Sargramostim (GM-CSF) and lenalidomide in castration-resistant prostate cancer (CRPC): results from a phase I-II clinical trial

Urol Oncol. 2014 Jan;32(1):33.e11-7. doi: 10.1016/j.urolonc.2012.12.004. Epub 2013 Mar 17.

Abstract

Background: Granulocyte-macrophage colony-stimulating factor (GM-CSF) is a pleiotropic cytokine that stimulates dendritic cells (DCs) and promotes uptake of tumor antigens by DCs leading to T-cell cross-priming. Lenalidomide (Revlimid) is an immunomodulatory analog of thalidomide with significant T-cell stimulatory and antiangiogenic properties. GM-CSF in combination with thalidomide induces prostate-specific antigen (PSA) responses in 20% to 25% of patients with castration-resistant prostate cancer (CRPC). In an effort to further evaluate the clinical and immune activity of GM-CSF and lenalidomide, we conducted a phase I-II trial in patients with CRPC.

Methods: Asymptomatic patients with CRPC were enrolled. Prior immunotherapy or chemotherapy was not allowed. All the patients received 250 μg of GM-CSF administered subcutaneously 3 times weekly along with 25mg/d of lenalidomide administered orally on days 1 to 21 of a 28-day cycle. The primary end points were objective, PSA response, and safety. Exploratory end points included activation of circulating DCs, regulatory T cells, and Th1 cytokine production.

Results: Thirty-two patients were enrolled in the study. No dose-limiting toxicities occurred in the phase I portion of the study. Although 81% of the patients achieved a decline in the levels of PSA while on therapy, only 4 achieved a PSA level decline of ≥ 50%. The overall response rate among 11 patients with response evaluation criteria in solid tumors-defined measurable disease was 18%. Overall toxicity was G1 and G2 in nature and included fatigue observed in 69% of the patients, nausea/vomiting in 34%, and diarrhea in 28% of the patients. Grade 3 or 4 toxicities occurred in 22% of the patients and were primarily thrombocytopenia (9%) or neutropenia (19%) or both.

Conclusions: Administration of GM-CSF and lenalidomide in patients with CRPC is safe with modest evidence of antitumor activity and no immune changes observed.

Keywords: Castration-resistant prostate cancer (CRPC); Granulocyte-macrophage colony-stimulating factor (GM-CSF); Immunomodulation; Lenalidomide.

Publication types

  • Clinical Trial, Phase I
  • Clinical Trial, Phase II
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Cytokines / metabolism
  • Dendritic Cells / cytology
  • Drug Administration Schedule
  • Granulocyte-Macrophage Colony-Stimulating Factor / administration & dosage*
  • Humans
  • Immunologic Factors / administration & dosage*
  • Immunotherapy / methods
  • Lenalidomide
  • Male
  • Middle Aged
  • Prostate-Specific Antigen / blood*
  • Prostatic Neoplasms, Castration-Resistant / drug therapy*
  • Prostatic Neoplasms, Castration-Resistant / surgery*
  • Recombinant Proteins / administration & dosage
  • Survival Analysis
  • T-Lymphocytes, Regulatory / cytology
  • Thalidomide / administration & dosage
  • Thalidomide / analogs & derivatives*
  • Time Factors
  • Treatment Outcome

Substances

  • Cytokines
  • Immunologic Factors
  • Recombinant Proteins
  • Thalidomide
  • sargramostim
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Prostate-Specific Antigen
  • Lenalidomide