Measurable Residual Disease Assessment and Allogeneic Transplantation as Consolidation Therapy in Adult Acute Lymphoblastic Leukemia in Colombia
Detectable minimal residual disease (MRD) after therapy for acute lymphoblastic leukemia (ALL) is the strongest predictor of hematologic relapse. The objective of the study was to assess disease-free survival (DFS) and overall survival (OS) of patients with ALL according with MRD status at the end o...
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Published in | Clinical lymphoma, myeloma and leukemia Vol. 21; no. 4; pp. e365 - e372 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.04.2021
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ISSN | 2152-2650 2152-2669 2152-2669 |
DOI | 10.1016/j.clml.2020.11.010 |
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Abstract | Detectable minimal residual disease (MRD) after therapy for acute lymphoblastic leukemia (ALL) is the strongest predictor of hematologic relapse. The objective of the study was to assess disease-free survival (DFS) and overall survival (OS) of patients with ALL according with MRD status at the end of induction therapy in a Colombian population.
We assessed a retrospective cohort to compare DFS and OS in adults with de novo ALL according to MRD status at the end of induction chemotherapy, and the type of postinduction consolidation strategy used.
A total of 165 adults with ALL were included in the MRD part of the study, 73 patients in the MRD-negative group and 92 in the MRD-positive group. Median DFS for the MRD-positive group was 11 months (95% confidence interval, 11.7-22.2) and was not reached for the MRD-negative group (P < .001). At 3 years, DFS was 18% and 55%, respectively (P < .001). The median OS for MRD-positive patients was 16 months (95% confidence interval, 8.8-23.15) and was not reached in the MRD-negative group. At 3 years, OS was 26% and 51% for the former and latter group, respectively. Among subjects who did not receive a transplant, median DFS was 21 months for MRD-negative patients and 9 months for MRD-positive patients (P < .001). The median DFS was not reached in either group, whereas 3-year DFS was 64% for MRD-negative and 70% for MRD-positive patients who underwent transplantation in first remission (P = .861).
MRD status at the end of induction is an independent prognostic factor for DFS and OS in adult ALL. Allogeneic transplantation in first remission could overcome the adverse prognostic impact of MRD.
A retrospective assessment of disease-free survival (DFS) and overall survival (OS) of adults with acute lymphoblastic leukemia (ALL) according to minimal residual disease (MRD) status at the end of induction therapy in a Colombian population found that MRD status was an independent prognostic factor for DFS and OS in ALL. Allogeneic transplantation in first remission could overcome the adverse prognostic impact of MRD. |
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AbstractList | Detectable minimal residual disease (MRD) after therapy for acute lymphoblastic leukemia (ALL) is the strongest predictor of hematologic relapse. The objective of the study was to assess disease-free survival (DFS) and overall survival (OS) of patients with ALL according with MRD status at the end of induction therapy in a Colombian population.
We assessed a retrospective cohort to compare DFS and OS in adults with de novo ALL according to MRD status at the end of induction chemotherapy, and the type of postinduction consolidation strategy used.
A total of 165 adults with ALL were included in the MRD part of the study, 73 patients in the MRD-negative group and 92 in the MRD-positive group. Median DFS for the MRD-positive group was 11 months (95% confidence interval, 11.7-22.2) and was not reached for the MRD-negative group (P < .001). At 3 years, DFS was 18% and 55%, respectively (P < .001). The median OS for MRD-positive patients was 16 months (95% confidence interval, 8.8-23.15) and was not reached in the MRD-negative group. At 3 years, OS was 26% and 51% for the former and latter group, respectively. Among subjects who did not receive a transplant, median DFS was 21 months for MRD-negative patients and 9 months for MRD-positive patients (P < .001). The median DFS was not reached in either group, whereas 3-year DFS was 64% for MRD-negative and 70% for MRD-positive patients who underwent transplantation in first remission (P = .861).
MRD status at the end of induction is an independent prognostic factor for DFS and OS in adult ALL. Allogeneic transplantation in first remission could overcome the adverse prognostic impact of MRD.
A retrospective assessment of disease-free survival (DFS) and overall survival (OS) of adults with acute lymphoblastic leukemia (ALL) according to minimal residual disease (MRD) status at the end of induction therapy in a Colombian population found that MRD status was an independent prognostic factor for DFS and OS in ALL. Allogeneic transplantation in first remission could overcome the adverse prognostic impact of MRD. Detectable minimal residual disease (MRD) after therapy for acute lymphoblastic leukemia (ALL) is the strongest predictor of hematologic relapse. The objective of the study was to assess disease-free survival (DFS) and overall survival (OS) of patients with ALL according with MRD status at the end of induction therapy in a Colombian population. We assessed a retrospective cohort to compare DFS and OS in adults with de novo ALL according to MRD status at the end of induction chemotherapy, and the type of postinduction consolidation strategy used. A total of 165 adults with ALL were included in the MRD part of the study, 73 patients in the MRD-negative group and 92 in the MRD-positive group. Median DFS for the MRD-positive group was 11 months (95% confidence interval, 11.7-22.2) and was not reached for the MRD-negative group (P < .001). At 3 years, DFS was 18% and 55%, respectively (P < .001). The median OS for MRD-positive patients was 16 months (95% confidence interval, 8.8-23.15) and was not reached in the MRD-negative group. At 3 years, OS was 26% and 51% for the former and latter group, respectively. Among subjects who did not receive a transplant, median DFS was 21 months for MRD-negative patients and 9 months for MRD-positive patients (P < .001). The median DFS was not reached in either group, whereas 3-year DFS was 64% for MRD-negative and 70% for MRD-positive patients who underwent transplantation in first remission (P = .861). MRD status at the end of induction is an independent prognostic factor for DFS and OS in adult ALL. Allogeneic transplantation in first remission could overcome the adverse prognostic impact of MRD. Detectable minimal residual disease (MRD) after therapy for acute lymphoblastic leukemia (ALL) is the strongest predictor of hematologic relapse. The objective of the study was to assess disease-free survival (DFS) and overall survival (OS) of patients with ALL according with MRD status at the end of induction therapy in a Colombian population.INTRODUCTIONDetectable minimal residual disease (MRD) after therapy for acute lymphoblastic leukemia (ALL) is the strongest predictor of hematologic relapse. The objective of the study was to assess disease-free survival (DFS) and overall survival (OS) of patients with ALL according with MRD status at the end of induction therapy in a Colombian population.We assessed a retrospective cohort to compare DFS and OS in adults with de novo ALL according to MRD status at the end of induction chemotherapy, and the type of postinduction consolidation strategy used.PATIENTS AND METHODSWe assessed a retrospective cohort to compare DFS and OS in adults with de novo ALL according to MRD status at the end of induction chemotherapy, and the type of postinduction consolidation strategy used.A total of 165 adults with ALL were included in the MRD part of the study, 73 patients in the MRD-negative group and 92 in the MRD-positive group. Median DFS for the MRD-positive group was 11 months (95% confidence interval, 11.7-22.2) and was not reached for the MRD-negative group (P < .001). At 3 years, DFS was 18% and 55%, respectively (P < .001). The median OS for MRD-positive patients was 16 months (95% confidence interval, 8.8-23.15) and was not reached in the MRD-negative group. At 3 years, OS was 26% and 51% for the former and latter group, respectively. Among subjects who did not receive a transplant, median DFS was 21 months for MRD-negative patients and 9 months for MRD-positive patients (P < .001). The median DFS was not reached in either group, whereas 3-year DFS was 64% for MRD-negative and 70% for MRD-positive patients who underwent transplantation in first remission (P = .861).RESULTSA total of 165 adults with ALL were included in the MRD part of the study, 73 patients in the MRD-negative group and 92 in the MRD-positive group. Median DFS for the MRD-positive group was 11 months (95% confidence interval, 11.7-22.2) and was not reached for the MRD-negative group (P < .001). At 3 years, DFS was 18% and 55%, respectively (P < .001). The median OS for MRD-positive patients was 16 months (95% confidence interval, 8.8-23.15) and was not reached in the MRD-negative group. At 3 years, OS was 26% and 51% for the former and latter group, respectively. Among subjects who did not receive a transplant, median DFS was 21 months for MRD-negative patients and 9 months for MRD-positive patients (P < .001). The median DFS was not reached in either group, whereas 3-year DFS was 64% for MRD-negative and 70% for MRD-positive patients who underwent transplantation in first remission (P = .861).MRD status at the end of induction is an independent prognostic factor for DFS and OS in adult ALL. Allogeneic transplantation in first remission could overcome the adverse prognostic impact of MRD.CONCLUSIONMRD status at the end of induction is an independent prognostic factor for DFS and OS in adult ALL. Allogeneic transplantation in first remission could overcome the adverse prognostic impact of MRD. |
Author | Arango, Marcos Orduz, Rocio Hernandez, Sonia Ramirez, Carlos Agudelo, Claudia Bautista, Leonardo Madera, Ana María Valdés, Jaime León, Guillermo Avila, Vladimir Moreno, Liliana Combariza, Juan Felipe Mejía, Fabian Díaz, Laura |
Author_xml | – sequence: 1 givenname: Juan Felipe surname: Combariza fullname: Combariza, Juan Felipe email: jfcombariza@colsanitas.com organization: Department of Hematology, Clínica Universitaria Colombia, Bogotá, Colombia – sequence: 2 givenname: Marcos orcidid: 0000-0002-5326-8022 surname: Arango fullname: Arango, Marcos organization: Department of Hematology, Hospital Pablo Tobón Uribe, Medellín, Colombia – sequence: 3 givenname: Laura surname: Díaz fullname: Díaz, Laura organization: Department of Hematology, Hospital Pablo Tobón Uribe, Medellín, Colombia – sequence: 4 givenname: Claudia surname: Agudelo fullname: Agudelo, Claudia organization: Department of Hematology, Clínica Universitaria Colombia, Bogotá, Colombia – sequence: 5 givenname: Sonia surname: Hernandez fullname: Hernandez, Sonia organization: Department of Hematology, Clínica Universitaria Colombia, Bogotá, Colombia – sequence: 6 givenname: Ana María surname: Madera fullname: Madera, Ana María organization: Department of Hematology, Clínica Universitaria Colombia, Bogotá, Colombia – sequence: 7 givenname: Guillermo surname: León fullname: León, Guillermo organization: Department of Hematology, Clínica Universitaria Colombia, Bogotá, Colombia – sequence: 8 givenname: Vladimir surname: Avila fullname: Avila, Vladimir organization: Department of Hematology, Clínica Universitaria Colombia, Bogotá, Colombia – sequence: 9 givenname: Leonardo surname: Bautista fullname: Bautista, Leonardo organization: Department of Hematology, Clínica Universitaria Colombia, Bogotá, Colombia – sequence: 10 givenname: Jaime surname: Valdés fullname: Valdés, Jaime organization: Department of Hematology, Clínica Universitaria Colombia, Bogotá, Colombia – sequence: 11 givenname: Rocio orcidid: 0000-0001-8983-7963 surname: Orduz fullname: Orduz, Rocio organization: Department of Pathology, Clínica Universitaria Colombia, Bogotá, Colombia – sequence: 12 givenname: Fabian surname: Mejía fullname: Mejía, Fabian organization: Department of Pathology, Clínica Universitaria Colombia, Bogotá, Colombia – sequence: 13 givenname: Liliana orcidid: 0000-0002-0264-3427 surname: Moreno fullname: Moreno, Liliana organization: Department of Pathology, Clínica Universitaria Colombia, Bogotá, Colombia – sequence: 14 givenname: Carlos surname: Ramirez fullname: Ramirez, Carlos organization: Department of Hematology, Clínica Reina Sofía, Bogotá, Colombia |
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Keywords | Prognosis Acute lymphoblastic leukemia Measurable residual disease Disease free survival Hematopoietic stem-cell transplantation |
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SubjectTerms | Acute lymphoblastic leukemia Adolescent Adult Aged Colombia - epidemiology Consolidation Chemotherapy - methods Disease free survival Female Follow-Up Studies Hematopoietic Stem Cell Transplantation Humans Induction Chemotherapy - methods Male Measurable residual disease Middle Aged Neoplasm Recurrence, Local - epidemiology Neoplasm, Residual Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy Prognosis Retrospective Studies Transplantation, Homologous Young Adult |
Title | Measurable Residual Disease Assessment and Allogeneic Transplantation as Consolidation Therapy in Adult Acute Lymphoblastic Leukemia in Colombia |
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