LOW-DOSE ARA-C IN MYELODYSPLASTIC SYNDROMES (MDS) AND ACUTE-LEUKEMIA FOLLOWING MDS - PROPOSAL FOR A PREDICTIVE MODEL

被引:10
作者
HELLSTROMLINDBERG, E
ROBERT, KH
GAHRTON, G
LINDBERG, G
FORSBLOM, AM
KOCK, Y
OST, A
机构
[1] Department of Medicine, Huddinge University Hospital, Huddinge
[2] Department of Pathology, Karolinska Hospital, Stockholm
关键词
MYELODYSPLASTIC SYNDROMES; LOW-DOSE ARA-C; PROGNOSTIC FACTORS;
D O I
10.3109/10428199409073775
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Patients with myelodysplastic syndromes (MDS) comprise an extremely heterogenous group. There is a need for decision models both for predicting the natural course of the disease and the outcomes of different treatment alternatives. In 102 consecutive patients with MDS or acute myelogenous leukemia (AML) following MDS, pre-treatment variables were studied in relation to the response to treatment with low-dose ara-C. Thirty patients (29%) responded with either a complete remission or a significant rise in the hemoglobin level. For the remaining 71%, the treatment was ineffective and in some cases hazardous. The factors associated with a poor response to treatment could be divided into two groups: one included low platelet counts and the presence of chromosomal aberrations, both signs of progressive MDS with a short survival, and the other comprised morphological findings, indicating ineffective hemopoiesis. Patients with platelet counts > 150 x 10(9)/l had a response rate of 55%, compared to 24% in patients with subnormal platelet counts. Logistic regression identified low bone marrow cellularity, absence of ring sideroblasts and <2 chromosomal aberrations as predictors of a favourable response in patients with platelet counts < 150 x 10(9)/l. These factors and the platelet count were combined in a predictive model which divided patients into dime groups with different probabilities of response: one favourable (38% of the patients), with a response rate of >50%; a second, intermediate group (33% of the patients), with a response rate of 24%; and a third, unfavourable group (29% of the patients) with only 3% responses. While low-dose ara-C is an effective treatment for some patients, it is ineffective and hazardous for others. We propose a model that can facilitate therapeutic decision-making in 2/3 of patients with MDS and MDS-AML by identifying diose who should not be treated with low-dose ara-C as well as those with a relatively high probability of response.
引用
收藏
页码:343 / 351
页数:9
相关论文
共 48 条
[1]  
Kerkhofs H., Hermans J., Haak H., Leeksma C., Utility of the FAB classification for myelodysplastic syndromes: Investigation of prognostic factors in 237 patients, Br. J. Haematol., 65, pp. 73-81, (1987)
[2]  
Bennett J., Catovsky D., Daniel M., Flandrin G., Galton D.A.G., Gralnick H., Sultan C., Proposals for the classification of the myelodysplastic syndromes, Br. J. Haematol., 51, pp. 189-199, (1982)
[3]  
Mufti G., Stevens J., Oscier D., Hamblin T., Machin D., Myelodysplastic syndromes: a scoring system with prognostic significants, Br. J. Haematol., 59, pp. 425-433, (1985)
[4]  
Worsely A., Oscier D., Stevens J., Darlow S., Fige A., Mufti G., Hamblin T., Prognostic features of chronic myelomonocytic leukemia: a modified Bournemouth score gives the best prediction of survival, Br. J. Haematol., 68, pp. 17-21, (1988)
[5]  
van der Weide M., Sizoo W., Nauta J.J.P., Krefft J., Langenhuijsen M.M.A.C., Myelodysplastic syndromes: analysis of clinical and prognostic features in 96 patients, Eur. J. Haematol., 41, pp. 115-122, (1988)
[6]  
Sanz G., Sanz M., Vallespi T., Canizo C., Torrabadella M., Garcia S., Irriguible D., San Miguel J., Two regression models and a scoring system for predicting survival and planning treatment in myelodysplastic syndromes: A tnultivariate analysis of prognostic factors in 370 patients, Blood, 74, pp. 395-408, (1989)
[7]  
Aul C., Gattermann N., Heyll A., Germing U., Derigs G., Schneider W., Primary myelodysplastic syndromes: analysis of prognostic factors in 235 patients and proposals for an improved scoring system, Leukemia, 6, pp. 52-59, (1992)
[8]  
Yunis J., Lobell M., Arnesen M., Oken M., Mayer M., Rydell R., Brunning R., Refined chromosome study helps define prognostic subgroups in most patients with primary myelodysplastic syndrome and acute leukemia, Br. J. Haematol., 68, pp. 189-194, (1988)
[9]  
Geddes A., Bowen D., Jacobs A., Clonal caryotypic abnormalities and clinical progress in the myelodysplastic syndromes, Br. J. Haematol., 76, pp. 194-202, (1990)
[10]  
White A.D., Culligan T.G., Hoy T.G., Jacobs A., Extended cytogenetic follow-up of patients with myelodysplastic syndrome (MDS), Br. J. Haematol., 81, pp. 499-502, (1992)