Survivin expression and its potential clinical significance in gastrointestinal stromal sarcoma

Int Immunopharmacol. 2011 Dec;11(12):2227-31. doi: 10.1016/j.intimp.2011.10.005. Epub 2011 Oct 20.

Abstract

This study was designed to determine the level of survivin expression and its clinical significance as a prognostic factor in gastrointestinal stromal sarcoma (GIST). Twenty patients (12 males and 8 females) ranging in age from 25 to 72, with a median age of 53 were evaluated. Failure of TKI treatment was higher in the survivin-positive group (p=0.06). The rate of metastasis was significantly higher in the survivin positive group vs. the negative group (80% vs. 30%, p=0.18). The median overall survival (OS) time was 114 (range 29-199)months, and the median disease-free survival (DFS) time was 88 (range 40-135) months. The median progression-free survival (PFS) time was 40 (range 24-55) months. Further, a comparison of patients with survivin positive versus negative tumors, revealed no significant difference for OS, DFS, and PFS (p=0.45, p=0.19, p=0.55, respectively), number of mitoses in 50 HPF (p=0.14), and tumor size (p=0.94). In conclusion, survivin was highly expressed in GISTs, although we found no correlation between survivin expression and PFS, DFS and OS, survivin may be a predictive marker in GISTs for disease progression. We believe that additional studies are warranted to determine the clinical significance of survivin expression as a prognostic or predictive marker in patients with GIST.

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Agents / therapeutic use
  • Benzamides
  • Biomarkers, Tumor / biosynthesis*
  • Combined Modality Therapy
  • Disease Progression
  • Disease-Free Survival
  • Female
  • Gastrointestinal Neoplasms / mortality
  • Gastrointestinal Neoplasms / pathology*
  • Gastrointestinal Neoplasms / therapy
  • Gastrointestinal Stromal Tumors / mortality
  • Gastrointestinal Stromal Tumors / pathology*
  • Gastrointestinal Stromal Tumors / therapy
  • Humans
  • Imatinib Mesylate
  • Indoles / therapeutic use
  • Inhibitor of Apoptosis Proteins / biosynthesis*
  • Male
  • Middle Aged
  • Mitosis
  • Piperazines / therapeutic use
  • Prognosis
  • Pyrimidines / therapeutic use
  • Pyrroles / therapeutic use
  • Retrospective Studies
  • Sunitinib
  • Survivin
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • BIRC5 protein, human
  • Benzamides
  • Biomarkers, Tumor
  • Indoles
  • Inhibitor of Apoptosis Proteins
  • Piperazines
  • Pyrimidines
  • Pyrroles
  • Survivin
  • Imatinib Mesylate
  • nilotinib
  • Sunitinib