Long-Term Outcome of Patients with Metastatic Breast Cancer Treated with High-Dose Chemotherapy and Transplantation of Purified Autologous Hematopoietic Stem Cells

被引:29
作者
Mueller, Antonia M. S. [1 ]
Kohrt, Holbrook E. K. [2 ]
Cha, Steven [2 ]
Laport, Ginna [1 ]
Klein, Jared [3 ]
Guardino, Alice E. [2 ]
Johnston, Laura J. [1 ]
Stockerl-Goldstein, Keith E. [4 ]
Hanania, Elie [5 ]
Juttner, Christopher [6 ]
Blume, Karl G. [1 ]
Negrin, Robert S. [1 ]
Weissman, Irving L. [7 ,8 ]
Shizuru, Judith A. [1 ,7 ,8 ]
机构
[1] Stanford Univ, Div Blood & Marrow Transplantat, Dept Med, Stanford, CA 94305 USA
[2] Stanford Univ, Div Oncol, Dept Med, Stanford, CA 94305 USA
[3] Banner Pediat Specialists Hematol & Oncol, Mesa, AZ USA
[4] Washington Univ, Div Oncol, St Louis, MO USA
[5] SAFC, Carlsbad, CA USA
[6] Australian Stem Cell Ctr, Clayton, Vic, Australia
[7] Stanford Univ, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[8] Stanford Univ, Ludwig Ctr Canc Stem Cell Res, Stanford, CA 94305 USA
关键词
Metastatic breast cancer; High-dose chemotherapy; Hematopoietic stem cell; Long-term; BONE-MARROW-TRANSPLANTATION; PERIPHERAL-BLOOD; TUMOR CONTAMINATION; RANDOMIZED-TRIAL; PROGENITOR CELLS; FREE SURVIVAL; SUPPORT; PRODUCTS; WOMEN; CYCLOPHOSPHAMIDE;
D O I
10.1016/j.bbmt.2011.07.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Metastatic breast cancer remains a major treatment challenge. The use of high-dose chemotherapy (HDCT) with rescue by autologous mobilized peripheral blood (MPB) is controversial, in part because of contamination of MPB by circulating tumor cells. CD34(+)Thy-1(+) selected hematopoietic stem cells (HSC) represent a graft source with a greater than 250,000-fold reduction in cancer cells. Here, we present the long-term outcome of a pilot study to determine feasibility and engraftment using HDCT and purified HSC in patients with metastatic breast cancer. Twenty-two patients who had been treated with standard chemotherapy were enrolled into a phase I/II trial between December 1996 and February 1998, and underwent HDCT followed by rescue with CD34(+)Thy-1(+) HSC isolated from autologous MPB. More than 12 years after the end of the study, 23% (5 of 22) of HSC recipients are alive, and 18% (4 of 22) are free of recurrence with normal hematopoietic function. Median progression-free survival (PFS) was 16 months, and median overall survival (OS) was 60 months. Retrospective comparison with 74 patients transplanted between February 1995 and June 1999 with the identical HDCT regimen but rescue with unmanipulated MPB indicated that 9% of patients are alive, and 7% are without disease. Median PFS was 10 months, and median OS was 28 months. In conclusion, cancer-depleted HSC following HDCT resulted in better than expected I 2- to 14-year PFS and OS in a cohort of metastatic breast cancer patients. These data prompt us to look once again at purified HSC transplantation in a protocol powered to test for efficacy in advanced-stage breast cancer patients. Biol Blood Marrow Transplant 18: 125-133 (2012) (C) 2012 American Society for Blood and Marrow Transplantation
引用
收藏
页码:125 / 133
页数:9
相关论文
共 43 条
[1]  
Armitage JO, 2009, THOMAS HEMATOPOIETIC, P8
[2]   PROGNOSTIC FACTORS FOR PROLONGED PROGRESSION-FREE SURVIVAL WITH HIGH-DOSE CHEMOTHERAPY WITH AUTOLOGOUS STEM-CELL SUPPORT FOR ADVANCED BREAST-CANCER [J].
AYASH, LJ ;
WHEELER, C ;
FAIRCLOUGH, D ;
SCHWARTZ, G ;
REICH, E ;
WARREN, D ;
SCHNIPPER, L ;
ANTMAN, K ;
FREI, E ;
ELIAS, A .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (08) :2043-2049
[3]   Pegase 03:: a prospective randomized phase III trial of FEC with or without high-dose thiotepa, cyclophosphamide and autologous stem cell transplantation in first-line treatment of metastatic breast cancer [J].
Biron, P. ;
Durand, M. ;
Roche, H. ;
Delozier, T. ;
Battista, C. ;
Fargeot, P. ;
Spaeth, D. ;
Bachelot, T. ;
Poiget, E. ;
Monnot, F. ;
Tanguy, M. L. ;
Cure, H. .
BONE MARROW TRANSPLANTATION, 2008, 41 (06) :555-562
[4]   Standardization of the immunocytochemical detection of cancer cells in BM and blood: I. establishment of objective criteria for the evaluation of immunostained cells [J].
Borgen, E ;
Naume, B ;
Nesland, JM ;
Kvalheim, G ;
Beiske, K ;
Fodstad, O ;
Diel, I ;
Solomayer, EF ;
Theocharous, P ;
Coombes, RC ;
Smith, BM ;
Wunder, E ;
Marolleau, JP ;
Garcia, J ;
Pantel, K .
CYTOTHERAPY, 1999, 1 (05) :377-388
[5]   A pooled analysis of bone marrow micrometastasis in breast cancer [J].
Braun, S ;
Vogl, FD ;
Naume, B ;
Janni, W ;
Osborne, MP ;
Coombes, RC ;
Schlimok, G ;
Diel, IJ ;
Gerber, B ;
Gebauer, G ;
Pierga, JY ;
Marth, C ;
Oruzio, D ;
Wiedswang, G ;
Solomayer, EF ;
Kundt, G ;
Strobl, B ;
Fehm, T ;
Wong, GYC ;
Bliss, J ;
Vincent-Salomon, A ;
Pantel, K .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (08) :793-802
[6]   GENE-MARKING TO TRACE ORIGIN OF RELAPSE AFTER AUTOLOGOUS BONE-MARROW TRANSPLANTATION [J].
BRENNER, MK ;
RILL, DR ;
MOEN, RC ;
KRANCE, RA ;
MIRRO, J ;
ANDERSON, WF ;
IHLE, JN .
LANCET, 1993, 341 (8837) :85-86
[7]  
Brockstein B E, 1996, J Hematother, V5, P617, DOI 10.1089/scd.1.1996.5.617
[8]  
BRUGGER W, 1994, BLOOD, V83, P636
[9]   Breast tumor contamination of PBSC harvests:: tumor depletion by positive selection of CD34+ cells [J].
Burgess, J ;
Mills, B ;
Griffith, M ;
Mansour, V ;
Weaver, CH ;
Schwartzberg, LS ;
Snyder, EL ;
Krause, DS ;
Yanovich, S ;
Prilutskaya, M ;
Umiel, T ;
Moss, TJ .
CYTOTHERAPY, 2001, 3 (04) :285-294
[10]  
Cheng YC, 2011, BREAST CANC