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These studies suggest that basal cell carcinoma and squamous cell carcinoma differ in chromosome loss patterns, prevalence, prognostic factors, and treatment options, with surgical removal being most effective for basal cell carcinoma and immunotherapeutic agents being developed for both.
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Basal cell carcinoma (BCC) and squamous cell carcinoma (SCC) are the two most common types of non-melanoma skin cancers. Both originate from the epidermis but exhibit distinct clinical, pathological, and molecular characteristics .
BCC is the most prevalent cancer in the United States, with an annual incidence nearing 2 million cases. In contrast, SCC, while also common, has a lower incidence rate. A population-based study in Olmsted County, Minnesota, reported age-adjusted incidence rates of 360.0 per 100,000 person-years for BCC in men and 292.9 in women, compared to 207.5 for SCC in men and 128.8 in women. The incidence of both cancers has been increasing over time, with a notable rise in SCC cases relative to BCC.
BCC and SCC exhibit distinct patterns of chromosome loss. BCCs typically show chromosome loss confined to a single chromosome arm, particularly 9q. In contrast, SCCs display more widespread chromosomal losses, including frequent loss of heterozygosity on chromosome arms 9p, 13q, 17p, 17q, and 3p. These differences suggest that the genetic mechanisms driving the development of these cancers are distinct.
The tumor microenvironment (TME) plays a crucial role in the progression of both BCC and SCC. Both types of carcinoma create an immunosuppressed environment by downregulating effector CD4+ and CD8+ T cells and promoting the release of pro-oncogenic Th2 cytokines. This understanding has led to the development of immunotherapeutic agents such as vismodegib for BCC and cemiplimab for SCC.
Clinically, BCCs are often less aggressive but can cause significant disfigurement if not treated properly. SCCs, on the other hand, have a higher potential for metastasis and recurrence. Histologically, BCCs and SCCs can sometimes be challenging to differentiate, especially poorly differentiated SCCs that may assume a basaloid phenotype. Immunohistochemical markers such as Ber-EP4 and MOC-31 are useful in distinguishing between these two types of carcinomas.
Surgical removal is considered the gold standard for treating BCC, but various other treatments are available, including photodynamic therapy and topical medications. The choice of treatment depends on multiple factors, including the patient's age, tumor size, and location. For SCC, treatment options also include surgical excision, radiation therapy, and systemic therapies for advanced cases.
Prognostic factors for both BCC and SCC include tumor size, depth of invasion, and histological subtype. SCCs have a higher risk of recurrence and metastasis compared to BCCs. The anatomical distribution of these cancers has also shifted over time, with BCCs now more commonly found on the torso and SCCs on the extremities.
While BCC and SCC share some similarities as non-melanoma skin cancers, they are distinct in their epidemiology, molecular characteristics, tumor microenvironment, clinical presentation, and treatment options. Understanding these differences is crucial for effective diagnosis, treatment, and management of these common skin cancers.
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