<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>150(3)</volume><submitter>Shijubou N</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Although immune checkpoint inhibitors (ICIs), together with cytotoxic chemotherapy (chemoimmunotherapy), have been adapted for the initial treatment of extensive-disease small-cell lung cancer (ED-SCLC), they have achieved limited success. In ED-SCLC, a subtype of SCLC, the expression of immune-related molecules and clinical data are not well understood in relation to ICI treatment efficiency.&lt;h4>Methods&lt;/h4>We examined lung biopsy specimens from patients diagnosed with ED-SCLC treated with chemoimmunotherapy or chemotherapy. SCLC subtype, expression of HLA class I, and infiltration of CD8-positive cells were examined using immunohistochemistry (IHC). Subsequently, the association between clinical factors, IHC results, and progression-free survival or overall survival was assessed.&lt;h4>Results&lt;/h4>Most of the cases showed the achaete-scute homolog 1 (ASCL1) subtype. Among the 75 SCLC cases, 29 expressed high levels of HLA class I, while 46 showed low levels or a negative result; 33 patients were characterized as CD8-high, whereas 42 were CD8-low. In the chemoimmunotherapy cohort, multivariate analysis revealed a correlation between CD8-high and improved survival. Specifically, patients in the CD8-high group of the chemoimmunotherapy cohort experienced enhanced survival compared to those in the chemotherapy cohort, which was attributed to ICI addition. IHC subtype analysis demonstrated a survival advantage in the SCLC-I and SCLC-A groups when ICI was combined with chemotherapy compared to chemotherapy alone.&lt;h4>Conclusion&lt;/h4>Our study highlights the predictive value of IHC-classified subtypes and CD8-positive cell infiltration in estimating outcomes for patients with ED-SCLC treated with chemoimmunotherapy as a first-line therapy. These findings have practical implications for daily clinical assessments and treatment decisions.</pubmed_abstract><journal>Journal of cancer research and clinical oncology</journal><pagination>125</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10940450</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Prognostic significance of immunohistochemical classification utilizing biopsy specimens in patients with extensive-disease small-cell lung cancer treated with first-line chemotherapy and immune checkpoint inhibitors.</pubmed_title><pmcid>PMC10940450</pmcid><pubmed_authors>Sasaki K</pubmed_authors><pubmed_authors>Kanaseki T</pubmed_authors><pubmed_authors>Chiba H</pubmed_authors><pubmed_authors>Tsukahara T</pubmed_authors><pubmed_authors>Murata K</pubmed_authors><pubmed_authors>Terai K</pubmed_authors><pubmed_authors>Ikeda T</pubmed_authors><pubmed_authors>Kubo T</pubmed_authors><pubmed_authors>Sumi T</pubmed_authors><pubmed_authors>Torigoe T</pubmed_authors><pubmed_authors>Hirohashi Y</pubmed_authors><pubmed_authors>Yamada Y</pubmed_authors><pubmed_authors>Shijubou N</pubmed_authors><pubmed_authors>Keira Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prognostic significance of immunohistochemical classification utilizing biopsy specimens in patients with extensive-disease small-cell lung cancer treated with first-line chemotherapy and immune checkpoint inhibitors.</name><description>&lt;h4>Purpose&lt;/h4>Although immune checkpoint inhibitors (ICIs), together with cytotoxic chemotherapy (chemoimmunotherapy), have been adapted for the initial treatment of extensive-disease small-cell lung cancer (ED-SCLC), they have achieved limited success. In ED-SCLC, a subtype of SCLC, the expression of immune-related molecules and clinical data are not well understood in relation to ICI treatment efficiency.&lt;h4>Methods&lt;/h4>We examined lung biopsy specimens from patients diagnosed with ED-SCLC treated with chemoimmunotherapy or chemotherapy. SCLC subtype, expression of HLA class I, and infiltration of CD8-positive cells were examined using immunohistochemistry (IHC). Subsequently, the association between clinical factors, IHC results, and progression-free survival or overall survival was assessed.&lt;h4>Results&lt;/h4>Most of the cases showed the achaete-scute homolog 1 (ASCL1) subtype. Among the 75 SCLC cases, 29 expressed high levels of HLA class I, while 46 showed low levels or a negative result; 33 patients were characterized as CD8-high, whereas 42 were CD8-low. In the chemoimmunotherapy cohort, multivariate analysis revealed a correlation between CD8-high and improved survival. Specifically, patients in the CD8-high group of the chemoimmunotherapy cohort experienced enhanced survival compared to those in the chemotherapy cohort, which was attributed to ICI addition. IHC subtype analysis demonstrated a survival advantage in the SCLC-I and SCLC-A groups when ICI was combined with chemotherapy compared to chemotherapy alone.&lt;h4>Conclusion&lt;/h4>Our study highlights the predictive value of IHC-classified subtypes and CD8-positive cell infiltration in estimating outcomes for patients with ED-SCLC treated with chemoimmunotherapy as a first-line therapy. These findings have practical implications for daily clinical assessments and treatment decisions.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-04-08T19:53:50.45Z</modification><creation>2025-04-05T12:05:47.824Z</creation></dates><accession>S-EPMC10940450</accession><cross_references><pubmed>38483588</pubmed><doi>10.1007/s00432-024-05652-2</doi></cross_references></HashMap>