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Recombinant Human Granulocyte-Macrophage Colony-Stimulating Factor (rhu GM-CSF) as Adjuvant Therapy for Invasive Fungal Diseases

BACKGROUND: Sargramostim (yeast-derived, glycosylated recombinant human granulocyte-macrophage colony-stimulating factor [rhu GM-CSF]) augments innate and adaptive immune responses and accelerates hematopoietic recovery of chemotherapy-induced neutropenia. However, considerably less is known about i...

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Autores principales: Chen, Tempe K, Batra, Jagmohan S, Michalik, David E, Casillas, Jacqueline, Patel, Ramesh, Ruiz, Maritza E, Hara, Harneet, Patel, Bhavita, Kadapakkam, Meena, Ch'Ng, James, Small, Catherine B, Zagaliotis, Panagiotis, Ragsdale, Carolyn E, Leal, Luis O, Roilides, Emmanuel, Walsh, Thomas J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9645583/
https://www.ncbi.nlm.nih.gov/pubmed/36381625
http://dx.doi.org/10.1093/ofid/ofac535
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author Chen, Tempe K
Batra, Jagmohan S
Michalik, David E
Casillas, Jacqueline
Patel, Ramesh
Ruiz, Maritza E
Hara, Harneet
Patel, Bhavita
Kadapakkam, Meena
Ch'Ng, James
Small, Catherine B
Zagaliotis, Panagiotis
Ragsdale, Carolyn E
Leal, Luis O
Roilides, Emmanuel
Walsh, Thomas J
author_facet Chen, Tempe K
Batra, Jagmohan S
Michalik, David E
Casillas, Jacqueline
Patel, Ramesh
Ruiz, Maritza E
Hara, Harneet
Patel, Bhavita
Kadapakkam, Meena
Ch'Ng, James
Small, Catherine B
Zagaliotis, Panagiotis
Ragsdale, Carolyn E
Leal, Luis O
Roilides, Emmanuel
Walsh, Thomas J
author_sort Chen, Tempe K
collection PubMed
description BACKGROUND: Sargramostim (yeast-derived, glycosylated recombinant human granulocyte-macrophage colony-stimulating factor [rhu GM-CSF]) augments innate and adaptive immune responses and accelerates hematopoietic recovery of chemotherapy-induced neutropenia. However, considerably less is known about its efficacy as adjunctive immunotherapy against invasive fungal diseases (IFDs). METHODS: The clinical courses of 15 patients with pediatric malignancies and IFDs treated adjunctively with sargramostim at a single institution were analyzed in a retrospective cohort review. Further, a systematic review of published reports of rhu GM-CSF for IFDs was also conducted. RESULTS: Among 65 cases, 15 were newly described pediatric patients and 50 were previously published cases of IFDs treated with rhu GM-CSF. Among the newly reported pediatric patients, IFDs were caused by Candida spp., Trichosporon sp., and molds (Aspergillus spp., Rhizopus sp., Lichtheimia sp., and Scedosporium sp). Twelve (80%) were neutropenic at baseline, and 12 (80%) were refractory to antifungal therapy. Among 12 evaluable patients, the overall response rate was 92% (8 [67%] complete responses, 3 [25%] partial responses, and 1 [8%] stable). Treatment is ongoing in the remaining 3 patients. Among 50 published cases (15 Candida spp., 13 Mucorales, 11 Aspergillus spp., 11 other organisms), 20 (40%) had baseline neutropenia and 36 (72%) were refractory to standard therapy before rhu GM-CSF administration. Consistent with responses in the newly reported patients, the overall response rate in the literature review was 82% (40 [80%] complete responses, 1 [2%] partial response, and 9 [18%] no response). CONCLUSIONS: Sargramostim may be a potential adjunctive immunomodulator for selected patients with hematological malignancies and refractory IFDs.
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spelling pubmed-96455832022-11-14 Recombinant Human Granulocyte-Macrophage Colony-Stimulating Factor (rhu GM-CSF) as Adjuvant Therapy for Invasive Fungal Diseases Chen, Tempe K Batra, Jagmohan S Michalik, David E Casillas, Jacqueline Patel, Ramesh Ruiz, Maritza E Hara, Harneet Patel, Bhavita Kadapakkam, Meena Ch'Ng, James Small, Catherine B Zagaliotis, Panagiotis Ragsdale, Carolyn E Leal, Luis O Roilides, Emmanuel Walsh, Thomas J Open Forum Infect Dis Major Article BACKGROUND: Sargramostim (yeast-derived, glycosylated recombinant human granulocyte-macrophage colony-stimulating factor [rhu GM-CSF]) augments innate and adaptive immune responses and accelerates hematopoietic recovery of chemotherapy-induced neutropenia. However, considerably less is known about its efficacy as adjunctive immunotherapy against invasive fungal diseases (IFDs). METHODS: The clinical courses of 15 patients with pediatric malignancies and IFDs treated adjunctively with sargramostim at a single institution were analyzed in a retrospective cohort review. Further, a systematic review of published reports of rhu GM-CSF for IFDs was also conducted. RESULTS: Among 65 cases, 15 were newly described pediatric patients and 50 were previously published cases of IFDs treated with rhu GM-CSF. Among the newly reported pediatric patients, IFDs were caused by Candida spp., Trichosporon sp., and molds (Aspergillus spp., Rhizopus sp., Lichtheimia sp., and Scedosporium sp). Twelve (80%) were neutropenic at baseline, and 12 (80%) were refractory to antifungal therapy. Among 12 evaluable patients, the overall response rate was 92% (8 [67%] complete responses, 3 [25%] partial responses, and 1 [8%] stable). Treatment is ongoing in the remaining 3 patients. Among 50 published cases (15 Candida spp., 13 Mucorales, 11 Aspergillus spp., 11 other organisms), 20 (40%) had baseline neutropenia and 36 (72%) were refractory to standard therapy before rhu GM-CSF administration. Consistent with responses in the newly reported patients, the overall response rate in the literature review was 82% (40 [80%] complete responses, 1 [2%] partial response, and 9 [18%] no response). CONCLUSIONS: Sargramostim may be a potential adjunctive immunomodulator for selected patients with hematological malignancies and refractory IFDs. Oxford University Press 2022-10-11 /pmc/articles/PMC9645583/ /pubmed/36381625 http://dx.doi.org/10.1093/ofid/ofac535 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Article
Chen, Tempe K
Batra, Jagmohan S
Michalik, David E
Casillas, Jacqueline
Patel, Ramesh
Ruiz, Maritza E
Hara, Harneet
Patel, Bhavita
Kadapakkam, Meena
Ch'Ng, James
Small, Catherine B
Zagaliotis, Panagiotis
Ragsdale, Carolyn E
Leal, Luis O
Roilides, Emmanuel
Walsh, Thomas J
Recombinant Human Granulocyte-Macrophage Colony-Stimulating Factor (rhu GM-CSF) as Adjuvant Therapy for Invasive Fungal Diseases
title Recombinant Human Granulocyte-Macrophage Colony-Stimulating Factor (rhu GM-CSF) as Adjuvant Therapy for Invasive Fungal Diseases
title_full Recombinant Human Granulocyte-Macrophage Colony-Stimulating Factor (rhu GM-CSF) as Adjuvant Therapy for Invasive Fungal Diseases
title_fullStr Recombinant Human Granulocyte-Macrophage Colony-Stimulating Factor (rhu GM-CSF) as Adjuvant Therapy for Invasive Fungal Diseases
title_full_unstemmed Recombinant Human Granulocyte-Macrophage Colony-Stimulating Factor (rhu GM-CSF) as Adjuvant Therapy for Invasive Fungal Diseases
title_short Recombinant Human Granulocyte-Macrophage Colony-Stimulating Factor (rhu GM-CSF) as Adjuvant Therapy for Invasive Fungal Diseases
title_sort recombinant human granulocyte-macrophage colony-stimulating factor (rhu gm-csf) as adjuvant therapy for invasive fungal diseases
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9645583/
https://www.ncbi.nlm.nih.gov/pubmed/36381625
http://dx.doi.org/10.1093/ofid/ofac535
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