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Case report reveals poor prognosis in alpha-fetoprotein-positive lung adenocarcinoma, suggesting targeted therapies.
We describe three cases of resection of embryonal lung adenocarcinoma, along with a literature review and immunohistochemical analyses of alpha-fetoprotein (AFP) levels. Generally, embryonal lung adenocarcinoma has a poor prognosis, which can be attributed to low programmed death-ligand 1 (PD-L1) expression, limiting the efficacy of immune checkpoint inhibitors. The cases showed varying intensities of AFP staining in the tumor tissues. Case 1 was initially negative for AFP, but positive at low levels upon re-staining; Case 2 was positive in a relatively small subset of cells; and Case 3 was intensely positive. Further, Case 3 showed elevated serum levels of AFP. Only Case 2 was positive for PD-L1 at relatively low levels. Patient 1 achieved >50-month overall survival, which can be attributed to early detection and complete resection. Cases 2 and 3 showed a poor prognosis. Our findings suggested that low or absent PD-L1 and moderate-to-high AFP expression may contribute to poor prognosis. AFP may train dendritic cells to promote differentiation of naïve T-cells to regulatory T-cells in the tumor microenvironment, which protects the tumor from adaptive immune responses. Therefore, combination therapy involving an AFP-targeted drug and an immune checkpoint inhibitor may be a viable treatment strategy for AFP-positive fetal lung adenocarcinoma.
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Nabe et al. (2026) studied this question.
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