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Open-Label Phase II Prospective, Randomized, Controlled Study of Romyelocel-L Myeloid Progenitor Cells to Reduce Infection During Induction Chemotherapy for Acute Myeloid Leukemia

Standard cytotoxic induction chemotherapy for acute myeloid leukemia (AML) results in prolonged neutropenia and risk of infection. Romyelocel-L is a universal, allogeneic myeloid progenitor cell product being studied to reduce infection during induction chemotherapy. PATIENTS AND METHODS: One hundre...

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Autores principales: Desai, Pinkal M., Brown, Janice, Gill, Saar, Solh, Melham M., Akard, Luke P., Hsu, Jack W., Ustun, Celalettin, Andreadis, Charalambos, Frankfurt, Olga, Foran, James M., Lister, John, Schiller, Gary J., Wieduwilt, Matthew J., Pagel, John M., Stiff, Patrick J., Liu, Delong, Khan, Irum, Stock, Wendy, Kambhampati, Suman, Tallman, Martin S., Morris, Lawrence, Edwards, John, Pusic, Iskra, Kantarjian, Hagop M., Mamelok, Richard, Wong, Alicia, Van Syoc, Rodney, Kellerman, Lois, Panuganti, Swapna, Mandalam, Ramkumar, Abboud, Camille N., Ravandi, Farhad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8500663/
https://www.ncbi.nlm.nih.gov/pubmed/34156898
http://dx.doi.org/10.1200/JCO.20.01739
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author Desai, Pinkal M.
Brown, Janice
Gill, Saar
Solh, Melham M.
Akard, Luke P.
Hsu, Jack W.
Ustun, Celalettin
Andreadis, Charalambos
Frankfurt, Olga
Foran, James M.
Lister, John
Schiller, Gary J.
Wieduwilt, Matthew J.
Pagel, John M.
Stiff, Patrick J.
Liu, Delong
Khan, Irum
Stock, Wendy
Kambhampati, Suman
Tallman, Martin S.
Morris, Lawrence
Edwards, John
Pusic, Iskra
Kantarjian, Hagop M.
Mamelok, Richard
Wong, Alicia
Van Syoc, Rodney
Kellerman, Lois
Panuganti, Swapna
Mandalam, Ramkumar
Abboud, Camille N.
Ravandi, Farhad
author_facet Desai, Pinkal M.
Brown, Janice
Gill, Saar
Solh, Melham M.
Akard, Luke P.
Hsu, Jack W.
Ustun, Celalettin
Andreadis, Charalambos
Frankfurt, Olga
Foran, James M.
Lister, John
Schiller, Gary J.
Wieduwilt, Matthew J.
Pagel, John M.
Stiff, Patrick J.
Liu, Delong
Khan, Irum
Stock, Wendy
Kambhampati, Suman
Tallman, Martin S.
Morris, Lawrence
Edwards, John
Pusic, Iskra
Kantarjian, Hagop M.
Mamelok, Richard
Wong, Alicia
Van Syoc, Rodney
Kellerman, Lois
Panuganti, Swapna
Mandalam, Ramkumar
Abboud, Camille N.
Ravandi, Farhad
author_sort Desai, Pinkal M.
collection PubMed
description Standard cytotoxic induction chemotherapy for acute myeloid leukemia (AML) results in prolonged neutropenia and risk of infection. Romyelocel-L is a universal, allogeneic myeloid progenitor cell product being studied to reduce infection during induction chemotherapy. PATIENTS AND METHODS: One hundred sixty-three patients with de novo AML (age ≥ 55 years) receiving induction chemotherapy were randomly assigned on day 0 (d0), of whom 120 were evaluable. Subjects received either romyelocel-L infusion on d9 with granulocyte colony-stimulating factor (G-CSF) starting daily d14 (treatment group) or G-CSF daily alone on d14 (control) until absolute neutrophil count recovery to 500/µL. End points included days in febrile episode, microbiologically defined infections, clinically diagnosed infection, and days in hospital. RESULTS: Mean days in febrile episode was shorter in the treatment arm from d15 through d28 (2.36 v 3.90; P = .02). Similarly, a trend toward decreased microbiologically defined infections and clinically diagnosed infection in the treatment arm was observed from d9 to d28 (35.6% v 47.5%; P = .09), reaching a statistically significant difference from d15 to d28 (6.8% v 27.9%; P = .002). Because of this, antibacterial or antifungal use for treatment of an infection was significantly less in the treatment group (d9-d28: 44.1% v 63.9%; P = .01). Significantly fewer patients in the treatment arm received empiric antifungals from d9 tod28 (42.4% v 63.9%; P = .02) and d15-d28 (42.4% v 62.3%; P = .02). Patients in the treatment arm also had 3.2 fewer hospital days compared with control (25.5 v 28.7; P = .001). Remission rates and days to absolute neutrophil count recovery were similar in the two groups. No patients in the romyelocel-L plus G-CSF group died because of infection compared with two patients in the control arm. No graft-versus-host disease was observed. CONCLUSION: Subjects receiving romyelocel-L showed a decreased incidence of infections, antimicrobial use, and hospitalization, suggesting that romyelocel-L may provide a new option to reduce infections in patients with AML undergoing induction therapy.
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spelling pubmed-85006632022-10-10 Open-Label Phase II Prospective, Randomized, Controlled Study of Romyelocel-L Myeloid Progenitor Cells to Reduce Infection During Induction Chemotherapy for Acute Myeloid Leukemia Desai, Pinkal M. Brown, Janice Gill, Saar Solh, Melham M. Akard, Luke P. Hsu, Jack W. Ustun, Celalettin Andreadis, Charalambos Frankfurt, Olga Foran, James M. Lister, John Schiller, Gary J. Wieduwilt, Matthew J. Pagel, John M. Stiff, Patrick J. Liu, Delong Khan, Irum Stock, Wendy Kambhampati, Suman Tallman, Martin S. Morris, Lawrence Edwards, John Pusic, Iskra Kantarjian, Hagop M. Mamelok, Richard Wong, Alicia Van Syoc, Rodney Kellerman, Lois Panuganti, Swapna Mandalam, Ramkumar Abboud, Camille N. Ravandi, Farhad J Clin Oncol ORIGINAL REPORTS Standard cytotoxic induction chemotherapy for acute myeloid leukemia (AML) results in prolonged neutropenia and risk of infection. Romyelocel-L is a universal, allogeneic myeloid progenitor cell product being studied to reduce infection during induction chemotherapy. PATIENTS AND METHODS: One hundred sixty-three patients with de novo AML (age ≥ 55 years) receiving induction chemotherapy were randomly assigned on day 0 (d0), of whom 120 were evaluable. Subjects received either romyelocel-L infusion on d9 with granulocyte colony-stimulating factor (G-CSF) starting daily d14 (treatment group) or G-CSF daily alone on d14 (control) until absolute neutrophil count recovery to 500/µL. End points included days in febrile episode, microbiologically defined infections, clinically diagnosed infection, and days in hospital. RESULTS: Mean days in febrile episode was shorter in the treatment arm from d15 through d28 (2.36 v 3.90; P = .02). Similarly, a trend toward decreased microbiologically defined infections and clinically diagnosed infection in the treatment arm was observed from d9 to d28 (35.6% v 47.5%; P = .09), reaching a statistically significant difference from d15 to d28 (6.8% v 27.9%; P = .002). Because of this, antibacterial or antifungal use for treatment of an infection was significantly less in the treatment group (d9-d28: 44.1% v 63.9%; P = .01). Significantly fewer patients in the treatment arm received empiric antifungals from d9 tod28 (42.4% v 63.9%; P = .02) and d15-d28 (42.4% v 62.3%; P = .02). Patients in the treatment arm also had 3.2 fewer hospital days compared with control (25.5 v 28.7; P = .001). Remission rates and days to absolute neutrophil count recovery were similar in the two groups. No patients in the romyelocel-L plus G-CSF group died because of infection compared with two patients in the control arm. No graft-versus-host disease was observed. CONCLUSION: Subjects receiving romyelocel-L showed a decreased incidence of infections, antimicrobial use, and hospitalization, suggesting that romyelocel-L may provide a new option to reduce infections in patients with AML undergoing induction therapy. Wolters Kluwer Health 2021-10-10 2021-06-22 /pmc/articles/PMC8500663/ /pubmed/34156898 http://dx.doi.org/10.1200/JCO.20.01739 Text en © 2021 by American Society of Clinical Oncology https://creativecommons.org/licenses/by-nc-nd/4.0/Creative Commons Attribution Non-Commercial No Derivatives 4.0 License: https://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle ORIGINAL REPORTS
Desai, Pinkal M.
Brown, Janice
Gill, Saar
Solh, Melham M.
Akard, Luke P.
Hsu, Jack W.
Ustun, Celalettin
Andreadis, Charalambos
Frankfurt, Olga
Foran, James M.
Lister, John
Schiller, Gary J.
Wieduwilt, Matthew J.
Pagel, John M.
Stiff, Patrick J.
Liu, Delong
Khan, Irum
Stock, Wendy
Kambhampati, Suman
Tallman, Martin S.
Morris, Lawrence
Edwards, John
Pusic, Iskra
Kantarjian, Hagop M.
Mamelok, Richard
Wong, Alicia
Van Syoc, Rodney
Kellerman, Lois
Panuganti, Swapna
Mandalam, Ramkumar
Abboud, Camille N.
Ravandi, Farhad
Open-Label Phase II Prospective, Randomized, Controlled Study of Romyelocel-L Myeloid Progenitor Cells to Reduce Infection During Induction Chemotherapy for Acute Myeloid Leukemia
title Open-Label Phase II Prospective, Randomized, Controlled Study of Romyelocel-L Myeloid Progenitor Cells to Reduce Infection During Induction Chemotherapy for Acute Myeloid Leukemia
title_full Open-Label Phase II Prospective, Randomized, Controlled Study of Romyelocel-L Myeloid Progenitor Cells to Reduce Infection During Induction Chemotherapy for Acute Myeloid Leukemia
title_fullStr Open-Label Phase II Prospective, Randomized, Controlled Study of Romyelocel-L Myeloid Progenitor Cells to Reduce Infection During Induction Chemotherapy for Acute Myeloid Leukemia
title_full_unstemmed Open-Label Phase II Prospective, Randomized, Controlled Study of Romyelocel-L Myeloid Progenitor Cells to Reduce Infection During Induction Chemotherapy for Acute Myeloid Leukemia
title_short Open-Label Phase II Prospective, Randomized, Controlled Study of Romyelocel-L Myeloid Progenitor Cells to Reduce Infection During Induction Chemotherapy for Acute Myeloid Leukemia
title_sort open-label phase ii prospective, randomized, controlled study of romyelocel-l myeloid progenitor cells to reduce infection during induction chemotherapy for acute myeloid leukemia
topic ORIGINAL REPORTS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8500663/
https://www.ncbi.nlm.nih.gov/pubmed/34156898
http://dx.doi.org/10.1200/JCO.20.01739
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