4.6 Article

Patterns of distant metastases in 215 Merkel cell carcinoma patients: Implications for prognosis and surveillance

期刊

CANCER MEDICINE
卷 9, 期 4, 页码 1374-1382

出版社

WILEY
DOI: 10.1002/cam4.2781

关键词

carcinoma; Merkel cell; dermatology; medical oncology; neoplasm metastasis; neoplasm staging; prognosis; radiology

类别

资金

  1. NIH/NCI [R01-CA162522, K24-CA139052]
  2. NIH/NCI Cancer Center Support Grant [P30-CA015704, 5P01-CA225517]
  3. MCC patient gift fund at University of Washington
  4. Kelsey Dickson Team Science Challenge Grant
  5. Prostate Cancer Foundation
  6. American Cancer Society Arlene Garrison Medical Student Summer Fellowship

向作者/读者索取更多资源

Approximately one-third of Merkel cell carcinoma (MCC) patients eventually develop distant metastatic disease. Little is known about whether the location of the primary lesion is predictive of initial distant metastatic site, or if survival likelihood differs depending on the metastatic site. Such data could inform imaging/surveillance practices and improve prognostic accuracy. Multivariate and competing-risk analyses were performed on a cohort of 215 MCC patients with distant metastases, 31% of whom had two or more initial sites of distant metastasis. At time of initial distant metastasis in the 215 patients, metastatic sites (n = 305) included non-regional lymph nodes (present in 41% of patients), skin/body wall (25%), liver (23%), bone (21%), pancreas (8%), lung (7%), and brain (5%). Among the 194 patients who presented with MCC limited to local or regional sites (stage I-III) but who ultimately developed distant metastases, distant progression occurred in 49% by 1 year and in 80% by 2 years following initial diagnosis. Primary MCC locations differed in how likely they were to metastasize to specific organs/sites (P < .001). For example, liver metastases were far more likely from a head/neck primary (43% of 58 patients) versus a lower limb primary (5% of 39 patients; P < .0001). Skin-only distant metastasis was associated with lower MCC-specific mortality as compared to metastases in multiple organs/sites (HR 2.7; P = .003), in the liver (HR 2.1; P = .05), or in distant lymph nodes (HR 2.0; P = .045). These data reflect outcomes before PD1-pathway inhibitor availability, which may positively impact survival. In conclusion, primary MCC location is associated with a pattern of distant spread, which may assist in optimizing surveillance. Because it is linked to survival, the site of initial distant metastasis should be considered when assessing prognosis.

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