Case report: A golden tail of immunotherapy: significant tail effect in a chemotherapy-resistant advanced pulmonary sarcomatoid carcinoma patient treated by Sintilimab combined with Anlotinib

Front Immunol. 2024 Nov 6:15:1452195. doi: 10.3389/fimmu.2024.1452195. eCollection 2024.

Abstract

Tail effect is a unique phenomenon in immunotherapy characterized by the prolonged maintenance of therapeutic efficacy. It can be observable even after treatment cessation. Immunotherapy has gradually become a vital regimen for the treatment of advanced lung cancer patients, among which immune-combined therapies based on immune checkpoint inhibitors (ICIs) have been applied clinically and demonstrates considerable clinical efficacy. In this case report, the patient was pathologically diagnosed with pulmonary sarcomatoid carcinoma (PSC), a rare and highly aggressive subtype of non-small cell lung cancer (NSCLC) known for its poor prognosis due to high invasiveness and metastatic potential. After developing resistance to chemotherapy, the patient was treated with a combined regimen of sintilimab and anlotinib, leading to initial clinical improvement. Following just three cycles of this regimen, treatment was discontinued, and the patient was discharged. Remarkably, over the subsequent months, the patient exhibited a significant tail effect, evidenced by sustained therapeutic stability, continuous tumor regression, stable low levels of serum carcinoembryonic antigen (CEA), and further improvement in clinical symptoms. Tail effect is a golden tail of immunotherapy. This case illustrates that the tail effect of immunotherapy can offer substantial survival benefits for patients with unresectable advanced lung cancer who have failed chemotherapy.

Keywords: ICI; PSC; Sintilimab; cancer therapy; immunotherapy; tail effect.

Publication types

  • Case Reports

MeSH terms

  • Antibodies, Monoclonal, Humanized* / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols* / therapeutic use
  • Carcinoma, Non-Small-Cell Lung / drug therapy
  • Carcinoma, Non-Small-Cell Lung / therapy
  • Drug Resistance, Neoplasm*
  • Humans
  • Immunotherapy / methods
  • Indoles* / therapeutic use
  • Lung Neoplasms* / drug therapy
  • Lung Neoplasms* / therapy
  • Quinolines* / administration & dosage
  • Quinolines* / therapeutic use
  • Treatment Outcome

Substances

  • anlotinib
  • Antibodies, Monoclonal, Humanized
  • Indoles
  • Quinolines
  • sintilimab

Grants and funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.