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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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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. |
format | Online Article Text |
id | pubmed-9645583 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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