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

Author:

Desai Pinkal M.1ORCID,Brown Janice2,Gill Saar3ORCID,Solh Melham M.4ORCID,Akard Luke P.5,Hsu Jack W.6,Ustun Celalettin7,Andreadis Charalambos8,Frankfurt Olga9,Foran James M.10,Lister John11ORCID,Schiller Gary J.12,Wieduwilt Matthew J.13ORCID,Pagel John M.14ORCID,Stiff Patrick J.15ORCID,Liu Delong16,Khan Irum17ORCID,Stock Wendy18ORCID,Kambhampati Suman19,Tallman Martin S.20,Morris Lawrence4,Edwards John5ORCID,Pusic Iskra21,Kantarjian Hagop M.22,Mamelok Richard23,Wong Alicia23,Van Syoc Rodney23,Kellerman Lois23,Panuganti Swapna23,Mandalam Ramkumar23,Abboud Camille N.21ORCID,Ravandi Farhad22

Affiliation:

1. Weill Cornell Medical College, New York, NY

2. Stanford University Medical Center, Stanford, CA

3. University of Pennsylvania, Philadelphia, PA

4. Northside Hospital, Atlanta, GA

5. Indiana Blood and Marrow Transplantation, Indianapolis, IN

6. University of Florida, Gainesville, FL

7. University of Minnesota, St Paul, MN

8. University of California San Francisco, San Francisco, CA

9. Northwestern University, Chicago, IL

10. Mayo Clinic, Jacksonville, FL

11. Allegheny Health Network, Pittsburgh, PA

12. David Geffen School of Medicine at UCLA, Los Angeles, CA

13. Stephenson Cancer Center, University of Oklahoma, Oklahoma City, OK

14. Swedish Cancer Institute, Seattle, WA

15. Loyola University Stritch School of Medicine, Maywood, IL

16. New York Medical College, Hawthorne, NY

17. University of Illinois Cancer Center, Chicago, IL

18. University of Chicago, Chicago, IL

19. Kansas City Veterans Affairs Medical Center, Kansas City, MO

20. Memorial Sloan Kettering Cancer Center, New York, NY

21. Washington University, St Louis, MO

22. The University of Texas MD Anderson Cancer Center, Houston, TX

23. Cellerant Therapeutics, San Carlos, CA

Abstract

PURPOSE 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.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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