Oesophageal cancer
Prepared with OnCo (onco.cc/prep/esophageal/). Orientation, not medical advice; your team knows your case.
My details
What I know, what is unclear, changes to discuss
Saved in this browserMy questions
34 on the sheet- 1.What is my exact diagnosis, stage, and grade, and which tests established them?
- 2.Which biomarkers have been tested on my tumour (for example PD-L1, HER2, EGFR, Histologydetermines the pathway, PD-L1), and what were the results?
- 3.Which subtype is my cancer, and does that change the recommended treatment?
- 4.Is germline (inherited) genetic testing recommended for me or my family?
- 5.For my situation (localised), which of the standard options do you recommend and why?
- 6.Am I a candidate for Nivolumab, and what side effects should I expect?
- 7.For my situation (advanced), which of the standard options do you recommend and why?
- 8.Am I a candidate for Pembrolizumab, Izalontamab brengitecan, and what side effects should I expect?
- 9.For my situation (prevention and screening), which of the standard options do you recommend and why?
- 10.For my situation (early (t1a, high-grade dysplasia)), which of the standard options do you recommend and why?
- 11.For my situation (resectable locally advanced (ct2-4a or n+)), which of the standard options do you recommend and why?
- 12.Am I a candidate for FLOT (5-FU, leucovorin, oxaliplatin, docetaxel), Nivolumab, and what side effects should I expect?
- 13.How do the results of CROSS and CheckMate 577 apply to someone like me?
- 14.For my situation (clinical complete response after chemoradiation), which of the standard options do you recommend and why?
- 15.How do the results of SANO apply to someone like me?
- 16.For my situation (unresectable locally advanced or cervical), which of the standard options do you recommend and why?
- 17.For my situation (advanced squamous cell carcinoma, first line), which of the standard options do you recommend and why?
- 18.Am I a candidate for Pembrolizumab, Nivolumab, Ipilimumab or related drugs, and what side effects should I expect?
- 19.How do the results of KEYNOTE-590 and CheckMate 648 apply to someone like me?
- 20.For my situation (advanced adenocarcinoma, first line), which of the standard options do you recommend and why?
- 21.Am I a candidate for Trastuzumab, Zanidatamab, Zolbetuximab, and what side effects should I expect?
- 22.How do the results of KEYNOTE-590 and CheckMate 649 apply to someone like me?
- 23.For my situation (second line, squamous cell carcinoma), which of the standard options do you recommend and why?
- 24.Am I a candidate for Izalontamab brengitecan, and what side effects should I expect?
- 25.How do the results of PANKU-Esophagus01 (BL-B01D1-305) apply to someone like me?
- 26.For my situation (second line, adenocarcinoma), which of the standard options do you recommend and why?
- 27.Am I a candidate for Trastuzumab deruxtecan, Ramucirumab, and what side effects should I expect?
- 28.How do the results of DESTINY-Gastric04 and CLARITY-Gastric 01 apply to someone like me?
- 29.For my situation (palliation of dysphagia), which of the standard options do you recommend and why?
- 30.Are there clinical trials I could join, for example of Izalontamab brengitecan, PF-08634404, HS-20093, QLC5508?
- 31.Would a second opinion at a high-volume centre change anything, and can you help arrange it?
- 32.What supportive care (symptom control, nutrition, exercise, mental health, financial help) is available from the start?
- 33.I read that “Late presentation”. How does that affect my plan?
- 34.I read that “Squamous cell carcinoma lacks targets beyond EGFR/HER3”. How does that affect my plan?
The words I may hear
- Barrett's oesophagus: A change in the lining of the lower oesophagus caused by acid reflux that can, in a minority, progress through dysplasia to adenocarcinoma.
- Squamous cell carcinoma vs adenocarcinoma of the oesophagus: Oesophageal cancer is two different diseases in one organ: squamous cell carcinoma (upper/mid oesophagus, tobacco and alcohol, dominant in Asia) and adenocarcinoma (lower oesophagus, reflux and obesity, dominant in the West).
- FLOT regimen (perioperative chemotherapy for gastric cancer): Four cycles of chemotherapy before and four after surgery for stomach and junction cancer, using fluorouracil, leucovorin, oxaliplatin and docetaxel.
- Oesophagectomy: Surgery that removes most of the food pipe (oesophagus) and rebuilds it by pulling the stomach up into the chest.
- Dysphagia (difficulty swallowing): Trouble swallowing, either because a tumour narrows the food pipe or throat, or because radiotherapy and surgery to the head, neck or chest have damaged the muscles and nerves that coordinate swallowing.
- Gastrectomy: Removing part (subtotal) or all (total) of the stomach for stomach cancer, with the bowel joined to what remains.
- Gastro-oesophageal junction (GEJ): Where the food pipe meets the stomach.
- Feeding tube (gastrostomy, PEG, jejunostomy): A tube placed into the stomach (gastrostomy, PEG) or small bowel (jejunostomy) so a patient who cannot swallow enough can still be fed through the gut.
- Mediastinum: The space in the middle of the chest between the two lungs, containing the heart, great vessels, windpipe, food pipe and the lymph nodes that lung cancer spreads to first.
- Siewert classification (GEJ tumours): A way of classifying cancers at the junction of the oesophagus and stomach by where their centre sits, which decides whether they are treated as oesophageal or gastric.
Tests and results to bring
Biomarker results to ask for: PD-L1, HER2 (adenocarcinoma), EGFR (squamous), Histology (squamous vs adenocarcinoma) determines the pathway, PD-L1 (CPS for adenocarcinoma/pembrolizumab; TAP score for tislelizumab in ESCC), HER2 IHC/ISH in adenocarcinoma, MSI/dMMR, CLDN18.2 in GEJ adenocarcinoma (gastric trials), Pathologic response after neoadjuvant therapy (residual disease → adjuvant nivolumab), Clinical complete response assessment (endoscopy, biopsy, PET-CT) for surveillance, EGFR and HER3 expression (not required for iza-bren).
Scans and tests linked to this cancer: Active surveillance, Companion diagnostics, Endoscopic resection (EMR / ESD), Endoscopic ultrasound and EBUS systems, Gastric cancer endoscopic screening (East Asia), Histopathology & immunohistochemistry.
Bring copies of scan reports, pathology and blood results, and a list of every medicine and supplement.
The treatments I may be offered
- Prevention and screening: Tobacco and alcohol control; endoscopic screening of high-risk populations in China and Japan (Lugol chromoendoscopy); surveillance of Barrett's oesophagus with ablation or resection of dysplasia; non-endoscopic capsule-sponge screening in trials (BEST4). (Endoscopic resection (EMR / ESD), Barrett's oesophagus, Non-endoscopic screening for Barrett's oesophagus and early adenocarcinoma)
- Localised: Neoadjuvant chemoradiation (CROSS) or perioperative FLOT → surgery → nivolumab if residual disease. (Nivolumab, IMRT / IGRT (modern external beam))
- Early (T1a, high-grade dysplasia): Endoscopic resection (EMR/ESD) with radiofrequency ablation of residual Barrett's; oesophagectomy for T1b with high-risk features. (Endoscopic resection (EMR / ESD))
- Resectable locally advanced (cT2-4a or N+): CROSS chemoradiation (carboplatin/paclitaxel + 41.4 Gy) then oesophagectomy for squamous and adenocarcinoma; perioperative FLOT for adenocarcinoma/GEJ (ESOPEC). Adjuvant nivolumab for residual disease after chemoradiation (CheckMate 577). (CROSS, CheckMate 577, FLOT (5-FU, leucovorin, oxaliplatin, docetaxel), Nivolumab, CROSS chemoradiation → surgery → adjuvant nivolumab if residual disease)
- Unresectable locally advanced or cervical: Definitive chemoradiation (50-50.4 Gy with cisplatin/5-FU or carboplatin/paclitaxel); PD-1 blockade added in trials. (IMRT / IGRT (modern external beam), Platinum agents)
- Advanced: Chemotherapy + pembrolizumab/nivolumab; iza-bren in trials. (Pembrolizumab, Izalontamab brengitecan)
- Clinical complete response after chemoradiation: Active surveillance with surgery on regrowth is a non-inferior option (SANO); requires intensive endoscopic and PET surveillance. (SANO, Active surveillance, Clinical complete response (cCR))
- Advanced squamous cell carcinoma, first line: Chemotherapy + pembrolizumab (KEYNOTE-590), nivolumab (CheckMate 648), or tislelizumab (RATIONALE-306, PD-L1 ≥1%); nivolumab + ipilimumab chemotherapy-free option; camrelizumab/sintilimab/toripalimab in China. (KEYNOTE-590, CheckMate 648, RATIONALE-306, ESCORT-1st, Pembrolizumab, Nivolumab, Ipilimumab, Tislelizumab, Camrelizumab)
- Advanced adenocarcinoma, first line: As for gastric cancer: chemotherapy + pembrolizumab or nivolumab (PD-L1 CPS ≥5 or ≥1); trastuzumab-based therapy if HER2-positive; zolbetuximab if CLDN18.2-positive (GEJ eligible in SPOTLIGHT/GLOW). (KEYNOTE-590, CheckMate 649, Trastuzumab, Zanidatamab, Zolbetuximab)
- Palliation of dysphagia: Self-expanding metal stent, brachytherapy, or external beam radiation; nutritional support; early palliative care. (Brachytherapy, IMRT / IGRT (modern external beam))
- Second line, squamous cell carcinoma: Izalontamab brengitecan after PD-(L)1 + platinum (PANKU-Esophagus01, OS and PFS benefit, 2026; approval pending); otherwise taxane or irinotecan; nivolumab/pembrolizumab if IO-naive. (PANKU-Esophagus01 (BL-B01D1-305), Izalontamab brengitecan)
- Second line, adenocarcinoma: T-DXd if HER2-positive (DESTINY-Gastric04); ramucirumab + paclitaxel; CLDN18.2 ADC after CLARITY-Gastric 01. (DESTINY-Gastric04, Trastuzumab deruxtecan, Ramucirumab, CLARITY-Gastric 01)
From the standard of care recorded for this cancer; which apply depends on your stage and biomarkers. Ask which the team recommends and why.