Lancet, The, ISSN 0140-6736, 2016, Volume 388, Issue 10044, pp. 565 - 575
Summary Background Mantle cell lymphoma is characterised by a poor long-term prognosis. The European Mantle Cell Lymphoma Network aimed to investigate whether...
Internal Medicine | 1ST-LINE TREATMENT | MEDICINE, GENERAL & INTERNAL | MULTICENTER | THERAPY | RESPONSE CRITERIA | FREE SURVIVAL | TEMSIROLIMUS | PLUS RITUXIMAB | FOLLOW-UP | CHOP | INDOLENT | Doxorubicin - therapeutic use | Humans | Middle Aged | Lymphoma, Mantle-Cell - drug therapy | Male | Combined Modality Therapy | Cytarabine - adverse effects | Cyclophosphamide - therapeutic use | Cytarabine - administration & dosage | Lymphoma, Mantle-Cell - therapy | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Immunotherapy | Treatment Failure | Vincristine - therapeutic use | Adult | Female | Immunosuppressive Agents - adverse effects | Hematopoietic Stem Cell Transplantation - methods | Transplantation Conditioning | Immunosuppressive Agents - administration & dosage | Prednisone - therapeutic use | Transplantation | Epidemiology | Stem cells | Tumors | Medical informatics | Clinical trials | Chemotherapy | Lymphomas | Clinical outcomes
Internal Medicine | 1ST-LINE TREATMENT | MEDICINE, GENERAL & INTERNAL | MULTICENTER | THERAPY | RESPONSE CRITERIA | FREE SURVIVAL | TEMSIROLIMUS | PLUS RITUXIMAB | FOLLOW-UP | CHOP | INDOLENT | Doxorubicin - therapeutic use | Humans | Middle Aged | Lymphoma, Mantle-Cell - drug therapy | Male | Combined Modality Therapy | Cytarabine - adverse effects | Cyclophosphamide - therapeutic use | Cytarabine - administration & dosage | Lymphoma, Mantle-Cell - therapy | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Immunotherapy | Treatment Failure | Vincristine - therapeutic use | Adult | Female | Immunosuppressive Agents - adverse effects | Hematopoietic Stem Cell Transplantation - methods | Transplantation Conditioning | Immunosuppressive Agents - administration & dosage | Prednisone - therapeutic use | Transplantation | Epidemiology | Stem cells | Tumors | Medical informatics | Clinical trials | Chemotherapy | Lymphomas | Clinical outcomes
Journal Article
Lancet Oncology, The, ISSN 1470-2045, 2010, Volume 11, Issue 11, pp. 1036 - 1047
Summary Background High-dose methotrexate is the standard of care for patients with newly diagnosed primary CNS lymphoma. The role of whole brain radiotherapy...
Hematology, Oncology and Palliative Medicine | DEFERRED RADIOTHERAPY | 1ST-LINE TREATMENT | ONCOLOGY-GROUP | COMBINED-MODALITY THERAPY | ONCOLOGY | CONSOLIDATION RADIOTHERAPY | CELL TRANSPLANTATION | INITIAL TREATMENT | CENTRAL-NERVOUS-SYSTEM | CEREBROSPINAL-FLUID | CHEMOTHERAPY | Humans | Middle Aged | Antineoplastic Combined Chemotherapy Protocols - adverse effects | Male | Lymphoma - mortality | Antimetabolites, Antineoplastic - administration & dosage | Central Nervous System Neoplasms - radiotherapy | Lymphoma - drug therapy | Time Factors | Dose Fractionation | Female | Lymphoma - radiotherapy | Radiotherapy, Adjuvant | Risk Assessment | Risk Factors | Kaplan-Meier Estimate | Proportional Hazards Models | Survival Rate | Treatment Outcome | Chi-Square Distribution | Cranial Irradiation - adverse effects | Cytarabine - administration & dosage | Disease-Free Survival | Methotrexate - adverse effects | Ifosfamide - administration & dosage | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Antimetabolites, Antineoplastic - adverse effects | Methotrexate - administration & dosage | Aged | Central Nervous System Neoplasms - drug therapy | Central Nervous System Neoplasms - mortality | Germany | Chemotherapy | Radiation | Product development | Lymphomas | Methotrexate | Radiotherapy | Biometry | Cancer
Hematology, Oncology and Palliative Medicine | DEFERRED RADIOTHERAPY | 1ST-LINE TREATMENT | ONCOLOGY-GROUP | COMBINED-MODALITY THERAPY | ONCOLOGY | CONSOLIDATION RADIOTHERAPY | CELL TRANSPLANTATION | INITIAL TREATMENT | CENTRAL-NERVOUS-SYSTEM | CEREBROSPINAL-FLUID | CHEMOTHERAPY | Humans | Middle Aged | Antineoplastic Combined Chemotherapy Protocols - adverse effects | Male | Lymphoma - mortality | Antimetabolites, Antineoplastic - administration & dosage | Central Nervous System Neoplasms - radiotherapy | Lymphoma - drug therapy | Time Factors | Dose Fractionation | Female | Lymphoma - radiotherapy | Radiotherapy, Adjuvant | Risk Assessment | Risk Factors | Kaplan-Meier Estimate | Proportional Hazards Models | Survival Rate | Treatment Outcome | Chi-Square Distribution | Cranial Irradiation - adverse effects | Cytarabine - administration & dosage | Disease-Free Survival | Methotrexate - adverse effects | Ifosfamide - administration & dosage | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Antimetabolites, Antineoplastic - adverse effects | Methotrexate - administration & dosage | Aged | Central Nervous System Neoplasms - drug therapy | Central Nervous System Neoplasms - mortality | Germany | Chemotherapy | Radiation | Product development | Lymphomas | Methotrexate | Radiotherapy | Biometry | Cancer
Journal Article
Blood, ISSN 0006-4971, 11/2013, Volume 122, Issue 21, pp. 1487 - 1487
Abstract Introduction In acute leukemias, specific cytogenetic aberrations frequently correlate with myeloid or lymphoid phenotype of blasts and influence risk...
Journal Article
British Journal of Haematology, ISSN 0007-1048, 02/2017, Volume 176, Issue 3, pp. 431 - 439
Summary This study analysed the outcome of 267 patients with relapse/refractory acute myeloid leukaemia (AML) who received sequential chemotherapy including...
sequential chemotherapy | reduced intensity conditioning | acute myeloid leukaemia | allogeneic haematopoietic stem cell transplantation | CYTOSINE-ARABINOSIDE | FREE SURVIVAL | BONE-MARROW-TRANSPLANTATION | 1ST COMPLETE REMISSION | MYELODYSPLASTIC SYNDROME | MATCHED UNRELATED DONORS | GRAFT-VERSUS-LEUKEMIA | HIGH-RISK | HLA-IDENTICAL SIBLINGS | HOST-DISEASE | HEMATOLOGY | Recurrence | Humans | Middle Aged | Male | Hematopoietic Stem Cell Transplantation - mortality | Leukemia, Myeloid, Acute - complications | Young Adult | Allografts | Hematopoietic Stem Cell Transplantation - adverse effects | Adult | Female | Surveys and Questionnaires | Retrospective Studies | Transplantation Conditioning - methods | Graft vs Host Disease - etiology | Leukemia, Myeloid, Acute - therapy | Antibodies - therapeutic use | Survival Rate | Treatment Outcome | Combined Modality Therapy | Leukemia, Myeloid, Acute - mortality | Antibodies - administration & dosage | Disease-Free Survival | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | T-Lymphocytes - immunology | Aged | Hematopoietic Stem Cell Transplantation - methods | Salvage Therapy - methods | Surveys | Viral antibodies | Chemotherapy | Relapse | Stem cells | Antibodies | Transplantation | T cells | Hematopoietic stem cells | Diseases | Cancer | Graft-versus-host reaction | Immunoglobulins | Transplants & implants | Leukemia | Stem cell transplantation | Transplants | Lymphocytes T | Multivariate analysis | Patients | Survival | Incidence | Cytarabine | Fludarabine | Donors | Conditioning
sequential chemotherapy | reduced intensity conditioning | acute myeloid leukaemia | allogeneic haematopoietic stem cell transplantation | CYTOSINE-ARABINOSIDE | FREE SURVIVAL | BONE-MARROW-TRANSPLANTATION | 1ST COMPLETE REMISSION | MYELODYSPLASTIC SYNDROME | MATCHED UNRELATED DONORS | GRAFT-VERSUS-LEUKEMIA | HIGH-RISK | HLA-IDENTICAL SIBLINGS | HOST-DISEASE | HEMATOLOGY | Recurrence | Humans | Middle Aged | Male | Hematopoietic Stem Cell Transplantation - mortality | Leukemia, Myeloid, Acute - complications | Young Adult | Allografts | Hematopoietic Stem Cell Transplantation - adverse effects | Adult | Female | Surveys and Questionnaires | Retrospective Studies | Transplantation Conditioning - methods | Graft vs Host Disease - etiology | Leukemia, Myeloid, Acute - therapy | Antibodies - therapeutic use | Survival Rate | Treatment Outcome | Combined Modality Therapy | Leukemia, Myeloid, Acute - mortality | Antibodies - administration & dosage | Disease-Free Survival | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | T-Lymphocytes - immunology | Aged | Hematopoietic Stem Cell Transplantation - methods | Salvage Therapy - methods | Surveys | Viral antibodies | Chemotherapy | Relapse | Stem cells | Antibodies | Transplantation | T cells | Hematopoietic stem cells | Diseases | Cancer | Graft-versus-host reaction | Immunoglobulins | Transplants & implants | Leukemia | Stem cell transplantation | Transplants | Lymphocytes T | Multivariate analysis | Patients | Survival | Incidence | Cytarabine | Fludarabine | Donors | Conditioning
Journal Article
Molecular Therapy, ISSN 1525-0016, 05/2011, Volume 19, Issue 5, pp. 990 - 999
The aim of this phase I/II nonrandomized trial was to assess feasibility, safety as well as immunological and clinical responses of a mRNA-based vaccination in...
CANCER PATIENTS | MEDICINE, RESEARCH & EXPERIMENTAL | DIRECT-INJECTION | RENAL-CELL CARCINOMA | CYTOTOXIC T-LYMPHOCYTES | TRANSFECTED DENDRITIC CELLS | MESSENGER-RNA | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | IN-VIVO | GENETICS & HEREDITY | TUMOR-DERIVED RNA | ANTIGEN | EPITOPES | Antigens, Neoplasm - genetics | Genetic Therapy | Enzyme-Linked Immunosorbent Assay | Adjuvants, Immunologic | Antigens, Neoplasm - immunology | Cancer Vaccines - administration & dosage | Humans | Middle Aged | RNA, Messenger - genetics | Carcinoma, Renal Cell - genetics | Male | Granulocyte-Macrophage Colony-Stimulating Factor - genetics | CD4-Positive T-Lymphocytes - immunology | Cancer Vaccines - genetics | Cancer Vaccines - immunology | Granulocyte-Macrophage Colony-Stimulating Factor - immunology | RNA, Messenger - administration & dosage | Carcinoma, Renal Cell - therapy | Female | Aged | CD8-Positive T-Lymphocytes - immunology | RNA, Messenger - therapeutic use | Original
CANCER PATIENTS | MEDICINE, RESEARCH & EXPERIMENTAL | DIRECT-INJECTION | RENAL-CELL CARCINOMA | CYTOTOXIC T-LYMPHOCYTES | TRANSFECTED DENDRITIC CELLS | MESSENGER-RNA | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | IN-VIVO | GENETICS & HEREDITY | TUMOR-DERIVED RNA | ANTIGEN | EPITOPES | Antigens, Neoplasm - genetics | Genetic Therapy | Enzyme-Linked Immunosorbent Assay | Adjuvants, Immunologic | Antigens, Neoplasm - immunology | Cancer Vaccines - administration & dosage | Humans | Middle Aged | RNA, Messenger - genetics | Carcinoma, Renal Cell - genetics | Male | Granulocyte-Macrophage Colony-Stimulating Factor - genetics | CD4-Positive T-Lymphocytes - immunology | Cancer Vaccines - genetics | Cancer Vaccines - immunology | Granulocyte-Macrophage Colony-Stimulating Factor - immunology | RNA, Messenger - administration & dosage | Carcinoma, Renal Cell - therapy | Female | Aged | CD8-Positive T-Lymphocytes - immunology | RNA, Messenger - therapeutic use | Original
Journal Article
Annals of Hematology, ISSN 0939-5555, 9/2014, Volume 93, Issue 9, pp. 1579 - 1586
Natural killer (NK)-cell alloreactivity after allogeneic hematopoietic cell transplantation (HCT) is influenced by the interaction of killer-cell...
Haploidentical hematopoietic cell transplantation | Oncology | KIR haplotype | Medicine & Public Health | Hematology | KIR-ligand model | NATURAL-KILLER-CELLS | IMMUNOGLOBULIN-LIKE RECEPTORS | FREE SURVIVAL | ACUTE GVHD | ACUTE MYELOGENOUS LEUKEMIA | HEMATOPOIETIC TRANSPLANTS | GROUP-A | STEM-CELL TRANSPLANTATION | HLA | HEMATOLOGY | T-CELLS | Haplotypes | Recurrence | Humans | Middle Aged | Blood Group Incompatibility - complications | Male | Antigens, CD19 - genetics | Transplantation, Homologous | Incidence | Young Adult | Hematopoietic Stem Cells - immunology | CD3 Complex - genetics | Hematopoietic Stem Cell Transplantation - adverse effects | Adult | Female | Transplantation Conditioning - adverse effects | Transplantation Conditioning - methods | Receptors, KIR - genetics | Cell Separation | Histocompatibility Testing | Hematopoietic Stem Cells - metabolism | Histocompatibility Antigens Class I - genetics | CD3 Complex - metabolism | Hematologic Neoplasms - surgery | Blood Group Incompatibility - genetics | Hematopoietic Stem Cells - cytology | Antigens, CD19 - metabolism | Hematologic Neoplasms - genetics | Histocompatibility antigens | Analysis | Mortality | HLA histocompatibility antigens | Genetic aspects | Transplantation | Hematopoietic stem cells
Haploidentical hematopoietic cell transplantation | Oncology | KIR haplotype | Medicine & Public Health | Hematology | KIR-ligand model | NATURAL-KILLER-CELLS | IMMUNOGLOBULIN-LIKE RECEPTORS | FREE SURVIVAL | ACUTE GVHD | ACUTE MYELOGENOUS LEUKEMIA | HEMATOPOIETIC TRANSPLANTS | GROUP-A | STEM-CELL TRANSPLANTATION | HLA | HEMATOLOGY | T-CELLS | Haplotypes | Recurrence | Humans | Middle Aged | Blood Group Incompatibility - complications | Male | Antigens, CD19 - genetics | Transplantation, Homologous | Incidence | Young Adult | Hematopoietic Stem Cells - immunology | CD3 Complex - genetics | Hematopoietic Stem Cell Transplantation - adverse effects | Adult | Female | Transplantation Conditioning - adverse effects | Transplantation Conditioning - methods | Receptors, KIR - genetics | Cell Separation | Histocompatibility Testing | Hematopoietic Stem Cells - metabolism | Histocompatibility Antigens Class I - genetics | CD3 Complex - metabolism | Hematologic Neoplasms - surgery | Blood Group Incompatibility - genetics | Hematopoietic Stem Cells - cytology | Antigens, CD19 - metabolism | Hematologic Neoplasms - genetics | Histocompatibility antigens | Analysis | Mortality | HLA histocompatibility antigens | Genetic aspects | Transplantation | Hematopoietic stem cells
Journal Article
British Journal of Haematology, ISSN 0007-1048, 11/2017, Volume 179, Issue 4, pp. 586 - 597
Summary We assessed the safety and efficacy of bortezomib, cyclophosphamide and dexamethasone (VCD) induction therapy in previously untreated multiple myeloma...
dexamethasone | cyclophosphamide | multiple myeloma | induction therapy | bortezomib | HIGH-RISK CYTOGENETICS | MULTIPARAMETER FLOW-CYTOMETRY | INDUCED PERIPHERAL NEUROPATHY | NEWLY-DIAGNOSED PATIENTS | PLUS DEXAMETHASONE | HIGH-DOSE THERAPY | STEM-CELL TRANSPLANTATION | HEMATOLOGY | MINIMAL RESIDUAL DISEASE | HOVON-65/GMMG-HD4 TRIAL | CHROMOSOMAL-ABERRATIONS | Risk Assessment - methods | Cyclophosphamide - administration & dosage | Dexamethasone - administration & dosage | Multiple Myeloma - mortality | Humans | Middle Aged | Induction Chemotherapy - methods | Antineoplastic Combined Chemotherapy Protocols - adverse effects | Male | Transplantation, Autologous | Consolidation Chemotherapy | Stem Cell Transplantation | Young Adult | Multiple Myeloma - drug therapy | Bortezomib - administration & dosage | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Adolescent | Survival Analysis | Cytogenetics | Adult | Female | Cyclophosphamide | Dexamethasone | Bortezomib | Analysis | Multiple myeloma | Stem cells | Clinical trials | Transplantation | Steroids | Thrombocytopenia | Autografts | Therapy | Risk groups | Abnormalities | Stem cell transplantation | Risk | Patients | Survival | Consolidation
dexamethasone | cyclophosphamide | multiple myeloma | induction therapy | bortezomib | HIGH-RISK CYTOGENETICS | MULTIPARAMETER FLOW-CYTOMETRY | INDUCED PERIPHERAL NEUROPATHY | NEWLY-DIAGNOSED PATIENTS | PLUS DEXAMETHASONE | HIGH-DOSE THERAPY | STEM-CELL TRANSPLANTATION | HEMATOLOGY | MINIMAL RESIDUAL DISEASE | HOVON-65/GMMG-HD4 TRIAL | CHROMOSOMAL-ABERRATIONS | Risk Assessment - methods | Cyclophosphamide - administration & dosage | Dexamethasone - administration & dosage | Multiple Myeloma - mortality | Humans | Middle Aged | Induction Chemotherapy - methods | Antineoplastic Combined Chemotherapy Protocols - adverse effects | Male | Transplantation, Autologous | Consolidation Chemotherapy | Stem Cell Transplantation | Young Adult | Multiple Myeloma - drug therapy | Bortezomib - administration & dosage | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Adolescent | Survival Analysis | Cytogenetics | Adult | Female | Cyclophosphamide | Dexamethasone | Bortezomib | Analysis | Multiple myeloma | Stem cells | Clinical trials | Transplantation | Steroids | Thrombocytopenia | Autografts | Therapy | Risk groups | Abnormalities | Stem cell transplantation | Risk | Patients | Survival | Consolidation
Journal Article
Annals of Hematology, ISSN 0939-5555, 10/2016, Volume 95, Issue 10, pp. 1627 - 1636
Allogeneic hematopoietic cell transplantation (allo-HCT) remains the only curative treatment option for myelofibrosis (MF) despite the emergence of novel...
Anti-thymocyte globulin | Hematopoietic cell transplantation | Myelofibrosis | Medicine & Public Health | Hematology | Oncology | Hepatic toxicity | Bilirubin | BONE-MARROW-TRANSPLANTATION | ANTITHYMOCYTE GLOBULIN | MECHANISMS | TOXICITY | VERSUS-HOST-DISEASE | IMPACT | HEPATIC VENOOCCLUSIVE DISEASE | HEMATOLOGY | AGE | Humans | Immunosuppressive Agents - therapeutic use | Middle Aged | Male | Liver - physiopathology | Case-Control Studies | Transplantation, Homologous | Iron Overload - blood | Iron Overload - etiology | Primary Myelofibrosis - blood | Young Adult | Liver - drug effects | Antilymphocyte Serum - therapeutic use | Adult | Female | Transplantation Conditioning - methods | Hyperbilirubinemia - etiology | Antilymphocyte Serum - adverse effects | Graft Rejection - prevention & control | Hematopoietic Stem Cell Transplantation | Transfusion Reaction | Hyperbilirubinemia - immunology | Graft vs Host Disease - prevention & control | Immunosuppressive Agents - adverse effects | T-Lymphocytes - immunology | Aged | Primary Myelofibrosis - therapy | Care and treatment | Hyperbilirubinemia | Analysis | Mortality | Liver | Transplantation | T cells | Hematopoietic stem cells | Index Medicus
Anti-thymocyte globulin | Hematopoietic cell transplantation | Myelofibrosis | Medicine & Public Health | Hematology | Oncology | Hepatic toxicity | Bilirubin | BONE-MARROW-TRANSPLANTATION | ANTITHYMOCYTE GLOBULIN | MECHANISMS | TOXICITY | VERSUS-HOST-DISEASE | IMPACT | HEPATIC VENOOCCLUSIVE DISEASE | HEMATOLOGY | AGE | Humans | Immunosuppressive Agents - therapeutic use | Middle Aged | Male | Liver - physiopathology | Case-Control Studies | Transplantation, Homologous | Iron Overload - blood | Iron Overload - etiology | Primary Myelofibrosis - blood | Young Adult | Liver - drug effects | Antilymphocyte Serum - therapeutic use | Adult | Female | Transplantation Conditioning - methods | Hyperbilirubinemia - etiology | Antilymphocyte Serum - adverse effects | Graft Rejection - prevention & control | Hematopoietic Stem Cell Transplantation | Transfusion Reaction | Hyperbilirubinemia - immunology | Graft vs Host Disease - prevention & control | Immunosuppressive Agents - adverse effects | T-Lymphocytes - immunology | Aged | Primary Myelofibrosis - therapy | Care and treatment | Hyperbilirubinemia | Analysis | Mortality | Liver | Transplantation | T cells | Hematopoietic stem cells | Index Medicus
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 08/2018, Volume 19, Issue 1, pp. 144 - 7
The PTEN-hamartoma-tumor-syndrome (PHTS) is caused by germline mutations in Phosphatase and Tensin homolog (PTEN) and predisposes to the development of several...
Malignant Peritoneal Mesothelioma | Hereditary Tumor Syndrome | PTEN-Hamartoma-Tumor-Syndrome | Verrucous Carcinoma | Case Report | Lung Neoplasms - genetics | PTEN Phosphohydrolase - genetics | Humans | Mesothelioma - genetics | Rare Diseases | Carcinoma, Verrucous - genetics | Germ-Line Mutation - genetics | Mouth Neoplasms - genetics | Case studies | Gene mutations | Tumor suppressor genes | Mesothelioma | Genetic aspects | Health aspects | Mouth cancer | Immunohistochemistry | Asbestos | Disease | Genes | AKT protein | Phosphatase | Kinases | Occupational exposure | Thyroid carcinoma | Clonal deletion | Surgery | Age | Tensin | Medical screening | 1-Phosphatidylinositol 3-kinase | Chemotherapy | Thyroid cancer | Molecular modelling | Medical prognosis | Mutation | Neoplasia | PTEN protein | Peritoneum | Tumors | Apoptosis
Malignant Peritoneal Mesothelioma | Hereditary Tumor Syndrome | PTEN-Hamartoma-Tumor-Syndrome | Verrucous Carcinoma | Case Report | Lung Neoplasms - genetics | PTEN Phosphohydrolase - genetics | Humans | Mesothelioma - genetics | Rare Diseases | Carcinoma, Verrucous - genetics | Germ-Line Mutation - genetics | Mouth Neoplasms - genetics | Case studies | Gene mutations | Tumor suppressor genes | Mesothelioma | Genetic aspects | Health aspects | Mouth cancer | Immunohistochemistry | Asbestos | Disease | Genes | AKT protein | Phosphatase | Kinases | Occupational exposure | Thyroid carcinoma | Clonal deletion | Surgery | Age | Tensin | Medical screening | 1-Phosphatidylinositol 3-kinase | Chemotherapy | Thyroid cancer | Molecular modelling | Medical prognosis | Mutation | Neoplasia | PTEN protein | Peritoneum | Tumors | Apoptosis
Journal Article
Annals of Hematology, ISSN 0939-5555, 5/2017, Volume 96, Issue 5, pp. 817 - 827
Disease relapse after one or more allogeneic hematopoietic cell transplantations (HCT) represents a therapeutic challenge with all options bearing a...
Haploidentical hematopoietic cell transplantation | Graft versus host disease | Relapse | Medicine & Public Health | Hematology | Oncology | Salvage therapy | AML | BONE-MARROW-TRANSPLANTATION | UNRELATED DONORS | PREVENTION | ACUTE MYELOID-LEUKEMIA | 1ST COMPLETE REMISSION | VERSUS-HOST-DISEASE | PREDICTION | INTERNATIONAL WORKSHOP | HEMATOLOGY | HEMATOLOGIC MALIGNANCIES | Haplotypes | Recurrence | Humans | Middle Aged | Salvage Therapy | Male | Lymphocyte Depletion | Transplantation, Homologous | Young Adult | Hematopoietic Stem Cells - immunology | Leukemia - complications | Hematopoietic Stem Cell Transplantation - adverse effects | Adult | Female | Graft vs Host Disease - etiology | T-Lymphocytes | Mortality | Kaplan-Meier Estimate | Leukemia - therapy | Graft Survival | Treatment Outcome | Combined Modality Therapy | Transplantation Chimera | Retreatment | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Adolescent | Leukemia - diagnosis | Graft vs Host Disease - prevention & control | Hematopoietic Stem Cell Transplantation - methods | Tissue Donors | Transplantation Conditioning | Leukemia - mortality | Complications and side effects | Care and treatment | Leukemia | Transplantation | T cells | Hematopoietic stem cells | Diseases
Haploidentical hematopoietic cell transplantation | Graft versus host disease | Relapse | Medicine & Public Health | Hematology | Oncology | Salvage therapy | AML | BONE-MARROW-TRANSPLANTATION | UNRELATED DONORS | PREVENTION | ACUTE MYELOID-LEUKEMIA | 1ST COMPLETE REMISSION | VERSUS-HOST-DISEASE | PREDICTION | INTERNATIONAL WORKSHOP | HEMATOLOGY | HEMATOLOGIC MALIGNANCIES | Haplotypes | Recurrence | Humans | Middle Aged | Salvage Therapy | Male | Lymphocyte Depletion | Transplantation, Homologous | Young Adult | Hematopoietic Stem Cells - immunology | Leukemia - complications | Hematopoietic Stem Cell Transplantation - adverse effects | Adult | Female | Graft vs Host Disease - etiology | T-Lymphocytes | Mortality | Kaplan-Meier Estimate | Leukemia - therapy | Graft Survival | Treatment Outcome | Combined Modality Therapy | Transplantation Chimera | Retreatment | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Adolescent | Leukemia - diagnosis | Graft vs Host Disease - prevention & control | Hematopoietic Stem Cell Transplantation - methods | Tissue Donors | Transplantation Conditioning | Leukemia - mortality | Complications and side effects | Care and treatment | Leukemia | Transplantation | T cells | Hematopoietic stem cells | Diseases
Journal Article
Clinical Lymphoma, Myeloma & Leukemia, ISSN 2152-2650, 2014, Volume 14, Issue 1, pp. e7 - e11
During the past decade, introduction of the novel agents in treatment of multiple myeloma disease resulted in a significant improvement in response and an...
Hematology, Oncology and Palliative Medicine | EBV | High-dose mephalan | Thalidomide | Secondary primary malignancy | B-cell clonality | Thalidomide - adverse effects | Hodgkin Disease - pathology | Humans | Middle Aged | Hodgkin Disease - etiology | B-Lymphocytes - drug effects | Thalidomide - analogs & derivatives | Multiple Myeloma - drug therapy | Multiple Myeloma - pathology | Female | Immunologic Factors - adverse effects | B-Lymphocytes - pathology | Thalidomide - therapeutic use | Immunologic Factors - therapeutic use
Hematology, Oncology and Palliative Medicine | EBV | High-dose mephalan | Thalidomide | Secondary primary malignancy | B-cell clonality | Thalidomide - adverse effects | Hodgkin Disease - pathology | Humans | Middle Aged | Hodgkin Disease - etiology | B-Lymphocytes - drug effects | Thalidomide - analogs & derivatives | Multiple Myeloma - drug therapy | Multiple Myeloma - pathology | Female | Immunologic Factors - adverse effects | B-Lymphocytes - pathology | Thalidomide - therapeutic use | Immunologic Factors - therapeutic use
Journal Article
Cellular Physiology and Biochemistry, ISSN 1015-8987, 2002, Volume 12, Issue 5-6, pp. 365 - 372
Erythrocyte diseases such as sickle cell anemia, thalassemia and glucose-6-phosphate dehydrogenase deficiency decrease the erythrocyte life span, an effect...
Original Paper | Oxidation | tBOOH | Cell volume | Osmotic cell shrinkage | Annexin | Glucose depletion | cell volume | ACTIVATION | PHAGOCYTOSIS | PHYSIOLOGY | osmotic cell shrinkage | RAT HEPATOCYTES | MACROPHAGES | VOLUME | oxidation | CELL BIOLOGY | SHRINKAGE | HYPERTONICITY | annexin | glucose depletion | PHOSPHATIDYLSERINE EXPOSURE | CHLORIDE CONDUCTANCE | NA+ CONDUCTANCE | Osmotic Pressure | Thalassemia - blood | Confidence Intervals | Glucosephosphate Dehydrogenase Deficiency - blood | Annexins - metabolism | Erythrocytes, Abnormal - drug effects | Humans | Oxidative Stress - physiology | Erythrocyte Membrane - metabolism | Hydrogen Peroxide - pharmacology | Erythrocytes, Abnormal - metabolism | Hydrogen Peroxide - chemistry | Glucose - deficiency | Erythrocytes, Abnormal - pathology | Flow Cytometry | Analysis of Variance | Ionomycin - pharmacology | Anemia, Sickle Cell - blood | Apoptosis - physiology | Phosphatidylserines - blood
Original Paper | Oxidation | tBOOH | Cell volume | Osmotic cell shrinkage | Annexin | Glucose depletion | cell volume | ACTIVATION | PHAGOCYTOSIS | PHYSIOLOGY | osmotic cell shrinkage | RAT HEPATOCYTES | MACROPHAGES | VOLUME | oxidation | CELL BIOLOGY | SHRINKAGE | HYPERTONICITY | annexin | glucose depletion | PHOSPHATIDYLSERINE EXPOSURE | CHLORIDE CONDUCTANCE | NA+ CONDUCTANCE | Osmotic Pressure | Thalassemia - blood | Confidence Intervals | Glucosephosphate Dehydrogenase Deficiency - blood | Annexins - metabolism | Erythrocytes, Abnormal - drug effects | Humans | Oxidative Stress - physiology | Erythrocyte Membrane - metabolism | Hydrogen Peroxide - pharmacology | Erythrocytes, Abnormal - metabolism | Hydrogen Peroxide - chemistry | Glucose - deficiency | Erythrocytes, Abnormal - pathology | Flow Cytometry | Analysis of Variance | Ionomycin - pharmacology | Anemia, Sickle Cell - blood | Apoptosis - physiology | Phosphatidylserines - blood
Journal Article