J.F.C Marques , A.C Vigorito , F.J.P Aranha , I Lorand-Metze , E.C.M Miranda , E.C Lima Filho , M Valbonesi , G Santini , C.A De Souza
{"title":"早期的总白细胞恢复是低单采数和良好的CD34+细胞产量的预测因子","authors":"J.F.C Marques , A.C Vigorito , F.J.P Aranha , I Lorand-Metze , E.C.M Miranda , E.C Lima Filho , M Valbonesi , G Santini , C.A De Souza","doi":"10.1016/S0955-3886(00)00072-2","DOIUrl":null,"url":null,"abstract":"<div><p><em>Objective</em><span>. We analysed peripheral blood progenitor cell (PBPC) mobilisation and collection in order to assess the main factors related to CD34</span><sup>+</sup><span> cell yields in patients affected by haematological malignancies.</span></p><p><em>Patients and Methods</em>. The features of CD34<sup>+</sup><span><span> cell mobilisation of patients with haematological malignancies that underwent autologous bone marrow transplantation were examined. Mobilisation chemotherapy consisted mainly of </span>cyclophosphamide (CY) 4 or 7 g/m</span><sup>2</sup> followed by growth factors. Leukapheresis was started when the WBC counts reached 1.0<!--> <!-->×<!--> <!-->10<sup>9</sup>/l with the aim to collect at least 5<!--> <!-->×<!--> <!-->10<sup>6</sup> CD34<sup>+</sup> cells/kg body weight. The aphereses were performed on continuous-flow blood cell separators. The analysed variables were: age, diagnosis, CT mobilisation regimen, type of growth factor, number of previous CT lines, prior radiotherapy, days for WBC recovery and number of aphereses procedures to achieve the target of CD34<sup>+</sup> cells.</p><p><em>Results</em><span>. There were 41 consecutive patients (26 M/15 F): 21 non-Hodgkin’s lymphoma (NHL), 15 Hodgkin’s disease (HD), two chronic myeloid leukaemia (CML) and three multiple myeloma (MM). Eleven patients could not collect the proposed threshold of CD34</span><sup>+</sup> cells. CY 4 mobilised patients recovered WBC counts in less days (<em>P</em>=0.03). By ANOVA, the days to WBC recovery had a linear function of the predictors “number of aphereses” and “type of mobilisation CT” (coefficients: 0.86 and 0.95, respectively). For the number of aphereses and WBC recovery after CT mobilisation, we obtained a correlation coefficient of 0.36 (<em>P</em>=0.02).</p><p><em>Conclusion</em>. This study shows that it is feasible to mobilise and collect PBPC in patients previously treated with CT with or without RT. There was a linear correlation between the days for WBC recovery and the number of aphereses needed to collect the target number of CD34<sup>+</sup> cells. The study suggests that early WBC recovery, using mainly CY 4 mobilisation chemotherapy, is an important predictor of a low number of aphereses to achieve a good CD34<sup>+</sup> yield.</p></div>","PeriodicalId":80242,"journal":{"name":"Transfusion science","volume":"23 2","pages":"Pages 91-100"},"PeriodicalIF":0.0000,"publicationDate":"2000-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0955-3886(00)00072-2","citationCount":"19","resultStr":"{\"title\":\"Early total white blood cell recovery is a predictor of low number of apheresis and good CD34+ cell yield\",\"authors\":\"J.F.C Marques , A.C Vigorito , F.J.P Aranha , I Lorand-Metze , E.C.M Miranda , E.C Lima Filho , M Valbonesi , G Santini , C.A De Souza\",\"doi\":\"10.1016/S0955-3886(00)00072-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><em>Objective</em><span>. We analysed peripheral blood progenitor cell (PBPC) mobilisation and collection in order to assess the main factors related to CD34</span><sup>+</sup><span> cell yields in patients affected by haematological malignancies.</span></p><p><em>Patients and Methods</em>. The features of CD34<sup>+</sup><span><span> cell mobilisation of patients with haematological malignancies that underwent autologous bone marrow transplantation were examined. Mobilisation chemotherapy consisted mainly of </span>cyclophosphamide (CY) 4 or 7 g/m</span><sup>2</sup> followed by growth factors. Leukapheresis was started when the WBC counts reached 1.0<!--> <!-->×<!--> <!-->10<sup>9</sup>/l with the aim to collect at least 5<!--> <!-->×<!--> <!-->10<sup>6</sup> CD34<sup>+</sup> cells/kg body weight. The aphereses were performed on continuous-flow blood cell separators. The analysed variables were: age, diagnosis, CT mobilisation regimen, type of growth factor, number of previous CT lines, prior radiotherapy, days for WBC recovery and number of aphereses procedures to achieve the target of CD34<sup>+</sup> cells.</p><p><em>Results</em><span>. There were 41 consecutive patients (26 M/15 F): 21 non-Hodgkin’s lymphoma (NHL), 15 Hodgkin’s disease (HD), two chronic myeloid leukaemia (CML) and three multiple myeloma (MM). Eleven patients could not collect the proposed threshold of CD34</span><sup>+</sup> cells. CY 4 mobilised patients recovered WBC counts in less days (<em>P</em>=0.03). By ANOVA, the days to WBC recovery had a linear function of the predictors “number of aphereses” and “type of mobilisation CT” (coefficients: 0.86 and 0.95, respectively). For the number of aphereses and WBC recovery after CT mobilisation, we obtained a correlation coefficient of 0.36 (<em>P</em>=0.02).</p><p><em>Conclusion</em>. This study shows that it is feasible to mobilise and collect PBPC in patients previously treated with CT with or without RT. There was a linear correlation between the days for WBC recovery and the number of aphereses needed to collect the target number of CD34<sup>+</sup> cells. The study suggests that early WBC recovery, using mainly CY 4 mobilisation chemotherapy, is an important predictor of a low number of aphereses to achieve a good CD34<sup>+</sup> yield.</p></div>\",\"PeriodicalId\":80242,\"journal\":{\"name\":\"Transfusion science\",\"volume\":\"23 2\",\"pages\":\"Pages 91-100\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2000-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0955-3886(00)00072-2\",\"citationCount\":\"19\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Transfusion science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0955388600000722\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transfusion science","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0955388600000722","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Early total white blood cell recovery is a predictor of low number of apheresis and good CD34+ cell yield
Objective. We analysed peripheral blood progenitor cell (PBPC) mobilisation and collection in order to assess the main factors related to CD34+ cell yields in patients affected by haematological malignancies.
Patients and Methods. The features of CD34+ cell mobilisation of patients with haematological malignancies that underwent autologous bone marrow transplantation were examined. Mobilisation chemotherapy consisted mainly of cyclophosphamide (CY) 4 or 7 g/m2 followed by growth factors. Leukapheresis was started when the WBC counts reached 1.0 × 109/l with the aim to collect at least 5 × 106 CD34+ cells/kg body weight. The aphereses were performed on continuous-flow blood cell separators. The analysed variables were: age, diagnosis, CT mobilisation regimen, type of growth factor, number of previous CT lines, prior radiotherapy, days for WBC recovery and number of aphereses procedures to achieve the target of CD34+ cells.
Results. There were 41 consecutive patients (26 M/15 F): 21 non-Hodgkin’s lymphoma (NHL), 15 Hodgkin’s disease (HD), two chronic myeloid leukaemia (CML) and three multiple myeloma (MM). Eleven patients could not collect the proposed threshold of CD34+ cells. CY 4 mobilised patients recovered WBC counts in less days (P=0.03). By ANOVA, the days to WBC recovery had a linear function of the predictors “number of aphereses” and “type of mobilisation CT” (coefficients: 0.86 and 0.95, respectively). For the number of aphereses and WBC recovery after CT mobilisation, we obtained a correlation coefficient of 0.36 (P=0.02).
Conclusion. This study shows that it is feasible to mobilise and collect PBPC in patients previously treated with CT with or without RT. There was a linear correlation between the days for WBC recovery and the number of aphereses needed to collect the target number of CD34+ cells. The study suggests that early WBC recovery, using mainly CY 4 mobilisation chemotherapy, is an important predictor of a low number of aphereses to achieve a good CD34+ yield.