<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Ma J</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>To compare effects and adverse events of anti-programmed cell death protein 1 (anti-PD-1) antibody combined with chemoradiotherapy (CRT) and CRT alone as the initial treatment in locally advanced esophageal squamous cell carcinoma (ESCC).&lt;h4>Methods&lt;/h4>We retrospectively reviewed locally advanced ESCC patients who received Anti-PD-1+CRT as initial treatment at 3 institutions. Primary outcomes of interest were progression-free survival (PFS) and overall survival (OS); secondary outcomes were objective response rate (ORR), disease control rate (DCR), duration of response (DoR), and treatment-related adverse events (AEs) including immune-related adverse events (irAEs).&lt;h4>Results&lt;/h4>At data cutoff, 81 patients were included (30 Anti-PD-1+CRT, 51 CRT). Median follow-up was 31.4 months. Anti-PD-1+CRT resulted in significant improvements in PFS (median, 18.6 &lt;i>vs.&lt;/i> 11.8 months, HR 0.48 [95% CI, 0.29-0.80], P = 0.008), and OS (median, 27.7 &lt;i>vs.&lt;/i> 17.4 months, HR 0.37 [95% CI, 0.22-0.63], P = 0.002), compared with CRT in ESCC. The ORR and DCR of patients treated with Anti-PD-1+CRT were also significantly higher than those treated with CRT (80.0% &lt;i>vs.&lt;/i> 56.9%, P = 0.034), (100% &lt;i>vs.&lt;/i> 82.4%, P = 0.023), respectively. Anti-PD-1+CRT had better durable response compared with CRT, with DoR (median,17.3 &lt;i>vs.&lt;/i> 11.1 months, P = 0.022). Treatment-related adverse event incidence was similar between the two groups (any Grade, 93.3% &lt;i>vs.&lt;/i> 92.2%; ≥Grade 3, 50.0% &lt;i>vs.&lt;/i> 33.3%).&lt;h4>Conclusion&lt;/h4>Anti-PD-1 plus chemoradiotherapy demonstrated promising antitumor activity and was well tolerated in locally advanced ESCC.</pubmed_abstract><journal>Frontiers in oncology</journal><pagination>1005856</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9947779</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Efficacy and safety of anti-PD-1 antibody plus chemoradiotherapy in locally advanced esophageal squamous cancer.</pubmed_title><pmcid>PMC9947779</pmcid><pubmed_authors>Yuan S</pubmed_authors><pubmed_authors>Tong S</pubmed_authors><pubmed_authors>Yao Y</pubmed_authors><pubmed_authors>Cui L</pubmed_authors><pubmed_authors>Yao N</pubmed_authors><pubmed_authors>Qin Z</pubmed_authors><pubmed_authors>Lu J</pubmed_authors><pubmed_authors>Ma J</pubmed_authors><pubmed_authors>Qu W</pubmed_authors><pubmed_authors>Li N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Efficacy and safety of anti-PD-1 antibody plus chemoradiotherapy in locally advanced esophageal squamous cancer.</name><description>&lt;h4>Objective&lt;/h4>To compare effects and adverse events of anti-programmed cell death protein 1 (anti-PD-1) antibody combined with chemoradiotherapy (CRT) and CRT alone as the initial treatment in locally advanced esophageal squamous cell carcinoma (ESCC).&lt;h4>Methods&lt;/h4>We retrospectively reviewed locally advanced ESCC patients who received Anti-PD-1+CRT as initial treatment at 3 institutions. Primary outcomes of interest were progression-free survival (PFS) and overall survival (OS); secondary outcomes were objective response rate (ORR), disease control rate (DCR), duration of response (DoR), and treatment-related adverse events (AEs) including immune-related adverse events (irAEs).&lt;h4>Results&lt;/h4>At data cutoff, 81 patients were included (30 Anti-PD-1+CRT, 51 CRT). Median follow-up was 31.4 months. Anti-PD-1+CRT resulted in significant improvements in PFS (median, 18.6 &lt;i>vs.&lt;/i> 11.8 months, HR 0.48 [95% CI, 0.29-0.80], P = 0.008), and OS (median, 27.7 &lt;i>vs.&lt;/i> 17.4 months, HR 0.37 [95% CI, 0.22-0.63], P = 0.002), compared with CRT in ESCC. The ORR and DCR of patients treated with Anti-PD-1+CRT were also significantly higher than those treated with CRT (80.0% &lt;i>vs.&lt;/i> 56.9%, P = 0.034), (100% &lt;i>vs.&lt;/i> 82.4%, P = 0.023), respectively. Anti-PD-1+CRT had better durable response compared with CRT, with DoR (median,17.3 &lt;i>vs.&lt;/i> 11.1 months, P = 0.022). Treatment-related adverse event incidence was similar between the two groups (any Grade, 93.3% &lt;i>vs.&lt;/i> 92.2%; ≥Grade 3, 50.0% &lt;i>vs.&lt;/i> 33.3%).&lt;h4>Conclusion&lt;/h4>Anti-PD-1 plus chemoradiotherapy demonstrated promising antitumor activity and was well tolerated in locally advanced ESCC.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-06T19:42:02.161Z</modification><creation>2025-04-06T19:42:02.161Z</creation></dates><accession>S-EPMC9947779</accession><cross_references><pubmed>36845696</pubmed><doi>10.3389/fonc.2023.1005856</doi></cross_references></HashMap>