共查询到20条相似文献,搜索用时 382 毫秒
1.
Fiona C. Malcomson BSc MRes PhD Christopher Wiggins BSc MRes Solange Parra-Soto BSc MSc Frederick K. Ho BSc PhD Carlos Celis-Morales BSc PhD Linda Sharp BSc MSc PhD John C. Mathers BSc Dip. Nutr. PhD 《Cancer》2023,129(17):2655-2670
Background
The World Cancer Research Fund/American Institute for Cancer Research Cancer Prevention Recommendations are lifestyle-based guidelines that aim to reduce cancer risk. A systematic review and meta-analysis of studies investigating associations between a score for adherence to the 2018 Cancer Prevention Recommendations and cancer risk was conducted.Methods
MEDLINE, Embase, Web of Science, and Scopus were searched for studies published to November 28, 2022. In meta-analysis, the estimated risk ratios and 95% CIs for adherence score as a continuous (per 1-point increment) and categorical (highest vs. lowest score category) variable using random-effects models were estimated.Results
Eighteen studies (11 cohort; seven case-control) were included investigating incidence of breast (n = 7), colorectal (n = 5), prostate (n = 2), lung (n = 2), pancreatic (n = 1), endometrial (n = 1), unknown primary cancer (n = 1), chronic lymphocytic leukemia (n = 1), and overall (any) cancer (n = 1). The summary risk ratio per 1-point increment in adherence score was 0.89 (95% CI, 0.85–0.93; I2 = 76.5%; n = 7) for breast cancer, 0.88 (95% CI, 0.84–0.91; I2 = 26.2%; n = 4) for colorectal cancer, and 0.92 (95% CI, 0.86–0.98, I2 = 66.0%; n = 2) for lung cancer. There were no significant associations with prostate or other cancers. Meta-analysis results using categorical adherence score variables were consistent with these findings.Conclusions
Greater adherence to the 2018 World Cancer Research Fund/American Institute for Cancer Research Cancer Prevention Recommendations was associated with lower risk of breast, colorectal, and lung cancers. Future studies investigating associations with risk of other forms of cancer are warranted.PROSPERO registration number
CRD42022313327. 相似文献2.
3.
《Psycho-oncology》2018,27(7):1735-1741
Objective
Depression is common among patients diagnosed with cancer. Patients with cancer and depression use more health care services compared with nondepressed cancer patients. The current study seeks to estimate the added cost of depression in cancer patients in the first year after cancer diagnosis.Methods
Health care charges were obtained for 2051 depressed and 11 182 nondepressed patients with an International Classification of Diseases, Ninth Revision, diagnosis of cancer in the 2014 calendar year from the University of California San Diego Healthcare System. The annual health care charges for cancer patients with and without depression were analyzed using generalized linear models with a log‐link function and gamma distribution, covarying for age, sex, race/ethnicity, comorbid diseases, and presence of metastatic disease. Total cost data were broken down into several categories including ambulatory care, emergency department visits, and hospital visits.Results
Depressed cancer patients had total annual health care charges that were 113% higher than nondepressed cancer patients (B = 0.76; P < .001). The estimated mean charges for depressed patients were $235 337 compared with $110 650 for nondepressed patients. Depressed cancer patients incurred greater charges than nondepressed patients in ambulatory care (B = 0.70; P < .001), emergency department charges (B = 0.31; P < .001), and hospital charges (B = 0.39; P < .001).Conclusions
Depressed cancer patients incur significantly higher health care charges across multiple cost categories including ambulatory care, emergency department visits, and hospital visits. Future research should investigate if interventions for detecting and treating depression are effective for reducing health care use and costs in cancer patients.4.
Zeynep Eroglu MD Shifra Krinshpun MS LCGC Ekaterina Kalashnikova PhD Sumedha Sudhaman PhD Turkan Ozturk Topcu MD Matt Nichols BS Justin Martin MS Katherine M. Bui MD Charuta C. Palsuledesai PhD Meenakshi Malhotra PhD Perry Olshan MA PhD Joseph Markowitz MD PhD Nikhil I. Khushalani MD Ahmad A. Tarhini MD PhD Jane L. Messina MD Alexey Aleshin MD MBA 《Cancer》2023,129(11):1723-1734
Background
Immune checkpoint inhibitors (ICIs) have substantially improved overall survival in patients with advanced melanoma; however, the lack of biomarkers to monitor treatment response and relapse remains an important clinical challenge. Thus, a reliable biomarker is needed that can risk-stratify patients for disease recurrence and predict response to treatment.Methods
A retrospective analysis using a personalized, tumor-informed circulating tumor DNA (ctDNA) assay on prospectively collected plasma samples (n = 555) from 69 patients with advanced melanoma was performed. Patients were divided into three cohorts: cohort A (N = 30), stage III patients receiving adjuvant ICI/observation; cohort B (N = 29), unresectable stage III/IV patients receiving ICI therapy; and cohort C (N = 10), stage III/IV patients on surveillance after planned completion of ICI therapy for metastatic disease.Results
In cohort A, compared to molecular residual disease (MRD)-negative patients, MRD-positivity was associated with significantly shorter distant metastasis-free survival (DMFS; hazard ratio [HR], 10.77; p = .01). Increasing ctDNA levels from the post-surgical or pre-treatment time point to after 6 weeks of ICI were predictive of shorter DMFS in cohort A (HR, 34.54; p < .0001) and shorter progression-free survival (PFS) in cohort B (HR, 22; p = .006). In cohort C, all ctDNA-negative patients remained progression-free for a median follow-up of 14.67 months, whereas ctDNA-positive patients experienced disease progression.Conclusion
Personalized and tumor-informed longitudinal ctDNA monitoring is a valuable prognostic and predictive tool that may be used throughout the clinical course of patients with advanced melanoma. 相似文献5.
6.
Sally Järvelä Immo Rantala Alejandra Rodriguez Heini Kallio Seppo Parkkila Vuokko L Kinnula Ylermi Soini Hannu Haapasalo 《BMC cancer》2010,10(1):104
Background
Peroxiredoxins (Prxs) have recently been suggested to have a role in tumorigenesis. 相似文献7.
Evaluation of kidney motion with and without a pneumatic abdominal compression belt: Considerations for stereotactic radiotherapy
下载免费PDF全文
![点击此处可从《Journal of Medical Imaging and Radiation Oncology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Kimberley West Majella Russo Elizabeth Brown Tamara Barry Cathy Hargrave David Pryor 《Journal of Medical Imaging and Radiation Oncology》2018,62(1):128-132
Introduction
The optimal delivery of stereotactic radiotherapy for kidney tumours requires an effective motion management strategy. This study assessed the effectiveness of a pneumatic abdominal compression belt in reducing kidney motion during free breathing.Methods
Thirteen patients, with four‐dimensional computed tomography (4DCT) of the abdomen in free breathing with and without a pneumatic abdominal compression belt, were retrospectively reviewed. Points of Interest (POI) were placed on each kidney to determine the greatest magnitude of displacement in all directions.Results
Without compression, all patients had >5.0 mm motion in the craniocaudal (CC) direction in at least one kidney. Median CC excursion of the left superior pole was reduced with compression from 8.0 mm (range 2.0 mm–18.0 mm) to 4.0 mm (range 2.0 mm–10.0 mm, P = 0.047) and right superior pole from 10.0 mm (range 4.0 mm–16.0 mm) to 6.0 mm (range 2.0 mm–10.0 mm, P=value 0.051). A benefit was less evident for the left and right inferior poles with median CC excursion of 6.0 mm versus 4.0 mm and 5.0 mm versus 4.0 mm without and with compression, respectively. Median displacement in the anteroposterior direction (≤3.2 mm) and lateral directions (≤1.3 mm) was similar for left and right kidneys and not significantly altered by compression. Overall, seven patients had kidney motion reduced by >5.0 mm with two reduced by 10.0 mm.Conclusion
A pneumatic abdominal compression belt reduced kidney motion by >5.0 mm in seven of thirteen patients. The relative benefit is patient and location specific and should be assessed on an individual basis. 相似文献8.
Kelly E. Rentscher PhD Traci N. Bethea PhD Wanting Zhai MS Brent J. Small PhD Xingtao Zhou MS Tim A. Ahles PhD Jaeil Ahn PhD Elizabeth C. Breen PhD Harvey Jay Cohen MD Martine Extermann MD Deena M. A. Graham MD Heather S. L. Jim PhD Brenna C. McDonald PsyD Zev M. Nakamura MD Sunita K. Patel PhD James C. Root PhD Andrew J. Saykin PsyD Kathleen Van Dyk PhD Jeanne S. Mandelblatt MD MPH Judith E. Carroll PhD 《Cancer》2023,129(17):2741-2753
Background
Cancer and its treatments may accelerate aging in survivors; however, research has not examined epigenetic markers of aging in longer term breast cancer survivors. This study examined whether older breast cancer survivors showed greater epigenetic aging than noncancer controls and whether epigenetic aging related to functional outcomes.Methods
Nonmetastatic breast cancer survivors (n = 89) enrolled prior to systemic therapy and frequency-matched controls (n = 101) ages 62 to 84 years provided two blood samples to derive epigenetic aging measures (Horvath, Extrinsic Epigenetic Age [EEA], PhenoAge, GrimAge, Dunedin Pace of Aging) and completed cognitive (Functional Assessment of Cancer Therapy-Cognitive Function) and physical (Medical Outcomes Study Short Form-12) function assessments at approximately 24 to 36 and 60 months after enrollment. Mixed-effects models tested survivor-control differences in epigenetic aging, adjusting for age and comorbidities; models for functional outcomes also adjusted for racial group, site, and cognitive reserve.Results
Survivors were 1.04 to 2.22 years biologically older than controls on Horvath, EEA, GrimAge, and DunedinPACE measures (p = .001–.04) at approximately 24 to 36 months after enrollment. Survivors exposed to chemotherapy were 1.97 to 2.71 years older (p = .001–.04), and among this group, an older EEA related to worse self-reported cognition (p = .047) relative to controls. An older epigenetic age related to worse physical function in all women (p < .001–.01). Survivors and controls showed similar epigenetic aging over time, but Black survivors showed accelerated aging over time relative to non-Hispanic White survivors.Conclusion
Older breast cancer survivors, particularly those exposed to chemotherapy, showed greater epigenetic aging than controls that may relate to worse outcomes. If replicated, measurement of biological aging could complement geriatric assessments to guide cancer care for older women. 相似文献9.
10.
Clinical benefit and residual kidney function of en bloc nephrectomy for perirenal retroperitoneal sarcoma
下载免费PDF全文
![点击此处可从《Asia-Pacific Journal of Clinical Oncology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Chan Woo Cho Kyo Won Lee Hyojun Park Hyung Joon Kim Jae Berm Park Yoon‐La Choi Jeong Il Yu Su Jin Lee Dong Il Choi Sung Joo Kim 《Asia-Pacific Journal of Clinical Oncology》2018,14(5):e465-e471
1 Aim
The purpose of this study was to evaluate the efficacy of en bloc nephrectomy for perirenal retroperitoneal sarcoma (RPS) with respect to postoperative kidney function and oncological benefits.2 Methods
We performed a comparative study of 114 patients undergoing surgery for primary RPS, classifying cases as nephrectomy (NPX, n = 65) versus no nephrectomy (no‐NPX, n = 49). The Δ and % change between preoperative and postoperative estimated glomerulus filtration rate (eGFR) were analyzed to compare renal function changes after surgery. Kaplan–Meier analysis was performed to verify the incidence of local relapse between the two groups.3 Results
During a median follow‐up of 29 months, median postoperative GFR of 65 patients in the NPX group decreased to 73.5% of preoperative eGFR. Although 38 patients (58%) in the NPX group experienced a progression in chronic kidney disease stage after nephrectomy, no patients progressed to end‐stage renal disease (ESRD). In French Federation of Cancer Centers Sarcoma grade 2, the NPX group had statistically significant local control benefits, compared with the no‐NPX group (P = 0.048).4 Conclusions
Residual renal function after en bloc nephrectomy was stabilized without progression to ESRD. Moreover, en bloc nephrectomy for perirenal RPS might secure a complete resection margin for local tumor control. 相似文献11.
Objective
To report the time trends of cancer incidence in urban Beijing from 1998 to 2007. 相似文献12.
Objective
The aim of the study was to detect the valuable ultrasonographic features in diagnosing prostate cancer. 相似文献13.
Objective
To analyze the relationship between KRAS, BRAF mutations and the response to Cetuximab in Chinese colorectal cancer patients. 相似文献14.
H. Tamagawa T. Oshima M. Numata N. Yamamoto M. Shiozawa S. Morinaga Y. Nakamura M. Yoshihara Y. Sakuma Y. Kameda M. Akaike N. Yukawa Y. Rino M. Masuda Y. Miyagi 《European journal of surgical oncology》2013
Background
We evaluated the methylation patterns of histone H3 lysine 27 (H3K27), H3 lysine 36 (H3K36) and the expression of H3K27 methylase EZH2 in patients with colorectal carcinomas with metachronous liver metastasis to search for biomarkers identifying these patients.Methods
Double 2-mm core tissue microarrays were made from 54 paraffin-embedded samples of primary colorectal adenocarcinomas and corresponding liver metastases and examined using an immunohistochemical analysis of dimethylation and trimethylation in H3K27, H3K36 and EZH2. Positive tumor cell staining for each histone modification (H-score) was used to classify patients into low- and high-staining groups, which were then examined to identify any correlations between the clinicopathological parameters and the clinical outcomes.Results
The H-scores of H3K27me2 were lower in the liver metastases than in the corresponding primary tumors, while the H-scores of H3K36me2 were higher in the liver metastases than in the corresponding primary tumors (P < 0.001). H3K27me2 in the primary tumors correlated with tumor size (P = 0.016), H3K36me2 in the primary tumors correlated with histological type (P = 0.038), and H3K36me3 in the primary tumors correlated with lymph node metastasis (P = 0.017). In addition, lower levels of H3K27me2 in the primary tumors correlated with poorer survival rates (P = 0.039). The multivariate survival analysis showed that the H3K27me2 status is an independent prognostic factor for colorectal cancer patients (P = 0.047).Conclusions
Our findings suggest that the methylation level of H3K27me2 detected with immunohistochemistry may be an independent prognostic factor for metachronous liver metastasis of colorectal carcinomas. 相似文献15.
Amanda Pigott Bena Brown Nicole White Steven McPhail Sandro Porceddu Howard Liu Claire Jeans Ben Panizza Jodie Nixon 《Asia-Pacific Journal of Clinical Oncology》2023,19(4):473-481
Introduction
Head and neck lymphedema can occur in the internal or external structures of the head and neck region. Little is known about the development of this condition over the course of treatment for head and neck cancer. This study aimed to observe the development of internal and external lymphedema from diagnosis to 12 weeks postacute treatment.Methods
A single center, prospective observational cohort study assessed participants for external lymphedema, internal lymphedema, quality of life, and symptom burden. Assessments were conducted prior to starting radiotherapy (RT), at the end of RT, 6 and 12 weeks after RT.Results
Forty-six participants were recruited. External lymphedema as measured by percentage water content, increased from 41.9 at baseline (95% CI: 39.3–44.4) to 50.4 (95% CI: 46.0–54.8) at 12 weeks following RT (p-value < .001). After adjusting for changes in weight and participant age at baseline, a general increase in tape measurements was observed over time with significant increases from baseline to 12 weeks post-RT for all measurement points. By 12 weeks post-RT, all participants had lymphedema present in eight of 13 internal sites assessed.Conclusions
Internal and external head and neck lymphedema was observed to increase from baseline to 12 weeks after completion of RT without abatement. People with head and neck cancer should be educated about the potentially extended duration of this treatment side effect. Further research is required to determine the point at which swelling symptoms recede. 相似文献16.
Mansoor R. Mirza MD Antonio González-Martín MD PhD Whitney S. Graybill MD David M. O’Malley MD Lydia Gaba MD Oi Wah Stephanie Yap MD Eva M. Guerra MD Peter G. Rose MD Jean-François Baurain MD PhD Sharad A. Ghamande MD MBBS Hannelore Denys MD PhD Emily Prendergast MD Carmela Pisano MD Philippe Follana MD Klaus Baumann MD Paula M. Calvert MB Bch BAO Jacob Korach MD Yong Li PhD Izabela A. Malinowska MD PhD Divya Gupta MD Bradley J. Monk MD 《Cancer》2023,129(12):1846-1855
Background
The PRIMA/ENGOT-OV26/GOG-3012 (NCT02655016) trial was amended to prospectively evaluate the safety and efficacy of an individualized starting dose (ISD) regimen of niraparib for first-line maintenance therapy in patients with newly diagnosed advanced ovarian cancer.Methods
In the phase 3 PRIMA trial, patients with newly diagnosed advanced ovarian cancer with a complete/partial response to first-line platinum-based chemotherapy (N = 733) were initially treated with a fixed starting dose (FSD) regimen of 300 mg once daily. Subsequently, the protocol was amended so newly enrolled patients received an ISD: 200 mg once daily in patients with baseline body weight < 77 kg or baseline platelet count < 150,000/µL, and 300 mg once daily in all other patients. Efficacy and safety outcomes were assessed by starting dose.Results
Overall, 475 (64.8%) patients were assigned to an FSD (niraparib, n = 317; placebo, n = 158) and 258 (35.2%) were assigned to an ISD (niraparib, n = 170; placebo, n = 88). Efficacy in patients who received FSD or ISD was similar for the overall (FSD hazard ratio [HR], 0.59 [95% CI, 0.46–0.76] vs. ISD HR, 0.69 [95% CI, 0.48–0.98]) and the homologous recombination–deficient (FSD HR, 0.44 [95% CI, 0.30–0.64] vs. ISD HR, 0.39 [95% CI, 0.22–0.72]) populations. In patients with low body weight/platelet count, rates of grades ≥3 and 4 hematologic treatment-emergent adverse events, dose interruptions, and dose reductions were lower for those who received ISD than for those who received FSD.Conclusions
In PRIMA, similar dose intensity, similar efficacy, and improved safety were observed with the ISD compared with the FSD regimen. 相似文献17.
18.
Tamta Makharadze MD Ruben G. W. Quek PhD Tamar Melkadze MD Miranda Gogishvili MD Cristina Ivanescu PhD Davit Giorgadze MD Mikhail Dvorkin MD Konstantin Penkov MD Konstantin Laktionov MD Gia Nemsadze MD Marina Nechaeva MD Irina Rozhkova MD Ewa Kalinka MD Christian Gessner MD Brizio Moreno-Jaime MD Rodolfo Passalacqua MD Gerasimos Konidaris MSc Petra Rietschel MD PhD Giuseppe Gullo MD 《Cancer》2023,129(14):2256-2265
Background
EMPOWER-Lung 3, a randomized 2:1 phase 3 trial, showed clinically meaningful and statistically significant overall survival improvement with cemiplimab plus platinum-doublet chemotherapy versus placebo plus chemotherapy for first-line treatment of advanced non–small cell lung cancer. This study evaluated patient-reported outcomes (PROs).Methods
PROs were assessed at day 1 (baseline), the start of each treatment cycle (every 3 weeks) for the first six doses, and then at start of every three cycles, using the European Organisation for Research and Treatment of Cancer (EORTC) Quality of Life-Core 30 (QLQ-C30) and Quality of Life-Lung Cancer Module (QLQ-LC13) questionnaires. Prespecified analyses included a longitudinal mixed-effect model comparing treatment arms and a time to definitive clinically meaningful deterioration (TTD) analysis performed for global health status/quality of life (GHS/QoL) and all scales from the questionnaires. Between-arm TTD comparisons were made using a stratified log-rank test and proportional hazards model.Results
A total of 312 patients were assigned to receive cemiplimab plus platinum-doublet chemotherapy and 154 to receive placebo plus chemotherapy; 391 (83.9%) were male and the median age was 63.0 years (range, 25–84). For pain symptoms (EORTC QLQ-C30), a statistically significant overall improvement from baseline (−4.98, 95% confidence interval [CI] −8.36 to −1.60, p = .004) and a statistically significant delay in TTD (hazard ratio, 0.39; 95% CI, 0.26–0.60, p < .0001) favoring cemiplimab plus chemotherapy were observed. Statistically significant delays in TTD, all favoring cemiplimab plus chemotherapy, were also observed in functioning and symptom scales. A significant overall improvement from baseline in GHS/QoL was seen for cemiplimab plus chemotherapy compared with nonsignificant overall change from baseline for placebo plus chemotherapy (1.69, 95% CI, 0.20–3.19 vs. 1.08, 95% CI, –1.34 to 3.51; between arms, p = .673). No analyses yielded statistically significant PRO results favoring placebo plus chemotherapy for any QLQ-C30 or QLQ-LC13 scale.Conclusion
Cemiplimab plus chemotherapy resulted in significant overall improvement in pain symptoms and delayed TTD in cancer-related and lung cancer–specific symptoms and functions. 相似文献19.
Peiman Haddad Mostafa Farzin Farnaz Amouzegar-Hashemi Bita Kalaghchi Shadi Babazadeh Hamid-Reza Mirzaei Ahmad Mousavizadeh Iraj Harirchi Jahangir Rafat 《Breast cancer (Tokyo, Japan)》2010,17(4):281-285
Background
We performed a cross-sectional multicentre study to assess the prevalence of lymphedema after breast cancer treatment in Iran. 相似文献20.
Clara Bodelon Margaret M. Madeleine Lynda F. Voigt Noel S. Weiss 《Cancer causes & control : CCC》2009,20(9):1779-1782