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Forced Transdifferentiation

Transdifferentiation, also known as lineage reprogramming, was first discovered by Selman and Kafatos in 1974 in silkmoths. They observed that the moths’ cuticle-producing cells transformed into salt-producing cells. Many such cases of natural transdifferentiation occur in organisms. In humans, pancreatic alpha cells can become beta cells. In newts, the loss of the eye’s lens causes the pigmented epithelial cells to transdifferentiate into the lens cells.
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Oligometastatic disease - a renaissance for surgery?

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Innovative Surgical Sciences
|March 27, 2025
PubMed
Summary

Metastatic esophageal, gastro-esophageal junction, and gastric cancers can be treated with multimodal therapy for oligometastatic disease. Combining systemic therapy with tumor and metastasis resection improves prognosis compared to systemic therapy alone.

Keywords:
cancer of the gastro-esophageal junctionesophageal cancergastric cancermultimodal therapeutic approacholigometastatic disease

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Area of Science:

  • Oncology
  • Gastroenterology
  • Surgical Oncology

Background:

  • Metastasis at diagnosis is common in esophageal, gastro-esophageal junction, and gastric cancers.
  • Metastatic disease is typically treated with palliative systemic therapy.
  • Oligometastatic disease, a state of low metastatic burden, presents a potential therapeutic target.

Purpose of the Study:

  • To review recent literature on multimodal therapies for oligometastatic esophageal, gastro-esophageal junction, and gastric cancers.
  • To evaluate the efficacy of combining systemic therapy with surgical resection for oligometastatic disease.
  • To highlight treatment strategies for specific subtypes, including esophageal squamous cell carcinomas and adenocarcinomas.

Main Methods:

  • Literature review of recent publications on multimodal treatment for oligometastatic cancers.
  • Analysis of studies comparing systemic therapy alone versus multimodal approaches.
  • Inclusion of a case report on curative-intent treatment for oligometastatic esophago-gastric junction cancer.

Main Results:

  • Multimodal therapy (systemic therapy + resection of primary tumor and metastases) is associated with a better prognosis than systemic therapy alone.
  • Specific focus on esophageal squamous cell carcinomas and adenocarcinomas of the gastro-esophageal junction and stomach.
  • Curative-intent treatment is possible for select patients with oligometastatic esophago-gastric junction cancer.

Conclusions:

  • Multimodal approaches for oligometastatic esophageal, gastro-esophageal junction, and gastric cancers show promising results.
  • Further evidence from ongoing randomized trials may support incorporating these strategies into European guidelines.
  • Aggressive, multimodal therapy offers improved outcomes for patients with limited metastatic disease.