<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Carr RA</submitter><funding>AHRQ HHS</funding><funding>NCI NIH HHS</funding><pagination>e538-e544</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8840992</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>277(3)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>To compare the efficacy and safety of induction FOLFOX followed by PET-directed nCRT, induction CP followed by PET-directed nCRT, and nCRT with CP alone in patients with EAC.&lt;h4>Summary of background data&lt;/h4>nCRT with CP is a standard treatment for locally advanced EAC. The results of cancer and leukemia group B 80803 support the use of induction chemotherapy followed by PET-directed chemo-radiation therapy.&lt;h4>Methods&lt;/h4>We retrospectively identified all patients with EAC who underwent the treatments above followed by esophagectomy. We assessed incidences of pathologic complete response (pCR), near-pCR (ypN0 with ≥90% response), and surgical complications between treatment groups using Fisher exact test and logistic regression; disease-free survival (DFS) and overall survival (OS) were estimated by the Kaplan-Meier method and evaluated using the log-rank test and extended Cox regression.&lt;h4>Results&lt;/h4>In total, 451 patients were included: 309 (69%) received induction chemotherapy before nCRT (FOLFOX, n = 70; CP, n = 239); 142 (31%) received nCRT with CP. Rates of pCR (33% vs. 16%, P = 0.004), near-pCR (57% vs. 33%, P &lt; 0.001), and 2-year DFS (68% vs. 50%, P = 0.01) were higher in the induction FOLFOX group than in the induction CP group. Similarly, the rate of near-pCR (57% vs. 42%, P = 0.04) and 2-year DFS (68% vs. 44%, P &lt; 0.001) were significantly higher in the FOLFOX group than in the no-induction group.&lt;h4>Conclusions&lt;/h4>Induction FOLFOX followed by PET-directed nCRT may result in better histopathologic response rates and DFS than either induction CP plus PET-directed nCRT or nCRT with CP alone.</pubmed_abstract><journal>Annals of surgery</journal><pubmed_title>Induction FOLFOX and PET-Directed Chemoradiation for Locally Advanced Esophageal Adenocarcinoma.</pubmed_title><pmcid>PMC8840992</pmcid><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>T32 HS000063</funding_grant_id><funding_grant_id>K12 CA184746</funding_grant_id><pubmed_authors>Janjigian YY</pubmed_authors><pubmed_authors>Tan KS</pubmed_authors><pubmed_authors>Bott MJ</pubmed_authors><pubmed_authors>Bains MS</pubmed_authors><pubmed_authors>Park BJ</pubmed_authors><pubmed_authors>Molena D</pubmed_authors><pubmed_authors>Sihag S</pubmed_authors><pubmed_authors>Carr RA</pubmed_authors><pubmed_authors>Wu AJ</pubmed_authors><pubmed_authors>Jones DR</pubmed_authors><pubmed_authors>Rusch VW</pubmed_authors><pubmed_authors>Ilson DH</pubmed_authors><pubmed_authors>Hsu M</pubmed_authors><pubmed_authors>Isbell JM</pubmed_authors><pubmed_authors>Maron SB</pubmed_authors><pubmed_authors>Harrington CA</pubmed_authors><pubmed_authors>Ku GY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Induction FOLFOX and PET-Directed Chemoradiation for Locally Advanced Esophageal Adenocarcinoma.</name><description>&lt;h4>Objective&lt;/h4>To compare the efficacy and safety of induction FOLFOX followed by PET-directed nCRT, induction CP followed by PET-directed nCRT, and nCRT with CP alone in patients with EAC.&lt;h4>Summary of background data&lt;/h4>nCRT with CP is a standard treatment for locally advanced EAC. The results of cancer and leukemia group B 80803 support the use of induction chemotherapy followed by PET-directed chemo-radiation therapy.&lt;h4>Methods&lt;/h4>We retrospectively identified all patients with EAC who underwent the treatments above followed by esophagectomy. We assessed incidences of pathologic complete response (pCR), near-pCR (ypN0 with ≥90% response), and surgical complications between treatment groups using Fisher exact test and logistic regression; disease-free survival (DFS) and overall survival (OS) were estimated by the Kaplan-Meier method and evaluated using the log-rank test and extended Cox regression.&lt;h4>Results&lt;/h4>In total, 451 patients were included: 309 (69%) received induction chemotherapy before nCRT (FOLFOX, n = 70; CP, n = 239); 142 (31%) received nCRT with CP. Rates of pCR (33% vs. 16%, P = 0.004), near-pCR (57% vs. 33%, P &lt; 0.001), and 2-year DFS (68% vs. 50%, P = 0.01) were higher in the induction FOLFOX group than in the induction CP group. Similarly, the rate of near-pCR (57% vs. 42%, P = 0.04) and 2-year DFS (68% vs. 44%, P &lt; 0.001) were significantly higher in the FOLFOX group than in the no-induction group.&lt;h4>Conclusions&lt;/h4>Induction FOLFOX followed by PET-directed nCRT may result in better histopathologic response rates and DFS than either induction CP plus PET-directed nCRT or nCRT with CP alone.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2025-04-18T16:57:13.265Z</modification><creation>2025-04-07T04:31:02.36Z</creation></dates><accession>S-EPMC8840992</accession><cross_references><pubmed>34387205</pubmed><doi>10.1097/sla.0000000000005163</doi><doi>10.1097/SLA.0000000000005163</doi></cross_references></HashMap>