Value of colony forming unit-granulocyte macrophage assay in predicting relapse in acute myeloid leukaemia. 1996

M C del Cañizo, and A Mota, and A Orfao, and J Galende, and M D Caballero, and M A Garcia Marcos, and J F San Miguel
Departamento de Medicina, Universidad de Salamanca, Spain.

OBJECTIVE To evaluate the validity of the colony forming unit-granulocyte macrophage (CFU-GM) assay for predicting relapse in patients with acute myeloid leukaemia (AML). METHODS The study population comprised 32 patients with AML in remission, followed for a median of 18 months. A mean of four studies was carried out per patient. Three patterns of in vitro growth based on the number of CFU-GM in normal bone marrow were defined: 1 = normal (normal number of CFU-GM and a cluster:colony ratio < 2); 2 = hypoplastic (low number of CFU-GM and a cluster:colony ratio < 2); 3 = anomalous (low or normal number of CFU-GM and a cluster:colony ratio > 2). RESULTS Eleven patients relapsed, all of whom had previously displayed an abnormal CFU-GM pattern: anomalous in nine and hypoplastic in two. The remaining 25 patients were in complete remission at the time of writing, 16 of whom had a normal growth pattern. The other nine had anomalous (eight patients) or hypoplastic (one patient) growth. The latter may be false positive results. The in vitro growth pattern was not constant during follow up analysis. All 15 patients in whom the growth pattern switched from abnormal to normal remain in complete remission. By contrast, of the five cases in whom the pattern changed from normal to abnormal, three have relapsed and the other two had other indicators of relapse. The growth pattern remained unchanged in the remaining 16 patients. CONCLUSIONS The present data show that the sequential investigation of the CFU-GM growth pattern may be of value in predicting relapse in patients with AML.

UI MeSH Term Description Entries
D012008 Recurrence The return of a sign, symptom, or disease after a remission. Recrudescence,Relapse,Recrudescences,Recurrences,Relapses
D001853 Bone Marrow The soft tissue filling the cavities of bones. Bone marrow exists in two types, yellow and red. Yellow marrow is found in the large cavities of large bones and consists mostly of fat cells and a few primitive blood cells. Red marrow is a hematopoietic tissue and is the site of production of erythrocytes and granular leukocytes. Bone marrow is made up of a framework of connective tissue containing branching fibers with the frame being filled with marrow cells. Marrow,Red Marrow,Yellow Marrow,Marrow, Bone,Marrow, Red,Marrow, Yellow
D003114 Colony-Forming Units Assay A cytologic technique for measuring the functional capacity of stem cells by assaying their activity. Clonogenic Cell Assay,Stem Cell Assay,Clonogenic Cell Assays,Colony Forming Units Assays,Colony-Forming Units Assays,Stem Cell Assays,Assay, Clonogenic Cell,Assay, Colony-Forming Units,Assay, Stem Cell,Assays, Clonogenic Cell,Assays, Colony-Forming Units,Assays, Stem Cell,Colony Forming Units Assay
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D015470 Leukemia, Myeloid, Acute Clonal expansion of myeloid blasts in bone marrow, blood, and other tissue. Myeloid leukemias develop from changes in cells that normally produce NEUTROPHILS; BASOPHILS; EOSINOPHILS; and MONOCYTES. Leukemia, Myelogenous, Acute,Leukemia, Nonlymphocytic, Acute,Myeloid Leukemia, Acute,Nonlymphocytic Leukemia, Acute,ANLL,Acute Myelogenous Leukemia,Acute Myeloid Leukemia,Acute Myeloid Leukemia with Maturation,Acute Myeloid Leukemia without Maturation,Leukemia, Acute Myelogenous,Leukemia, Acute Myeloid,Leukemia, Myeloblastic, Acute,Leukemia, Myelocytic, Acute,Leukemia, Myeloid, Acute, M1,Leukemia, Myeloid, Acute, M2,Leukemia, Nonlymphoblastic, Acute,Myeloblastic Leukemia, Acute,Myelocytic Leukemia, Acute,Myelogenous Leukemia, Acute,Myeloid Leukemia, Acute, M1,Myeloid Leukemia, Acute, M2,Nonlymphoblastic Leukemia, Acute,Acute Myeloblastic Leukemia,Acute Myeloblastic Leukemias,Acute Myelocytic Leukemia,Acute Myelocytic Leukemias,Acute Myelogenous Leukemias,Acute Myeloid Leukemias,Acute Nonlymphoblastic Leukemia,Acute Nonlymphoblastic Leukemias,Acute Nonlymphocytic Leukemia,Acute Nonlymphocytic Leukemias,Leukemia, Acute Myeloblastic,Leukemia, Acute Myelocytic,Leukemia, Acute Nonlymphoblastic,Leukemia, Acute Nonlymphocytic,Leukemias, Acute Myeloblastic,Leukemias, Acute Myelocytic,Leukemias, Acute Myelogenous,Leukemias, Acute Myeloid,Leukemias, Acute Nonlymphoblastic,Leukemias, Acute Nonlymphocytic,Myeloblastic Leukemias, Acute,Myelocytic Leukemias, Acute,Myelogenous Leukemias, Acute,Myeloid Leukemias, Acute,Nonlymphoblastic Leukemias, Acute,Nonlymphocytic Leukemias, Acute
D018450 Disease Progression The worsening and general progression of a disease over time. This concept is most often used for chronic and incurable diseases where the stage of the disease is an important determinant of therapy and prognosis. Clinical Course,Clinical Progression,Disease Exacerbation,Exacerbation, Disease,Progression, Clinical,Progression, Disease

Related Publications

M C del Cañizo, and A Mota, and A Orfao, and J Galende, and M D Caballero, and M A Garcia Marcos, and J F San Miguel
December 2001, Toxicology in vitro : an international journal published in association with BIBRA,
M C del Cañizo, and A Mota, and A Orfao, and J Galende, and M D Caballero, and M A Garcia Marcos, and J F San Miguel
February 1986, Scandinavian journal of haematology,
M C del Cañizo, and A Mota, and A Orfao, and J Galende, and M D Caballero, and M A Garcia Marcos, and J F San Miguel
April 1997, British journal of haematology,
M C del Cañizo, and A Mota, and A Orfao, and J Galende, and M D Caballero, and M A Garcia Marcos, and J F San Miguel
March 1984, [Rinsho ketsueki] The Japanese journal of clinical hematology,
M C del Cañizo, and A Mota, and A Orfao, and J Galende, and M D Caballero, and M A Garcia Marcos, and J F San Miguel
August 2006, Toxicology in vitro : an international journal published in association with BIBRA,
M C del Cañizo, and A Mota, and A Orfao, and J Galende, and M D Caballero, and M A Garcia Marcos, and J F San Miguel
November 1994, Journal of internal medicine,
M C del Cañizo, and A Mota, and A Orfao, and J Galende, and M D Caballero, and M A Garcia Marcos, and J F San Miguel
July 2014, Transfusion,
M C del Cañizo, and A Mota, and A Orfao, and J Galende, and M D Caballero, and M A Garcia Marcos, and J F San Miguel
December 1998, Leukemia research,
M C del Cañizo, and A Mota, and A Orfao, and J Galende, and M D Caballero, and M A Garcia Marcos, and J F San Miguel
January 1998, Acta haematologica,
M C del Cañizo, and A Mota, and A Orfao, and J Galende, and M D Caballero, and M A Garcia Marcos, and J F San Miguel
February 1998, Chinese medical journal,
Copied contents to your clipboard!