# Two cases of gastric cancer with elevated serum levels of KL-6

**Authors:** Naoe Yanagisawa, Naohiko Koide, Harunari Fukai, Yoshinori Koyama, Yuu Ogihara, Maki Ohya

PMC · DOI: 10.1186/s40792-024-01883-0 · 2024-04-09

## TL;DR

Two gastric cancer patients with elevated KL-6 levels showed tumor and biomarker response to chemotherapy, suggesting KL-6 may also act as a cancer marker.

## Contribution

Reports two rare gastric cancer cases with elevated KL-6 and demonstrates KL-6's potential as a tumor marker in metastatic gastric cancer.

## Key findings

- Elevated KL-6 levels in gastric cancer patients decreased with chemotherapy, indicating treatment response.
- KL-6 may serve as a tumor marker in metastatic gastric cancer, beyond its role in interstitial pneumonia.
- Chemotherapy response correlated with KL-6 reduction in both patients, though one later developed interstitial pneumonia.

## Abstract

The serum level of Krebs von den Lungen-6 (sKL-6) is a biomarker of interstitial pneumonia and has been reported to be elevated in patients with cancers. However, there have been few cases of gastric cancer (GC) with elevated sKL-6 that were treated by chemotherapy. We herein report two cases of GC with elevated sKL-6 that were treated with oxaliplatin plus S-1 (SOX) chemotherapy and discussed the resulting changes in sKL-6.

The first patient was a 79-year-old woman complaining of loss of appetite. Esophagogastroduodenoscopy (EGD) showed a type-3 tumor in the gastric antrum and biopsy specimens showed adenocarcinoma. Computed tomography (CT) showed multiple liver metastases. sKL-6 was elevated to 1,292 U/ml, but a CT revealed no obvious lesions of the lungs, including interstitial pneumonia. The tumor was diagnosed as GC with liver metastases and elevated sKL-6. Respiratory function data were normal. SOX therapy using oxaliplatin and S-1 was performed. After 3 courses of SOX therapy, CT showed reductions of the liver metastases as well as the primary tumor, and sKL-6 was decreased to 201 U/ml. After the 44 courses, sKL-6 was slightly elevated. Chest CT showed interstitial pneumonia and chemotherapy was stopped. The patient is still alive without any metastasis 72 months later. The second patient was a 69-year-old woman complaining of upper abdominal pain. EGD revealed a type-3 tumor in the gastric antrum showing adenocarcinoma with HER2-positive pathology. CT showed multiple node metastases around the abdominal aorta. sKL-6 was elevated to 2,239 U/ml, but a respiratory function test showed no abnormalities, and CT of the lungs showed no obvious lesions. The tumor was diagnosed as GC with distant node metastases and elevated sKL-6. The patient received SOX therapy combined with trastuzumab. After 6 courses, the size of the primary tumor and multiple node metastases were reduced, and sKL-6 was decreased to 284 U/ml.

These two cases suggest that sKL-6 may be important not only as an indicator of interstitial pneumonia in chemotherapeutic courses, but also as a tumor marker in GC patients with multiple metastases.

## Linked entities

- **Proteins:** MUC1 (mucin 1, cell surface associated)
- **Chemicals:** oxaliplatin (PubChem CID 9887053), S-1 (PubChem CID 1497102)
- **Diseases:** gastric cancer (MONDO:0001056), adenocarcinoma (MONDO:0004970)

## Full-text entities

- **Genes:** MUC1 (mucin 1, cell surface associated) [NCBI Gene 4582] {aka ADMCKD, ADMCKD1, ADTKD2, CA 15-3, CD227, Ca15-3}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}
- **Diseases:** abdominal pain (MESH:D015746), distant node metastases (MESH:D008207), GC (MESH:D013274), PRESENTATION (MESH:D001946), adenocarcinoma (MESH:D000230), loss of appetite (MESH:D001068), liver metastases (MESH:D009362), cancers (MESH:D009369), type-3 tumor (MESH:C565335), interstitial pneumonia (MESH:D017563)
- **Chemicals:** S-1 (-), trastuzumab (MESH:D000068878), oxaliplatin (MESH:D000077150)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11003941/full.md

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Source: https://tomesphere.com/paper/PMC11003941