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

Author:

Chen Tempe K12ORCID,Batra Jagmohan S12ORCID,Michalik David E12ORCID,Casillas Jacqueline34ORCID,Patel Ramesh34,Ruiz Maritza E34,Hara Harneet34,Patel Bhavita34,Kadapakkam Meena34,Ch'Ng James34ORCID,Small Catherine B5,Zagaliotis Panagiotis567,Ragsdale Carolyn E8ORCID,Leal Luis O8ORCID,Roilides Emmanuel6ORCID,Walsh Thomas J59

Affiliation:

1. Department of Pediatric Infectious Diseases, MemorialCare Miller Children's & Women's Hospital Long Beach , Long Beach, California , USA

2. Department of Pediatrics, Division of Infectious Diseases, University of California Irvine School of Medicine , Irvine, California , USA

3. Department of Pediatric Hematology/Oncology, MemorialCare Miller Children's & Women's Hospital Long Beach , Long Beach, California , USA

4. Division of Hematology/Oncology, Department of Pediatrics, David Geffen School of Medicine at University of California Los Angeles , Los Angeles, California , USA

5. Transplantation-Oncology Infectious Diseases Program, Weill Cornell Medicine , New York, New York , USA

6. Infectious Diseases Unit, 3rd Department of Pediatrics, Faculty of Medicine, Aristotle University School of Health Sciences, Hippokration General Hospital , Thessaloniki , Greece

7. Department of Pharmacology and Therapeutics, School of Pharmacy, Aristotle University of Thessaloniki , Thessaloniki , Greece

8. Partner Therapeutics, Inc. , Lexington, Massachusetts , USA

9. Center for Innovative Therapeutics and Diagnostics , Richmond, Virginia , USA

Abstract

Abstract 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.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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