Sintilimab plus GemOx is an effective salvage therapy in patients with refractory/relapsing nodal peripheral T cell lymphomas.

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  • Author(s): Xiao X;Xiao X; Hu M; Hu M; Jiang H; Jiang H; Chen P; Chen P; Lei H; Lei H
  • Source:
    Journal of cancer research and clinical oncology [J Cancer Res Clin Oncol] 2024 Sep 19; Vol. 150 (9), pp. 425. Date of Electronic Publication: 2024 Sep 19.
  • Publication Type:
    Journal Article
  • Language:
    English
  • Additional Information
    • Source:
      Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 7902060 Publication Model: Electronic Cited Medium: Internet ISSN: 1432-1335 (Electronic) Linking ISSN: 01715216 NLM ISO Abbreviation: J Cancer Res Clin Oncol Subsets: MEDLINE
    • Publication Information:
      Original Publication: Berlin ; New York : Springer-Verlag.
    • Subject Terms:
    • Abstract:
      Purpose: The retrospective study was to explore the effectiveness and safety of GemOx (gemcitabine, oxaliplatin) plus sintilimab (belongs to the class of drugs known as immune checkpoint inhibitors, particularly targeting the PD-1 receptor) in relapse or refractory nodal PTCLs.
      Methods: Patients with nodal PTCL who initiated salvage therapy with sintilimab and GemOx between January 2020 to September 2021 were identified from the database of the hematology department of the Second Affiliated Hospital of Zhejiang University School of Medicine. All patients received 2-4 cycles (3 weeks/cycle) of treatment of sintilimab (200 mg, I.V, D1) in combination with GemOx. Treatment response was assessed every six weeks during the salvage treatment phase. Eligible patients received maintenance therapy according to the investigator's decision. Follow-ups were routinely conducted every three months.
      Results: 31 patients with r/r nodal PTCLs were enrolled, including 23 PTCL-NOS, 4 AITL, and 4 ALCL. 21 (67.7%) patients received at least two lines of therapy. 71.0% (95% CI, 53.4%-83.9%) of patients documented objective response of 2-4 cycles of sintilimab plus GemOx therapy, including 9 complete response and 13 partial response. 21 (67.7%) patients received consolidation therapy, including 5 autologous stem-cell transplantation and 12 histone deacetylase inhibitors. After a median 25.6 months follow-up, the median PFS was 22.0 (95% CI,11.8-24.7) months, and the median OS was 26.2 (95% CI, 24.4 -NA) months. 29 (93.5%) patients experienced at least one adverse event, and 26 (83.9% patients only had mild (grade 1-2) AEs.Univariable Cox regression showed the progression risk of AITL is 22.7 (3.9- 131.0, p < 0.01) times of PTCL-NOS, while the HR of ALCL was 1.14 (0.33-3.96,p = 0.833).
      Conclusion: Sintilimab plus GemOx showed encouraging activity and manageable toxicity for patients with r/r PTCL.
      (© 2024. The Author(s).)
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    • Contributed Indexing:
      Keywords: Chemoimmunotherapy; GemOx; PTCL; Salvage therapy; Sintilimab
    • Accession Number:
      8FU7FQ8UPK (sintilimab)
      0 (Antibodies, Monoclonal, Humanized)
      0 (Gemcitabine)
      0W860991D6 (Deoxycytidine)
      04ZR38536J (Oxaliplatin)
      0 (Organoplatinum Compounds)
    • Subject Terms:
      gemcitabine-oxaliplatin regimen
    • Publication Date:
      Date Created: 20240919 Date Completed: 20240919 Latest Revision: 20240921
    • Publication Date:
      20240921
    • Accession Number:
      10.1007/s00432-024-05956-3
    • Accession Number:
      39299973