3.9 Article Proceedings Paper

High incidence of head and neck squamous cell carcinoma in patients with Fanconi Anemia

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AMER MEDICAL ASSOC
DOI: 10.1001/archotol.129.1.106

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  1. NATIONAL CANCER INSTITUTE [T32CA009685, R01CA082678] Funding Source: NIH RePORTER
  2. NATIONAL CENTER FOR RESEARCH RESOURCES [M01RR000102, M01RR006020] Funding Source: NIH RePORTER
  3. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R37HL032987] Funding Source: NIH RePORTER
  4. NCI NIH HHS [R01 CA82678, 5T32 CA09685] Funding Source: Medline
  5. NCRR NIH HHS [M01-RR00102, M01-RR06020] Funding Source: Medline
  6. NHLBI NIH HHS [R37 HL32987] Funding Source: Medline

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Background: Fanconi anemia (FA) is a rare autosomal recessive disorder characterized by a high degree of genomic instability and predisposition to cancer development. Recent evidence suggests that the incidence of head and neck squamous cell carcinoma (HNSCC) may be increased in patients with FA. Objective: To determine the cumulative incidence, tumor distribution, and outcome of HNSCC in patients with FA. Design and Setting: We analyzed data from 754 subjects from the International Fanconi Anemia Registry, a prospectively collected database of patients with FA. Main Outcome Measures: Cumulative incidence of HNSCC and 2-year overall, relapse-free and disease-specific survival. Results: Of the 754 patients in the International Fanconi Anemia Registry, 19 (3%) had HNSCC. This is a significantly higher incidence of HNSCC compared with that observed in the general population (standardized incidence ratio, 500; 95% confidence interval, 300-781) (P<.001). The patients' age ranged from 15 to 49 years (median, 31 years), and there was a 2:1 female predominance. Surgical treatment was well tolerated (n = 17); however, radiation therapy and chemotherapy were associated with significant morbidity and mortality. Of the 19 patients, 10 (53%) developed locoregional recurrences within a median of 16 months from diagnosis. The median follow-up was 29 months. The 2-year disease-specific, overall, and relapse-free survival rates were 49%, 49%, and 42%, respectively. The cumulative incidence of relapse by the age of 40 years was 50%. Conclusions: in patients with FA, there is a high incidence of aggressive HNSCC at a young age. Surgery remains the mainstay of treatment because patients with FA tolerate radiation therapy and chemotherapy poorly, with significant morbidity. An increased understanding of FA-associated malignancies is not only important in the clinical management of patients with FA but can also elucidate the role of chromosomal instability in the development of HNSCC in general.

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