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Survival between synchronous and non-synchronous multiple primary cutaneous melanomas-a SEER database analysis
Jie Xiong1,2, Yanlin Su3, Zhitong Bing4
1Department of Mathematics and Computer Science, Changsha University, Changsha, Hunan, China.
Synchronous multiple primary cutaneous melanomas (MPMs) occurring within 2 months have significantly poorer survival rates. This finding helps distinguish synchronous from non-synchronous MPMs and identify a key risk factor for cutaneous melanoma prognosis.
Area of Science:
- Oncology
- Dermatology
- Biostatistics
Background:
- Distinguishing synchronous and non-synchronous multiple primary cutaneous melanomas (MPMs) lacks established criteria.
- Accurate differentiation is crucial for prognostic assessment and treatment planning in melanoma patients.
Purpose of the Study:
- To establish criteria for distinguishing synchronous from non-synchronous MPMs.
- To compare the survival outcomes between synchronous and non-synchronous MPMs.
- To identify the prognostic significance of synchronous MPM occurrence.
Main Methods:
- Utilized the Surveillance, Epidemiology, and End Results (SEER) database.
- Applied piecewise linear regression to the time interval between first and second primary cutaneous melanomas (TIFtS) distribution.
- Employed Kaplan-Meier and Cox proportional hazard models for survival analysis, treating synchronous MPM occurrence as a time-dependent variable.
Main Results:
- The time interval distribution suggested a 2-month threshold for defining synchronous MPMs.
- Synchronous MPMs demonstrated significantly inferior overall and melanoma-specific survival compared to non-synchronous MPMs (P < 0.0001).
- The occurrence of synchronous MPM was identified as a significant risk factor for overall survival in cutaneous melanoma (HR: 2.213, P < 0.0001).
Conclusions:
- Provides data-driven evidence supporting the use of a 2-month interval to differentiate synchronous MPMs.
- Confirms that synchronous MPM occurrence is a critical risk factor impacting patient prognosis in cutaneous melanoma.
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