2019
DOI: 10.1002/cam4.2276
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Prognosis and cure of long‐term cancer survivors: A population‐based estimation

Abstract: Background Increasing evidence of cure for some neoplasms has emerged in recent years. The study aimed to estimate population‐based indicators of cancer cure. Methods Information on more than half a million cancer patients aged 15‐74 years collected by population‐based Italian cancer registries and mixture cure models were used to estimate the life expectancy of fatal tumors (LEFT), proportions of patients with similar death rates of the general population (cure fractio… Show more

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Cited by 27 publications
(29 citation statements)
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References 32 publications
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“…This study used data collected by the network of population-based Italian cancer registries [8], which agreed to participate in the study and with at least 18 years of cancer registration as of December 31, 2011 (i.e., Ferrara, Genova, Modena, Parma, Ragusa, Sassari, Varese, and Veneto, representing 10% of the entire Italian population in 2010) [8], [12].…”
Section: Methodsmentioning
confidence: 99%
“…This study used data collected by the network of population-based Italian cancer registries [8], which agreed to participate in the study and with at least 18 years of cancer registration as of December 31, 2011 (i.e., Ferrara, Genova, Modena, Parma, Ragusa, Sassari, Varese, and Veneto, representing 10% of the entire Italian population in 2010) [8], [12].…”
Section: Methodsmentioning
confidence: 99%
“…In 2019 it was estimated that about 3.5 million Italians (5.3% of the entire population) are living after a cancer diagnosis [1]. Improvements in medical treatments have led to a substantial increase in the proportion of cancer patients with death rates similar to those of the general Italian population [2].…”
Section: Introductionmentioning
confidence: 99%
“…A limitation of this study is that the Barcelona Clinic system routinely used by clinicians to stage HCC is not usually available in population-based cancer registry [51]. A further limitation is related to the lack of information for population-based cancer registries on the aetiology of primary liver tumours (viral, non-viral), which is relevant for clinical progression.…”
Section: Discussionmentioning
confidence: 99%
“…Clinical registries play an import role in identifying priorities to improve access to care [55][56][57] and clinical outcomes [10,58,59] of liver cancer patients with poor access to care. This study emphasises how populationbased cancer registries can play a supportive role in meeting the increasing need to prioritise cancer control measures [46].…”
Section: Discussionmentioning
confidence: 99%