Myeloablative versus Reduced-Intensity Conditioning for Hematopoietic Cell Transplantation in Acute Myelogenous Leukemia and Myelodysplastic Syndromes—Long-Term Follow-Up of the BMT CTN 0901 Clinical Trial
•There was a higher rate of treatment-related mortality with myeloablative conditioning, but this was offset by a much higher rate of relapse with reduced-intensity conditioning.•There was no difference in survival following relapse based on conditioning intensity.•Myeloablative conditioning led to...
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Published in | Transplantation and cellular therapy Vol. 27; no. 6; pp. 483.e1 - 483.e6 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.06.2021
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Online Access | Get full text |
ISSN | 2666-6367 2666-6375 2666-6367 |
DOI | 10.1016/j.jtct.2021.02.031 |
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Abstract | •There was a higher rate of treatment-related mortality with myeloablative conditioning, but this was offset by a much higher rate of relapse with reduced-intensity conditioning.•There was no difference in survival following relapse based on conditioning intensity.•Myeloablative conditioning led to improved overall survival in patients with myelodysplastic syndrome or acute myelogenous leukemia who underwent allogeneic transplantation.
Several prospective randomized trials comparing conditioning intensity before allogeneic hematopoietic cell transplantation (HCT) have been performed, with conflicting results. Although reduced-intensity conditioning (RIC) leads to lower treatment-related mortality (TRM), this is offset by higher rates of relapse. Long-term follow-up of randomized comparative trials are limited. Here we present long-term follow-up of a randomized comparison of myeloablative conditioning (MAC) compared with RIC before HCT for acute myelogenous leukemia (AML) or myelodysplasia (MDS). Long-term comparative analyses of overall survival, relapse, and relapse-free survival were performed. Patients age 18 to 65 years with <5% marrow myeloblasts were randomized to receive MAC (n = 135) or RIC (n = 137), followed by HCT from an HLA-matched donor. The primary endpoint of the trial was an 18-month pointwise comparison of overall survival. The analyses were performed using a proportional hazards model. The median follow-up of the entire cohort was 51 months. At 4 years, the transplant-related mortality (TRM) was 25.1% for MAC, compared with 9.9% for RIC (P < .001). Patients who received RIC had a significantly higher risk of relapse compared to those who received MAC (hazard ratio [HR], 4.06; 95% CI, 2.59 to 6.35; P < 0.001). Among the patients who relapsed after HCT, postrelapse survival was similar at 3 years (24% for MAC and 26% for RIC). Overall survival was superior for patients who received MAC compared to those who received RIC (HR, 1.54; 95% CI, 1.07 to 2.2; P = .03). Our data show that patients who received MAC were at higher risk of late TRM compared with those who received RIC; however, because of the exceedingly high rates of relapse in the RIC arm, overall survival remained significantly better for patients who received MAC. Among patients with MDS or AML eligible for either MAC or RIC regimens, long-term follow up demonstrates a survival advantage for patients who received MAC. |
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AbstractList | •There was a higher rate of treatment-related mortality with myeloablative conditioning, but this was offset by a much higher rate of relapse with reduced-intensity conditioning.•There was no difference in survival following relapse based on conditioning intensity.•Myeloablative conditioning led to improved overall survival in patients with myelodysplastic syndrome or acute myelogenous leukemia who underwent allogeneic transplantation.
Several prospective randomized trials comparing conditioning intensity before allogeneic hematopoietic cell transplantation (HCT) have been performed, with conflicting results. Although reduced-intensity conditioning (RIC) leads to lower treatment-related mortality (TRM), this is offset by higher rates of relapse. Long-term follow-up of randomized comparative trials are limited. Here we present long-term follow-up of a randomized comparison of myeloablative conditioning (MAC) compared with RIC before HCT for acute myelogenous leukemia (AML) or myelodysplasia (MDS). Long-term comparative analyses of overall survival, relapse, and relapse-free survival were performed. Patients age 18 to 65 years with <5% marrow myeloblasts were randomized to receive MAC (n = 135) or RIC (n = 137), followed by HCT from an HLA-matched donor. The primary endpoint of the trial was an 18-month pointwise comparison of overall survival. The analyses were performed using a proportional hazards model. The median follow-up of the entire cohort was 51 months. At 4 years, the transplant-related mortality (TRM) was 25.1% for MAC, compared with 9.9% for RIC (P < .001). Patients who received RIC had a significantly higher risk of relapse compared to those who received MAC (hazard ratio [HR], 4.06; 95% CI, 2.59 to 6.35; P < 0.001). Among the patients who relapsed after HCT, postrelapse survival was similar at 3 years (24% for MAC and 26% for RIC). Overall survival was superior for patients who received MAC compared to those who received RIC (HR, 1.54; 95% CI, 1.07 to 2.2; P = .03). Our data show that patients who received MAC were at higher risk of late TRM compared with those who received RIC; however, because of the exceedingly high rates of relapse in the RIC arm, overall survival remained significantly better for patients who received MAC. Among patients with MDS or AML eligible for either MAC or RIC regimens, long-term follow up demonstrates a survival advantage for patients who received MAC. Several prospective randomized trials comparing conditioning intensity before allogeneic hematopoietic cell transplantation (HCT) have been performed, with conflicting results. Although reduced-intensity conditioning (RIC) leads to lower treatment-related mortality (TRM), this is offset by higher rates of relapse. Long-term follow-up of randomized comparative trials are limited. Here we present long-term follow-up of a randomized comparison of myeloablative conditioning (MAC) compared with RIC before HCT for acute myelogenous leukemia (AML) or myelodysplasia (MDS). Long-term comparative analyses of overall survival, relapse, and relapse-free survival were performed. Patients age 18 to 65 years with <5% marrow myeloblasts were randomized to receive MAC (n = 135) or RIC (n = 137), followed by HCT from an HLA-matched donor. The primary endpoint of the trial was an 18-month pointwise comparison of overall survival. The analyses were performed using a proportional hazards model. The median follow-up of the entire cohort was 51 months. At 4 years, the transplant-related mortality (TRM) was 25.1% for MAC, compared with 9.9% for RIC (P < .001). Patients who received RIC had a significantly higher risk of relapse compared to those who received MAC (hazard ratio [HR], 4.06; 95% CI, 2.59 to 6.35; P < 0.001). Among the patients who relapsed after HCT, postrelapse survival was similar at 3 years (24% for MAC and 26% for RIC). Overall survival was superior for patients who received MAC compared to those who received RIC (HR, 1.54; 95% CI, 1.07 to 2.2; P = .03). Our data show that patients who received MAC were at higher risk of late TRM compared with those who received RIC; however, because of the exceedingly high rates of relapse in the RIC arm, overall survival remained significantly better for patients who received MAC. Among patients with MDS or AML eligible for either MAC or RIC regimens, long-term follow up demonstrates a survival advantage for patients who received MAC. Several prospective randomized trials comparing conditioning intensity before allogeneic hematopoietic cell transplantation (HCT) have been performed, with conflicting results. Although reduced-intensity conditioning (RIC) leads to lower treatment-related mortality (TRM), this is offset by higher rates of relapse. Long-term follow-up of randomized comparative trials are limited. Here we present long-term follow-up of a randomized comparison of myeloablative conditioning (MAC) compared with RIC before HCT for acute myelogenous leukemia (AML) or myelodysplasia (MDS). Long-term comparative analyses of overall survival, relapse, and relapse-free survival were performed. Patients age 18 to 65 years with <5% marrow myeloblasts were randomized to receive MAC (n = 135) or RIC (n = 137), followed by HCT from an HLA-matched donor. The primary endpoint of the trial was an 18-month pointwise comparison of overall survival. The analyses were performed using a proportional hazards model. The median follow-up of the entire cohort was 51 months. At 4 years, the transplant-related mortality (TRM) was 25.1% for MAC, compared with 9.9% for RIC (P < .001). Patients who received RIC had a significantly higher risk of relapse compared to those who received MAC (hazard ratio [HR], 4.06; 95% CI, 2.59 to 6.35; P < 0.001). Among the patients who relapsed after HCT, postrelapse survival was similar at 3 years (24% for MAC and 26% for RIC). Overall survival was superior for patients who received MAC compared to those who received RIC (HR, 1.54; 95% CI, 1.07 to 2.2; P = .03). Our data show that patients who received MAC were at higher risk of late TRM compared with those who received RIC; however, because of the exceedingly high rates of relapse in the RIC arm, overall survival remained significantly better for patients who received MAC. Among patients with MDS or AML eligible for either MAC or RIC regimens, long-term follow up demonstrates a survival advantage for patients who received MAC.Several prospective randomized trials comparing conditioning intensity before allogeneic hematopoietic cell transplantation (HCT) have been performed, with conflicting results. Although reduced-intensity conditioning (RIC) leads to lower treatment-related mortality (TRM), this is offset by higher rates of relapse. Long-term follow-up of randomized comparative trials are limited. Here we present long-term follow-up of a randomized comparison of myeloablative conditioning (MAC) compared with RIC before HCT for acute myelogenous leukemia (AML) or myelodysplasia (MDS). Long-term comparative analyses of overall survival, relapse, and relapse-free survival were performed. Patients age 18 to 65 years with <5% marrow myeloblasts were randomized to receive MAC (n = 135) or RIC (n = 137), followed by HCT from an HLA-matched donor. The primary endpoint of the trial was an 18-month pointwise comparison of overall survival. The analyses were performed using a proportional hazards model. The median follow-up of the entire cohort was 51 months. At 4 years, the transplant-related mortality (TRM) was 25.1% for MAC, compared with 9.9% for RIC (P < .001). Patients who received RIC had a significantly higher risk of relapse compared to those who received MAC (hazard ratio [HR], 4.06; 95% CI, 2.59 to 6.35; P < 0.001). Among the patients who relapsed after HCT, postrelapse survival was similar at 3 years (24% for MAC and 26% for RIC). Overall survival was superior for patients who received MAC compared to those who received RIC (HR, 1.54; 95% CI, 1.07 to 2.2; P = .03). Our data show that patients who received MAC were at higher risk of late TRM compared with those who received RIC; however, because of the exceedingly high rates of relapse in the RIC arm, overall survival remained significantly better for patients who received MAC. Among patients with MDS or AML eligible for either MAC or RIC regimens, long-term follow up demonstrates a survival advantage for patients who received MAC. Several prospective randomized trials comparing conditioning intensity before allogeneic hematopoietic cell transplantation (HCT) have been performed, with conflicting results. Although reduced-intensity conditioning (RIC) leads to lower treatment-related mortality (TRM), this is offset by higher rates of relapse. Long-term follow-up of randomized comparative trials are limited. Here we present long-term follow-up of a randomized comparison of myeloablative conditioning (MAC) compared with RIC before HCT for acute myelogenous leukemia (AML) or myelodysplasia (MDS). Long-term comparative analyses of overall survival, relapse, and relapse-free survival were performed. Patients age 18 to 65 years with <5% marrow myeloblasts were randomized to receive MAC (n = 135) or RIC (n = 137), followed by HCT from an HLA-matched donor. The primary endpoint of the trial was an 18-month pointwise comparison of overall survival. The analyses were performed using a proportional hazards model. The median follow-up of the entire cohort was 51 months. At 4 years, the transplant-related mortality (TRM) was 25.1% for MAC, compared with 9.9% for RIC ( P < .001). Patients who received RIC had a significantly higher risk of relapse compared to those who received MAC (hazard ratio [HR], 4.06; 95% CI, 2.59 to 6.35; P < 0.001). Among the patients who relapsed after HCT, postrelapse survival was similar at 3 years (24% for MAC and 26% for RIC). Overall survival was superior for patients who received MAC compared to those who received RIC (HR, 1.54; 95% CI, 1.07 to 2.2; P = .03). Our data show that patients who received MAC were at higher risk of late TRM compared with those who received RIC; however, because of the exceedingly high rates of relapse in the RIC arm, overall survival remained significantly better for patients who received MAC. Among patients with MDS or AML eligible for either MAC or RIC regimens, long-term follow up demonstrates a survival advantage for patients who received MAC. |
Author | Geller, Nancy L. Hourigan, Christopher S. Horowitz, Mary M. Hamadani, Mehdi Porter, David L. Scott, Bart L. Warlick, Erica Fernandez, Hugo F. Gui, Gege Horwitz, Mitchell E. Fei, Mingwei Devine, Steve M. Maziarz, Richard T. Bashey, Asad Fraser, Raphael Leifer, Eric Wu, Juan Pasquini, Marcelo C. Soiffer, Robert J. Alyea, Edwin Mendizabal, Adam Giralt, Sergio Deeg, H. Joachim |
AuthorAffiliation | 8 Moffitt Cancer Center, Tampa, Florida 4 The Ohio State University Comprehensive Cancer Center, Columbus, Ohio 10 Duke University, Durham, North Carolina 13 National Heart Lung and Blood Institute, Bethesda, Maryland 3 The Emmes Corporation, Rockville, Maryland 2 BMT & Cellular Therapy Program, Medical College of Wisconsin, Milwaukee, Wisconsin 7 University of Minnesota, Minneapolis, Minnesota 9 Dana Farber Cancer Institute, Boston, Massachusetts 1 Fred Hutchinson Cancer Research Center, Seattle, Washington 12 Memorial Sloan Kettering Cancer Center, New York, New York 11 Northside Hospital Cancer Institute, Atlanta, Georgia 5 University of Pennsylvania, Philadelphia, Pennsylvania 6 Orgeon Health and Science University, Portland, Oregon |
AuthorAffiliation_xml | – name: 3 The Emmes Corporation, Rockville, Maryland – name: 12 Memorial Sloan Kettering Cancer Center, New York, New York – name: 7 University of Minnesota, Minneapolis, Minnesota – name: 13 National Heart Lung and Blood Institute, Bethesda, Maryland – name: 9 Dana Farber Cancer Institute, Boston, Massachusetts – name: 5 University of Pennsylvania, Philadelphia, Pennsylvania – name: 1 Fred Hutchinson Cancer Research Center, Seattle, Washington – name: 6 Orgeon Health and Science University, Portland, Oregon – name: 11 Northside Hospital Cancer Institute, Atlanta, Georgia – name: 4 The Ohio State University Comprehensive Cancer Center, Columbus, Ohio – name: 10 Duke University, Durham, North Carolina – name: 8 Moffitt Cancer Center, Tampa, Florida – name: 2 BMT & Cellular Therapy Program, Medical College of Wisconsin, Milwaukee, Wisconsin |
Author_xml | – sequence: 1 givenname: Bart L. surname: Scott fullname: Scott, Bart L. email: bscott@fhcrc.org organization: Fred Hutchinson Cancer Research Center, Seattle, Washington – sequence: 2 givenname: Marcelo C. surname: Pasquini fullname: Pasquini, Marcelo C. organization: BMT & Cellular Therapy Program, Medical College of Wisconsin, Milwaukee, Wisconsin – sequence: 3 givenname: Mingwei surname: Fei fullname: Fei, Mingwei organization: BMT & Cellular Therapy Program, Medical College of Wisconsin, Milwaukee, Wisconsin – sequence: 4 givenname: Raphael surname: Fraser fullname: Fraser, Raphael organization: BMT & Cellular Therapy Program, Medical College of Wisconsin, Milwaukee, Wisconsin – sequence: 5 givenname: Juan surname: Wu fullname: Wu, Juan organization: The Emmes Corporation, Rockville, Maryland – sequence: 6 givenname: Steve M. surname: Devine fullname: Devine, Steve M. organization: The Ohio State University Comprehensive Cancer Center, Columbus, Ohio – sequence: 7 givenname: David L. surname: Porter fullname: Porter, David L. organization: University of Pennsylvania, Philadelphia, Pennsylvania – sequence: 8 givenname: Richard T. surname: Maziarz fullname: Maziarz, Richard T. organization: Orgeon Health and Science University, Portland, Oregon – sequence: 9 givenname: Erica surname: Warlick fullname: Warlick, Erica organization: University of Minnesota, Minneapolis, Minnesota – sequence: 10 givenname: Hugo F. surname: Fernandez fullname: Fernandez, Hugo F. organization: Moffitt Cancer Center, Tampa, Florida – sequence: 11 givenname: Robert J. surname: Soiffer fullname: Soiffer, Robert J. organization: Dana Farber Cancer Institute, Boston, Massachusetts – sequence: 12 givenname: Edwin surname: Alyea fullname: Alyea, Edwin organization: Duke University, Durham, North Carolina – sequence: 13 givenname: Mehdi surname: Hamadani fullname: Hamadani, Mehdi organization: BMT & Cellular Therapy Program, Medical College of Wisconsin, Milwaukee, Wisconsin – sequence: 14 givenname: Asad surname: Bashey fullname: Bashey, Asad organization: Northside Hospital Cancer Institute, Atlanta, Georgia – sequence: 15 givenname: Sergio surname: Giralt fullname: Giralt, Sergio organization: Memorial Sloan Kettering Cancer Center, New York, New York – sequence: 16 givenname: Nancy L. surname: Geller fullname: Geller, Nancy L. organization: National Heart Lung and Blood Institute, Bethesda, Maryland – sequence: 17 givenname: Eric surname: Leifer fullname: Leifer, Eric organization: National Heart Lung and Blood Institute, Bethesda, Maryland – sequence: 18 givenname: Christopher S. surname: Hourigan fullname: Hourigan, Christopher S. organization: National Heart Lung and Blood Institute, Bethesda, Maryland – sequence: 19 givenname: Gege surname: Gui fullname: Gui, Gege organization: National Heart Lung and Blood Institute, Bethesda, Maryland – sequence: 20 givenname: Adam surname: Mendizabal fullname: Mendizabal, Adam organization: The Emmes Corporation, Rockville, Maryland – sequence: 21 givenname: Mary M. surname: Horowitz fullname: Horowitz, Mary M. organization: BMT & Cellular Therapy Program, Medical College of Wisconsin, Milwaukee, Wisconsin – sequence: 22 givenname: H. Joachim surname: Deeg fullname: Deeg, H. Joachim organization: Fred Hutchinson Cancer Research Center, Seattle, Washington – sequence: 23 givenname: Mitchell E. surname: Horwitz fullname: Horwitz, Mitchell E. organization: Duke University, Durham, North Carolina |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33775615$$D View this record in MEDLINE/PubMed |
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Keywords | Acute myelogenous leukemia Hematopoietic cell transplantation Myelodysplastic syndrome Conditioning intensity |
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PublicationDateYYYYMMDD | 2021-06-01 |
PublicationDate_xml | – month: 06 year: 2021 text: 2021-06-01 day: 01 |
PublicationDecade | 2020 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States |
PublicationTitle | Transplantation and cellular therapy |
PublicationTitleAlternate | Transplant Cell Ther |
PublicationYear | 2021 |
Publisher | Elsevier Inc |
Publisher_xml | – name: Elsevier Inc |
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Title | Myeloablative versus Reduced-Intensity Conditioning for Hematopoietic Cell Transplantation in Acute Myelogenous Leukemia and Myelodysplastic Syndromes—Long-Term Follow-Up of the BMT CTN 0901 Clinical Trial |
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