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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://dk.um.si/IzpisGradiva.php?id=94340"><dc:title>Tumor-infiltrating lymphocytes in breast and female genital tract cancers</dc:title><dc:creator>Skok,	Kristijan	(Avtor)
	</dc:creator><dc:creator>Maccio,	Umberto	(Avtor)
	</dc:creator><dc:creator>Martin,	Spencer D.	(Avtor)
	</dc:creator><dc:creator>Bräutigam,	Konstantin	(Avtor)
	</dc:creator><dc:subject>breast cancer</dc:subject><dc:subject>endometrial cancer</dc:subject><dc:subject>fallopian tube</dc:subject><dc:subject>immunotherapy</dc:subject><dc:subject>ovarian cancer</dc:subject><dc:subject>review</dc:subject><dc:subject>tumor microenvironment (TME)</dc:subject><dc:subject>tumor‐infiltrating lymphocytes (TILs)</dc:subject><dc:subject>vulvar cancer</dc:subject><dc:description>Background: The growing success of cancer immunotherapies has led to significant advances in oncology. However, despite these promising developments, cancer-related mortality remains high for common cancer types such as breast and lower female genital tract cancers. Method: Here, we synthesize recent findings on the prognostic relevance of tumor-infiltrating lymphocytes (TILs) in breast, endometrial, tubo-ovarian, and vulvar cancer. Our analysis covers the relationship between TIL counts and density, immune cell subtype combinations, immunotherapy approaches, and patient outcomes. Results: High TIL infiltration, especially CD8+ T-cells, generally correlates with improved outcomes such as in endometrial cancer (especially the POLE-ultramutated subgroup), invasive breast cancer, and ovarian epithelial tumors. However, in ductal carcinoma in situ (DCIS) of the breast, elevated TIL counts are linked to a worse prognosis. Ethnicity, the tumor microenvironment (TME), and molecular profiles further complicate the prognostic utility of TILs. Conclusions: TIL-based therapies have shown potential in personalized immunotherapy, particularly in recurrent, refractory ovarian cancer. Limited research on rarer gynecologic tumors hinders broader clinical applications.</dc:description><dc:publisher>John Wiley &amp; Sons Ltd.</dc:publisher><dc:date>2025</dc:date><dc:date>2025-08-14 03:29:14</dc:date><dc:type>Znanstveno delo</dc:type><dc:identifier>94340</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
