrastim was given at 10 μg/kg/d s.c. from day 5 until the completion of peripheral blood stem cell harvest. Fourteen of 32 patients had measurable or evaluable disease before mobilization therapy and were assessed for response. In nine (64%) of the 14 patients, treatment response was demonstrated, and these patients received a second cycle of mobilization therapy. The target CD34+ cell dose (>8 × 106 cells/kg) was achieved with a median of one apheresis (range 1–5). A median of 25.1 (range 8.0–122.5) × 106 CD34+ cells/kg body weight was collected. Non-hematologic toxicity was limited to grade 2 renal dysfunction in one patient and grade 2 hepatic dysfunction in three patients. In this patient group, high-dose ifosfamide plus etoposide with filgrastim support was well tolerated, lead to successful stem cell harvest and had antitumor activity. Bone Marrow Transplantation (2000) 25, 1137–1140.
引用
收藏
页码:1137 / 1140
页数:3
相关论文
共 78 条
  • [1] Legros M(1997)High-dose chemotherapy with hematopoietic rescue in patients with stage III and IV ovarian cancer: long term results J Clin Oncol 15 1302-1308
  • [2] Dauplat J(1997)High-dose chemotherapy with autologous transplantation for persistent/relapsed ovarian cancer: a multivariate analysis of survival for 100 consecutively treated patients J Clin Oncol 15 1291-1293
  • [3] Fleury H(1995)Engraftment kinetics and long term stability of hematopoiesis following autografting of peripheral blood stem cells Haemotologica 80 115-122
  • [4] Stiff PJ(1995)Engraftment of patients with lymphoid malignancies transplanted with autologous bone marrow, peripheral blood stem cells or both Bone Marrow Transplant 15 241-246
  • [5] Bayer R(1992)Comparison of hematological recovery times and supportive care requirements of autologous recovery phase peripheral blood transplants, autologous bone marrow transplants and allogeneic bone marrow transplants Bone Marrow Transplant 9 277-284
  • [6] Kerger C(1994)Bone marrow reconstitution after high-dose chemotherapy and autologous peripheral blood progenitor cell transplantation: effect of graft size Ann Oncol 5 795-802
  • [7] Indovina A(1995)An analysis of engraftment kinetics as a function of the CD34 content of peripheral blood progenitor cell collections in 692 patients after the administration of myeloblative chemotherapy Blood 86 3961-3969
  • [8] Majolino I(1994)Combined chemotherapy and granulocyte colony-stimulating factor (G-CSF) mobilize large numbers of peripheral blood progenitor cells in treated patients Leuk Lymphoma 15 91-97
  • [9] Buscemi F(1996)Mobilization of peripheral blood progenitor cells with high-dose cyclophosphamide (4 or 7gm/m Bone Marrow Transplant 17 691-697
  • [10] Langenmayer I(1995)) and granulocyte colony stimulation factor in patients with multiple myeloma Bone Marrow Transplant 16 359-363