Martín Angel, Berenice Freile, Andres Rodriguez, Federico Cayol, Ray Manneh Kopp, Patricia Rioja, Tomas Soule, Federico Losco, Laura Bernal Vaca, Jose Mauricio Penaloza, Maycos Leandro Zapata Muñoz, Silvia Patricia Neciosup, Roger Rodrigo Sanchez, Carolina Passarella, Elvio Guerreño, Diego Farelluk, Ernesto Maturana Leiva, Martin Zarba, Maria Teresa Bourlon, Mauricio Mora Pineda, Juan Pablo Sade
{"title":"拉丁美洲人群中的前列腺癌基因组图谱。","authors":"Martín Angel, Berenice Freile, Andres Rodriguez, Federico Cayol, Ray Manneh Kopp, Patricia Rioja, Tomas Soule, Federico Losco, Laura Bernal Vaca, Jose Mauricio Penaloza, Maycos Leandro Zapata Muñoz, Silvia Patricia Neciosup, Roger Rodrigo Sanchez, Carolina Passarella, Elvio Guerreño, Diego Farelluk, Ernesto Maturana Leiva, Martin Zarba, Maria Teresa Bourlon, Mauricio Mora Pineda, Juan Pablo Sade","doi":"10.1200/GO.24.00072","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>This study aims to describe genomic characteristics of patients with metastatic prostate cancer (mPC).</p><p><strong>Patients and methods: </strong>This study is a retrospective, multicenter cohort study of patients with mPC and reports on genomic testing. Patients were included from 12 academic centers in five countries.</p><p><strong>Results: </strong>A total of 349 patients with PC were included in this study. Most patients (209, 59.9%) were de novo metastatic. Genomic analysis was performed in 233 (66.6%) patients in the metastatic castration-resistant prostate cancer (mCRPC) setting, and only 115 (32.8%) patients had a tumor evaluation in the metastatic hormone sensitive prostate cancer scenario. The evaluation of somatic and/or germline mutations was performed through multigene panel analyses in 290 (83.09%) patients, and next-generation sequencing of <i>BRCA1</i> and <i>BRCA2</i> genes was performed in 59 (16.91%) patients. Analyzing the mCRPC subgroup, with a median follow-up of 15.6 months (IQR, 14-19.06), the median progression-free survival (PFS) was not reached (NR) and the PFS at 16 months was 58.7% (95% CI, 50.8 to 67.8). When comparing patients with <i>BRCA</i> mutations with those who are not <i>BRCA</i>-mutated in the mCRPC scenario, the median PFS was NR (95% CI, 14 to NR) and 26.3 months (95% CI, 16.7 to 36.5; <i>P</i> = .2), respectively. Two of six patients with <i>BRCA</i> mutations were treated with targeted therapies (poly-ADP-ribose polymerase inhibitors).</p><p><strong>Conclusion: </strong>Our study, to the best of our knowledge, represents one of the larger data sets for somatic testing in patients with PC in Latin America (LATAM). It adds valuable information to the growing body of knowledge about the genomic landscape of advanced PC in real-world daily practice scenarios in LATAM countries, which are not always well-represented in large-scale randomized clinical trials.</p>","PeriodicalId":14806,"journal":{"name":"JCO Global Oncology","volume":"10 ","pages":"e2400072"},"PeriodicalIF":3.2000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genomic Landscape in Prostate Cancer in a Latin American Population.\",\"authors\":\"Martín Angel, Berenice Freile, Andres Rodriguez, Federico Cayol, Ray Manneh Kopp, Patricia Rioja, Tomas Soule, Federico Losco, Laura Bernal Vaca, Jose Mauricio Penaloza, Maycos Leandro Zapata Muñoz, Silvia Patricia Neciosup, Roger Rodrigo Sanchez, Carolina Passarella, Elvio Guerreño, Diego Farelluk, Ernesto Maturana Leiva, Martin Zarba, Maria Teresa Bourlon, Mauricio Mora Pineda, Juan Pablo Sade\",\"doi\":\"10.1200/GO.24.00072\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>This study aims to describe genomic characteristics of patients with metastatic prostate cancer (mPC).</p><p><strong>Patients and methods: </strong>This study is a retrospective, multicenter cohort study of patients with mPC and reports on genomic testing. Patients were included from 12 academic centers in five countries.</p><p><strong>Results: </strong>A total of 349 patients with PC were included in this study. Most patients (209, 59.9%) were de novo metastatic. Genomic analysis was performed in 233 (66.6%) patients in the metastatic castration-resistant prostate cancer (mCRPC) setting, and only 115 (32.8%) patients had a tumor evaluation in the metastatic hormone sensitive prostate cancer scenario. The evaluation of somatic and/or germline mutations was performed through multigene panel analyses in 290 (83.09%) patients, and next-generation sequencing of <i>BRCA1</i> and <i>BRCA2</i> genes was performed in 59 (16.91%) patients. Analyzing the mCRPC subgroup, with a median follow-up of 15.6 months (IQR, 14-19.06), the median progression-free survival (PFS) was not reached (NR) and the PFS at 16 months was 58.7% (95% CI, 50.8 to 67.8). When comparing patients with <i>BRCA</i> mutations with those who are not <i>BRCA</i>-mutated in the mCRPC scenario, the median PFS was NR (95% CI, 14 to NR) and 26.3 months (95% CI, 16.7 to 36.5; <i>P</i> = .2), respectively. Two of six patients with <i>BRCA</i> mutations were treated with targeted therapies (poly-ADP-ribose polymerase inhibitors).</p><p><strong>Conclusion: </strong>Our study, to the best of our knowledge, represents one of the larger data sets for somatic testing in patients with PC in Latin America (LATAM). 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引用次数: 0
摘要
目的:本研究旨在描述转移性前列腺癌(mPC)患者的基因组特征:本研究是一项针对mPC患者的回顾性多中心队列研究,并报告了基因组检测结果。患者来自五个国家的12个学术中心:本研究共纳入了 349 名 PC 患者。大多数患者(209人,占59.9%)为新发转移灶。233例(66.6%)转移性去势抵抗性前列腺癌(mCRPC)患者进行了基因组分析,只有115例(32.8%)转移性激素敏感性前列腺癌患者进行了肿瘤评估。290例(83.09%)患者通过多基因面板分析进行了体细胞和/或种系突变评估,59例(16.91%)患者进行了BRCA1和BRCA2基因的新一代测序。分析mCRPC亚组,中位随访时间为15.6个月(IQR,14-19.06),中位无进展生存期(PFS)未达到(NR),16个月时的PFS为58.7%(95% CI,50.8-67.8)。在mCRPC方案中,将BRCA突变患者与未发生BRCA突变的患者进行比较,中位PFS分别为NR(95% CI,14至NR)和26.3个月(95% CI,16.7至36.5;P = .2)。6名BRCA突变患者中有2名接受了靶向治疗(聚ADP核糖聚合酶抑制剂):据我们所知,我们的研究代表了拉丁美洲(LATAM)PC 患者体细胞检测的较大数据集之一。它为拉丁美洲和加勒比海地区国家日益增长的有关晚期 PC 基因组情况的知识库增添了宝贵的信息,而这些国家在大规模随机临床试验中的代表性并不总是很强。
Genomic Landscape in Prostate Cancer in a Latin American Population.
Purpose: This study aims to describe genomic characteristics of patients with metastatic prostate cancer (mPC).
Patients and methods: This study is a retrospective, multicenter cohort study of patients with mPC and reports on genomic testing. Patients were included from 12 academic centers in five countries.
Results: A total of 349 patients with PC were included in this study. Most patients (209, 59.9%) were de novo metastatic. Genomic analysis was performed in 233 (66.6%) patients in the metastatic castration-resistant prostate cancer (mCRPC) setting, and only 115 (32.8%) patients had a tumor evaluation in the metastatic hormone sensitive prostate cancer scenario. The evaluation of somatic and/or germline mutations was performed through multigene panel analyses in 290 (83.09%) patients, and next-generation sequencing of BRCA1 and BRCA2 genes was performed in 59 (16.91%) patients. Analyzing the mCRPC subgroup, with a median follow-up of 15.6 months (IQR, 14-19.06), the median progression-free survival (PFS) was not reached (NR) and the PFS at 16 months was 58.7% (95% CI, 50.8 to 67.8). When comparing patients with BRCA mutations with those who are not BRCA-mutated in the mCRPC scenario, the median PFS was NR (95% CI, 14 to NR) and 26.3 months (95% CI, 16.7 to 36.5; P = .2), respectively. Two of six patients with BRCA mutations were treated with targeted therapies (poly-ADP-ribose polymerase inhibitors).
Conclusion: Our study, to the best of our knowledge, represents one of the larger data sets for somatic testing in patients with PC in Latin America (LATAM). It adds valuable information to the growing body of knowledge about the genomic landscape of advanced PC in real-world daily practice scenarios in LATAM countries, which are not always well-represented in large-scale randomized clinical trials.