AI Article Synopsis

  • Pulmonary sarcomatoid carcinoma (PSC) is a rare type of aggressive lung cancer that often spreads quickly and is hard to treat, especially with standard therapies.
  • A case study of a 29-year-old male showed that he had both PSC and lung adenocarcinoma, which quickly metastasized; he had a gene fusion and high PD-L1 expression found in both tumors.
  • A combination of targeted chemotherapy and immunotherapy was introduced after initial treatment failure, leading to significant symptom relief and partial remission, highlighting the importance of genetic testing and PD-L1 monitoring in treating PSC.

Article Abstract

Pulmonary sarcomatoid carcinoma (PSC) is a rare form of poorly differentiated non-small-cell lung cancer that is prone to distant metastases. PSC is therapeutically challenging, with low sensitivity to conventional radiotherapy and a poor overall prognosis. The present study reported on the case of a 29-year-old male non-smoker diagnosed with both PSC and lung adenocarcinoma; the cancer had a complex etiology and rapidly metastasized after surgery. The patient presented with an EML4-ALK gene fusion in both tumors with high programmed death ligand-1 (PD-L1) expression. After initial treatment failure, Alectinib, Anlotinib and Tirelizumab were combined, which rapidly resolved the patient's symptoms and led to partial remission of disease at 6 weeks and effective control of the disease 7 months into the treatment. This case exemplifies the efficacy of combining targeted chemotherapy with immunotherapy for patients with PSC. Furthermore, this outcome suggests the usefulness of genetic testing and monitoring PD-L1 expression to identify patients with PSC who may be candidates likely to respond to this combined therapeutic regimen. The present study provides evidence of the success of a novel therapeutic strategy for patients with PSC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434725PMC
http://dx.doi.org/10.3892/ol.2022.13463DOI Listing

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