MACOP-B Chemotherapy for the treatment of high grade and intermediate grade Non Hodgkin's lymphoma
Summary Between Nov. 1985 and Nov. 1988, sixty-three patients with high grade malignant (hg) and intermediate grade malignant (img) Non Hodgkin's Lymphoma (NHL) were treated with MACOP-B (methotrexate, doborubicin, cyclophosphamide, vincristine, prednison and bleomycin). Thirty-seven patients r...
Ausführliche Beschreibung
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Englisch |
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1990 |
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5 |
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Springer Online Journal Archives 1860-2002 |
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in: Annals of hematology - 1955, 60(1990) vom: Jan., Seite 23-27 |
Übergeordnetes Werk: |
volume:60 ; year:1990 ; month:01 ; pages:23-27 ; extent:5 |
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NLEJ202967662 |
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520 | |a Summary Between Nov. 1985 and Nov. 1988, sixty-three patients with high grade malignant (hg) and intermediate grade malignant (img) Non Hodgkin's Lymphoma (NHL) were treated with MACOP-B (methotrexate, doborubicin, cyclophosphamide, vincristine, prednison and bleomycin). Thirty-seven patients received MACOP-B as an upfront treatment modality, whereas twenty-six patients had relapsed disease and received MACOP-B as a salvage protocol. Four weeks after termination of therapy, 75% of patients with de novo NHL and 72% of the patients with relapsed NHL were in complete remission (CR). In the group of newly diagnosed NHL, 22% achieved partial remission (PR) and 3% no change (NC), whereas in the group with relapsed disease 14% had PR and 14% had progressive disease (PD). At a medium follow-up of 12 months (range 1 month to 33 months), 74% of patients with de novo NHL continued to be in CR whereas the continuous CR rate in patients with relapsed disease was 35%. Overall survival after 30 months of observation for the patient group with de novo NHL was 75% and 40% for patients with relapsed NHL. The mean duration for completion of the projected 12 chemotherapy cycles, given in weekly intervals, was 12.9 and 13.5 weeks in upfront or salvage therapy, respectively. With low incidence of major toxicities, application of drugs on an outpatient basis, and high efficacy, MACOP-B shows substantial advantges for therapy of de novo and relapsed NHL. | ||
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700 | 1 | |a Oster, W. |4 oth | |
700 | 1 | |a Forsthuber, T. |4 oth | |
700 | 1 | |a Hennekeuser, H. H. |4 oth | |
700 | 1 | |a Gamm, H. |4 oth | |
700 | 1 | |a Lindemann, A. |4 oth | |
700 | 1 | |a Schmitz, G. |4 oth | |
700 | 1 | |a Fuhr, H. -G. |4 oth | |
700 | 1 | |a Hinterberger, R. |4 oth | |
700 | 1 | |a Kreiter, H. |4 oth | |
700 | 1 | |a Thoenes, W. |4 oth | |
700 | 1 | |a Herrmann, F. |4 oth | |
700 | 1 | |a Mertelsmann, R. |4 oth | |
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(DE-627)NLEJ202967662 DE-627 ger DE-627 rakwb eng MACOP-B Chemotherapy for the treatment of high grade and intermediate grade Non Hodgkin's lymphoma 1990 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Summary Between Nov. 1985 and Nov. 1988, sixty-three patients with high grade malignant (hg) and intermediate grade malignant (img) Non Hodgkin's Lymphoma (NHL) were treated with MACOP-B (methotrexate, doborubicin, cyclophosphamide, vincristine, prednison and bleomycin). Thirty-seven patients received MACOP-B as an upfront treatment modality, whereas twenty-six patients had relapsed disease and received MACOP-B as a salvage protocol. Four weeks after termination of therapy, 75% of patients with de novo NHL and 72% of the patients with relapsed NHL were in complete remission (CR). In the group of newly diagnosed NHL, 22% achieved partial remission (PR) and 3% no change (NC), whereas in the group with relapsed disease 14% had PR and 14% had progressive disease (PD). At a medium follow-up of 12 months (range 1 month to 33 months), 74% of patients with de novo NHL continued to be in CR whereas the continuous CR rate in patients with relapsed disease was 35%. Overall survival after 30 months of observation for the patient group with de novo NHL was 75% and 40% for patients with relapsed NHL. The mean duration for completion of the projected 12 chemotherapy cycles, given in weekly intervals, was 12.9 and 13.5 weeks in upfront or salvage therapy, respectively. With low incidence of major toxicities, application of drugs on an outpatient basis, and high efficacy, MACOP-B shows substantial advantges for therapy of de novo and relapsed NHL. Springer Online Journal Archives 1860-2002 Oster, W. oth Forsthuber, T. oth Hennekeuser, H. H. oth Gamm, H. oth Lindemann, A. oth Schmitz, G. oth Fuhr, H. -G. oth Hinterberger, R. oth Kreiter, H. oth Thoenes, W. oth Herrmann, F. oth Mertelsmann, R. oth in Annals of hematology 1955 60(1990) vom: Jan., Seite 23-27 (DE-627)NLEJ18898836X (DE-600)1458429-3 1432-0584 nnns volume:60 year:1990 month:01 pages:23-27 extent:5 http://dx.doi.org/10.1007/BF01720198 GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE AR 60 1990 1 23-27 5 |
spelling |
(DE-627)NLEJ202967662 DE-627 ger DE-627 rakwb eng MACOP-B Chemotherapy for the treatment of high grade and intermediate grade Non Hodgkin's lymphoma 1990 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Summary Between Nov. 1985 and Nov. 1988, sixty-three patients with high grade malignant (hg) and intermediate grade malignant (img) Non Hodgkin's Lymphoma (NHL) were treated with MACOP-B (methotrexate, doborubicin, cyclophosphamide, vincristine, prednison and bleomycin). Thirty-seven patients received MACOP-B as an upfront treatment modality, whereas twenty-six patients had relapsed disease and received MACOP-B as a salvage protocol. Four weeks after termination of therapy, 75% of patients with de novo NHL and 72% of the patients with relapsed NHL were in complete remission (CR). In the group of newly diagnosed NHL, 22% achieved partial remission (PR) and 3% no change (NC), whereas in the group with relapsed disease 14% had PR and 14% had progressive disease (PD). At a medium follow-up of 12 months (range 1 month to 33 months), 74% of patients with de novo NHL continued to be in CR whereas the continuous CR rate in patients with relapsed disease was 35%. Overall survival after 30 months of observation for the patient group with de novo NHL was 75% and 40% for patients with relapsed NHL. The mean duration for completion of the projected 12 chemotherapy cycles, given in weekly intervals, was 12.9 and 13.5 weeks in upfront or salvage therapy, respectively. With low incidence of major toxicities, application of drugs on an outpatient basis, and high efficacy, MACOP-B shows substantial advantges for therapy of de novo and relapsed NHL. Springer Online Journal Archives 1860-2002 Oster, W. oth Forsthuber, T. oth Hennekeuser, H. H. oth Gamm, H. oth Lindemann, A. oth Schmitz, G. oth Fuhr, H. -G. oth Hinterberger, R. oth Kreiter, H. oth Thoenes, W. oth Herrmann, F. oth Mertelsmann, R. oth in Annals of hematology 1955 60(1990) vom: Jan., Seite 23-27 (DE-627)NLEJ18898836X (DE-600)1458429-3 1432-0584 nnns volume:60 year:1990 month:01 pages:23-27 extent:5 http://dx.doi.org/10.1007/BF01720198 GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE AR 60 1990 1 23-27 5 |
allfields_unstemmed |
(DE-627)NLEJ202967662 DE-627 ger DE-627 rakwb eng MACOP-B Chemotherapy for the treatment of high grade and intermediate grade Non Hodgkin's lymphoma 1990 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Summary Between Nov. 1985 and Nov. 1988, sixty-three patients with high grade malignant (hg) and intermediate grade malignant (img) Non Hodgkin's Lymphoma (NHL) were treated with MACOP-B (methotrexate, doborubicin, cyclophosphamide, vincristine, prednison and bleomycin). Thirty-seven patients received MACOP-B as an upfront treatment modality, whereas twenty-six patients had relapsed disease and received MACOP-B as a salvage protocol. Four weeks after termination of therapy, 75% of patients with de novo NHL and 72% of the patients with relapsed NHL were in complete remission (CR). In the group of newly diagnosed NHL, 22% achieved partial remission (PR) and 3% no change (NC), whereas in the group with relapsed disease 14% had PR and 14% had progressive disease (PD). At a medium follow-up of 12 months (range 1 month to 33 months), 74% of patients with de novo NHL continued to be in CR whereas the continuous CR rate in patients with relapsed disease was 35%. Overall survival after 30 months of observation for the patient group with de novo NHL was 75% and 40% for patients with relapsed NHL. The mean duration for completion of the projected 12 chemotherapy cycles, given in weekly intervals, was 12.9 and 13.5 weeks in upfront or salvage therapy, respectively. With low incidence of major toxicities, application of drugs on an outpatient basis, and high efficacy, MACOP-B shows substantial advantges for therapy of de novo and relapsed NHL. Springer Online Journal Archives 1860-2002 Oster, W. oth Forsthuber, T. oth Hennekeuser, H. H. oth Gamm, H. oth Lindemann, A. oth Schmitz, G. oth Fuhr, H. -G. oth Hinterberger, R. oth Kreiter, H. oth Thoenes, W. oth Herrmann, F. oth Mertelsmann, R. oth in Annals of hematology 1955 60(1990) vom: Jan., Seite 23-27 (DE-627)NLEJ18898836X (DE-600)1458429-3 1432-0584 nnns volume:60 year:1990 month:01 pages:23-27 extent:5 http://dx.doi.org/10.1007/BF01720198 GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE AR 60 1990 1 23-27 5 |
allfieldsGer |
(DE-627)NLEJ202967662 DE-627 ger DE-627 rakwb eng MACOP-B Chemotherapy for the treatment of high grade and intermediate grade Non Hodgkin's lymphoma 1990 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Summary Between Nov. 1985 and Nov. 1988, sixty-three patients with high grade malignant (hg) and intermediate grade malignant (img) Non Hodgkin's Lymphoma (NHL) were treated with MACOP-B (methotrexate, doborubicin, cyclophosphamide, vincristine, prednison and bleomycin). Thirty-seven patients received MACOP-B as an upfront treatment modality, whereas twenty-six patients had relapsed disease and received MACOP-B as a salvage protocol. Four weeks after termination of therapy, 75% of patients with de novo NHL and 72% of the patients with relapsed NHL were in complete remission (CR). In the group of newly diagnosed NHL, 22% achieved partial remission (PR) and 3% no change (NC), whereas in the group with relapsed disease 14% had PR and 14% had progressive disease (PD). At a medium follow-up of 12 months (range 1 month to 33 months), 74% of patients with de novo NHL continued to be in CR whereas the continuous CR rate in patients with relapsed disease was 35%. Overall survival after 30 months of observation for the patient group with de novo NHL was 75% and 40% for patients with relapsed NHL. The mean duration for completion of the projected 12 chemotherapy cycles, given in weekly intervals, was 12.9 and 13.5 weeks in upfront or salvage therapy, respectively. With low incidence of major toxicities, application of drugs on an outpatient basis, and high efficacy, MACOP-B shows substantial advantges for therapy of de novo and relapsed NHL. Springer Online Journal Archives 1860-2002 Oster, W. oth Forsthuber, T. oth Hennekeuser, H. H. oth Gamm, H. oth Lindemann, A. oth Schmitz, G. oth Fuhr, H. -G. oth Hinterberger, R. oth Kreiter, H. oth Thoenes, W. oth Herrmann, F. oth Mertelsmann, R. oth in Annals of hematology 1955 60(1990) vom: Jan., Seite 23-27 (DE-627)NLEJ18898836X (DE-600)1458429-3 1432-0584 nnns volume:60 year:1990 month:01 pages:23-27 extent:5 http://dx.doi.org/10.1007/BF01720198 GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE AR 60 1990 1 23-27 5 |
allfieldsSound |
(DE-627)NLEJ202967662 DE-627 ger DE-627 rakwb eng MACOP-B Chemotherapy for the treatment of high grade and intermediate grade Non Hodgkin's lymphoma 1990 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Summary Between Nov. 1985 and Nov. 1988, sixty-three patients with high grade malignant (hg) and intermediate grade malignant (img) Non Hodgkin's Lymphoma (NHL) were treated with MACOP-B (methotrexate, doborubicin, cyclophosphamide, vincristine, prednison and bleomycin). Thirty-seven patients received MACOP-B as an upfront treatment modality, whereas twenty-six patients had relapsed disease and received MACOP-B as a salvage protocol. Four weeks after termination of therapy, 75% of patients with de novo NHL and 72% of the patients with relapsed NHL were in complete remission (CR). In the group of newly diagnosed NHL, 22% achieved partial remission (PR) and 3% no change (NC), whereas in the group with relapsed disease 14% had PR and 14% had progressive disease (PD). At a medium follow-up of 12 months (range 1 month to 33 months), 74% of patients with de novo NHL continued to be in CR whereas the continuous CR rate in patients with relapsed disease was 35%. Overall survival after 30 months of observation for the patient group with de novo NHL was 75% and 40% for patients with relapsed NHL. The mean duration for completion of the projected 12 chemotherapy cycles, given in weekly intervals, was 12.9 and 13.5 weeks in upfront or salvage therapy, respectively. With low incidence of major toxicities, application of drugs on an outpatient basis, and high efficacy, MACOP-B shows substantial advantges for therapy of de novo and relapsed NHL. Springer Online Journal Archives 1860-2002 Oster, W. oth Forsthuber, T. oth Hennekeuser, H. H. oth Gamm, H. oth Lindemann, A. oth Schmitz, G. oth Fuhr, H. -G. oth Hinterberger, R. oth Kreiter, H. oth Thoenes, W. oth Herrmann, F. oth Mertelsmann, R. oth in Annals of hematology 1955 60(1990) vom: Jan., Seite 23-27 (DE-627)NLEJ18898836X (DE-600)1458429-3 1432-0584 nnns volume:60 year:1990 month:01 pages:23-27 extent:5 http://dx.doi.org/10.1007/BF01720198 GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE AR 60 1990 1 23-27 5 |
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Oster, W. @@oth@@ Forsthuber, T. @@oth@@ Hennekeuser, H. H. @@oth@@ Gamm, H. @@oth@@ Lindemann, A. @@oth@@ Schmitz, G. @@oth@@ Fuhr, H. -G. @@oth@@ Hinterberger, R. @@oth@@ Kreiter, H. @@oth@@ Thoenes, W. @@oth@@ Herrmann, F. @@oth@@ Mertelsmann, R. @@oth@@ |
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The mean duration for completion of the projected 12 chemotherapy cycles, given in weekly intervals, was 12.9 and 13.5 weeks in upfront or salvage therapy, respectively. With low incidence of major toxicities, application of drugs on an outpatient basis, and high efficacy, MACOP-B shows substantial advantges for therapy of de novo and relapsed NHL.</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="f">Springer Online Journal Archives 1860-2002</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Oster, W.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Forsthuber, T.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Hennekeuser, H. 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macop-b chemotherapy for the treatment of high grade and intermediate grade non hodgkin's lymphoma |
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MACOP-B Chemotherapy for the treatment of high grade and intermediate grade Non Hodgkin's lymphoma |
abstract |
Summary Between Nov. 1985 and Nov. 1988, sixty-three patients with high grade malignant (hg) and intermediate grade malignant (img) Non Hodgkin's Lymphoma (NHL) were treated with MACOP-B (methotrexate, doborubicin, cyclophosphamide, vincristine, prednison and bleomycin). Thirty-seven patients received MACOP-B as an upfront treatment modality, whereas twenty-six patients had relapsed disease and received MACOP-B as a salvage protocol. Four weeks after termination of therapy, 75% of patients with de novo NHL and 72% of the patients with relapsed NHL were in complete remission (CR). In the group of newly diagnosed NHL, 22% achieved partial remission (PR) and 3% no change (NC), whereas in the group with relapsed disease 14% had PR and 14% had progressive disease (PD). At a medium follow-up of 12 months (range 1 month to 33 months), 74% of patients with de novo NHL continued to be in CR whereas the continuous CR rate in patients with relapsed disease was 35%. Overall survival after 30 months of observation for the patient group with de novo NHL was 75% and 40% for patients with relapsed NHL. The mean duration for completion of the projected 12 chemotherapy cycles, given in weekly intervals, was 12.9 and 13.5 weeks in upfront or salvage therapy, respectively. With low incidence of major toxicities, application of drugs on an outpatient basis, and high efficacy, MACOP-B shows substantial advantges for therapy of de novo and relapsed NHL. |
abstractGer |
Summary Between Nov. 1985 and Nov. 1988, sixty-three patients with high grade malignant (hg) and intermediate grade malignant (img) Non Hodgkin's Lymphoma (NHL) were treated with MACOP-B (methotrexate, doborubicin, cyclophosphamide, vincristine, prednison and bleomycin). Thirty-seven patients received MACOP-B as an upfront treatment modality, whereas twenty-six patients had relapsed disease and received MACOP-B as a salvage protocol. Four weeks after termination of therapy, 75% of patients with de novo NHL and 72% of the patients with relapsed NHL were in complete remission (CR). In the group of newly diagnosed NHL, 22% achieved partial remission (PR) and 3% no change (NC), whereas in the group with relapsed disease 14% had PR and 14% had progressive disease (PD). At a medium follow-up of 12 months (range 1 month to 33 months), 74% of patients with de novo NHL continued to be in CR whereas the continuous CR rate in patients with relapsed disease was 35%. Overall survival after 30 months of observation for the patient group with de novo NHL was 75% and 40% for patients with relapsed NHL. The mean duration for completion of the projected 12 chemotherapy cycles, given in weekly intervals, was 12.9 and 13.5 weeks in upfront or salvage therapy, respectively. With low incidence of major toxicities, application of drugs on an outpatient basis, and high efficacy, MACOP-B shows substantial advantges for therapy of de novo and relapsed NHL. |
abstract_unstemmed |
Summary Between Nov. 1985 and Nov. 1988, sixty-three patients with high grade malignant (hg) and intermediate grade malignant (img) Non Hodgkin's Lymphoma (NHL) were treated with MACOP-B (methotrexate, doborubicin, cyclophosphamide, vincristine, prednison and bleomycin). Thirty-seven patients received MACOP-B as an upfront treatment modality, whereas twenty-six patients had relapsed disease and received MACOP-B as a salvage protocol. Four weeks after termination of therapy, 75% of patients with de novo NHL and 72% of the patients with relapsed NHL were in complete remission (CR). In the group of newly diagnosed NHL, 22% achieved partial remission (PR) and 3% no change (NC), whereas in the group with relapsed disease 14% had PR and 14% had progressive disease (PD). At a medium follow-up of 12 months (range 1 month to 33 months), 74% of patients with de novo NHL continued to be in CR whereas the continuous CR rate in patients with relapsed disease was 35%. Overall survival after 30 months of observation for the patient group with de novo NHL was 75% and 40% for patients with relapsed NHL. The mean duration for completion of the projected 12 chemotherapy cycles, given in weekly intervals, was 12.9 and 13.5 weeks in upfront or salvage therapy, respectively. With low incidence of major toxicities, application of drugs on an outpatient basis, and high efficacy, MACOP-B shows substantial advantges for therapy of de novo and relapsed NHL. |
collection_details |
GBV_USEFLAG_U ZDB-1-SOJ GBV_NL_ARTICLE |
title_short |
MACOP-B Chemotherapy for the treatment of high grade and intermediate grade Non Hodgkin's lymphoma |
url |
http://dx.doi.org/10.1007/BF01720198 |
remote_bool |
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author2 |
Oster, W. Forsthuber, T. Hennekeuser, H. H. Gamm, H. Lindemann, A. Schmitz, G. Fuhr, H. -G. Hinterberger, R. Kreiter, H. Thoenes, W. Herrmann, F. Mertelsmann, R. |
author2Str |
Oster, W. Forsthuber, T. Hennekeuser, H. H. Gamm, H. Lindemann, A. Schmitz, G. Fuhr, H. -G. Hinterberger, R. Kreiter, H. Thoenes, W. Herrmann, F. Mertelsmann, R. |
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up_date |
2024-07-06T09:24:15.843Z |
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7.400093 |