当前位置: 首页 >> 检索结果
共有 3027 条符合本次的查询结果, 用时 9.1662888 秒

2801. A systematic review and meta-analysis of intravenous palonosetron in the prevention of chemotherapy-induced nausea and vomiting in adults.

作者: Zhou Likun.;Jing Xiang.;Ba Yi.;Duan Xin.;Zheng Liu Tao.
来源: Oncologist. 2011年16卷2期207-16页
We performed a systematic review and meta-analysis to compare treatment effectiveness and adverse effects in cancer patients receiving chemotherapy with palonosetron to prevent chemotherapy-induced nausea and vomiting (CINV).

2802. ERCC1 and ERCC2 polymorphisms predict clinical outcomes of oxaliplatin-based chemotherapies in gastric and colorectal cancer: a systemic review and meta-analysis.

作者: Ming Yin.;Jingrong Yan.;Eva Martinez-Balibrea.;Francesco Graziano.;Heinz-Josef Lenz.;Hyo-Jin Kim.;Jacques Robert.;Seock-Ah Im.;Wei-Shu Wang.;Marie-Christine Etienne-Grimaldi.;Qingyi Wei.
来源: Clin Cancer Res. 2011年17卷6期1632-40页
Nucleotide excision repair (NER) modulates platinum-based chemotherapeutic efficacy by removing drug-produced DNA damage. To summarize published data on the association between polymorphisms of NER genes (ERCC1 and ERCC2) and responses to oxaliplatin-based chemotherapies, we carried out a meta-analysis of gastric and colorectal cancer for commonly studied polymorphisms ERCC1 rs11615C>T and ERCC2 rs13181T>G.

2803. Treatment including anthracyclines versus treatment not including anthracyclines for childhood cancer.

作者: Elvira C van Dalen.;Martine F Raphaël.;Huib N Caron.;Leontien Cm Kremer.
来源: Cochrane Database Syst Rev. 2011年1期CD006647页
One of the most important adverse effects of anthracyclines is cardiotoxicity. A well-informed decision on the use of anthracyclines in the treatment of childhood cancers should be based on evidence regarding both antitumour efficacy and cardiotoxicity.

2804. Quality-of-life measurement in randomized clinical trials in breast cancer: an updated systematic review (2001-2009).

作者: Julie Lemieux.;Pamela J Goodwin.;Louise J Bordeleau.;Sophie Lauzier.;Valérie Théberge.
来源: J Natl Cancer Inst. 2011年103卷3期178-231页
Quality-of-life (QOL) measurement is often incorporated into randomized clinical trials in breast cancer. The objectives of this systematic review were to assess the incremental effect of QOL measurement in addition to traditional endpoints (such as disease-free survival or toxic effects) on clinical decision making and to describe the extent of QOL reporting in randomized clinical trials of breast cancer.

2805. The safety and efficacy of EGFR TKIs monotherapy versus single-agent chemotherapy using third-generation cytotoxics as the first-line treatment for patients with advanced non-small cell lung cancer and poor performance status.

作者: Shan Liu.;Deqiang Wang.;Bo Chen.;Yan Wang.;Weihong Zhao.;Jianqing Wu.
来源: Lung Cancer. 2011年73卷2期203-10页
To assess the risk/benefit profiles of EGFR TKIs monotherapy using erlotinib or gefitinib in comparison with single-agent chemotherapy using third-generation cytotoxics (gemcitabine, vinorelbine, taxanes) as the first-line treatment for chemonaÏve patients with advanced non-small cell lung cancer (ANSCLC) and poor performance status (PS).

2806. Filling in the gaps: reporting of concurrent supportive care therapies in breast cancer chemotherapy trials.

作者: Orit Freedman.;Eitan Amir.;Camilla Zimmermann.;Mark Clemons.
来源: Support Care Cancer. 2011年19卷3期315-22页
Supportive care interventions can have a substantial impact on side effects of chemotherapy. Consequently, accurate reporting of such interventions is essential when interpreting clinical trial results. This study determined the prevalence and quality of reporting of supportive care treatment for common chemotherapy-induced toxicities in phase III, breast cancer chemotherapy trials.

2807. Measures of chemotherapy-induced peripheral neuropathy: a systematic review of psychometric properties.

作者: Kathleen A Griffith.;Ingemar S J Merkies.;Elizabeth E Hill.;David R Cornblath.
来源: J Peripher Nerv Syst. 2010年15卷4期314-25页
Chemotherapy-induced peripheral neuropathy (CIPN) remains the principal dose-limiting toxicity of many agents. This systematic review evaluates available CIPN measures and provides rationale for selection of measures in this field. Searches of Medline (1966-2010), CINAHL (1966-2010), Embase (1966-2010), and Cochrane (1988-2010) databases were performed. To be selected, studies had to include (1) subjects receiving peripheral neurotoxic chemotherapy for cancer and (2) a primary purpose of psychometric evaluation of CIPN measures. A modified Quality of Diagnostic Accuracy Studies (QUADAS) tool coded psychometric study quality, with 0-7 score overall possible (higher score indicating better quality). A total of 15 studies qualified for evaluation. Overall studies were of moderate quality, with 10 of 15 receiving a 4-5 QUADAS score. Averaged quality scores for two repeatedly studied measures, Total Neuropathy Score (TNS) versions and Functional Assessment of Cancer-Gynecologic Oncology Group, neurotoxicity (FACT/GOG-Ntx), were 5.4 and 4.5, respectively. Two measures emerged as potentially useful for clinical trials and patient care. The FACT/GOG-Ntx is a subjective measure of CIPN-related quality of life (QoL). TNS clinical versions incorporate both subjective measures and objective examinations of nerve function. However, to improve QUADAS scoring, additional research is needed focusing on other psychometric aspects such as responsiveness of CIPN outcome measures.

2808. Efficacy and safety of vandetanib, a dual VEGFR and EGFR inhibitor, in advanced non-small-cell lung cancer: a systematic review and meta-analysis.

作者: Xinji Zhang.;Yingyi Qin.;Hui Li.;Chong Bai.;Tianyi Zhu.;Jinfang Xu.;Cheng Wu.;Mengjie Wu.;Chaoxiang Wang.;Hualing Song.;Lixin Wei.;Jia He.
来源: Asian Pac J Cancer Prev. 2011年12卷11期2857-63页
Vandetanib, an oral inhibitor of vascular endothelial growth factor receptor and epidermal growth factor receptor signaling, has attracted wide interest in treatment of advanced non-small-cell lung cancer (NSCLC). We aimed to assess its efficacy and safety via a systematic review and meta-analysis.

2809. Rituximab in Hodgkin lymphoma: is the target always a hit?

作者: Kamal S Saini.;Hatem A Azim.;Emilia Cocorocchio.;Anna Vanazzi.;Monika Lamba Saini.;Paola Rafaniello Raviele.;Giancarlo Pruneri.;Fedro A Peccatori.
来源: Cancer Treat Rev. 2011年37卷5期385-90页
In 1997, the anti-CD20 monoclonal antibody (MAb) rituximab became the first MAb approved for clinical use in oncology, and ushered in a new era of rationally designed targeted agents in cancer therapeutics. It is currently approved for use in non-Hodgkin lymphoma (NHL), chronic lymphoid leukemia (CLL), and rheumatoid arthritis (RA). Rituximab is non-mutagenic, associated with low treatment-related toxicity, and few, if any, long term adverse events, making it an attractive agent to be tried in off-label settings like Hodgkin lymphoma (HL). HL consists of two distinct subtypes - classic HL (cHL) and lymphocyte predominant HL (LPHL). CD20 is present in virtually all patients with LPHL, and in a significant minority of patients with cHL. In this CD20 positive sub-population, the use of rituximab is a rational intervention strategy. Rituximab has been used in patients with cHL as well as LPHL with good efficacy. In this article, we provide a clinically-oriented overview of the use of rituximab in the different sub-types of HL, and report updated results of our series of 8 LPHL patients treated with rituximab. A systematic review of the literature is also presented.

2810. Managing bone health with zoledronic acid: a review of randomized clinical study results.

作者: P Hadji.
来源: Climacteric. 2011年14卷3期321-32页
To systematically review randomized, controlled clinical trials for managing osteoporosis, cancer treatment-induced bone loss, and bone metastases from breast cancer using zoledronic acid (ZOL).

2811. Biomechanical analysis of hyoid bone displacement in videofluoroscopy: a systematic review of intervention effects.

作者: Jolien G J van der Kruis.;Laura W J Baijens.;Renée Speyer.;Iris Zwijnenberg.
来源: Dysphagia. 2011年26卷2期171-82页
This systematic review explores studies using biomechanical analysis of hyoid bone displacement in videofluoroscopy of swallowing as a spatial outcome parameter to evaluate intervention effects. Two authors independently carried out the literature search using the electronic databases Embase, PubMed, and Cochrane Library. Differences in their search findings were settled by discussion. The search was limited to publications in the English, German, French, Spanish, or Dutch language. MeSH terms were used, supplemented by free-text words to identify the most recent publications. In addition, reference lists were searched by hand. Only studies using videofluoroscopy to evaluate the biomechanical effects of swallowing interventions in dysphagic subjects were included in the review. While the body of literature on measuring hyoid bone displacement in videofluoroscopy has grown, only 12 studies met the inclusion criteria. Several of the 12 studies had methodological shortcomings. In general, the conclusions could not be compared across the studies because of their heterogeneous designs and outcome measures. Overall, several intervention effect studies reported significant results. In particular, bolus modification and swallowing maneuvers showed a greater range of hyoid bone displacement. In light of this review, further research on hyoid bone displacement as a spatial variable in well-defined patient populations using well-defined videofluoroscopic protocols to measure intervention effects is recommended.

2812. Criteria of evidence to move potential chemopreventive agents into late phase clinical trials.

作者: Ronan J Kelly.;Ariel Lopez-Chavez.;Eva Szabo.
来源: Curr Drug Targets. 2011年12卷13期1983-8页
Preclinical models and data from clinical trials suggest that cancer is a preventable disease. However, demonstration of a preventive effect requires large phase III clinical trials of long duration and involves many thousands of participants. The decision to proceed with phase III studies therefore must be informed by robust efficacy and safety data. This requires a systematic review of all available preclinical, epidemiological, and clinical data, along with a mechanistic understanding of the biology of the disease under study. In this review we identify the issues that are critical to decision-making prior to embarking on late phase prevention clinical trials and provide a framework for making such decisions.

2813. Interventions for preventing oral mucositis for patients with cancer receiving treatment.

作者: Helen V Worthington.;Jan E Clarkson.;Gemma Bryan.;Susan Furness.;Anne-Marie Glenny.;Anne Littlewood.;Martin G McCabe.;Stefan Meyer.;Tasneem Khalid.
来源: Cochrane Database Syst Rev. 2010年12期CD000978页
Treatment of cancer is increasingly more effective but is associated with short and long term side effects. Oral side effects remain a major source of illness despite the use of a variety of agents to prevent them. One of these side effects is oral mucositis (mouth ulcers).

2814. Risk/benefit profile of bevacizumab in metastatic colon cancer: a systematic review and meta-analysis.

作者: Elena Galfrascoli.;Sheila Piva.;Michela Cinquini.;Antonio Rossi.;Nicla La Verde.;Annalisa Bramati.;Anna Moretti.;Andrea Manazza.;Giovanna Damia.;Valter Torri.;Gaetana Muserra.;Gabriella Farina.;Marina Chiara Garassino.; .
来源: Dig Liver Dis. 2011年43卷4期286-94页
Bevacizumab, an anti vascular endothelial growth factor antibody is licensed in several tumours and widely used in colorectal cancer. However, bevacizumab has several adverse effects which may appear unexpectedly and differ according to the tumour.

2815. Gonadotropin-releasing hormone analog cotreatment for preservation of ovarian function during gonadotoxic chemotherapy: a systematic review and meta-analysis.

作者: Mohamed A Bedaiwy.;Ahmed M Abou-Setta.;Nina Desai.;William Hurd.;David Starks.;Sherif A El-Nashar.;Hesham G Al-Inany.;Tommaso Falcone.
来源: Fertil Steril. 2011年95卷3期906-14.e1-4页
To determine whether gonadotropin-releasing hormone (GnRH) analog cotreatment with chemotherapy provides better reproductive outcomes for women at risk of premature ovarian failure (POF) as a side-effect of gonadotoxic chemotherapy.

2816. A systematic review of the literature on the effects of dexamethasone on the brain from in vivo human-based studies: implications for physiological brain imaging of patients with intracranial tumors.

作者: Christina Kotsarini.;Paul D Griffiths.;Iain D Wilkinson.;Nigel Hoggard.
来源: Neurosurgery. 2010年67卷6期1799-815; discussion 1815页
Among glucocorticoids, dexamethasone is most widely used for treatment of cerebral edema because of its long biological half-life and its low mineralocorticoid activity (sodium retaining).

2817. Dose-dense chemotherapy in nonmetastatic breast cancer: a systematic review and meta-analysis of randomized controlled trials.

作者: Luisa Bonilla.;Irit Ben-Aharon.;Liat Vidal.;Anat Gafter-Gvili.;Leonard Leibovici.;Salomon M Stemmer.
来源: J Natl Cancer Inst. 2010年102卷24期1845-54页
Dose-dense chemotherapy has become a mainstay regimen in the adjuvant setting for women with high-risk breast cancer. We performed a systematic review and meta-analysis of the existing data from randomized controlled trials regarding the efficacy and toxicity of the dose-dense chemotherapy approach in nonmetastatic breast cancer.

2818. Increased risk of serious hemorrhage with bevacizumab in cancer patients: a meta-analysis.

作者: Sanjaykumar Hapani.;Amna Sher.;David Chu.;Shenhong Wu.
来源: Oncology. 2010年79卷1-2期27-38页
The role of the widely-used angiogenesis inhibitor bevacizumab in the development of serious hemorrhage is not well defined in cancer patients. This study was conducted to determine the overall risk of hemorrhage with bevacizumab by a systematic review and meta-analysis of randomized controlled trials (RCT).

2819. A systematic review of drug-induced subacute cutaneous lupus erythematosus.

作者: G C Lowe.;C L Henderson.;R H Grau.;C B Hansen.;R D Sontheimer.
来源: Br J Dermatol. 2011年164卷3期465-72页
The initial appearance of subacute cutaneous lupus erythematosus (SCLE) skin lesions in conjunction with Ro/SS-A autoantibodies occurring as an adverse reaction to hydrochlorothiazide [i.e. drug-induced SCLE (DI-SCLE)] was first reported in 1985. Over the past decade an increasing number of drugs in different classes has been implicated as triggers for DI-SCLE. The management of DI-SCLE can be especially challenging in patients taking multiple medications capable of triggering DI-SCLE. Our objectives were to review the published English language literature on DI-SCLE and use the resulting summary data pool to address questions surrounding drug-induced SCLE and to develop guidelines that might be of value to clinicians in the diagnosis and management of DI-SCLE. A systematic review of the Medline/PubMed-cited literature on DI-SCLE up to August 2009 was performed. Our data collection and analysis strategies were prospectively designed to answer a series of questions related to the clinical, prognostic and pathogenetic significance of DI-SCLE. One hundred and seventeen cases of DI-SCLE were identified and reviewed. White women made up the large majority of cases, and the mean overall age was 58·0 years. Triggering drugs fell into a number of different classes, highlighted by antihypertensives and antifungals. Time intervals ('incubation period') between drug exposure and appearance of DI-SCLE varied greatly and were drug class dependent. Most cases of DI-SCLE spontaneously resolved within weeks of drug withdrawal. Ro/SS-A autoantibodies were present in 80% of the cases in which such data were reported and most remained positive after resolution of SCLE skin disease activity. No significant differences in the clinical, histopathological or immunopathological features between DI-SCLE and idiopathic SCLE were detected. There is now adequate published experience to suggest that DI-SCLE does not differ clinically, histopathologically or immunologically from idiopathic SCLE. It should be recognized as a distinct clinical constellation differing clinically and immunologically from the classical form of drug-induced systemic lupus erythematosus.

2820. 5-α-Reductase inhibitors for prostate cancer chemoprevention: an updated Cochrane systematic review.

作者: Timothy J Wilt.;Roderick Macdonald.;Karen Hagerty.;Paul Schellhammer.;James Tacklind.;Mark R Somerfield.;Barnett S Kramer.
来源: BJU Int. 2010年106卷10期1444-51页
• To estimate the benefits and harms of 5-α-reductase inhibitors (5-α-RIs) in preventing prostate cancer.
共有 3027 条符合本次的查询结果, 用时 9.1662888 秒