首页 > 最新文献

Onkologie最新文献

英文 中文
Fatigue in the general population of Colombia - normative values for the multidimensional fatigue inventory MFI-20. 哥伦比亚普通人群的疲劳程度——多维疲劳量表MFI-20的规范性值。
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2013-01-01 Epub Date: 2013-06-28 DOI: 10.1159/000353606
Andreas Hinz, Carolyn Finck Barboza, Susana Barradas, Annett Körner, Volker Beierlein, Susanne Singer

Background: Fatigue is a frequent symptom in cancer patients. In Europe and Northern America fatigue questionnaires were developed and tested, but their generalizability to other cultural contexts is largely unknown. The aim of this study is to provide normative values for the Multidimensional Fatigue Inventory (MFI-20) based on a representative sample of the general population in Colombia and to test psychometric properties.

Methods: 1,500 individuals completed a questionnaire that contained the MFI-20, as well as other questionnaires, and questions on sociodemographic variables and chronic diseases.

Results: The mean values of the scales were marginally higher than those for 2 European samples. The mean value of the total score was 44.3 ± 14.1. Women were affected by fatigue more than men, and there was an almost linear age trend, with higher mean scores for older subjects. People with chronic diseases were affected by fatigue more than people without chronic conditions. The best psychometric properties were obtained for the total scale (sum score) of the MFI-20.

Conclusion: The normative values presented here can help us to assess the individual burden of fatigue in a Latin American context. Psychometric properties of the MFI-20 in Colombia are similar to those obtained in Europe.

背景:疲劳是癌症患者的常见症状。在欧洲和北美,人们开发并测试了疲劳问卷,但它们在其他文化背景下的普遍性在很大程度上是未知的。本研究的目的是为多维疲劳量表(MFI-20)提供基于哥伦比亚普通人群代表性样本的规范性值,并测试心理测量特性。方法:对1500名个体进行问卷调查,问卷内容包括MFI-20、其他问卷、社会人口学变量和慢性病问题。结果:量表的平均值略高于2个欧洲样本。总评分平均值为44.3±14.1。女性比男性更容易受到疲劳的影响,而且年龄几乎呈线性趋势,年龄越大的受试者平均得分越高。患有慢性疾病的人比没有慢性疾病的人更容易受到疲劳的影响。MFI-20总量表(总分)的心理测量学性质最好。结论:这里提出的规范性值可以帮助我们评估拉丁美洲背景下的个人疲劳负担。哥伦比亚的MFI-20的心理测量特性与欧洲的相似。
{"title":"Fatigue in the general population of Colombia - normative values for the multidimensional fatigue inventory MFI-20.","authors":"Andreas Hinz,&nbsp;Carolyn Finck Barboza,&nbsp;Susana Barradas,&nbsp;Annett Körner,&nbsp;Volker Beierlein,&nbsp;Susanne Singer","doi":"10.1159/000353606","DOIUrl":"https://doi.org/10.1159/000353606","url":null,"abstract":"<p><strong>Background: </strong>Fatigue is a frequent symptom in cancer patients. In Europe and Northern America fatigue questionnaires were developed and tested, but their generalizability to other cultural contexts is largely unknown. The aim of this study is to provide normative values for the Multidimensional Fatigue Inventory (MFI-20) based on a representative sample of the general population in Colombia and to test psychometric properties.</p><p><strong>Methods: </strong>1,500 individuals completed a questionnaire that contained the MFI-20, as well as other questionnaires, and questions on sociodemographic variables and chronic diseases.</p><p><strong>Results: </strong>The mean values of the scales were marginally higher than those for 2 European samples. The mean value of the total score was 44.3 ± 14.1. Women were affected by fatigue more than men, and there was an almost linear age trend, with higher mean scores for older subjects. People with chronic diseases were affected by fatigue more than people without chronic conditions. The best psychometric properties were obtained for the total scale (sum score) of the MFI-20.</p><p><strong>Conclusion: </strong>The normative values presented here can help us to assess the individual burden of fatigue in a Latin American context. Psychometric properties of the MFI-20 in Colombia are similar to those obtained in Europe.</p>","PeriodicalId":19684,"journal":{"name":"Onkologie","volume":"36 7-8","pages":"403-7"},"PeriodicalIF":0.3,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000353606","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31638491","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 22
Primary intracranial small cell carcinoma: a case report and review of the literature. 原发性颅内小细胞癌1例报告及文献复习。
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2013-01-01 Epub Date: 2013-07-08 DOI: 10.1159/000353566
Sheng Zhang, Qian Cai, Li Fan, Ruiguang Zhang, Yingchao Zhao, Gang Wu, Xiaorong Dong

Background: Extrapulmonary small cell carcinoma is a distinct clinicopathological entity accounting for only 2.5-4% of small cell carcinomas. Here we present a case of primary intracranial small cell carcinoma.

Case report: A 69-year-old woman with an isolated brain lesion presented with progressive headaches, confusion, nausea, and vomiting. A magnetic resonance imaging scan of the brain revealed a 4 × 3 × 5-cm solitary cystic tumor in the right frontoparietal lobe, accompanied by a midline shift. The mass was resected and pathologically proven to be a small cell carcinoma. The patient was given adjuvant radiotherapy but refused any chemotherapy. At the 12-month follow-up the patient was alive and well.

Conclusion: Primary intracranial small cell carcinoma presenting as an isolated lesion is extremely rare. While there are no standard treatment guidelines for these patients, the authors believe multimodality treatment including tumorectomy and postoperative radiotherapy should be recommended.

背景:肺外小细胞癌是一种独特的临床病理实体,仅占小细胞癌的2.5-4%。我们报告一例原发性颅内小细胞癌。病例报告:一名69岁女性,孤立脑损伤,表现为进行性头痛,意识不清,恶心和呕吐。脑磁共振成像扫描示右侧额顶叶一个4 × 3 × 5厘米的孤立囊性肿瘤,伴中线移位。肿块被切除,病理证实为小细胞癌。患者接受辅助放疗,但拒绝化疗。在12个月的随访中,患者活得很好。结论:原发性颅内小细胞癌表现为孤立病灶是极为罕见的。虽然这些患者没有标准的治疗指南,但作者认为应该推荐包括肿瘤切除术和术后放疗在内的多模式治疗。
{"title":"Primary intracranial small cell carcinoma: a case report and review of the literature.","authors":"Sheng Zhang,&nbsp;Qian Cai,&nbsp;Li Fan,&nbsp;Ruiguang Zhang,&nbsp;Yingchao Zhao,&nbsp;Gang Wu,&nbsp;Xiaorong Dong","doi":"10.1159/000353566","DOIUrl":"https://doi.org/10.1159/000353566","url":null,"abstract":"<p><strong>Background: </strong>Extrapulmonary small cell carcinoma is a distinct clinicopathological entity accounting for only 2.5-4% of small cell carcinomas. Here we present a case of primary intracranial small cell carcinoma.</p><p><strong>Case report: </strong>A 69-year-old woman with an isolated brain lesion presented with progressive headaches, confusion, nausea, and vomiting. A magnetic resonance imaging scan of the brain revealed a 4 × 3 × 5-cm solitary cystic tumor in the right frontoparietal lobe, accompanied by a midline shift. The mass was resected and pathologically proven to be a small cell carcinoma. The patient was given adjuvant radiotherapy but refused any chemotherapy. At the 12-month follow-up the patient was alive and well.</p><p><strong>Conclusion: </strong>Primary intracranial small cell carcinoma presenting as an isolated lesion is extremely rare. While there are no standard treatment guidelines for these patients, the authors believe multimodality treatment including tumorectomy and postoperative radiotherapy should be recommended.</p>","PeriodicalId":19684,"journal":{"name":"Onkologie","volume":"36 7-8","pages":"428-31"},"PeriodicalIF":0.3,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000353566","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31638495","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
[Oncological therapies - what are the patient relative outcomes?]. [肿瘤治疗-患者的相对结果是什么?]。
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2013-01-01 Epub Date: 2013-08-12 DOI: 10.1159/000353716
Michael Ehmann, Martin Härter, Ralf Rambach, Eva Winkler
3 Patientengruppen unterscheiden [1–3]: Etwa ein Drittel dieser Patienten praferiert eine rein symptomatische, auf die Lebensqualitat ausgerichtete Behandlung, ein Drittel wunscht bis zum Lebensende eine maximale Therapie und ein Drittel ist zunachst unentschieden, praferiert aber mit fortschreitender Erkrankung eine primar an der Lebensqualitat orientierte Behandlung. Zwischen den Patientengruppen zeigen sich Unterschiede bei der Krankheitsbewaltigung. So scheinen Patienten, die sehr lange an einer maximalen Therapie festhalten, haufiger eine unrealistische Prognoseeinschatzung zu haben als jene, die sich fur eine symptomorientierte Behandlung entscheiden [1, 4]. Die Diskrepanz zwischen dem Therapieziel des Arztes und dem des Patienten kann auf einer faktischen oder einer normativen Differenz beruhen: (1) Die faktische Differenz basiert darauf, dass der Patient seine Krankheitssituation nicht realistisch sieht [4, 5]. (2) Eine normative Differenz besteht, wenn der Patient die Situation zwar realistisch sieht, sie aber fur sich anders bewertet als der Arzt. Dies ist gerade bei schwerkranken Patienten haufiger der Fall, die eher bereit sind, belastende Therapien zu ertragen als Gesunde [6, 7]. Aus Sicht des Behandlers stellt sich in solchen Situationen die Frage, ob ein Therapieverzicht gegen den Patientenwillen ethisch begrundbar ist bzw. ob er intensiver behandeln sollte, als er es fur sinnvoll halt, weil der Patient dies wunscht. Eine weitere Frage ist, ob es legitim ist, dem Patienten eine intensivere Therapie gar nicht anzubieten, weil sie aus arztlicher Sicht nicht infrage kommt. Klassischerweise stutzt sich die Therapieentscheidung auf die medizinische Indikation und den Patientenwillen. Lehnt der Patient eine Behandlung ab, darf diese nicht durchgefuhrt werden. Die Frage bleibt, ob der Arzt eine Therapie anbieten muss, die er nicht fur indiziert halt bzw. fur die es keine ausreichenden Wirknachweise gibt. Aus ethischer Sicht ist es wichtig, dass die TherapieentTeil 1: Bedurfnisse der Patienten integrieren Verantwortliche Autoren: Martin Harter, Hamburg, Eva Winkler, Heidelberg
{"title":"[Oncological therapies - what are the patient relative outcomes?].","authors":"Michael Ehmann,&nbsp;Martin Härter,&nbsp;Ralf Rambach,&nbsp;Eva Winkler","doi":"10.1159/000353716","DOIUrl":"https://doi.org/10.1159/000353716","url":null,"abstract":"3 Patientengruppen unterscheiden [1–3]: Etwa ein Drittel dieser Patienten praferiert eine rein symptomatische, auf die Lebensqualitat ausgerichtete Behandlung, ein Drittel wunscht bis zum Lebensende eine maximale Therapie und ein Drittel ist zunachst unentschieden, praferiert aber mit fortschreitender Erkrankung eine primar an der Lebensqualitat orientierte Behandlung. Zwischen den Patientengruppen zeigen sich Unterschiede bei der Krankheitsbewaltigung. So scheinen Patienten, die sehr lange an einer maximalen Therapie festhalten, haufiger eine unrealistische Prognoseeinschatzung zu haben als jene, die sich fur eine symptomorientierte Behandlung entscheiden [1, 4]. Die Diskrepanz zwischen dem Therapieziel des Arztes und dem des Patienten kann auf einer faktischen oder einer normativen Differenz beruhen: (1) Die faktische Differenz basiert darauf, dass der Patient seine Krankheitssituation nicht realistisch sieht [4, 5]. (2) Eine normative Differenz besteht, wenn der Patient die Situation zwar realistisch sieht, sie aber fur sich anders bewertet als der Arzt. Dies ist gerade bei schwerkranken Patienten haufiger der Fall, die eher bereit sind, belastende Therapien zu ertragen als Gesunde [6, 7]. Aus Sicht des Behandlers stellt sich in solchen Situationen die Frage, ob ein Therapieverzicht gegen den Patientenwillen ethisch begrundbar ist bzw. ob er intensiver behandeln sollte, als er es fur sinnvoll halt, weil der Patient dies wunscht. Eine weitere Frage ist, ob es legitim ist, dem Patienten eine intensivere Therapie gar nicht anzubieten, weil sie aus arztlicher Sicht nicht infrage kommt. Klassischerweise stutzt sich die Therapieentscheidung auf die medizinische Indikation und den Patientenwillen. Lehnt der Patient eine Behandlung ab, darf diese nicht durchgefuhrt werden. Die Frage bleibt, ob der Arzt eine Therapie anbieten muss, die er nicht fur indiziert halt bzw. fur die es keine ausreichenden Wirknachweise gibt. Aus ethischer Sicht ist es wichtig, dass die TherapieentTeil 1: Bedurfnisse der Patienten integrieren Verantwortliche Autoren: Martin Harter, Hamburg, Eva Winkler, Heidelberg","PeriodicalId":19684,"journal":{"name":"Onkologie","volume":"36 Suppl 6 ","pages":"5-8"},"PeriodicalIF":0.3,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000353716","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31693499","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Anxiety, posttraumatic stress, and fear of cancer progression in patients with melanoma in cancer aftercare. 癌症后护理中黑色素瘤患者的焦虑、创伤后应激和对癌症进展的恐惧。
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2013-01-01 Epub Date: 2013-09-17 DOI: 10.1159/000355137
Yesim Erim, Carmen Loquai, Ulrike Schultheis, Marion Lindner, Mingo Beckmann, Corinna Schadendorf, Wolfgang Senf

Unlabelled: Several studies have described mental distress and anxiety in patients with melanoma. The findings of these studies varied from patients with a quality of life similar to the general population and those with increased mental distress. In the present study, we investigated anxiety, posttraumatic stress, and fear of cancer progression to gain a detailed picture of the burdens of these patients.

Patients and methods: 70 patients with malignant melanoma who attended cancer aftercare were surveyed using the psychometric instruments Hospital Anxiety and Depression Scale (HADS), Posttraumatic Symptom Scale (PTSS-10), and Fear of Progression Questionnaire (FoP-Q). The questionnaires were evaluated and an analysis of the single items carried out.

Results: The scores for the three anxiety parameters were low, but 7% of the patients presented an increased HADS score, and 17% an increased PTSS-10 value. An analysis of the items showed that patients feared physical disabilities more than mental distress or lack of social support.

Conclusion: Most of the patients perceived themselves as stable, and relied on the assistance of their families. However, a small group of patients suffered from clinically relevant anxiety; these patients should be given the support indicated for their specific distress.

未标记:一些研究描述了黑色素瘤患者的精神痛苦和焦虑。这些研究的结果从生活质量与一般人群相似的患者到精神压力增加的患者各不相同。在本研究中,我们调查了焦虑、创伤后应激和对癌症进展的恐惧,以获得这些患者负担的详细情况。患者和方法:采用医院焦虑抑郁量表(HADS)、创伤后症状量表(ptsd -10)和进展恐惧问卷(op - q)对70例恶性黑色素瘤患者进行癌症后护理调查。对问卷进行了评估,并对单个项目进行了分析。结果:3项焦虑参数得分均较低,但有7%的患者出现HADS评分升高,17%的患者出现ptsd -10值升高。对这些项目的分析表明,患者更担心身体残疾,而不是精神痛苦或缺乏社会支持。结论:大多数患者认为自己病情稳定,并依赖于家人的帮助。然而,一小部分患者患有临床相关焦虑;这些患者应根据其具体的痛苦情况给予相应的支持。
{"title":"Anxiety, posttraumatic stress, and fear of cancer progression in patients with melanoma in cancer aftercare.","authors":"Yesim Erim,&nbsp;Carmen Loquai,&nbsp;Ulrike Schultheis,&nbsp;Marion Lindner,&nbsp;Mingo Beckmann,&nbsp;Corinna Schadendorf,&nbsp;Wolfgang Senf","doi":"10.1159/000355137","DOIUrl":"https://doi.org/10.1159/000355137","url":null,"abstract":"<p><strong>Unlabelled: </strong>Several studies have described mental distress and anxiety in patients with melanoma. The findings of these studies varied from patients with a quality of life similar to the general population and those with increased mental distress. In the present study, we investigated anxiety, posttraumatic stress, and fear of cancer progression to gain a detailed picture of the burdens of these patients.</p><p><strong>Patients and methods: </strong>70 patients with malignant melanoma who attended cancer aftercare were surveyed using the psychometric instruments Hospital Anxiety and Depression Scale (HADS), Posttraumatic Symptom Scale (PTSS-10), and Fear of Progression Questionnaire (FoP-Q). The questionnaires were evaluated and an analysis of the single items carried out.</p><p><strong>Results: </strong>The scores for the three anxiety parameters were low, but 7% of the patients presented an increased HADS score, and 17% an increased PTSS-10 value. An analysis of the items showed that patients feared physical disabilities more than mental distress or lack of social support.</p><p><strong>Conclusion: </strong>Most of the patients perceived themselves as stable, and relied on the assistance of their families. However, a small group of patients suffered from clinically relevant anxiety; these patients should be given the support indicated for their specific distress.</p>","PeriodicalId":19684,"journal":{"name":"Onkologie","volume":"36 10","pages":"540-4"},"PeriodicalIF":0.3,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000355137","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31793715","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 19
Far upstream element-binding protein 1 (FUBP1) is overexpressed in human gastric cancer tissue compared to non-cancerous tissue. 远上游元件结合蛋白1 (FUBP1)在人胃癌组织中与非癌组织相比过表达。
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2013-01-01 Epub Date: 2013-10-14 DOI: 10.1159/000355659
Fucheng Zhang, Qin Tian, Yaojun Wang

Background: The aim of this study was to investigate the role of far upstream element-binding protein 1 (FUBP1) in gastric cancer development.

Patients and methods: Using immunohistochemistry, we detected FUBP1 expression in 18 chronic superficial gastritis patients, 33 chronic atrophic gastritis patients, 21 moderate and severe gastric dysplasia patients, and 31 gastric cancer patients. FUBP1 mRNA expression in gastric cancer tissue and paraneoplastic tissue was measured with fluorescent quantitative reverse transcription polymerase chain reaction.

Results: The FUBP1 expression rates in the chronic atrophic gastritis, moderate and severe dysplasia, and gastric cancer patients were 51.51% (17/33), 76.19% (16/21), and 90.32% (28/31), respectively; these were higher than the expression rate of the chronic superficial gastritis patients (11.11%, 2/18). FUBP1 expression in the gastric cancer patients was significantly higher than that in the chronic atrophic gastritis patients. The relative amount (0.2593 ± 0.1209) of FUBP1 mRNA in the gastric cancer tissue was higher than that in paraneoplastic tissue (0.1969 ± 0.0211) (p < 0.05). There was a statistically significant correlation between overall survival rates and age, sex, lymph node metastasis, and distant metastasis (p < 0.05).

Conclusion: FUBP1 expression differs among gastric tissues. There is a correlation between overall survival rates and age, sex, lymph node metastasis, and distant metastasis.

背景:本研究旨在探讨远上游元件结合蛋白1 (FUBP1)在胃癌发生发展中的作用。患者及方法:应用免疫组化技术检测18例慢性浅表性胃炎、33例慢性萎缩性胃炎、21例中重度胃发育不良、31例胃癌患者中FUBP1的表达。荧光定量逆转录聚合酶链反应检测胃癌组织和副肿瘤组织中FUBP1 mRNA的表达。结果:FUBP1在慢性萎缩性胃炎、中重度非典型增生和胃癌患者中的表达率分别为51.51%(17/33)、76.19%(16/21)和90.32% (28/31);其表达率高于慢性浅表性胃炎患者(11.11%,2/18)。胃癌患者中FUBP1的表达明显高于慢性萎缩性胃炎患者。胃癌组织中FUBP1 mRNA的相对表达量(0.2593±0.1209)高于副肿瘤组织(0.1969±0.0211)(p < 0.05)。总生存率与年龄、性别、淋巴结转移及远处转移有统计学意义(p < 0.05)。结论:FUBP1在胃组织中的表达存在差异。总生存率与年龄、性别、淋巴结转移和远处转移有关。
{"title":"Far upstream element-binding protein 1 (FUBP1) is overexpressed in human gastric cancer tissue compared to non-cancerous tissue.","authors":"Fucheng Zhang,&nbsp;Qin Tian,&nbsp;Yaojun Wang","doi":"10.1159/000355659","DOIUrl":"https://doi.org/10.1159/000355659","url":null,"abstract":"<p><strong>Background: </strong>The aim of this study was to investigate the role of far upstream element-binding protein 1 (FUBP1) in gastric cancer development.</p><p><strong>Patients and methods: </strong>Using immunohistochemistry, we detected FUBP1 expression in 18 chronic superficial gastritis patients, 33 chronic atrophic gastritis patients, 21 moderate and severe gastric dysplasia patients, and 31 gastric cancer patients. FUBP1 mRNA expression in gastric cancer tissue and paraneoplastic tissue was measured with fluorescent quantitative reverse transcription polymerase chain reaction.</p><p><strong>Results: </strong>The FUBP1 expression rates in the chronic atrophic gastritis, moderate and severe dysplasia, and gastric cancer patients were 51.51% (17/33), 76.19% (16/21), and 90.32% (28/31), respectively; these were higher than the expression rate of the chronic superficial gastritis patients (11.11%, 2/18). FUBP1 expression in the gastric cancer patients was significantly higher than that in the chronic atrophic gastritis patients. The relative amount (0.2593 ± 0.1209) of FUBP1 mRNA in the gastric cancer tissue was higher than that in paraneoplastic tissue (0.1969 ± 0.0211) (p < 0.05). There was a statistically significant correlation between overall survival rates and age, sex, lymph node metastasis, and distant metastasis (p < 0.05).</p><p><strong>Conclusion: </strong>FUBP1 expression differs among gastric tissues. There is a correlation between overall survival rates and age, sex, lymph node metastasis, and distant metastasis.</p>","PeriodicalId":19684,"journal":{"name":"Onkologie","volume":"36 11","pages":"650-5"},"PeriodicalIF":0.3,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000355659","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31834778","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 22
[Status of clinical trials in oncology--2013 and onwards]. 【肿瘤临床试验现状——2013年及以后】。
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2013-01-01 DOI: 10.1159/000348257
Bernhard Wörmann, Mathias Freund, Friedrich Overkamp, Gerhard Ehninger

Clinical trials connect basic science with patient care. They form the backbone of evidence-based medicine and clinical guidelines. The unprecedented implementation of new methods in oncology over the past 40 years has only been possible on the basis of multiple well-organized clinical study groups. The continued existence of these study groups in their current multitude is in danger. Far-reaching changes in the legal framework, underfunding, new definitions of patient-related outcome and shifts in the organization of cancer patient care ask for critical reappraisal and new concepts.

临床试验将基础科学与病人护理联系起来。它们构成了循证医学和临床指南的支柱。在过去的40年里,肿瘤学中前所未有的新方法的实施只有在多个组织良好的临床研究小组的基础上才有可能。这些学习小组以目前的人数继续存在是危险的。法律框架的深远变化、资金不足、对患者相关结果的新定义以及癌症患者护理组织的转变,都要求对其进行批判性的重新评估和新概念。
{"title":"[Status of clinical trials in oncology--2013 and onwards].","authors":"Bernhard Wörmann,&nbsp;Mathias Freund,&nbsp;Friedrich Overkamp,&nbsp;Gerhard Ehninger","doi":"10.1159/000348257","DOIUrl":"https://doi.org/10.1159/000348257","url":null,"abstract":"<p><p>Clinical trials connect basic science with patient care. They form the backbone of evidence-based medicine and clinical guidelines. The unprecedented implementation of new methods in oncology over the past 40 years has only been possible on the basis of multiple well-organized clinical study groups. The continued existence of these study groups in their current multitude is in danger. Far-reaching changes in the legal framework, underfunding, new definitions of patient-related outcome and shifts in the organization of cancer patient care ask for critical reappraisal and new concepts.</p>","PeriodicalId":19684,"journal":{"name":"Onkologie","volume":"36 Suppl 2 ","pages":"3-8"},"PeriodicalIF":0.3,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000348257","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40243224","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
[Application for academic multicenter studies at German ethical review boards]. [德国伦理审查委员会多中心学术研究申请]。
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2013-01-01 DOI: 10.1159/000348270
Nicola Gökbuget, Ralph Naumann

Before the start of a clinical trial, approval by the responsible institutional ethical review board (IRB) is required. In Germany, nearly 50 independent IRBs may be responsible for the different participating sites of a multicenter study. In trials for rare diseases, the participation of many centers is required. Therefore, the application procedure for academic multicenter trials in malignant hematologic diseases is often a bureaucratic nightmare. Different aspects of IRB application and possible approaches for improvement are presented.

在开始临床试验之前,需要得到负责的机构伦理审查委员会(IRB)的批准。在德国,近50个独立的irb可能负责多中心研究的不同参与站点。在罕见疾病的试验中,需要许多中心的参与。因此,恶性血液病的学术多中心试验的申请程序往往是官僚主义的噩梦。介绍了IRB应用的不同方面和可能的改进方法。
{"title":"[Application for academic multicenter studies at German ethical review boards].","authors":"Nicola Gökbuget,&nbsp;Ralph Naumann","doi":"10.1159/000348270","DOIUrl":"https://doi.org/10.1159/000348270","url":null,"abstract":"<p><p>Before the start of a clinical trial, approval by the responsible institutional ethical review board (IRB) is required. In Germany, nearly 50 independent IRBs may be responsible for the different participating sites of a multicenter study. In trials for rare diseases, the participation of many centers is required. Therefore, the application procedure for academic multicenter trials in malignant hematologic diseases is often a bureaucratic nightmare. Different aspects of IRB application and possible approaches for improvement are presented.</p>","PeriodicalId":19684,"journal":{"name":"Onkologie","volume":"36 Suppl 2 ","pages":"29-35"},"PeriodicalIF":0.3,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000348270","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40244229","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
[The economic dilemma]. (经济困境)。
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2013-01-01 DOI: 10.1159/000348256
Friedrich Overkamp, Anja Bröker

Clinical studies have been situated very well in Germany during the last 10 years; oncologists in practices and clinics are highly motivated. However, the financing of clinical trials is desolate so that disillusionment spreads in many centers. This paper would like to give some impetus to the discussion on better and more adequate financing. Facts and backgrounds concerning unsatisfactory financing of clinical trials are demonstrated; costs are analyzed in a detailed way. It seems to be very important to establish tools for a better calculation of costs. First approaches have been defined.

在过去的10年里,临床研究在德国得到了很好的发展;肿瘤学家在实践和诊所的积极性很高。然而,临床试验的融资是荒凉的,因此幻灭在许多中心蔓延。本文希望对更好和更充足的融资问题的讨论提供一些推动。证明了临床试验经费不足的事实和背景;详细地分析了成本。建立更好地计算成本的工具似乎是非常重要的。第一种方法已经确定。
{"title":"[The economic dilemma].","authors":"Friedrich Overkamp,&nbsp;Anja Bröker","doi":"10.1159/000348256","DOIUrl":"https://doi.org/10.1159/000348256","url":null,"abstract":"<p><p>Clinical studies have been situated very well in Germany during the last 10 years; oncologists in practices and clinics are highly motivated. However, the financing of clinical trials is desolate so that disillusionment spreads in many centers. This paper would like to give some impetus to the discussion on better and more adequate financing. Facts and backgrounds concerning unsatisfactory financing of clinical trials are demonstrated; costs are analyzed in a detailed way. It seems to be very important to establish tools for a better calculation of costs. First approaches have been defined.</p>","PeriodicalId":19684,"journal":{"name":"Onkologie","volume":"36 Suppl 2 ","pages":"41-4"},"PeriodicalIF":0.3,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000348256","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40244231","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Practical management of everolimus-related toxicities in patients with advanced solid tumors. 晚期实体瘤患者依维莫司相关毒性的实际管理。
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2013-01-01 Epub Date: 2013-04-05 DOI: 10.1159/000350625
Viktor Grünwald, Steffen Weikert, Marianne E Pavel, Dieter Hörsch, Diana Lüftner, Wolfgang Janni, Matthias Geberth, Matthias M Weber

Everolimus is an orally administered inhibitor of the mammalian target of rapamycin (mTOR), an intracellular protein kinase downstream of the phosphatidylinositol 3-kinase/AKT pathway involved in key components of tumorigenesis, including cell growth, proliferation, and angiogenesis. In the advanced cancer setting, based on favorable results from phase III trials, everolimus is indicated for the treatment of advanced renal cell carcinoma, advanced neuroendocrine tumors of pancreatic origin, and advanced hormone receptor-positive, human epidermal growth factor receptor 2-negative breast cancer. Additional oncology indications for everolimus include renal angiomyolipoma with tuberous sclerosis complex and subependymal giant-cell astrocytoma. Although it is generally well tolerated, with most adverse events of mild to moderate severity and manageable, everolimus exhibits a distinct adverse event profile that warrants guidance for proper diagnostic and medical management. This guidance is particularly important given the potential for widespread long-term use of everolimus. This review will focus on the most relevant toxicities associated with mTOR inhibitors and on their management. Practical treatment recommendations are presented for stomatitis, noninfectious pneumonitis, rash, selected metabolic abnormalities, and infections. Provided these events are rapidly identified and treated, the vast majority should resolve with minimal effect on treatment outcomes and patients' quality of life.

依维莫司是哺乳动物雷帕霉素靶蛋白(mTOR)的口服抑制剂,雷帕霉素是一种细胞内蛋白激酶,位于磷脂酰肌醇3-激酶/AKT通路的下游,参与肿瘤发生的关键成分,包括细胞生长、增殖和血管生成。在晚期癌症方面,基于III期试验的有利结果,依维莫司适用于晚期肾细胞癌、晚期胰腺源神经内分泌肿瘤和晚期激素受体阳性、人表皮生长因子受体2阴性的乳腺癌的治疗。依维莫司的其他肿瘤适应症包括肾血管平滑肌脂肪瘤合并结节性硬化症和室管膜下巨细胞星形细胞瘤。尽管依维莫司通常耐受性良好,大多数不良事件的严重程度为轻度至中度且可控,但依维莫司表现出独特的不良事件概况,为正确的诊断和医疗管理提供了指导。鉴于依维莫司可能被广泛长期使用,这一指导尤为重要。本综述将重点关注与mTOR抑制剂相关的最相关的毒性及其管理。实用的治疗建议提出了口炎,非传染性肺炎,皮疹,选定的代谢异常和感染。如果这些事件得到迅速识别和治疗,绝大多数应该在对治疗结果和患者生活质量影响最小的情况下得到解决。
{"title":"Practical management of everolimus-related toxicities in patients with advanced solid tumors.","authors":"Viktor Grünwald,&nbsp;Steffen Weikert,&nbsp;Marianne E Pavel,&nbsp;Dieter Hörsch,&nbsp;Diana Lüftner,&nbsp;Wolfgang Janni,&nbsp;Matthias Geberth,&nbsp;Matthias M Weber","doi":"10.1159/000350625","DOIUrl":"https://doi.org/10.1159/000350625","url":null,"abstract":"<p><p>Everolimus is an orally administered inhibitor of the mammalian target of rapamycin (mTOR), an intracellular protein kinase downstream of the phosphatidylinositol 3-kinase/AKT pathway involved in key components of tumorigenesis, including cell growth, proliferation, and angiogenesis. In the advanced cancer setting, based on favorable results from phase III trials, everolimus is indicated for the treatment of advanced renal cell carcinoma, advanced neuroendocrine tumors of pancreatic origin, and advanced hormone receptor-positive, human epidermal growth factor receptor 2-negative breast cancer. Additional oncology indications for everolimus include renal angiomyolipoma with tuberous sclerosis complex and subependymal giant-cell astrocytoma. Although it is generally well tolerated, with most adverse events of mild to moderate severity and manageable, everolimus exhibits a distinct adverse event profile that warrants guidance for proper diagnostic and medical management. This guidance is particularly important given the potential for widespread long-term use of everolimus. This review will focus on the most relevant toxicities associated with mTOR inhibitors and on their management. Practical treatment recommendations are presented for stomatitis, noninfectious pneumonitis, rash, selected metabolic abnormalities, and infections. Provided these events are rapidly identified and treated, the vast majority should resolve with minimal effect on treatment outcomes and patients' quality of life.</p>","PeriodicalId":19684,"journal":{"name":"Onkologie","volume":"36 5","pages":"295-302"},"PeriodicalIF":0.3,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000350625","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31443257","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 33
[Developmental history: bendamustine yesterday, today, tomorrow]. [发展史:苯达莫司汀的昨天,今天,明天]。
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2013-01-01 Epub Date: 2013-01-28 DOI: 10.1159/000346104
Walter Werner, Michael Herold, Klaus Ruffert, Karlheinz Merkle, Axel Brakhage, Lorenzo Leoni, Bruce D Cheson
a WERNER BioAgents, Jena, b 4. Medizinische Klinik, HELIOS Klinikum Erfurt, c Überörtliche Gemeinschaftspraxis für Hämatologie und Internistische Onkologie, Jena, d Oncology Consulting, Miesbach, e Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie (HKI), Jena, Deutschland f AGIRE Stiftung, Manno, Schweiz g Georgetown University Hospital, Lombardi Comprehensive Cancer Center, Washington, DC, USA
{"title":"[Developmental history: bendamustine yesterday, today, tomorrow].","authors":"Walter Werner,&nbsp;Michael Herold,&nbsp;Klaus Ruffert,&nbsp;Karlheinz Merkle,&nbsp;Axel Brakhage,&nbsp;Lorenzo Leoni,&nbsp;Bruce D Cheson","doi":"10.1159/000346104","DOIUrl":"https://doi.org/10.1159/000346104","url":null,"abstract":"a WERNER BioAgents, Jena, b 4. Medizinische Klinik, HELIOS Klinikum Erfurt, c Überörtliche Gemeinschaftspraxis für Hämatologie und Internistische Onkologie, Jena, d Oncology Consulting, Miesbach, e Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie (HKI), Jena, Deutschland f AGIRE Stiftung, Manno, Schweiz g Georgetown University Hospital, Lombardi Comprehensive Cancer Center, Washington, DC, USA","PeriodicalId":19684,"journal":{"name":"Onkologie","volume":"36 Suppl 1 ","pages":"2-10"},"PeriodicalIF":0.3,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000346104","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31361574","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
期刊
Onkologie
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1