Background: C-reactive protein (CRP), considered as a prototypical inflammatory cytokine, has beenproposed to be involved in tumor progression through inflammation. Recent studies have indicated CRP asa progostic predictor for urological cancers, but the results remain controversial. Materials and Methods: Asystematic search of Medline, Scopus and the Cochrane Library was performed to identify eligible studiespublished between Jan 1, 2001 and Sep 1, 2013. Outcomes of interest were collected from studies comparingoverall survival (OS), cancer-specific survival (CSS) and relapse-free survival (RFS) in patients with elevatedCRP levels and those having lower levels. Studies were pooled, and combined hazard ratio (HR) of CRP withits 95% confidence interval (CI) for survival were used for the effect size estimate. Results: A total of 43 studies(7,490 patients) were included in this meta-analysis (25 for RCC, 10 for UC, and 8 for PC). Our pooled resultsshowed that elevated serum CRP level was associated with poor OS (HR: 1.26, 95%CI: 1.22-1.30) and RFS (HR:1.38 95%CI: 1.29-1.47), respectively. For CSS the pooled HR (HR: 1.33, 95%CI: 1.28-1.39) for higher CRPexpression could strongly predict poorer survival in urological cancers. Simultaneously, elevated serum CRPwas also significantly associated with poor prognosis in the subgroup analysis. Conclusions: Our pooled resultsdemonstrate that a high serum level of CRP as an inflammation biomarker denotes a poor prognosis of patientswith urological cancers. Further large prospective studies should be performed to confirm whether CRP, as abiomarker of inflammation, has a prognostic role in urological cancer progression. 相似文献
Introduction: Sarcopenia, the degenerative and systemic loss of skeletal muscle mass, develops as a consequence of the progression of cancer cachexia. Recent studies suggest that sarcopenia may be used as a biomarker in the management of patients with several cancers.
Areas covered: In this article, the authors review 1) the methods to simply and optimally evaluate and define sarcopenia using computed tomography images in daily clinical practice and 2) the impact of sarcopenia in the management of urological cancers, specifically focusing on the usefulness in predicting treatment-related complications and prognosis. The authors also discuss the prognostic importance of changes in skeletal muscle mass in the course of treatment and the potential roles of nutritional support and exercise to prevent progression of sarcopenia.
Expert commentary: Sarcopenia is associated with treatment-related complications and unfavorable prognosis in urological cancer patients. Nutritional support and exercise might be helpful in improving sarcopenia. The impact of these interventions on clinical outcomes would be elucidated by ongoing or future clinical studies. 相似文献
Purpose: The parapelvic renal cyst is a relatively common finding on routine urological examination, butonly rarely needs treatment. We here examined all parapelvic renal cyst patients who consulted our Departmentbetween April 1998 and December 2004 with the focus on potential for malignant development. Materials andMethods: A total of 73 patients were diagnosed as having parapelvic renal cysts by ultrasonography, incombination with computed tomography, and/or drip infusion urography in our Department. The backgroundto diagnosis was suspicion of hydronephrosis in 15, flank and/or back pain in 15, and macroscopic hematuriaand/or occult blood urine in 12. Results: There were 3 patients with renal pelvic cancer, and one patient withureteral cancer. Nephro-ureterectomy was performed for all of these 4 cases. There were 10 patients with renalstones, three of which were given extracorporeal shock wave lithotripsy and one pyelonephrolithotomy. A furtherthree underwent parapelvic renal cyst puncture, performed to preserve renal function or obtain release fromsymptoms. The remaining 3 cases were symptomless, diagnosed after routine examinations, and were simplyfollowed up, as with the other 59 cases with no stones or cancer. Conclusions: Unless a parapelvic renal cystcauses pyelonephritis, symptomatic renal stones, or back discomfort, treatment is not indicated. However, thepossibility that urological malignant disease may be encountered should be borne in mind and appropriatediagnostic measures should be performed. Furthermore, careful follow up of parapelvic renal cyst patients maybe required. 相似文献
What’s known on the subject? and What does the study add? Metastatic bladder cancer is a devastating disease that often proves fatal. Systemic chemotherapy with MVAC (methotrexate, vinblastine, adriamycin, cisplatin) has been the first choice of treatment for many years but toxicity can be severe and overall survival poor. The search for more effective drug combinations continues. Clinical data indicate that gemcitabine has activity in this disease in terms of tumour response and overall survival. This systematic review comprehensively presents the available clinical evidence on gemcitabine chemotherapy for the management of metastatic bladder cancer. Limited data from randomized trials suggest that cisplatin plus gemcitabine may be considered a viable first‐line option for this disease and that the less toxic combination of gemcitabine plus carboplatin may be suitable for patients with poor renal function or low performance status. Data from observational studies highlight the wide variation in drug combinations and schedules used and the need for a systematic approach to clinical research with gemcitabine.
OBJECTIVE
? To systematically review the literature on gemcitabine chemotherapy for advanced or metastatic bladder cancer.
MATERIALS AND METHODS
? The Medical Literature Analysis and Retrieval System Onlinedatabase (MEDLINE), the Excerpta Medicadatabase (EMBASE), the Cumulative Index to Nursing and Allied Health Literature database(CIHNAL), the Cochrane database of randomized trials, the Literatura Latino‐Americana e do Caribe emCiências da Saúdedatabase (LILACS), and Web of Science were searched to identify trials of gemcitabine for metastatic bladder cancer. Also searched were international guidelines on metastatic prostate cancer, trial registries, and recent systematic reviews. Data on trial design, survival, tumour response and toxicity outcomes were extracted from relevant studies.
RESULTS
? This review identified six randomized trials of combined chemotherapy with gemcitabine for the management of unresectable, locally advanced or metastatic bladder cancer. ? One trial compared gemcitabine plus cisplatin (GCis) with methotrexate/vinblastine/doxorubicin/cisplatin(MVAC) and found no difference in overall survival (OS; hazard ratio 1.09) but a better safety profile with GCis, which was suggested as the treatment of choice. ? A second trial evaluated GCis against gemcitabine plus carboplatin (GCarbo) and reported similar median OS (12.8 vs 9.8 months), disease progression (8.3 vs 7.3 months) and tumour response rates (66% vs 56%) for the two patient groups. ? A third trial compared GCis with GCis plus paclitaxel (GCisPac) and showed no significant difference in median OS (12.3 vs 15.3 months) and response rates (44% vs 43%) but greater toxicity with GCisPac. ? A fourth trial assessed GCarbo against methotrexate plus carboplatin plus vinblastine in patients unfit for cisplatin‐based chemotherapy and found similar tumour response rates for each regime (38% vs 20%) but the triplet regime was more toxic. ? Two other randomized studies compared a 2‐weekly maintenance regime of gemcitabine plus paclitaxel with a 3‐weelky regime given for a maximum of six cycles and found that the maintenance schedule did not confer any additional survival benefit. ? In all, 53observational studies of gemcitabine chemotherapy were identified that varied considerably in the drug combinations used and schedules. Overall response rates (17–78%) and median OS (6.4–24.0 months) were variable with no combination being clearly superior.
CONCLUSIONS
? Gemcitabine combined chemotherapy is active in the management of metastatic bladder cancer. ? GCis may be considered an alternative regime to MVAC. ? GCarbo should be considered for patients unfit for cisplatin‐based therapy. 相似文献
IntroductionSurgical oncology strives to remove the primary cancer tumor together with its local lymphatic tissue. One of the techniques improving the staging of lymph nodes is sentinel node biopsy. The most common agent used in SNB is indocyanine green (ICG). Indocyanine green is characterized by its high affinity for human serum albumin (HSA). In practice, the visualization of the sentinel node is enhanced by attaching a relatively large carrier to the ICG molecule. The aim of this study was to investigate whether the covalent linking of ICG to a nanocolloid would extend the time of detection of the dye as it binds to HSA, assessed by fluorescence measurements in vitro.Material and methodsThe influence of the molar concentration of ICG on its ability to form a complex with HSA was investigated. The dye luminescence was measured, with an increasing amount of dye in the presence of a constant concentration of HSA. The stability of the ICG:HSA complex was also investigated.ResultsThe binding of ICG and human protein in a solution ratio of 3 : 1 made it possible to detect the ICG luminescence with better and prolonged visibility. In the case of the two lowest ratios, complex formation was not observed. The use of ICG bound to a nanocolloid based on human serum albumin increases the luminescence of the HSA : ICG complex up to 98%.ConclusionsProperly selected proportions of human albumin protein and ICH allowed higher and longer luminescence to be achieved. Nevertheless, further studies are necessary to establish the optimal concentration ratio. 相似文献