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Tumor Progression02:07

Tumor Progression

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Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
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[Progress in pulmonary enteric adenocarcinoma].

Y Zuo1, H Bai1, J M Ying2

  • 1Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.

Zhonghua Zhong Liu Za Zhi [Chinese Journal of Oncology]
|April 21, 2022
PubMed
Summary
This summary is machine-generated.

Pulmonary enteric adenocarcinoma (PEAC) is a rare lung cancer subtype mimicking colorectal cancer. Current research highlights its distinct molecular profile and clinical features, guiding treatment towards non-small cell lung cancer (NSCLC) therapies.

Keywords:
Clinical pathologyEnteric adenocarcinomaLung neoplasmsPathogenesis

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Area of Science:

  • Pulmonary Medicine
  • Oncology
  • Pathology

Background:

  • Pulmonary enteric adenocarcinoma (PEAC) is a rare histologic subtype of primary lung adenocarcinoma, characterized by an enteric component exceeding 50%.
  • PEAC shares morphological and immunohistochemical features with colorectal cancer, posing diagnostic challenges in differentiating it from lung metastatic colorectal cancer.
  • Potential origins include intestinal metaplasia of respiratory basal cells, possibly influenced by factors like smoking.

Purpose of the Study:

  • To summarize the key characteristics of pulmonary enteric adenocarcinoma.
  • To highlight diagnostic challenges and current understanding of its molecular and clinical features.
  • To inform treatment strategies and identify areas for future research.

Main Methods:

  • Review of existing literature on pulmonary enteric adenocarcinoma.
  • Analysis of reported immunohistochemical markers (CK7, CDX2, CK20, TTF1).
  • Compilation of clinical data including age, sex, smoking history, and lesion location.

Main Results:

  • KRAS mutations are frequently observed, while other driver mutations are rare.
  • Immunohistochemistry shows high positivity for CK7 (88.2%) and CDX2 (78.1%), with lower rates for CK20 (48.2%) and TTF1 (38.8%).
  • Clinical features include a mean onset age of 62 years, male predominance (56.5%), high smoking prevalence (78.8%), and frequent upper right lobe location (41.4%).

Conclusions:

  • Pulmonary enteric adenocarcinoma presents unique diagnostic and therapeutic considerations.
  • Current treatment recommendations align with non-small cell lung cancer (NSCLC) regimens.
  • Further research into molecular features, pathogenesis, and optimal therapies, including targeted and immunotherapy, is urgently needed.