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Thymosin-alpha-1

Thymalfasin, Zadaxin, Thymosin α1

Quick Stats
Studies 759
Trials 63
Score 3
2017 pubmed

Thymalfasin, a promising adjuvant therapy in small hepatocellular carcinoma after liver resection.

He. Chao C; Peng. Wei W; Li. Chuan C; Wen. Tian-Fu TF

Key Findings

  • Thymosin‑alpha‑1 given after liver resection raised 5‑year overall survival from ~63% to ~83%.
  • Recurrence‑free survival at 5 years improved from ~32% to ~53% with the peptide.
  • Multivariate analysis showed thymosin‑alpha‑1 independently cut the risk of death by about 65% and the risk of recurrence by about 44%.

Practical Outcomes

  • For patients who have had surgery to remove a small liver tumor, adding thymosin‑alpha‑1 may improve survival and lower the chance the cancer comes back. This evidence comes from a retrospective study, so it isn’t a proven standard of care yet. Anyone considering it should discuss it with a liver‑cancer specialist and weigh the limited data against potential costs and side‑effects.

Summary

A study of 206 patients with small liver cancer who had surgery found that those who also received the peptide thymosin‑alpha‑1 (called thymalfasin) lived longer and had fewer cancer recurrences than those who had surgery alone.

Abstract

There is limited information available concerning the effect of thymalfasin (Tα1) as an adjuvant therapy in hepatocellular carcinoma (HCC) patient who received liver resection. The present study aimed to evaluate whether Tα1 can improve the prognosis of small HCC patients after liver resection.A total of 206 patients with small HCC who underwent liver resection were analyzed in our retrospective cohort study. Patients were divided into 2 groups: group A (resection + Tα1, n = 44) and group B (resection, n = 162). Clinical data, overall survival (OS), and recurrence-free survival (RFS) were compared. Prognostic factors were identified using multivariate analysis.After a median follow-up of 47.0 months, 134 patients (65%) had recurrence, and 62 patients (30.09%) died. The 1, 3, and 5-year OS rate of patients in group A was 97.7%, 90.6%, and 82.9%, respectively, and 95.1%, 80.5%, and 62.9%, respectively, for patients in group B (P = .014). The 1, 3, and 5-year RFS rate of patients in group A was 70.5%, 56.8%, and 53.3%, respectively, and 65.8%, 41.3%, and 32.1%, respectively, for patients in group B (P = .015). Multivariate analysis indicated that Tα1 was an independent prognostic factor for both OS (P = .015, hazard ratio 0.349, 95% confidence interval 0.149-0.816) and RFS (P = .019, hazard ratio 0.564, 95% confidence interval 0.349-0.910).Tα1 as an adjuvant therapy after liver resection may improve the prognosis of small HCC patients after liver resection.

Study Information

Provider

pubmed

Year

2017

DOI

10.1097/md.0000000000006606