Cyclophosphamide, doxorubicin, vincristine, prednisone dose intensification with granulocyte colony-stimulating factor markedly depletes stem cell reserve for autologous bone marrow transplantation

被引:37
作者
Freedman, A
Neuberg, D
Mauch, P
Gribben, J
Soiffer, R
Anderson, K
Robertson, M
Fisher, DC
Schlossman, R
Kroon, M
Rhuda, C
Kuhlman, C
Ritz, J
Nadler, L
机构
[1] BRIGHAM & WOMENS HOSP,DEPT RADIAT THERAPY,BOSTON,MA 02115
[2] HARVARD UNIV,SCH MED,DEPT MED,BOSTON,MA
[3] HARVARD UNIV,SCH MED,DEPT RADIAT ONCOL,BOSTON,MA
关键词
D O I
10.1182/blood.V90.12.4996.4996_4996_5001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hematopoietic growth factors allow dose escalation of chemotherapy. This approach may potentially reduce the quality and quantity of hematopoietic stem cells. The capacity of stem cells recovered after dose intensification to support myeloablative therapy is unknown. In patients with previously untreated advanced follicular lymphoma, trilineage hematopoietic engraftment was compared in two sequential trials of induction therapy (standard dose cyclophosphamide, doxorubicin, vincristine. prednisone [CHOP] without growth factors or dose intensification CHOP supported by granulocyte colony-stimulating factor [G-CSF]) followed by identical myeloablative therapy and autologous stem cell support. Neutrophil, platelet, and red blood cell (RBC) engraftment were compared on days 100, 180, and 360 after stem cell reinfusion. Despite similar patient characteristics including reinfusion of comparable numbers of marrow mononuclear cells, after stem cell transplantation. a highly significant prolongation of neutrophil and platelet engraftment was seen in patients who received high dose CHOP and G-CSF in comparison to standard dose CHOP. These findings suggest that dose intensified chemotherapy and G-CSF recruited stem cells into a proliferative phase and that G-CSF allowed retreatment at a time when stem cells were susceptible to damage by cytotoxic therapy. Such inadequate hematologic engraftment after myeloablative therapy might be avoided by either shortening the time that growth factor support is administered, lengthening the interval between cycles, or attempting to repetitively harvest additional stem cells either from the marrow or peripheral blood. Therefore, intensification of chemotherapy with growth factor support must be used with caution if stem cells are to be used to support myeloablative therapy. (C) 1997 by The American Society of Hematology.
引用
收藏
页码:4996 / 5001
页数:6
相关论文
共 28 条
[1]   EFFECT OF RECOMBINANT HUMAN GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR ON CHEMOTHERAPY-INDUCED MYELOSUPPRESSION [J].
ANTMAN, KS ;
GRIFFIN, JD ;
ELIAS, A ;
SOCINSKI, MA ;
RYAN, L ;
CANNISTRA, SA ;
OETTE, D ;
WHITLEY, M ;
FREI, E ;
SCHNIPPER, LE .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 319 (10) :593-598
[2]   A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in multiple myeloma [J].
Attal, M ;
Harousseau, JL ;
Stoppa, AM ;
Sotto, JJ ;
Fuzibet, JG ;
Rossi, JF ;
Casassus, P ;
Maisonneuve, H ;
Facon, T ;
Ifrah, N ;
Payen, C ;
Bataille, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (02) :91-97
[3]   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
[4]   LONG-TERM FOLLOW-UP OF PATIENTS WITH LOW-GRADE MALIGNANT-LYMPHOMAS TREATED WITH DOXORUBICIN-BASED CHEMOTHERAPY OR CHEMOIMMUNOTHERAPY [J].
DANA, BW ;
DAHLBERG, S ;
NATHWANI, BN ;
CHASE, E ;
COLTMAN, C ;
MILLER, TP ;
FISHER, RI .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (04) :644-651
[5]   AUTOLOGOUS PROGENITOR-CELL TRANSPLANTATION - PRIOR EXPOSURE TO STEM CELL-TOXIC DRUGS DETERMINES YIELD AND ENGRAFTMENT OF PERIPHERAL-BLOOD PROGENITOR-CELL BUT NOT OF BONE-MARROW GRAFTS [J].
DREGER, P ;
KLOSS, M ;
PETERSEN, B ;
HAFERLACH, T ;
LOFFLER, H ;
LOEFFLER, M ;
SCHMITZ, N .
BLOOD, 1995, 86 (10) :3970-3978
[6]  
FREEDMAN AS, 1991, BLOOD, V77, P2524
[7]   High-dose therapy and autologous bone marrow transplantation in patients with follicular lymphoma during first remission [J].
Freedman, AS ;
Gribben, JG ;
Neuberg, D ;
Mauch, P ;
Soiffer, RJ ;
Anderson, KC ;
Pandite, L ;
Robertson, MJ ;
Kroon, M ;
Ritz, J ;
Nadler, LM .
BLOOD, 1996, 88 (07) :2780-2786
[8]  
FREEDMAN AS, 1990, J CLIN ONCOL, V8, P1
[9]   DOSE - A CRITICAL FACTOR IN CANCER-CHEMOTHERAPY [J].
FREI, E ;
CANELLOS, GP .
AMERICAN JOURNAL OF MEDICINE, 1980, 69 (04) :585-594
[10]   PHASE-I STUDY OF GRANULOCYTE COLONY-STIMULATING FACTOR IN PATIENTS WITH TRANSITIONAL CELL-CARCINOMA OF THE UROTHELIUM [J].
GABRILOVE, JL ;
JAKUBOWSKI, A ;
FAIN, K ;
GROUS, J ;
SCHER, H ;
STERNBERG, C ;
YAGODA, A ;
CLARKSON, B ;
BONILLA, MA ;
OETTGEN, HF ;
ALTON, K ;
BOONE, T ;
ALTROCK, B ;
WELTE, K ;
SOUZA, L .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (04) :1454-1461