Rare and aggressive form of adenocarcinoma with cells that resemble signet rings.
Colon and rectum
Signet ring cell
Origin: Glandular cells
Grade: High
Severity: High
Molecular Marker: KRAS, BRAF, MSI
Age Range: 20-70 years
Life Expectancy: 1-2 years
Signet Ring Cell Carcinoma (SRCC) is a rare and aggressive form of colorectal cancer characterized by the presence of signet ring cells. These cells contain a large vacuole, displacing the nucleus to one side, resembling a signet ring. This carcinoma typically occurs in the colon and rectum, but can also be found in other parts of the gastrointestinal tract.
Patients with Signet Ring Cell Carcinoma may experience symptoms similar to other forms of colorectal cancer, including:
Due to its aggressive nature, symptoms may progress rapidly, often leading to a late-stage diagnosis.
Surgery: Surgical resection of the tumor is the primary treatment for localized SRCC. Depending on the location and extent of the cancer, procedures may include partial colectomy or proctectomy.
Chemotherapy: Adjuvant chemotherapy is often recommended, particularly for advanced stages. Common regimens include:
Radiation Therapy: This can be used in combination with surgery and chemotherapy, especially in rectal cancer, to shrink the tumor before surgery or eliminate remaining cancer cells post-surgery.
Immunotherapy: Some studies are exploring the use of checkpoint inhibitors like pembrolizumab for treating SRCC, especially in cases with high microsatellite instability (MSI). These treatments are still largely experimental for SRCC but have shown promise in other types of cancer.
Clinical Trials: Ongoing trials are investigating new drug combinations, immunotherapy, and novel targeted therapies specifically for SRCC, aiming to improve outcomes for this aggressive cancer type.
As research progresses, the understanding and management of Signet Ring Cell Carcinoma continue to evolve, offering hope for improved outcomes through innovative treatments.