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Esophageal adenocarcinoma is described in the packet as a malignant tumor with glandular differentiation arising predominantly from Barrett mucosa in the lower third of the esophagus. Rare examples deriving from ectopic gastric mucosa in the upper esophagus have also been reported. The packet lists three related entries: esophageal adenoid cystic carcinoma, Barrett adenocarcinoma and mucoepidermoid esophageal carcinoma. Orphanet-derived prevalence in the packet is categorized as uncommon, at 1 to 9 per 100,000. No genes, inheritance pattern or onset category are listed in the packet.
The packet's phenotype list includes gastroesophageal reflux, Barrett esophagus, nausea and vomiting, chest pain and cough, and lymphadenopathy at a lower reported frequency. Annotated frequencies for some entries in this list appear unreliable for this condition and are not reproduced here, and the list is not a complete description of how the condition presents. The definition describes grossly visible tumors similar to esophageal squamous cell carcinomas and, microscopically, typically papillary or tubular growth in the setting of Barrett esophagus.
The packet lists no genes, inheritance pattern or molecular mechanism, so these are unknown in this packet. The definition describes the tumor as arising predominantly from Barrett mucosa in the lower third of the esophagus, with rare examples arising from ectopic gastric mucosa in the upper esophagus.
The packet supplies no diagnostic criteria or testing information. It describes the tumor microscopically as typically papillary and/or tubular when arising in the setting of Barrett esophagus. Clinical trial records in the packet include a study titled as multi-site detection of Barrett's esophagus in patients without chronic GERD symptoms (NCT06687603); a title does not establish diagnostic performance.
The packet contains one active FDA approval record, for nivolumab (Opdivo), approved under a BLA through CDER on 2014-12-22. The approval record does not state an indication. A related orphan drug record for Opdivo gives an indication of gastric cancer and gastro-esophageal junction cancer, so approval specifically for esophageal adenocarcinoma is not established by this packet. The packet also lists tezacitabine with orphan designation for adenocarcinoma of the esophagus and stomach; a designation is not an approval. The packet supplies no management guidance beyond these records.
113 trials found
The packet's definition states that the prognosis is poor. No survival figures or stage-specific outcomes are supplied in this packet.
The packet lists a large number of active clinical trial records for esophageal adenocarcinoma, ten of which have details supplied. Examples include NCT05677490, a phase 3 study sponsored by the Alliance for Clinical Trials in Oncology and recruiting, titled as mFOLFIRINOX versus mFOLFOX with or without nivolumab in advanced HER2-negative esophageal, gastroesophageal junction and gastric adenocarcinoma (2023-01-31 to 2028-11-08); NCT05152147, a phase 3 study sponsored by Jazz Pharmaceuticals, active and not recruiting, titled as zanidatamab with chemotherapy with or without tislelizumab in HER2-positive advanced or metastatic gastric and esophageal cancers; and NCT07090499, a phase 1 study sponsored by Pfizer in advanced solid tumors. Several records concern Barrett's esophagus, including NCT06732388, a phase 2 study sponsored by the National Cancer Institute titled as itraconazole with ablation for prevention of esophageal cancer in high-risk Barrett's esophagus, and NCT05753748, titled as surveillance versus endoscopic therapy for Barrett's esophagus with low-grade dysplasia. Trial titles describe the studies and do not establish safety or efficacy. The packet's research digest classifies 359 publications, mostly reviews and meta-analyses.
Data assembled from 6 of 12 sources · Last updated Nov 3, 2026, 3:00 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
AI-curated news mentioning esophageal adenocarcinoma
Updated Aug 25, 2026
Ziihera receives approval for use as an initial treatment for all HER2-positive gastroesophageal adenocarcinomas, significantly broadening its market potential. This approval positions the drug for potential blockbuster sales in a competitive oncology landscape.
A case study highlights a fatal instance of esophageal adenocarcinoma in a pregnant woman, initially misdiagnosed as gestational hyperemesis. This research underscores the importance of accurate diagnosis in pregnant patients presenting with gastrointestinal symptoms.
A recent study highlights recurrent steroid-responsive exophthalmos as a paraneoplastic manifestation of esophageal adenocarcinoma. This discovery may enhance understanding of the disease's systemic effects and guide future research.