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Stereotactic ablative body radiotherapy versus conventionally fractionated radiotherapy for early stage large cell neuroendocrine carcinoma of the lung. 立体定向消融体放疗对早期肺大细胞神经内分泌癌的分级放疗比较。
IF 2.8 Q3 Medicine Pub Date : 2020-04-21 DOI: 10.2217/lmt-2020-0004
Rodney E Wegner, Stephen Abel, Athanasios Colonias

Aim: Some patients with early stage large cell neuroendocrine carcinoma (LCNEC) of the lung are not surgical candidates and will be managed with radiotherapy. We used the national cancer database to identify predictors of stereotactic radiotherapy and compare outcomes.

Materials & methods: We queried national cancer database for T1-2N0 LCNEC treated with radiation. Logistic regression and Cox regression identified predictors of stereotactic ablative body radiotherapy (SABR) and survival, respectively.

Results: We identified 754 patients, with 238 (32%) treated with SABR. Predictors of SABR were distance to facility, no chemotherapy, academic center, T1 and recent year. After propensity matching, median survival was 34.7 months compared with 23.7 months in favor of SABR (p = 0.02).

Conclusion: SABR for LCNEC has increased over time and was associated with improved survival.

目的:一些早期肺大细胞神经内分泌癌(LCNEC)患者不适合手术治疗,需要放疗治疗。我们使用国家癌症数据库来确定立体定向放疗的预测因素并比较结果。材料与方法:我们查询国家癌症数据库中放疗的T1-2N0 LCNEC。Logistic回归和Cox回归分别确定了立体定向消融体放疗(SABR)和生存的预测因子。结果:我们确定了754例患者,其中238例(32%)接受了SABR治疗。SABR的预测因子为离医院距离、未接受化疗、学术中心、T1和最近一年。倾向匹配后,中位生存期为34.7个月,而SABR组为23.7个月(p = 0.02)。结论:LCNEC的SABR随着时间的推移而增加,并与生存率的提高有关。
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引用次数: 4
Welcome to Volume 9 of Lung Cancer Management. 欢迎来到《肺癌管理》第九卷。
IF 2.8 Q3 Medicine Pub Date : 2020-03-24 DOI: 10.2217/lmt-2020-0007
Katherine Gordon
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引用次数: 1
Switching from first or second generation EGFR-TKI to osimertinib in EGFR mutation-positive NSCLC. EGFR突变阳性NSCLC从第一代或第二代EGFR- tki切换到奥西替尼。
IF 2.8 Q3 Medicine Pub Date : 2020-03-19 DOI: 10.2217/lmt-2020-0005
Fumio Imamura, Takako Inoue, Kei Kunimasa, Aki Kubota, Hanako Kuhara, Motohiro Tamiya, Kazumi Nishino, Madoka Kimura, Kika Kuno, Hayato Kawachi, Toru Kumagai

Aim: We evaluated the efficacy of a novel switch protocol for EGFR-TKIs for EGFR mutation-positive NSCLC.

Materials & methods: Clinical records were collected from the patients who had received one of two sequential combination strategies of EGFR-TKIs: Salvage use of osimertinib for T790M-mediated acquired resistance to an prior EGFR-TKI or switch use of osimertinib where an EGFR-TKI was switched to osimertinib before disease progression.

Results: Progression-free survival of osimertinib and time from the start of treatment until progression to osimertinib was comparable between the salvage use and switch use of osimertinib.

Conclusion: Switch use of osimertinib seemed to produce improved efficacy for patients with activating EGFR mutations, because of the lack of patient selection via T790M.

目的:我们评估了一种新的EGFR- tkis开关方案对EGFR突变阳性NSCLC的疗效。材料与方法:从接受两种EGFR-TKI顺序联合策略之一的患者中收集临床记录:挽救使用奥西替尼治疗t790m介导的对先前EGFR-TKI的获得性耐药,或在疾病进展前将EGFR-TKI转换为奥西替尼。结果:奥西替尼的无进展生存期和从开始治疗到进展到奥西替尼的时间在挽救使用和切换使用奥西替尼之间是相当的。结论:由于缺乏通过T790M对患者的选择,切换使用奥西替尼似乎可以提高EGFR激活突变患者的疗效。
{"title":"Switching from first or second generation EGFR-TKI to osimertinib in <i>EGFR</i> mutation-positive NSCLC.","authors":"Fumio Imamura,&nbsp;Takako Inoue,&nbsp;Kei Kunimasa,&nbsp;Aki Kubota,&nbsp;Hanako Kuhara,&nbsp;Motohiro Tamiya,&nbsp;Kazumi Nishino,&nbsp;Madoka Kimura,&nbsp;Kika Kuno,&nbsp;Hayato Kawachi,&nbsp;Toru Kumagai","doi":"10.2217/lmt-2020-0005","DOIUrl":"https://doi.org/10.2217/lmt-2020-0005","url":null,"abstract":"<p><strong>Aim: </strong>We evaluated the efficacy of a novel switch protocol for EGFR-TKIs for <i>EGFR</i> mutation-positive NSCLC.</p><p><strong>Materials & methods: </strong>Clinical records were collected from the patients who had received one of two sequential combination strategies of EGFR-TKIs: Salvage use of osimertinib for <i>T790M</i>-mediated acquired resistance to an prior EGFR-TKI or switch use of osimertinib where an EGFR-TKI was switched to osimertinib before disease progression.</p><p><strong>Results: </strong>Progression-free survival of osimertinib and time from the start of treatment until progression to osimertinib was comparable between the salvage use and switch use of osimertinib.</p><p><strong>Conclusion: </strong>Switch use of osimertinib seemed to produce improved efficacy for patients with activating <i>EGFR</i> mutations, because of the lack of patient selection via <i>T790M</i>.</p>","PeriodicalId":43551,"journal":{"name":"Lung Cancer Management","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2020-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/lmt-2020-0005","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37882476","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: 4
Cost analysis of the management of brain metastases in patients with advanced ALK+ NSCLC: alectinib versus crizotinib. 晚期ALK+ NSCLC患者脑转移治疗的成本分析:阿勒替尼与克唑替尼
IF 2.8 Q3 Medicine Pub Date : 2020-03-04 DOI: 10.2217/lmt-2019-0011
Dolores Isla, Bartomeu Massuti, Martín Lázaro, Lucía Ruiz de Alda, Rocio Gordo, Nuria Ortega-Joaquín, Itziar Oyagüez

Aim: To estimate management cost of NSCLC ALK+ patients with and without brain metastasis (BM), and to compare annual costs in patients treated with alectinib or crizotinib.

Methods: Management cost/year (€ 2018) in patients with and without BM was estimated with disaggregated resource consumption provided by local oncologists, including medical visits, hospitalizations, diagnostic/laboratory tests, imaging techniques and surgical procedures. The comparison of costs/year with alectinib and crizotinib, considered the cumulative 12-month incidence of BM in ALEX trial (9.4 and 41.4%, respectively).

Results: Management cost was €6173.42/patient-year without BM and €21,637.50/patient-year with BM. With alectinib, average cost/patient was lower than crizotinib (€4948.51/patient-year).

Conclusion: Prevention of BM with alectinib may result in reductions of cost/year in the management of advanced ALK+ NSCLC.

目的:评估伴有和不伴有脑转移(BM)的NSCLC ALK+患者的管理成本,并比较阿勒替尼或克唑替尼治疗患者的年成本。方法:根据当地肿瘤学家提供的分类资源消耗,包括就诊、住院、诊断/实验室检查、成像技术和外科手术,估计有和没有BM的患者的管理成本/年(€2018)。与阿勒替尼和克唑替尼的成本/年比较,考虑了ALEX试验中累积12个月的BM发病率(分别为9.4%和41.4%)。结果:无BM的管理成本为6173.42欧元/患者-年,有BM的管理成本为21637.50欧元/患者-年。使用阿勒替尼,每位患者的平均成本低于克唑替尼(4948.51欧元/患者年)。结论:阿勒替尼预防脑转移可降低晚期ALK+ NSCLC治疗的年成本。
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引用次数: 1
Risk of brain metastases in T1-3N0 NSCLC: a population-based analysis. T1-3N0 NSCLC脑转移风险:基于人群的分析
IF 2.8 Q3 Medicine Pub Date : 2020-02-25 DOI: 10.2217/lmt-2019-0010
Michael T Milano, James E Bates, Justin Budnik, Haoming Qiu, Sara Hardy, Michael A Cummings, Megan A Baumgart, Ronald J Maggiore, Deborah A Mulford, Kenneth Y Usuki

Aim: Several consensus guidelines recommend against routine brain imaging at diagnosis of T1-3N0 non-small cell lung cancer (NSCLC).

Methods: From the Surveillance, Epidemiology and End Results registry, patients with pathologically confirmed T1-3N0 NSCLC were identified. Risks of brain metastases at time of initial diagnosis were analyzed.

Results: Patients selected to not undergo primary NSCLC resection had approximately tenfold greater incidence of brain metastases versus those who did. Younger age, adenocarcinoma histology, higher tumor stage and higher histologic grade were all significantly (p < 0.0001) associated with greater likelihood of presenting with brain metastases.

Conclusion: Given the morbidity and mortality of brain metastases, routine brain screening after NSCLC diagnosis (particularly adenocarcinoma) may be justifiable, though more refined cost-benefit analyses are warranted.

目的:一些一致的指南建议在诊断T1-3N0非小细胞肺癌(NSCLC)时不进行常规脑成像。方法:从监测、流行病学和最终结果登记中,确定病理证实的T1-3N0 NSCLC患者。分析初诊时脑转移的风险。结果:选择不进行原发性非小细胞肺癌切除术的患者的脑转移发生率大约是接受手术的患者的10倍。年龄较小、腺癌组织学、较高的肿瘤分期和较高的组织学分级与出现脑转移的可能性均显著相关(p < 0.0001)。结论:考虑到脑转移的发病率和死亡率,非小细胞肺癌(特别是腺癌)诊断后的常规脑筛查可能是合理的,尽管需要更精确的成本-收益分析。
{"title":"Risk of brain metastases in T1-3N0 NSCLC: a population-based analysis.","authors":"Michael T Milano,&nbsp;James E Bates,&nbsp;Justin Budnik,&nbsp;Haoming Qiu,&nbsp;Sara Hardy,&nbsp;Michael A Cummings,&nbsp;Megan A Baumgart,&nbsp;Ronald J Maggiore,&nbsp;Deborah A Mulford,&nbsp;Kenneth Y Usuki","doi":"10.2217/lmt-2019-0010","DOIUrl":"https://doi.org/10.2217/lmt-2019-0010","url":null,"abstract":"<p><strong>Aim: </strong>Several consensus guidelines recommend against routine brain imaging at diagnosis of T1-3N0 non-small cell lung cancer (NSCLC).</p><p><strong>Methods: </strong>From the Surveillance, Epidemiology and End Results registry, patients with pathologically confirmed T1-3N0 NSCLC were identified. Risks of brain metastases at time of initial diagnosis were analyzed.</p><p><strong>Results: </strong>Patients selected to not undergo primary NSCLC resection had approximately tenfold greater incidence of brain metastases versus those who did. Younger age, adenocarcinoma histology, higher tumor stage and higher histologic grade were all significantly (p < 0.0001) associated with greater likelihood of presenting with brain metastases.</p><p><strong>Conclusion: </strong>Given the morbidity and mortality of brain metastases, routine brain screening after NSCLC diagnosis (particularly adenocarcinoma) may be justifiable, though more refined cost-benefit analyses are warranted.</p>","PeriodicalId":43551,"journal":{"name":"Lung Cancer Management","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2020-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/lmt-2019-0010","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37808519","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: 6
Status of correlation between BMI and response to immunocheck-point inhibitor in advanced non-small-cell lung cancer. 晚期非小细胞肺癌患者BMI与免疫检查点抑制剂应答的相关性研究
IF 2.8 Q3 Medicine Pub Date : 2020-02-25 DOI: 10.2217/lmt-2019-0016
Alain Gelibter, Mario Occhipinti, Simona Pisegna, Alessio Cortellini, Enrico Cortesi, Paolo Marchetti
Alain Gelibter*,1, Mario Occhipinti1 , Simona Pisegna1, Alessio Cortellini2,3, Enrico Cortesi1 & Paolo Marchetti1,4 1Medical Oncology Unit, Policlinico Umberto I, Sapienza University of Rome, Rome, Italy 2Medical Oncology Unit, St. Salvatore Hospital, L’Aquila, Italy 3Department of Biotechnological & Applied Clinical Sciences, University of L’Aquila, L’Aquila, Italy 4U.O.C. Oncologia Medica, Azienda Ospedaliero Universitaria Sant’Andrea, Rome, Italy *Author for correspondence: alain.gelibter@uniroma1.it
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引用次数: 9
Optimizing molecular residual disease detection using liquid biopsy postoperatively in early stage lung cancer. 早期肺癌术后液体活检分子残留检测优化
IF 2.8 Q3 Medicine Pub Date : 2020-02-21 DOI: 10.2217/lmt-2019-0017
Anna L McGuire, Curtis B Hughesman, Melissa K McConechy, Barb Melosky, Stephen Lam, Renelle Myers, John Yee, Ernest Tang, Stephen Yip
Anna L McGuire*,1, Curtis B Hughesman2, Melissa K McConechy3, Barb Melosky4,5, Stephen Lam4,6, Renelle Myers4,6, John Yee1, Ernest Tang1 & Stephen Yip2,7 1Department of Surgery, Division of Thoracic Surgery, Vancouver General Hospital, University of British Columbia, Vancouver V5Z1M9, BC, Canada 2Department of Pathology and Laboratory Medicine, BC Cancer, Cancer Genetics & Genomics Laboratory, Vancouver, BC, Canada 3Contextual Genomics Inc., Vancouver, BC, Canada 4Department of Medical Oncology, BC Cancer Agency, Vancouver, British Columbia, Vancouver, BC, Canada 5Medical Oncology, University of British Columbia, Vancouver, BC, Canada 6Department of Medicine, Divisions of Respiratory Medicine, University of British Columbia, Vancouver, BC, Canada 7Department of Pathology & Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada *Author for correspondence: anna.mcguire@vch.ca
{"title":"Optimizing molecular residual disease detection using liquid biopsy postoperatively in early stage lung cancer.","authors":"Anna L McGuire,&nbsp;Curtis B Hughesman,&nbsp;Melissa K McConechy,&nbsp;Barb Melosky,&nbsp;Stephen Lam,&nbsp;Renelle Myers,&nbsp;John Yee,&nbsp;Ernest Tang,&nbsp;Stephen Yip","doi":"10.2217/lmt-2019-0017","DOIUrl":"https://doi.org/10.2217/lmt-2019-0017","url":null,"abstract":"Anna L McGuire*,1, Curtis B Hughesman2, Melissa K McConechy3, Barb Melosky4,5, Stephen Lam4,6, Renelle Myers4,6, John Yee1, Ernest Tang1 & Stephen Yip2,7 1Department of Surgery, Division of Thoracic Surgery, Vancouver General Hospital, University of British Columbia, Vancouver V5Z1M9, BC, Canada 2Department of Pathology and Laboratory Medicine, BC Cancer, Cancer Genetics & Genomics Laboratory, Vancouver, BC, Canada 3Contextual Genomics Inc., Vancouver, BC, Canada 4Department of Medical Oncology, BC Cancer Agency, Vancouver, British Columbia, Vancouver, BC, Canada 5Medical Oncology, University of British Columbia, Vancouver, BC, Canada 6Department of Medicine, Divisions of Respiratory Medicine, University of British Columbia, Vancouver, BC, Canada 7Department of Pathology & Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada *Author for correspondence: anna.mcguire@vch.ca","PeriodicalId":43551,"journal":{"name":"Lung Cancer Management","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2020-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/lmt-2019-0017","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37882474","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: 2
Chemotherapy and/or immune checkpoint inhibitors in NSCLC first-line setting: what is the best approach? 化疗和/或免疫检查点抑制剂在非小细胞肺癌一线:什么是最好的方法?
IF 2.8 Q3 Medicine Pub Date : 2020-02-12 DOI: 10.2217/lmt-2019-0018
Luigi Della Gravara, Ciro Battiloro, Rosa Cantile, Antonietta Letizia, Fabiana Vitiello, Vincenzo Montesarchio, Danilo Rocco
Luigi Della Gravara1, Ciro Battiloro2, Rosa Cantile2, Antonietta Letizia2, Fabiana Vitiello2, Vincenzo Montesarchio3 & Danilo Rocco*,2 1Department of Experimental Medicine, Università degli Studi della Campania “Luigi Vanvitelli”, Caserta, Italy 2Division of Pulmonary Oncology, AORN dei Colli Monaldi, Naples, Italy 3Division of Medical Oncology, AORN dei Colli Monaldi, Naples, Italy *Author for correspondence: danilorocc@yahoo.it
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引用次数: 15
Practical challenges in patients with stage III NSCLC receiving checkpoint inhibitors after chemoradiation. 化疗后接受检查点抑制剂的III期非小细胞肺癌患者的实际挑战。
IF 2.8 Q3 Medicine Pub Date : 2020-02-06 DOI: 10.2217/lmt-2020-0001
Nikhil A Shukla, Nasser H Hanna
NSCLC accounts for 80% of all lung cancer diagnoses, and approximately a third of patients present with locally advanced (stage III) disease [1]. The optimal therapy for fit patients with unresectable and/or inoperable stage III disease has evolved over the last three decades from radiation alone to sequential chemoradiation (CRT) to concurrent CRT followed by checkpoint inhibitor therapy (CPI). The recently reported PACIFIC trial generated a paradigm shift in the treatment of such patients, with a 3-year overall survival (OS) of 57% for patients receiving consolidation durvalumab compared with 43.5% for those receiving placebo [2–4]. Similar outcomes were reported with consolidation pembrolizumab in a Hoosier Cancer Research Network (HCRN) Phase II Trial [5]. In this article, we explore key clinical challenges that arise when treating patients with consolidation CPI after CRT for patients with stage III NSCLC; namely, the management of CPI-related pneumonitis, timing of consolidation CPI and their role in patients with PD-L1 TPS <1% and distinguishing local progression versus pseudoprogression.
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引用次数: 1
Convex endobronchial ultrasound: same coin, two faces. Challenging biopsy and staging for non-small-cell lung cancer. 支气管内凸超声:同一枚硬币,两面。非小细胞肺癌具有挑战性的活检和分期。
IF 2.8 Q3 Medicine Pub Date : 2020-01-16 DOI: 10.2217/lmt-2019-0008
Konstantinos Sapalidis, Konstantinos Romanidis, Panagoula Oikonomou, Paul Zarogoulidis, Athanasios Katsaounis, Aikaterini Amaniti, Nikolaos Michalopoulos, Charilaos Koulouris, Kosmas Tsakiridis, Dimitrios Giannakidis, Isaak Kesisoglou, Aris Ioannidis, Iason Nikolaos-Katsios, Anastasios Vagionas, Wolfgang Hohenforst-Schmidt, Haidong Huang, Chong Bai, Alexandru Marian Goganau, Christoforos Kosmidis

Lung cancer is still diagnosed at a late stage due to lack of early disease symptoms. Despite the development of new diagnostic endoscopic tools, such as radial/convex endobronchial ultrasounds (EBUS) and electromagnetic navigation, most patients are still diagnosed at advanced stage disease. Most of the patients refer to their doctor only if they cough blood or their cough changes character. There are challenging cases in the diagnosis and staging of a patient, such as the one that we will present. We present a case of lung cancer that was diagnosed through a biopsy from the main lesion, with access from the esophagus, through transbronchial needle aspiration with EBUS, under general anesthesia and intubation. Staging with transbronchial needle aspiration with EBUS was also performed at the same session.

由于缺乏早期疾病症状,肺癌的诊断仍处于晚期。尽管有了新的内镜诊断工具,如径向/凸支气管超声(EBUS)和电磁导航,但大多数患者仍在晚期诊断。大多数患者只有在咳嗽带血或咳嗽改变特征时才会去看医生。在病人的诊断和分期中有一些具有挑战性的病例,比如我们将要介绍的这个病例。我们报告了一个肺癌病例,在全身麻醉和插管下,通过主要病变的活检诊断,从食道进入,通过经支气管穿刺EBUS穿刺。在同一会议上也进行了经支气管针抽吸EBUS的分期。
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引用次数: 5
期刊
Lung Cancer Management
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