# A Dilemma in Staging of Esophageal Cancer: How Should We Stage ypT0 N2 M0 Esophageal Cancer after Neoadjuvant Therapy?

**Authors:** Sebahattin Celik, Remzi Erten, Abdulsamed Batur, Burak Suvak

PMC · DOI: 10.1155/2015/158626 · Case Reports in Pathology · 2015-08-06

## TL;DR

This paper discusses the challenges in staging esophageal cancer after neoadjuvant therapy when the tumor appears completely responded but lymph nodes are affected.

## Contribution

It highlights the need for new protocols to evaluate pathology reports in ypT0 N2 M0 cases after neoadjuvant therapy.

## Key findings

- Complete pathological response in the esophagus does not guarantee lymph nodes are tumor-free.
- Current staging systems lack guidance for ypT0 N2 M0 esophageal cancer cases.
- New studies are needed to address the dilemma in staging after neoadjuvant therapy.

## Abstract

Background. Since neoadjuvant treatment in esophageal cancer began to become popular, a complete pathological response at the primary tumour site has been commonly reported. An issue of conflict is whether complete response in the esophageal lumen means that the esophagus is completely tumour-free. Another important issue is whether lymph nodes that are retrieved from pathologically complete response cases are also tumour-free or not. There is a gap in the esophageal cancer staging system for ypT0 N2 M0 tumours that have received neoadjuvant therapy. Here, we will discuss the problem about staging of esophageal cancer associated with neoadjuvant therapy. Case. A female aged 40 years complaining of dysphagia was diagnosed as having locally advanced thoracic esophageal cancer. Neoadjuvant therapy decision was taken by oncology committee. Six weeks after neoadjuvant therapy, with a curative intention, minimal invasive surgery was performed. The pathology report was as follows. “There were no neoplastic cells in the suspected area of the esophageal mucosa upon examination with all staining. There was no cancer at resection margins. Four metastatic lymph nodes were infiltrated with squamous cell cancer.” Conclusion. Despite the growing use of neoadjuvant treatment in locally advanced esophageal cancer in world, we do not have a protocol for the evaluation of these patients' pathology reports. We believe that new studies and new ideas are needed to resolve this dilemma associated with neoadjuvant therapy.

## Linked entities

- **Diseases:** esophageal cancer (MONDO:0007576)

## Full-text entities

- **Genes:** TP63 (tumor protein p63) [NCBI Gene 8626] {aka AIS, B(p51A), B(p51B), EEC3, KET, LMS}
- **Diseases:** esophageal mass (MESH:C536030), dysphagia (MESH:D003680), squamous cell cancer (MESH:D018307), inflammation (MESH:D007249), ulcer (MESH:D014456), oncologic (MESH:D000072716), esophageal adenocarcinoma (MESH:D000230), metastases (MESH:D009362), Cancer (MESH:D009369), node (MESH:D012804), tachycardia (MESH:D013610), Esophageal Cancer (MESH:D004938), fibrosis (MESH:D005355), lymph (MESH:D000072717), TNM (MESH:D008207), metastatic disease (MESH:D000092182)
- **Chemicals:** methylene blue (MESH:D008751), H&amp;E (MESH:D006371), Carboplatin (MESH:D016190), Paclitaxel (MESH:D017239)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC4544951/full.md

## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC4544951/full.md

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Source: https://tomesphere.com/paper/PMC4544951