Lethal Prostate Cancer in Mexico: Data from the Can.Prost Mexican Registry and a Project for Early Detection
Epidemiological data are crucial for adopting primary and secondary prevention strategies and to develop screening protocols against prostate cancer (PCa). Despite the comprehensive characterization of PCa across White and Black men, there is a lack of data from the Mexican population. This manuscri...
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creator | Jimenez Rios, Miguel Angel Scavuzzo, Anna Noverón, Nancy Reynoso García Arango, Caleb Calvo Vazquez, Ivan Hurtado Vázquez, Alonso Arrieta Rodriguez, Oscar Gerardo Davila, Miguel Angel Jimenez Sighinolfi, Maria Chiara Rocco, Bernardo |
description | Epidemiological data are crucial for adopting primary and secondary prevention strategies and to develop screening protocols against prostate cancer (PCa). Despite the comprehensive characterization of PCa across White and Black men, there is a lack of data from the Mexican population. This manuscript presents data from the Can.Prost registry that captures PCa trends over the past two decades in Mexico City; furthermore, we aimed to compare clinical differences and oncological outcomes before and after the promotion of early detection actions through a campaign against PCa that occurred in 2014.
A retrospective observational study on newly diagnosed Mexican PCa patients was carried out at the Instituto Nacional de Cancerología (INCan) in Mexico City. During 2014 and 2015, a project for the early diagnosis of PCa ("OPUS program") was launched in the aforementioned tertiary hospital. Starting at the age of 45 years, all men were invited for a PSA measurement and a specialist urologist consultation. All individuals with clinical or biochemical suspicion of PCa (PSA > 4 ng/mL), in the context of age and prostate volume, underwent ultrasound-guided transrectal prostate biopsy. Then, patients with pathologically confirmed prostate cancer were stratified according to the year of diagnosis: Group A accounted for those diagnosed between 2000 and 2014 and Group B for those patients diagnosed in the timeframe of 2015-2021. Comparisons of PCa characteristics, treatment modalities and oncologic outcomes between Group A and B were performed.
Overall, we collected data from 2759 PCa patients from 2000 to 2021. The median PSA at baseline was 32 ng/mL, and 25% had a family history of PCa. Overall, 25.8% were asymptomatic and 46% had a non-metastatic presentation. After the OPUS campaign, PSA at diagnosis was significantly lower across all age groups. The incidence of PCa diagnosis in asymptomatic men was higher (31.4% vs. 19.9%) and a higher proportion of men were diagnosed with organ-confined, palpable disease (46% vs. 28%) (
< 0.001). The rate of patients eligible for active/radical treatment was higher after the OPUS campaign (patients who received surgery increased from 12.78% to 32.41%; patients who underwent radiation increased from 28.38% to 49.61%). The proportion of patients diagnosed with non-clinically significant disease was negligible and remained stable across time.
PCa in Mexican patients displays aggressive features at diagnosis, whereas the rate of non-sig |
doi_str_mv | 10.3390/cancers16213675 |
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A retrospective observational study on newly diagnosed Mexican PCa patients was carried out at the Instituto Nacional de Cancerología (INCan) in Mexico City. During 2014 and 2015, a project for the early diagnosis of PCa ("OPUS program") was launched in the aforementioned tertiary hospital. Starting at the age of 45 years, all men were invited for a PSA measurement and a specialist urologist consultation. All individuals with clinical or biochemical suspicion of PCa (PSA > 4 ng/mL), in the context of age and prostate volume, underwent ultrasound-guided transrectal prostate biopsy. Then, patients with pathologically confirmed prostate cancer were stratified according to the year of diagnosis: Group A accounted for those diagnosed between 2000 and 2014 and Group B for those patients diagnosed in the timeframe of 2015-2021. Comparisons of PCa characteristics, treatment modalities and oncologic outcomes between Group A and B were performed.
Overall, we collected data from 2759 PCa patients from 2000 to 2021. The median PSA at baseline was 32 ng/mL, and 25% had a family history of PCa. Overall, 25.8% were asymptomatic and 46% had a non-metastatic presentation. After the OPUS campaign, PSA at diagnosis was significantly lower across all age groups. The incidence of PCa diagnosis in asymptomatic men was higher (31.4% vs. 19.9%) and a higher proportion of men were diagnosed with organ-confined, palpable disease (46% vs. 28%) (
< 0.001). The rate of patients eligible for active/radical treatment was higher after the OPUS campaign (patients who received surgery increased from 12.78% to 32.41%; patients who underwent radiation increased from 28.38% to 49.61%). The proportion of patients diagnosed with non-clinically significant disease was negligible and remained stable across time.
PCa in Mexican patients displays aggressive features at diagnosis, whereas the rate of non-significant disease is negligible. The introduction of early detection strategies may lead to lower symptomatic and metastatic PCa and higher opportunities for radical treatment. This emphasizes the need for public awareness and for adjustment of screening strategies to the peculiarities of the Mexican population.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers16213675</identifier><identifier>PMID: 39518113</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Age groups ; Asymptomatic ; Biopsy ; Cancer therapies ; Chemotherapy ; Education ; Epidemiology ; Family medical history ; Hospitals ; Metastases ; Metastasis ; Mortality ; Prostate cancer ; Radiation therapy ; Risk factors ; Surgery ; Ultrasonic imaging</subject><ispartof>Cancers, 2024-10, Vol.16 (21), p.3675</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2024 by the authors. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c373t-4b897fe9afb822db2fb43b585a3518a44008c87b86746ece9583c1f5bcd5158f3</cites><orcidid>0000-0001-9558-8086</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11544922/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11544922/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39518113$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jimenez Rios, Miguel Angel</creatorcontrib><creatorcontrib>Scavuzzo, Anna</creatorcontrib><creatorcontrib>Noverón, Nancy Reynoso</creatorcontrib><creatorcontrib>García Arango, Caleb</creatorcontrib><creatorcontrib>Calvo Vazquez, Ivan</creatorcontrib><creatorcontrib>Hurtado Vázquez, Alonso</creatorcontrib><creatorcontrib>Arrieta Rodriguez, Oscar Gerardo</creatorcontrib><creatorcontrib>Davila, Miguel Angel Jimenez</creatorcontrib><creatorcontrib>Sighinolfi, Maria Chiara</creatorcontrib><creatorcontrib>Rocco, Bernardo</creatorcontrib><title>Lethal Prostate Cancer in Mexico: Data from the Can.Prost Mexican Registry and a Project for Early Detection</title><title>Cancers</title><addtitle>Cancers (Basel)</addtitle><description>Epidemiological data are crucial for adopting primary and secondary prevention strategies and to develop screening protocols against prostate cancer (PCa). Despite the comprehensive characterization of PCa across White and Black men, there is a lack of data from the Mexican population. This manuscript presents data from the Can.Prost registry that captures PCa trends over the past two decades in Mexico City; furthermore, we aimed to compare clinical differences and oncological outcomes before and after the promotion of early detection actions through a campaign against PCa that occurred in 2014.
A retrospective observational study on newly diagnosed Mexican PCa patients was carried out at the Instituto Nacional de Cancerología (INCan) in Mexico City. During 2014 and 2015, a project for the early diagnosis of PCa ("OPUS program") was launched in the aforementioned tertiary hospital. Starting at the age of 45 years, all men were invited for a PSA measurement and a specialist urologist consultation. All individuals with clinical or biochemical suspicion of PCa (PSA > 4 ng/mL), in the context of age and prostate volume, underwent ultrasound-guided transrectal prostate biopsy. Then, patients with pathologically confirmed prostate cancer were stratified according to the year of diagnosis: Group A accounted for those diagnosed between 2000 and 2014 and Group B for those patients diagnosed in the timeframe of 2015-2021. Comparisons of PCa characteristics, treatment modalities and oncologic outcomes between Group A and B were performed.
Overall, we collected data from 2759 PCa patients from 2000 to 2021. The median PSA at baseline was 32 ng/mL, and 25% had a family history of PCa. Overall, 25.8% were asymptomatic and 46% had a non-metastatic presentation. After the OPUS campaign, PSA at diagnosis was significantly lower across all age groups. The incidence of PCa diagnosis in asymptomatic men was higher (31.4% vs. 19.9%) and a higher proportion of men were diagnosed with organ-confined, palpable disease (46% vs. 28%) (
< 0.001). The rate of patients eligible for active/radical treatment was higher after the OPUS campaign (patients who received surgery increased from 12.78% to 32.41%; patients who underwent radiation increased from 28.38% to 49.61%). The proportion of patients diagnosed with non-clinically significant disease was negligible and remained stable across time.
PCa in Mexican patients displays aggressive features at diagnosis, whereas the rate of non-significant disease is negligible. The introduction of early detection strategies may lead to lower symptomatic and metastatic PCa and higher opportunities for radical treatment. This emphasizes the need for public awareness and for adjustment of screening strategies to the peculiarities of the Mexican population.</description><subject>Age groups</subject><subject>Asymptomatic</subject><subject>Biopsy</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Education</subject><subject>Epidemiology</subject><subject>Family medical history</subject><subject>Hospitals</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Mortality</subject><subject>Prostate cancer</subject><subject>Radiation therapy</subject><subject>Risk factors</subject><subject>Surgery</subject><subject>Ultrasonic imaging</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptks9vVCEQx4nR2Kb27M2QePGy28cDHuDFNNv6I1mjMXomPN6wy-Y9qMAa97-X3a21bYQDk5nPfGGYQeglaeaUqubCmmAhZdK1hHaCP0GnbSPaWdcp9vSefYLOc940dVFKRCeeoxOqOJGE0FM0LqGszYi_ppiLKYAXB1HsA_4Mv72Nb_GVKQa7FCdc1of4_AAf4ybgb7DyuaQdNmHAZq-0AVuwiwlfmzTu8BWU6vAxvEDPnBkznN-eZ-jH--vvi4-z5ZcPnxaXy5mlgpYZ66USDpRxvWzboW9dz2jPJTe0Ptsw1jTSStHLTrAOLCguqSWO93bghEtHz9C7o-7Ntp9gsBBKMqO-SX4yaaej8fphJPi1XsVfmhDOmGrbqvDmViHFn1vIRU8-WxhHEyBus6aklYKx7oC-foRu4jaFWt-e4kpx1qh_1MqMoH1wsV5s96L6UhJOGaOSVmr-H6ruAabaiwDOV_-DhItjgq0tyQncXZGk0fsh0Y-GpGa8uv83d_zfkaB_AN5at10</recordid><startdate>20241030</startdate><enddate>20241030</enddate><creator>Jimenez Rios, Miguel Angel</creator><creator>Scavuzzo, Anna</creator><creator>Noverón, Nancy Reynoso</creator><creator>García Arango, Caleb</creator><creator>Calvo Vazquez, Ivan</creator><creator>Hurtado Vázquez, Alonso</creator><creator>Arrieta Rodriguez, Oscar Gerardo</creator><creator>Davila, Miguel Angel Jimenez</creator><creator>Sighinolfi, Maria Chiara</creator><creator>Rocco, Bernardo</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9558-8086</orcidid></search><sort><creationdate>20241030</creationdate><title>Lethal Prostate Cancer in Mexico: Data from the Can.Prost Mexican Registry and a Project for Early Detection</title><author>Jimenez Rios, Miguel Angel ; Scavuzzo, Anna ; Noverón, Nancy Reynoso ; García Arango, Caleb ; Calvo Vazquez, Ivan ; Hurtado Vázquez, Alonso ; Arrieta Rodriguez, Oscar Gerardo ; Davila, Miguel Angel Jimenez ; Sighinolfi, Maria Chiara ; Rocco, Bernardo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c373t-4b897fe9afb822db2fb43b585a3518a44008c87b86746ece9583c1f5bcd5158f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Age groups</topic><topic>Asymptomatic</topic><topic>Biopsy</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Education</topic><topic>Epidemiology</topic><topic>Family medical history</topic><topic>Hospitals</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Mortality</topic><topic>Prostate cancer</topic><topic>Radiation therapy</topic><topic>Risk factors</topic><topic>Surgery</topic><topic>Ultrasonic imaging</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jimenez Rios, Miguel Angel</creatorcontrib><creatorcontrib>Scavuzzo, Anna</creatorcontrib><creatorcontrib>Noverón, Nancy Reynoso</creatorcontrib><creatorcontrib>García Arango, Caleb</creatorcontrib><creatorcontrib>Calvo Vazquez, Ivan</creatorcontrib><creatorcontrib>Hurtado Vázquez, Alonso</creatorcontrib><creatorcontrib>Arrieta Rodriguez, Oscar Gerardo</creatorcontrib><creatorcontrib>Davila, Miguel Angel Jimenez</creatorcontrib><creatorcontrib>Sighinolfi, Maria Chiara</creatorcontrib><creatorcontrib>Rocco, Bernardo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jimenez Rios, Miguel Angel</au><au>Scavuzzo, Anna</au><au>Noverón, Nancy Reynoso</au><au>García Arango, Caleb</au><au>Calvo Vazquez, Ivan</au><au>Hurtado Vázquez, Alonso</au><au>Arrieta Rodriguez, Oscar Gerardo</au><au>Davila, Miguel Angel Jimenez</au><au>Sighinolfi, Maria Chiara</au><au>Rocco, Bernardo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lethal Prostate Cancer in Mexico: Data from the Can.Prost Mexican Registry and a Project for Early Detection</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2024-10-30</date><risdate>2024</risdate><volume>16</volume><issue>21</issue><spage>3675</spage><pages>3675-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>Epidemiological data are crucial for adopting primary and secondary prevention strategies and to develop screening protocols against prostate cancer (PCa). Despite the comprehensive characterization of PCa across White and Black men, there is a lack of data from the Mexican population. This manuscript presents data from the Can.Prost registry that captures PCa trends over the past two decades in Mexico City; furthermore, we aimed to compare clinical differences and oncological outcomes before and after the promotion of early detection actions through a campaign against PCa that occurred in 2014.
A retrospective observational study on newly diagnosed Mexican PCa patients was carried out at the Instituto Nacional de Cancerología (INCan) in Mexico City. During 2014 and 2015, a project for the early diagnosis of PCa ("OPUS program") was launched in the aforementioned tertiary hospital. Starting at the age of 45 years, all men were invited for a PSA measurement and a specialist urologist consultation. All individuals with clinical or biochemical suspicion of PCa (PSA > 4 ng/mL), in the context of age and prostate volume, underwent ultrasound-guided transrectal prostate biopsy. Then, patients with pathologically confirmed prostate cancer were stratified according to the year of diagnosis: Group A accounted for those diagnosed between 2000 and 2014 and Group B for those patients diagnosed in the timeframe of 2015-2021. Comparisons of PCa characteristics, treatment modalities and oncologic outcomes between Group A and B were performed.
Overall, we collected data from 2759 PCa patients from 2000 to 2021. The median PSA at baseline was 32 ng/mL, and 25% had a family history of PCa. Overall, 25.8% were asymptomatic and 46% had a non-metastatic presentation. After the OPUS campaign, PSA at diagnosis was significantly lower across all age groups. The incidence of PCa diagnosis in asymptomatic men was higher (31.4% vs. 19.9%) and a higher proportion of men were diagnosed with organ-confined, palpable disease (46% vs. 28%) (
< 0.001). The rate of patients eligible for active/radical treatment was higher after the OPUS campaign (patients who received surgery increased from 12.78% to 32.41%; patients who underwent radiation increased from 28.38% to 49.61%). The proportion of patients diagnosed with non-clinically significant disease was negligible and remained stable across time.
PCa in Mexican patients displays aggressive features at diagnosis, whereas the rate of non-significant disease is negligible. The introduction of early detection strategies may lead to lower symptomatic and metastatic PCa and higher opportunities for radical treatment. This emphasizes the need for public awareness and for adjustment of screening strategies to the peculiarities of the Mexican population.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>39518113</pmid><doi>10.3390/cancers16213675</doi><orcidid>https://orcid.org/0000-0001-9558-8086</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Age groups Asymptomatic Biopsy Cancer therapies Chemotherapy Education Epidemiology Family medical history Hospitals Metastases Metastasis Mortality Prostate cancer Radiation therapy Risk factors Surgery Ultrasonic imaging |
title | Lethal Prostate Cancer in Mexico: Data from the Can.Prost Mexican Registry and a Project for Early Detection |
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