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Breast cancer pathology, receptor status, and patterns of metastasis in a rural appalachian population. 阿巴拉契亚农村人口乳腺癌病理、受体状态和转移模式。
IF 1.8 Q2 Medicine Pub Date : 2014-01-01 Epub Date: 2014-01-09 DOI: 10.1155/2014/170634
Linda Vona-Davis, David P Rose, Vijaya Gadiyaram, Barbara Ducatman, Gerald Hobbs, Hannah Hazard, Sobha Kurian, Jame Abraham

Breast cancer patients in rural Appalachia have a high prevalence of obesity and poverty, together with more triple-negative phenotypes. We reviewed clinical records for tumor receptor status and time to distant metastasis. Body mass index, tumor size, grade, nodal status, and receptor status were related to metastatic patterns. For 687 patients, 13.8% developed metastases to bone (n = 42) or visceral sites (n = 53). Metastases to viscera occurred within five years, a latent period which was shorter than that for bone (P = 0.042). More women with visceral metastasis presented with grade 3 tumors compared with the bone and nonmetastatic groups (P = 0.0002). There were 135/574 women (23.5%) with triple-negative breast cancer, who presented with lymph node involvement and visceral metastases (68.2% versus 24.3%; P = 0.033). Triple-negative tumors that metastasized to visceral sites were larger (P = 0.007). Developing a visceral metastasis within 10 years was higher among women with triple-negative tumors. Across all breast cancer receptor subtypes, the probability of remaining distant metastasis-free was greater for brain and liver than for lung. The excess risk of metastatic spread to visceral organs in triple-negative breast cancers, even in the absence of positive nodes, was combined with the burden of larger and more advanced tumors.

阿巴拉契亚农村地区的乳腺癌患者肥胖和贫困发生率较高,同时三阴性表型较多。我们回顾了肿瘤受体状态和远处转移时间的临床记录。身体质量指数、肿瘤大小、分级、淋巴结状态和受体状态与转移模式相关。在687例患者中,13.8%的患者发生骨转移(n = 42)或内脏转移(n = 53)。脏器转移在5年内发生,潜伏期短于骨转移(P = 0.042)。与骨转移组和非转移组相比,有内脏转移的女性更多出现3级肿瘤(P = 0.0002)。135/574名女性(23.5%)患有三阴性乳腺癌,表现为淋巴结受累和内脏转移(68.2%对24.3%;P = 0.033)。转移到内脏部位的三阴性肿瘤更大(P = 0.007)。三阴性肿瘤患者在10年内发生内脏转移的比例更高。在所有乳腺癌受体亚型中,脑和肝无远处转移的可能性大于肺。在三阴性乳腺癌中,即使没有阳性淋巴结,转移扩散到内脏器官的风险也很高,这与更大、更晚期肿瘤的负担相结合。
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引用次数: 23
Epidemic of non-hodgkin lymphoma in new zealand remains unexplained. 非霍奇金淋巴瘤在新西兰的流行仍未得到解释。
IF 1.8 Q2 Medicine Pub Date : 2014-01-01 Epub Date: 2014-04-01 DOI: 10.1155/2014/315378
Brian Cox, Chih-Wei Liu, Mary J Sneyd, Claire M Cameron

Background. Non-Hodgkin lymphoma (NHL) incidence rates have increased considerably in New Zealand. Methods. Incidence and mortality rates for NHL from 1981 to 2010 were calculated. Trends in age-specific rates were analysed and age-period-cohort models fitted to explore generation-specific changes in incidence and mortality. Results. NHL incidence increased by 67% for men and 74% for women between the 1981-1985 and 2006-2010 time periods in New Zealand. For women born about 1936 and men born about 1946, NHL incidence and mortality have diverged suggesting an improved prognosis for recent generations. Conclusion. The strong generation effects suggest that an exposure before 25 years of age is of major importance in determining the lifetime risk of NHL in New Zealand. NHL incidence rates in New Zealand will continue to increase in the future and probably more in females than males, as generations with increased risk age. Current hypotheses for the cause of NHL do not explain the trends observed. A decline in the prevalence of a protective factor may have also contributed to these trends. Examination of trends for subtypes of NHL and innovative testable hypotheses that may explain these trends are needed.

背景。非霍奇金淋巴瘤(NHL)的发病率在新西兰显著增加。方法。计算1981 - 2010年NHL的发病率和死亡率。分析了特定年龄发病率的趋势,并采用年龄-时期-队列模型来探索发病率和死亡率的代际变化。结果。1981-1985年和2006-2010年期间,新西兰NHL发病率男性增加67%,女性增加74%。在1936年前后出生的女性和1946年前后出生的男性中,NHL的发病率和死亡率存在差异,这表明近几代人的预后有所改善。结论。强代效应表明,25岁之前的暴露对于确定新西兰NHL的终生风险具有重要意义。新西兰的NHL发病率将在未来继续增加,并且随着患病风险的增加,女性的发病率可能会高于男性。目前关于NHL病因的假设并不能解释观察到的趋势。一种保护性因素的流行率下降也可能是造成这些趋势的原因之一。需要检查NHL亚型的趋势和可能解释这些趋势的创新的可检验的假设。
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引用次数: 2
Cancer incidence in egypt: results of the national population-based cancer registry program. 埃及癌症发病率:国家基于人口的癌症登记项目的结果。
IF 1.8 Q2 Medicine Pub Date : 2014-01-01 Epub Date: 2014-09-21 DOI: 10.1155/2014/437971
Amal S Ibrahim, Hussein M Khaled, Nabiel Nh Mikhail, Hoda Baraka, Hossam Kamel

Background. This paper aims to present cancer incidence rates at national and regional level of Egypt, based upon results of National Cancer Registry Program (NCRP). Methods. NCRP stratified Egypt into 3 geographical strata: lower, middle, and upper. One governorate represented each region. Abstractors collected data from medical records of cancer centers, national tertiary care institutions, Health Insurance Organization, Government-Subsidized Treatment Program, and death records. Data entry was online. Incidence rates were calculated at a regional and a national level. Future projection up to 2050 was also calculated. Results. Age-standardized incidence rates per 100,000 were 166.6 (both sexes), 175.9 (males), and 157.0 (females). Commonest sites were liver (23.8%), breast (15.4%), and bladder (6.9%) (both sexes): liver (33.6%) and bladder (10.7%) among men, and breast (32.0%) and liver (13.5%) among women. By 2050, a 3-fold increase in incident cancer relative to 2013 was estimated. Conclusion. These data are the only available cancer rates at national and regional levels of Egypt. The pattern of cancer indicated the increased burden of liver cancer. Breast cancer occupied the second rank. Study of rates of individual sites of cancer might help in giving clues for preventive programs.

背景。本文旨在根据国家癌症登记计划(NCRP)的结果,介绍埃及国家和地区一级的癌症发病率。方法。NCRP将埃及划分为3个地理层:下、中、上。每个地区有一个省代表。作者收集了癌症中心、国家三级保健机构、健康保险组织、政府补贴治疗计划和死亡记录的医疗记录。数据输入在线。发病率是在区域和国家一级计算的。还计算了到2050年的未来预测。结果。每10万人的年龄标准化发病率分别为166.6(男女)、175.9(男性)和157.0(女性)。最常见的部位是肝脏(23.8%)、乳房(15.4%)和膀胱(6.9%)(两性);男性中肝脏(33.6%)和膀胱(10.7%),女性中乳房(32.0%)和肝脏(13.5%)。据估计,到2050年,癌症发病率将比2013年增加3倍。结论。这些数据是埃及国家和区域一级唯一可用的癌症发病率。癌症类型表明肝癌负担增加。乳腺癌排在第二位。研究个别癌症部位的发病率可能有助于为预防计划提供线索。
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引用次数: 866
Breast Cancer Survival Defined by the ER/PR/HER2 Subtypes and a Surrogate Classification according to Tumor Grade and Immunohistochemical Biomarkers. 乳腺癌生存由ER/PR/HER2亚型和肿瘤分级和免疫组织化学生物标志物的替代分类定义。
IF 1.8 Q2 Medicine Pub Date : 2014-01-01 Epub Date: 2014-05-26 DOI: 10.1155/2014/469251
Carol A Parise, Vincent Caggiano

Introduction. ER, PR, and HER2 are routinely available in breast cancer specimens. The purpose of this study is to contrast breast cancer-specific survival for the eight ER/PR/HER2 subtypes with survival of an immunohistochemical surrogate for the molecular subtype based on the ER/PR/HER2 subtypes and tumor grade. Methods. We identified 123,780 cases of stages 1-3 primary female invasive breast cancer from California Cancer Registry. The surrogate classification was derived using ER/PR/HER2 and tumor grade. Kaplan-Meier survival analysis and Cox proportional hazards modeling were used to assess differences in survival and risk of mortality for the ER/PR/HER2 subtypes and surrogate classification within each stage. Results. The luminal B/HER2- surrogate classification had a higher risk of mortality than the luminal B/HER2+ for all stages of disease. There was no difference in risk of mortality between the ER+/PR+/HER2- and ER+/PR+/HER2+ in stage 3. With one exception in stage 3, the ER-negative subtypes all had an increased risk of mortality when compared with the ER-positive subtypes. Conclusions. Assessment of survival using ER/PR/HER2 illustrates the heterogeneity of HER2+ subtypes. The surrogate classification provides clear separation in survival and adjusted mortality but underestimates the wide variability within the subtypes that make up the classification.

介绍。ER, PR和HER2在乳腺癌标本中常规检测。本研究的目的是比较8种ER/PR/HER2亚型的乳腺癌特异性生存率与基于ER/PR/HER2亚型和肿瘤分级的分子亚型的免疫组化替代生存率。方法。我们从加州癌症登记处确定了123,780例1-3期原发性女性浸润性乳腺癌。根据ER/PR/HER2和肿瘤分级得出替代分类。使用Kaplan-Meier生存分析和Cox比例风险模型来评估ER/PR/HER2亚型的生存和死亡风险的差异,并在每个阶段进行替代分类。结果。在所有疾病阶段,管腔B/HER2-替代分类比管腔B/HER2+分类具有更高的死亡率风险。在第3期,ER+/PR+/HER2-和ER+/PR+/HER2+之间的死亡风险没有差异。除了第3阶段的一个例外,与er阳性亚型相比,er阴性亚型的死亡率都增加了。结论。使用ER/PR/HER2评估生存率说明了HER2+亚型的异质性。替代分类在生存率和调整死亡率方面提供了明确的区分,但低估了构成分类的亚型之间的广泛变异性。
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引用次数: 232
Smokeless tobacco and oral cancer in South Asia: a systematic review with meta-analysis. 南亚的无烟烟草与口腔癌:系统回顾与荟萃分析。
IF 1.8 Q2 Medicine Pub Date : 2014-01-01 Epub Date: 2014-07-06 DOI: 10.1155/2014/394696
Zohaib Khan, Justus Tönnies, Steffen Müller

Introduction. Smokeless tobacco is considered one of the major risk factors for oral cancer. It is estimated that over 90% of the global smokeless tobacco use burden is in South Asia. This paper aims to systematically review publications reporting epidemiological observational studies published in South Asia from 1984 till 2013. Methods. An electronic search in "Medline" and "ISI Web of Knowledge" yielded 734 publications out of which 21 were included in this review. All publications were assessed for quality using a standard quality assessment tool. Effect estimates (odds ratios (OR)) were abstracted or calculated from the given data. A random effects meta-analysis was performed to assess the risk of oral cancer with the use of different forms of smokeless tobacco. Results and Conclusion. The pooled OR for chewing tobacco and risk of oral cancer was 4.7 [3.1-7.1] and for paan with tobacco and risk of oral cancer was 7.1 [4.5-11.1]. The findings of this study suggest a strong causal link between oral cancer and various forms of smokeless tobacco. Public health policies in affected countries should consider SLT specific cessation programs in addition to campaigns and activities incorporated into smoking cessation programs.

介绍。无烟烟草被认为是口腔癌的主要风险因素之一。据估计,全球无烟烟草使用负担的 90% 以上发生在南亚。本文旨在系统回顾 1984 年至 2013 年在南亚发表的流行病学观察性研究报告。研究方法通过在 "Medline "和 "ISI Web of Knowledge "上进行电子检索,共获得 734 篇出版物,其中 21 篇被纳入本综述。使用标准质量评估工具对所有出版物进行了质量评估。从给定数据中抽取或计算出效果估计值(几率比(OR))。随机效应荟萃分析评估了使用不同形式的无烟烟草患口腔癌的风险。结果和结论。咀嚼烟草与口腔癌风险的汇总 OR 值为 4.7 [3.1-7.1],含烟草的派糖与口腔癌风险的汇总 OR 值为 7.1 [4.5-11.1]。本研究结果表明,口腔癌与各种形式的无烟烟草之间存在密切的因果关系。受影响国家的公共卫生政策除了考虑戒烟计划中的宣传和活动外,还应考虑针对无烟烟草的戒烟计划。
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引用次数: 0
Characterization of pediatric acute lymphoblastic leukemia survival patterns by age at diagnosis. 按诊断年龄划分的小儿急性淋巴细胞白血病存活模式。
IF 1.8 Q3 ONCOLOGY Pub Date : 2014-01-01 Epub Date: 2014-09-17 DOI: 10.1155/2014/865979
Md Jobayer Hossain, Li Xie, Suzanne M McCahan

Age at diagnosis is a key prognostic factor in pediatric acute lymphoblastic leukemia (ALL) survivorship. However, literature providing adequate assessment of the survival variability by age at diagnosis is scarce. The aim of this study is to assess the impact of this prognostic factor in pediatric ALL survival. We estimated incidence rate of mortality, 5-year survival rate, Kaplan-Meier survival function, and hazard ratio using the Surveillance Epidemiology and End Results (SEER) data during 1973-2009. There was significant variability in pediatric ALL survival by age at diagnosis. Survival peaked among children diagnosed at 1-4 years and steadily declined among those diagnosed at older ages. Infants (<1 year) had the lowest survivorship. In a multivariable Cox proportional hazard model stratified by year of diagnosis, those diagnosed in age groups 1-4, 5-9, 10-14, and 15-19 years were 82%, 75%, 57%, and 32% less likely to die compared to children diagnosed in infancy, respectively. Age at diagnosis remained to be a crucial determinant of the survival variability of pediatric ALL patients, after adjusting for sex, race, radiation therapy, primary tumor sites, immunophenotype, and year of diagnosis. Further research is warranted to disentangle the effects of age-dependent biological and environmental processes on this association.

诊断年龄是影响小儿急性淋巴细胞白血病(ALL)存活率的关键预后因素。然而,能够充分评估诊断年龄对存活率影响的文献却很少。本研究旨在评估这一预后因素对小儿急性淋巴细胞白血病存活率的影响。我们利用1973-2009年间的监测、流行病学和最终结果(SEER)数据估算了死亡率、5年生存率、卡普兰-梅耶生存函数和危险比。小儿 ALL 的存活率因诊断年龄的不同而存在很大差异。确诊年龄在1-4岁的儿童存活率最高,而确诊年龄较大的儿童存活率则稳步下降。婴儿
{"title":"Characterization of pediatric acute lymphoblastic leukemia survival patterns by age at diagnosis.","authors":"Md Jobayer Hossain, Li Xie, Suzanne M McCahan","doi":"10.1155/2014/865979","DOIUrl":"10.1155/2014/865979","url":null,"abstract":"<p><p>Age at diagnosis is a key prognostic factor in pediatric acute lymphoblastic leukemia (ALL) survivorship. However, literature providing adequate assessment of the survival variability by age at diagnosis is scarce. The aim of this study is to assess the impact of this prognostic factor in pediatric ALL survival. We estimated incidence rate of mortality, 5-year survival rate, Kaplan-Meier survival function, and hazard ratio using the Surveillance Epidemiology and End Results (SEER) data during 1973-2009. There was significant variability in pediatric ALL survival by age at diagnosis. Survival peaked among children diagnosed at 1-4 years and steadily declined among those diagnosed at older ages. Infants (<1 year) had the lowest survivorship. In a multivariable Cox proportional hazard model stratified by year of diagnosis, those diagnosed in age groups 1-4, 5-9, 10-14, and 15-19 years were 82%, 75%, 57%, and 32% less likely to die compared to children diagnosed in infancy, respectively. Age at diagnosis remained to be a crucial determinant of the survival variability of pediatric ALL patients, after adjusting for sex, race, radiation therapy, primary tumor sites, immunophenotype, and year of diagnosis. Further research is warranted to disentangle the effects of age-dependent biological and environmental processes on this association. </p>","PeriodicalId":15366,"journal":{"name":"Journal of Cancer Epidemiology","volume":"2014 ","pages":"865979"},"PeriodicalIF":1.8,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182848/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32742033","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Incidence and outcomes of desmoplastic small round cell tumor: results from the surveillance, epidemiology, and end results database. 结缔组织增生小圆细胞瘤的发病率和预后:来自监测、流行病学和最终结果数据库的结果。
IF 1.8 Q2 Medicine Pub Date : 2014-01-01 Epub Date: 2014-11-05 DOI: 10.1155/2014/680126
Christina K Lettieri, Pamela Garcia-Filion, Pooja Hingorani

Desmoplastic small round cell tumor (DSRCT) is a rare but highly fatal malignancy. Due to the rarity of this neoplasm, no large population based studies exist. Procedure. This is a retrospective cohort analysis. Incidence rates were calculated based on sex and ethnicity and compared statistically. Gender-, ethnicity-, and treatment- based survival were calculated using the Kaplan-Meier method. Results. A total of 192 cases of DSRCT were identified. Peak incidence age was between 20 and 24 years. Age-adjusted incidence rate for blacks was 0.5 cases/million and for whites was 0.2 cases/million (P = 0.037). There was no statistically significant difference in survival based on gender or ethnicity. When adjusted for age, there was no statistically significant difference in survival amongst patients who received radiation therapy compared to those who did not (HRadj = 0.73; 95% CI 0.49, 1.11). There was a statistically significant survival advantage for patients who received radiation after surgery compared to those who did not (HR 0.49; 95% CI 0.30, 0.79). Conclusion. DSRCT is more common in males and in people of African-American descent. Although overall survival remains poor, radiation therapy following surgery seems to improve outcome in these patients.

结缔组织增生小圆细胞瘤(DSRCT)是一种罕见但高度致命的恶性肿瘤。由于这种肿瘤的罕见性,没有大规模的基于人群的研究存在。过程。这是一项回顾性队列分析。发病率根据性别和种族计算,并进行统计比较。使用Kaplan-Meier方法计算基于性别、种族和治疗的生存率。结果。共发现192例DSRCT。发病高峰年龄为20 ~ 24岁。黑人年龄调整后的发病率为0.5例/百万,白人为0.2例/百万(P = 0.037)。基于性别或种族的生存率没有统计学上的显著差异。经年龄调整后,接受放射治疗的患者与未接受放射治疗的患者的生存率无统计学意义差异(HRadj = 0.73;95% ci 0.49, 1.11)。术后接受放射治疗的患者与未接受放射治疗的患者相比有统计学上显著的生存优势(HR 0.49;95% ci 0.30, 0.79)。结论。DSRCT在男性和非裔美国人后裔中更为常见。尽管总体生存率仍然很低,但手术后放射治疗似乎改善了这些患者的预后。
{"title":"Incidence and outcomes of desmoplastic small round cell tumor: results from the surveillance, epidemiology, and end results database.","authors":"Christina K Lettieri,&nbsp;Pamela Garcia-Filion,&nbsp;Pooja Hingorani","doi":"10.1155/2014/680126","DOIUrl":"https://doi.org/10.1155/2014/680126","url":null,"abstract":"<p><p>Desmoplastic small round cell tumor (DSRCT) is a rare but highly fatal malignancy. Due to the rarity of this neoplasm, no large population based studies exist. Procedure. This is a retrospective cohort analysis. Incidence rates were calculated based on sex and ethnicity and compared statistically. Gender-, ethnicity-, and treatment- based survival were calculated using the Kaplan-Meier method. Results. A total of 192 cases of DSRCT were identified. Peak incidence age was between 20 and 24 years. Age-adjusted incidence rate for blacks was 0.5 cases/million and for whites was 0.2 cases/million (P = 0.037). There was no statistically significant difference in survival based on gender or ethnicity. When adjusted for age, there was no statistically significant difference in survival amongst patients who received radiation therapy compared to those who did not (HRadj = 0.73; 95% CI 0.49, 1.11). There was a statistically significant survival advantage for patients who received radiation after surgery compared to those who did not (HR 0.49; 95% CI 0.30, 0.79). Conclusion. DSRCT is more common in males and in people of African-American descent. Although overall survival remains poor, radiation therapy following surgery seems to improve outcome in these patients. </p>","PeriodicalId":15366,"journal":{"name":"Journal of Cancer Epidemiology","volume":"2014 ","pages":"680126"},"PeriodicalIF":1.8,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2014/680126","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32843429","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 75
Cancer in the elderly. 老年人的癌症。
IF 1.8 Q2 Medicine Pub Date : 2014-01-01 Epub Date: 2014-04-30 DOI: 10.1155/2014/872029
Frank Buntinx, Christine Campbell, Marjan van den Akker
Part 1 Introduction: sickness and health in old age, R.E.Irvine epidemiology of cancer in the elderly, D.W.Lamont hopes and fears of the elderly cancer patient, I.B.Brewin. Part 2 Principles of management of cancer in the elderly: principles of surgery, Henry Tankel principles of radiotherapy, Thurston Brewin principles of chemotherapy, Craig Lewis, Kaye & Calman terminal care, J.Welsh. Part 3 Complications of cancer in the elderly: metabolic aspects, H.M.Hodkinson paraneoplastic CNS syndromes, Chen-Ya Huang. Part 4 Organs and systems: breast cancer, Allan Langlands bronchus lung tumours, Gordon P.Canning and F.J. Caird Oesophagus, P.T.D. Symonds stomach gastric cancers, Alan Jewkes, Simon Rowley and T.J. & Priestman colon, and rectum and anus, Philip F.Schofield liver, gallbladder, and pancreas, John Chalstrey kidney, ureter and bladder, Philip P.Clark cancer of the prostate, Malcolm A.Bagshaw gynaecological cancer malignancy, L.N.Hudson skin, Rona M.MacKie lymphoma and leukaemia and malignant, John M.Dagg myeloma, J.S.Malpas, Wallace Stewart eye ophthalmic neoplasia, Bertil E.Damato and Foulds malignant disorders of bone, Frank J.Frassica, Lester E.Wold and Franklin H. & Sim head and neck cancer, D.F.N.Harrison brain and spinal cord, David A.Stewart and F.J.Caird.
{"title":"Cancer in the elderly.","authors":"Frank Buntinx,&nbsp;Christine Campbell,&nbsp;Marjan van den Akker","doi":"10.1155/2014/872029","DOIUrl":"https://doi.org/10.1155/2014/872029","url":null,"abstract":"Part 1 Introduction: sickness and health in old age, R.E.Irvine epidemiology of cancer in the elderly, D.W.Lamont hopes and fears of the elderly cancer patient, I.B.Brewin. Part 2 Principles of management of cancer in the elderly: principles of surgery, Henry Tankel principles of radiotherapy, Thurston Brewin principles of chemotherapy, Craig Lewis, Kaye & Calman terminal care, J.Welsh. Part 3 Complications of cancer in the elderly: metabolic aspects, H.M.Hodkinson paraneoplastic CNS syndromes, Chen-Ya Huang. Part 4 Organs and systems: breast cancer, Allan Langlands bronchus lung tumours, Gordon P.Canning and F.J. Caird Oesophagus, P.T.D. Symonds stomach gastric cancers, Alan Jewkes, Simon Rowley and T.J. & Priestman colon, and rectum and anus, Philip F.Schofield liver, gallbladder, and pancreas, John Chalstrey kidney, ureter and bladder, Philip P.Clark cancer of the prostate, Malcolm A.Bagshaw gynaecological cancer malignancy, L.N.Hudson skin, Rona M.MacKie lymphoma and leukaemia and malignant, John M.Dagg myeloma, J.S.Malpas, Wallace Stewart eye ophthalmic neoplasia, Bertil E.Damato and Foulds malignant disorders of bone, Frank J.Frassica, Lester E.Wold and Franklin H. & Sim head and neck cancer, D.F.N.Harrison brain and spinal cord, David A.Stewart and F.J.Caird.","PeriodicalId":15366,"journal":{"name":"Journal of Cancer Epidemiology","volume":"2014 ","pages":"872029"},"PeriodicalIF":1.8,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2014/872029","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32380996","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 88
Colorectal cancer incidence and mortality disparities in new Mexico. 新墨西哥州结直肠癌发病率和死亡率差异。
IF 1.8 Q2 Medicine Pub Date : 2014-01-01 Epub Date: 2014-01-02 DOI: 10.1155/2014/239619
Richard M Hoffman, David K Espey, Robert L Rhyne, Melissa Gonzales, Ashwani Rajput, Shiraz I Mishra, S Noell Stone, Charles L Wiggins

Background. Previous analyses indicated that New Mexican Hispanics and American Indians (AI) did not experience the declining colorectal cancer (CRC) incidence and mortality rates observed among non-Hispanic whites (NHW). We evaluated more recent data to determine whether racial/ethnic differences persisted. Methods. We used New Mexico Surveillance Epidemiology and End Results data from 1995 to 2009 to calculate age-specific incidence rates and age-adjusted incidence rates overall and by tumor stage. We calculated mortality rates using National Center for Health Statistics' data. We used joinpoint regression to determine annual percentage change (APC) in age-adjusted incidence rates. Analyses were stratified by race/ethnicity and gender. Results. Incidence rates continued declining in NHW (APC -1.45% men, -1.06% women), while nonsignificantly increasing for AI (1.67% men, 1.26% women) and Hispanic women (0.24%). The APC initially increased in Hispanic men through 2001 (3.33%, P = 0.06), before declining (-3.10%, P = 0.003). Incidence rates declined in NHW and Hispanics aged 75 and older. Incidence rates for distant-stage cancer remained stable for all groups. Mortality rates declined significantly in NHW and Hispanics. Conclusions. Racial/ethnic disparities in CRC persist in New Mexico. Incidence differences could be related to risk factors or access to screening; mortality differences could be due to patterns of care for screening or treatment.

背景。先前的分析表明,新墨西哥西班牙裔和美洲印第安人(AI)没有经历在非西班牙裔白人(NHW)中观察到的结直肠癌(CRC)发病率和死亡率下降。我们评估了最近的数据,以确定种族/民族差异是否持续存在。方法。我们使用1995年至2009年的新墨西哥州监测流行病学和最终结果数据来计算年龄特异性发病率和年龄调整后的总体发病率和肿瘤分期。我们使用国家卫生统计中心的数据计算死亡率。我们使用连接点回归来确定年龄调整后发病率的年百分比变化(APC)。分析按种族/民族和性别分层。结果。NHW的发病率继续下降(APC男性-1.45%,女性-1.06%),而AI(男性1.67%,女性1.26%)和西班牙裔女性(0.24%)的发病率无显著增加。2001年,西班牙裔男性的APC开始上升(3.33%,P = 0.06),然后下降(-3.10%,P = 0.003)。75岁及以上的非裔美国人和西班牙裔美国人的发病率下降。所有组的晚期癌症发病率保持稳定。美国黑人和西班牙裔的死亡率显著下降。结论。新墨西哥州CRC的种族/民族差异依然存在。发病率差异可能与风险因素或接受筛查的机会有关;死亡率的差异可能是由于筛查或治疗的护理模式。
{"title":"Colorectal cancer incidence and mortality disparities in new Mexico.","authors":"Richard M Hoffman, David K Espey, Robert L Rhyne, Melissa Gonzales, Ashwani Rajput, Shiraz I Mishra, S Noell Stone, Charles L Wiggins","doi":"10.1155/2014/239619","DOIUrl":"10.1155/2014/239619","url":null,"abstract":"<p><p>Background. Previous analyses indicated that New Mexican Hispanics and American Indians (AI) did not experience the declining colorectal cancer (CRC) incidence and mortality rates observed among non-Hispanic whites (NHW). We evaluated more recent data to determine whether racial/ethnic differences persisted. Methods. We used New Mexico Surveillance Epidemiology and End Results data from 1995 to 2009 to calculate age-specific incidence rates and age-adjusted incidence rates overall and by tumor stage. We calculated mortality rates using National Center for Health Statistics' data. We used joinpoint regression to determine annual percentage change (APC) in age-adjusted incidence rates. Analyses were stratified by race/ethnicity and gender. Results. Incidence rates continued declining in NHW (APC -1.45% men, -1.06% women), while nonsignificantly increasing for AI (1.67% men, 1.26% women) and Hispanic women (0.24%). The APC initially increased in Hispanic men through 2001 (3.33%, P = 0.06), before declining (-3.10%, P = 0.003). Incidence rates declined in NHW and Hispanics aged 75 and older. Incidence rates for distant-stage cancer remained stable for all groups. Mortality rates declined significantly in NHW and Hispanics. Conclusions. Racial/ethnic disparities in CRC persist in New Mexico. Incidence differences could be related to risk factors or access to screening; mortality differences could be due to patterns of care for screening or treatment. </p>","PeriodicalId":15366,"journal":{"name":"Journal of Cancer Epidemiology","volume":"2014 ","pages":"239619"},"PeriodicalIF":1.8,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2014/239619","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32115235","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 14
Associations of census-tract poverty with subsite-specific colorectal cancer incidence rates and stage of disease at diagnosis in the United States. 美国人口普查区贫困与特定地区结直肠癌发病率和诊断时疾病阶段的关系。
IF 1.8 Q2 Medicine Pub Date : 2014-01-01 Epub Date: 2014-08-03 DOI: 10.1155/2014/823484
Kevin A Henry, Recinda L Sherman, Kaila McDonald, Christopher J Johnson, Ge Lin, Antoinette M Stroup, Francis P Boscoe

Background. It remains unclear whether neighborhood poverty contributes to differences in subsite-specific colorectal cancer (CRC) incidence. We examined associations between census-tract poverty and CRC incidence and stage by anatomic subsite and race/ethnicity. Methods. CRC cases diagnosed between 2005 and 2009 from 15 states and Los Angeles County (N = 278,097) were assigned to 1 of 4 groups based on census-tract poverty. Age-adjusted and stage-specific CRC incidence rates (IRs) and incidence rate ratios (IRRs) were calculated. Analyses were stratified by subsite (proximal, distal, and rectum), sex, race/ethnicity, and poverty. Results. Compared to the lowest poverty areas, CRC IRs were significantly higher in the most impoverished areas for men (IRR = 1.14 95% CI 1.12-1.17) and women (IRR = 1.06 95% CI 1.05-1.08). Rate differences between high and low poverty were strongest for distal colon (male IRR = 1.24 95% CI 1.20-1.28; female IRR = 1.14 95% CI 1.10-1.18) and weakest for proximal colon. These rate differences were significant for non-Hispanic whites and blacks and for Asian/Pacific Islander men. Inverse associations between poverty and IRs of all CRC and proximal colon were found for Hispanics. Late-to-early stage CRC IRRs increased monotonically with increasing poverty for all race/ethnicity groups. Conclusion. There are differences in subsite-specific CRC incidence by poverty, but associations were moderated by race/ethnicity.

背景。邻里贫困是否会导致特定部位结直肠癌(CRC)发病率的差异,目前仍不清楚。我们按解剖学亚部位和种族/人种研究了人口普查区贫困与 CRC 发病率和分期之间的关系。研究方法将 15 个州和洛杉矶县 2005 年至 2009 年期间确诊的 CRC 病例(N = 278,097 例)根据人口普查区的贫困程度分为 4 组。计算经年龄调整和分期的 CRC 发病率 (IR) 和发病率比 (IRR)。分析按部位(近端、远端和直肠)、性别、种族/民族和贫困程度进行分层。结果显示与贫困程度最低的地区相比,最贫困地区的男性(IRR = 1.14 95% CI 1.12-1.17)和女性(IRR = 1.06 95% CI 1.05-1.08)CRC IRs 明显更高。远端结肠和近端结肠的贫困率差异最大(男性 IRR = 1.24 95% CI 1.20-1.28;女性 IRR = 1.14 95% CI 1.10-1.18),而近端结肠的差异最小。在非西班牙裔白人、黑人和亚裔/太平洋岛民男性中,这些比率差异显著。在西班牙裔中,贫困与所有 CRC 和近端结肠的 IR 之间存在反向关系。在所有种族/族裔群体中,晚期至早期 CRC IRR 随贫困程度的增加而单调增加。结论。不同贫困程度的亚特异性 CRC 发病率存在差异,但相关性受种族/人种的影响而有所缓和。
{"title":"Associations of census-tract poverty with subsite-specific colorectal cancer incidence rates and stage of disease at diagnosis in the United States.","authors":"Kevin A Henry, Recinda L Sherman, Kaila McDonald, Christopher J Johnson, Ge Lin, Antoinette M Stroup, Francis P Boscoe","doi":"10.1155/2014/823484","DOIUrl":"10.1155/2014/823484","url":null,"abstract":"<p><p>Background. It remains unclear whether neighborhood poverty contributes to differences in subsite-specific colorectal cancer (CRC) incidence. We examined associations between census-tract poverty and CRC incidence and stage by anatomic subsite and race/ethnicity. Methods. CRC cases diagnosed between 2005 and 2009 from 15 states and Los Angeles County (N = 278,097) were assigned to 1 of 4 groups based on census-tract poverty. Age-adjusted and stage-specific CRC incidence rates (IRs) and incidence rate ratios (IRRs) were calculated. Analyses were stratified by subsite (proximal, distal, and rectum), sex, race/ethnicity, and poverty. Results. Compared to the lowest poverty areas, CRC IRs were significantly higher in the most impoverished areas for men (IRR = 1.14 95% CI 1.12-1.17) and women (IRR = 1.06 95% CI 1.05-1.08). Rate differences between high and low poverty were strongest for distal colon (male IRR = 1.24 95% CI 1.20-1.28; female IRR = 1.14 95% CI 1.10-1.18) and weakest for proximal colon. These rate differences were significant for non-Hispanic whites and blacks and for Asian/Pacific Islander men. Inverse associations between poverty and IRs of all CRC and proximal colon were found for Hispanics. Late-to-early stage CRC IRRs increased monotonically with increasing poverty for all race/ethnicity groups. Conclusion. There are differences in subsite-specific CRC incidence by poverty, but associations were moderated by race/ethnicity. </p>","PeriodicalId":15366,"journal":{"name":"Journal of Cancer Epidemiology","volume":"2014 ","pages":"823484"},"PeriodicalIF":1.8,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4137551/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32620692","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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