𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A population-based analysis of risk factors for a second primary cutaneous melanoma among melanoma survivors

✍ Scribed by William B. Goggins; Hensin Tsao


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
79 KB
Volume
97
Category
Article
ISSN
0008-543X

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

BACKGROUND

The results of several studies have provided evidence that patients diagnosed with cutaneous melanoma (CM) are at a higher risk of developing a second primary CM than the general population. In this study, the authors examined how the risk of a second primary tumor varied with time from diagnosis of CM and examined the patient‐specific factors that modify a CM patient's risk of developing a second primary tumor.

METHODS

Survival curves for time from first CM to second CM were calculated using the Kaplan–Meier method. The Cox proportional hazards model was used to determine which demographic‐ and disease‐related factors influence the risk of a second CM.

RESULTS

Approximately 0.5% of Surveillance, Epidemiology, and End Results (SEER) CM patients were found to have synchronous second primaries. The estimated cumulative probability of having a second primary CM was 0.99% at 1 year after initial CM diagnosis, 2.06% at 5 years, 3.17% at 10 years, and 5.34% at 20 years. Risk was significantly greater for males; older patients; patients with first CM on the face, neck, or trunk; those from the Atlanta, Hawaii, or Connecticut registries; and more recently diagnosed patients. Risk was lower for patients from the Utah registry and those with Stage IV disease.

CONCLUSIONS

The elevated risk for CM among CM survivors appears to be greatest in the first few months, and then subsequently declines. However, the risk for a second CM among CM survivors was found to remain substantially higher than the risk for a first CM in the general population throughout the observation period (> 20 years). Demographic‐ and disease‐related factors substantially modify the risk of a second primary CM. Cancer 2003;97:639–43. © 2003 American Cancer Society.

DOI 10.1002/cncr.11116


📜 SIMILAR VOLUMES


Nuclear PTEN expression and clinicopatho
✍ David C. Whiteman; Xiao-Ping Zhou; Margaret C. Cummings; Sandra Pavey; Nicholas 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 French ⚖ 438 KB

## Abstract Germline mutations of the __PTEN__ tumor‐suppressor gene, on 10q23, cause Cowden syndrome, an inherited hamartoma syndrome with a high risk of breast, thyroid and endometrial carcinomas and, some suggest, melanoma. To date, most studies which strongly implicate PTEN in the etiology of s

Melanocortin 1 receptor and risk of cuta
✍ Patricia F. Williams; Catherine M. Olsen; Nicholas K. Hayward; David C. Whiteman 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 French ⚖ 472 KB 👁 1 views

Polymorphisms in the melanocortin 1 receptor (MC1R) gene have been associated with increased risks of melanoma, but different approaches to study design, analysis, and reporting have hindered comparisons of findings. We aimed to harmonize the published data by conducting a systematic review and meta

Invasive cutaneous malignant melanoma in
✍ Christer Lindholm; Ronny Andersson; Monika Dufmats; Johan Hansson; Christian Ing 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 268 KB 👁 1 views

## Abstract ## BACKGROUND The objective of the current study was to compile prospective, population‐based data on cutaneous invasive melanomas in Sweden during the period from 1990 to 1999, to describe and analyze survival data and prognostic factors, and to make comparisons with previously publis

Risk of radiation-related salivary gland
✍ Houda Boukheris; Elaine Ron; Graça M. Dores; Marilyn Stovall; Susan A. Smith; Ro 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 87 KB 👁 2 views

## Abstract ## BACKGROUND. Radiotherapy for Hodgkin lymphoma (HL) increases the risk of salivary gland carcinomas (SGC). To the authors' knowledge, however, the magnitude of the risk has not been assessed to date. ## METHODS. The risks of SGC among 20,928 1‐year survivors of HL who were diagnose