Randomized placebo-controlled double-blind phase II study of zaltoprofen for patients with diffuse-type and unresectable localized tenosynovial giant cell tumors: a study protocol

BMC Musculoskelet Disord. 2019 Feb 9;20(1):68. doi: 10.1186/s12891-019-2453-z.

Abstract

Background: A tenosynovial giant cell tumor (TGCT) is a locally aggressive benign neoplasm arising from intra- or extra-articular tissue. Diffuse TGCT (D-TGCT) most commonly develops in the knee, followed by the hip, ankle, elbow, and shoulder. Surgical removal is the only effective treatment option for the patients. However, a local recurrence rate as high as 47% has been reported. Recently, we revealed that zaltoprofen, a nonsteroidal anti-inflammatory drug possessing the ability to activate peroxisome proliferator-activated receptor gamma (PPARγ), can inhibit the proliferation of TGCT stromal cells via PPARγ. PPARγ is a ligand-activated transcription factor that belongs to the nuclear hormone receptor superfamily. It plays an important role in the differentiation of adipocytes from precursor cells and exhibits antitumorigenic effects on certain malignancies. Therefore, we are conducting this investigator-initiated clinical trial to evaluate whether zaltoprofen is safe and effective for patients with D-TGCT or unresectable localized TGCT (L-TGCT).

Methods: This study is a randomized, placebo-controlled, double-blind, multicenter trial to evaluate the safety and efficacy of zaltoprofen for patients with D-TGCT or L-TGCT. For the treatment group, zaltoprofen 480 mg/day will be administered for 48 weeks; the placebo group will receive similar dosages without zaltoprofen. Twenty participants in each group are needed in this trial (40 participants total). The primary outcome is the progression-free rate at 48 weeks after treatment administration. "Progression" is defined as any serious events (1. Repetitive joint swelling due to hemorrhage, 2. Joint range of motion limitation, 3. Invasion of adjacent cartilage or bone, 4. Severe joint space narrowing, 5. Increase in tumor size) requiring surgical interventions. We hypothesize that the zaltoprofen group will have a higher progression-free rate compared to that of the placebo group at 48 weeks.

Discussion: This is the first study to evaluate the efficacy of zaltoprofen in patients with D-TGCT or unresectable L-TGCT. We believe that the results of this trial will validate a novel treatment option, zaltoprofen, to stabilize disease progression for TGCT patients.

Trial registration: University Hospital Medical Information Network (UMIN) Clinical Trials Registry ( UMIN000025901 ) registered on 4/01/2017.

Keywords: Clinical trial; Non-steroidal; Randomized control trial; Tenosynovial giant cell tumor; Zaltoprofen.

Publication types

  • Clinical Trial Protocol

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / therapeutic use*
  • Benzopyrans / adverse effects
  • Benzopyrans / therapeutic use*
  • Clinical Trials, Phase II as Topic
  • Disease Progression
  • Double-Blind Method
  • Female
  • Giant Cell Tumor of Tendon Sheath / diagnostic imaging
  • Giant Cell Tumor of Tendon Sheath / drug therapy*
  • Giant Cell Tumor of Tendon Sheath / metabolism
  • Giant Cell Tumor of Tendon Sheath / pathology
  • Humans
  • Japan
  • Male
  • Middle Aged
  • Multicenter Studies as Topic
  • PPAR gamma / agonists
  • PPAR gamma / metabolism
  • Progression-Free Survival
  • Propionates / adverse effects
  • Propionates / therapeutic use*
  • Randomized Controlled Trials as Topic
  • Time Factors
  • Young Adult

Substances

  • Antineoplastic Agents
  • Benzopyrans
  • PPAR gamma
  • PPARG protein, human
  • Propionates
  • pyranoprofen