Pub Date : 2017-11-01Epub Date: 2017-11-17DOI: 10.2217/lmt-2017-0006
Mark T Corkum, George B Rodrigues
Treatment of extensive-stage small-cell lung cancer remains a challenge with poor local control and overall survival. Chemotherapy is the mainstay of treatment, consisting of a combination of a platinum agent plus etoposide. The role of consolidative chest radiotherapy in extensive-stage small-cell lung cancer remains controversial. Two randomized clinical trials have been published demonstrating improved intrathoracic disease control with a small survival benefit, though interpretation and application of these results to clinical practice has been debated. These two trials examined different radiotherapy techniques and doses, with a third trial treating consolidative chest and oligometastatic disease having closed prematurely due to an interim analysis demonstrating treatment futility plus increased toxicity. Patients with residual intrathoracic disease after chemotherapy appear to benefit the most from consolidative chest radiotherapy, offering a potential tool to help select appropriate patients.
{"title":"Patient selection for thoracic radiotherapy in extensive-stage small-cell lung cancer.","authors":"Mark T Corkum, George B Rodrigues","doi":"10.2217/lmt-2017-0006","DOIUrl":"10.2217/lmt-2017-0006","url":null,"abstract":"<p><p>Treatment of extensive-stage small-cell lung cancer remains a challenge with poor local control and overall survival. Chemotherapy is the mainstay of treatment, consisting of a combination of a platinum agent plus etoposide. The role of consolidative chest radiotherapy in extensive-stage small-cell lung cancer remains controversial. Two randomized clinical trials have been published demonstrating improved intrathoracic disease control with a small survival benefit, though interpretation and application of these results to clinical practice has been debated. These two trials examined different radiotherapy techniques and doses, with a third trial treating consolidative chest and oligometastatic disease having closed prematurely due to an interim analysis demonstrating treatment futility plus increased toxicity. Patients with residual intrathoracic disease after chemotherapy appear to benefit the most from consolidative chest radiotherapy, offering a potential tool to help select appropriate patients.</p>","PeriodicalId":43551,"journal":{"name":"Lung Cancer Management","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2017-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310308/pdf/lmt-06-47.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36854077","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}
Pub Date : 2017-07-01Epub Date: 2017-05-19DOI: 10.2217/lmt-2016-0019
Satya Das, Leora Horn
The identification of driver mutations in patients with advanced non-small-cell lung cancer has changed the treatment outcomes for patients with actionable driver mutations. Lack of tissue at diagnosis, however, remains a central obstacle in making optimal treatment decisions in patients with advanced disease. Although the US FDA has approved one plasma-based test for detecting epidermal growth factor receptor mutations in patients with advanced stage disease, sensitivity of these assays remains mediocre, necessitating additional tissue testing and possible delays in patients with negative results. Serial monitoring for response and early detection of acquired resistance to targeted therapies is also possible with cell-free DNA, however the benefit of switching therapy prior to detection of changes on imaging is unknown currently.
{"title":"Plasma genotyping in patients with non-small-cell lung cancer: simplifying or confusing the diagnosis?","authors":"Satya Das, Leora Horn","doi":"10.2217/lmt-2016-0019","DOIUrl":"https://doi.org/10.2217/lmt-2016-0019","url":null,"abstract":"<p><p>The identification of driver mutations in patients with advanced non-small-cell lung cancer has changed the treatment outcomes for patients with actionable driver mutations. Lack of tissue at diagnosis, however, remains a central obstacle in making optimal treatment decisions in patients with advanced disease. Although the US FDA has approved one plasma-based test for detecting epidermal growth factor receptor mutations in patients with advanced stage disease, sensitivity of these assays remains mediocre, necessitating additional tissue testing and possible delays in patients with negative results. Serial monitoring for response and early detection of acquired resistance to targeted therapies is also possible with cell-free DNA, however the benefit of switching therapy prior to detection of changes on imaging is unknown currently.</p>","PeriodicalId":43551,"journal":{"name":"Lung Cancer Management","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2017-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/lmt-2016-0019","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36854073","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}
Pub Date : 2017-07-01Epub Date: 2017-07-14DOI: 10.2217/lmt-2016-0020
Anjali Gera, David Olayinka Kamson, Victoria M Villaflor, Rimas V Lukas
Diagnosis of paraneoplastic neurologic disorder (PND) synthesizes the clinical picture (including the temporal relationship to the cancer diagnosis), detection of onconeural antibodies and exclusion of alternative causes. The mainstay of brain imaging of PNDs is MRI. There is also an increasingly recognized role of PET using radiotracer 18F-Fluorodeoxyglucose (FDG) in the evaluation of the brain. We describe a 67-year-old female with a 50-year smoking history and small-cell lung cancer developing subacute encephalopathy with MRI and PET abnormalities identifying paraneoplastic encephalitis. PET may complement conventional tools in diagnosing a subset of patients with PND.
{"title":"Added diagnostic utility of PET in a patient with subacute encephalopathy and small-cell lung cancer.","authors":"Anjali Gera, David Olayinka Kamson, Victoria M Villaflor, Rimas V Lukas","doi":"10.2217/lmt-2016-0020","DOIUrl":"https://doi.org/10.2217/lmt-2016-0020","url":null,"abstract":"<p><p>Diagnosis of paraneoplastic neurologic disorder (PND) synthesizes the clinical picture (including the temporal relationship to the cancer diagnosis), detection of onconeural antibodies and exclusion of alternative causes. The mainstay of brain imaging of PNDs is MRI. There is also an increasingly recognized role of PET using radiotracer <sup>18</sup>F-Fluorodeoxyglucose (FDG) in the evaluation of the brain. We describe a 67-year-old female with a 50-year smoking history and small-cell lung cancer developing subacute encephalopathy with MRI and PET abnormalities identifying paraneoplastic encephalitis. PET may complement conventional tools in diagnosing a subset of patients with PND.</p>","PeriodicalId":43551,"journal":{"name":"Lung Cancer Management","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2017-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/lmt-2016-0020","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36864628","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}
Pub Date : 2017-07-01Epub Date: 2017-07-14DOI: 10.2217/lmt-2017-0003
Akshjot Puri, Ly Ma, Gary V Walker, John Chang, Ron Z Shinar, Madappa N Kundranda
Aim: The frequency of pancreatic cancer in association with cancer of other organs ranges from 1 to 20%, with the most common ones being gastric, colon, thyroid and genitourinary. The presence of synchronous lung and pancreatic cancers is extremely rare.
Case series: Two patients with extensive smoking history and variable presentations were found to have simultaneous lung and pancreatic masses both lesions being different histologically and on immunohistochemical staining. After individualized treatment plans, the first patient remains free of disease and the second patient is being treated with a palliative intent.
Conclusion: The early recognition and treatment is important as there exists a significant survival difference in patients who have synchronous primaries as opposed to those with metastatic pancreatic adenocarcinoma.
{"title":"Synchronous primary adenocarcinoma of the lung and pancreas: a case series and review of the literature.","authors":"Akshjot Puri, Ly Ma, Gary V Walker, John Chang, Ron Z Shinar, Madappa N Kundranda","doi":"10.2217/lmt-2017-0003","DOIUrl":"https://doi.org/10.2217/lmt-2017-0003","url":null,"abstract":"<p><strong>Aim: </strong>The frequency of pancreatic cancer in association with cancer of other organs ranges from 1 to 20%, with the most common ones being gastric, colon, thyroid and genitourinary. The presence of synchronous lung and pancreatic cancers is extremely rare.</p><p><strong>Case series: </strong>Two patients with extensive smoking history and variable presentations were found to have simultaneous lung and pancreatic masses both lesions being different histologically and on immunohistochemical staining. After individualized treatment plans, the first patient remains free of disease and the second patient is being treated with a palliative intent.</p><p><strong>Conclusion: </strong>The early recognition and treatment is important as there exists a significant survival difference in patients who have synchronous primaries as opposed to those with metastatic pancreatic adenocarcinoma.</p>","PeriodicalId":43551,"journal":{"name":"Lung Cancer Management","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2017-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/lmt-2017-0003","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36864627","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}
Pub Date : 2017-07-01Epub Date: 2017-07-14DOI: 10.2217/lmt-2016-0017
Tamara A Sussman, Monica Khunger, Vamsidhar Velcheti
We report a case of crizotinib-induced esophageal ulcers in a 45-year-old woman with metastatic anaplastic lymphoma kinase-positive non-small-cell lung cancer after 10 weeks of therapy. Endoscopic and pathologic findings were consistent with active inflammation with mid-esophageal ulceration and consistent with drug-induced esophagitis. Crizotinib was held and had a complete clinical and radiographic resolution of her symptoms. Patient was started on treatment with another anaplastic lymphoma kinase-targeted agent alectinib and has been tolerating it well without evidence of recurrence of esophagitis.
{"title":"A case of crizotinib-induced esophageal ulcers.","authors":"Tamara A Sussman, Monica Khunger, Vamsidhar Velcheti","doi":"10.2217/lmt-2016-0017","DOIUrl":"https://doi.org/10.2217/lmt-2016-0017","url":null,"abstract":"We report a case of crizotinib-induced esophageal ulcers in a 45-year-old woman with metastatic anaplastic lymphoma kinase-positive non-small-cell lung cancer after 10 weeks of therapy. Endoscopic and pathologic findings were consistent with active inflammation with mid-esophageal ulceration and consistent with drug-induced esophagitis. Crizotinib was held and had a complete clinical and radiographic resolution of her symptoms. Patient was started on treatment with another anaplastic lymphoma kinase-targeted agent alectinib and has been tolerating it well without evidence of recurrence of esophagitis.","PeriodicalId":43551,"journal":{"name":"Lung Cancer Management","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2017-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/lmt-2016-0017","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36864623","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}
Association For The Fight Against Lung Cancer in Poland, Gdansk, Poland Lung Cancer Europe (LuCE), Bern, Switzerland MAS, MBA, Focus patient Ltd, Baden, Austria *Author for correspondence: Tel.: +39 0119 026 980; stefania.vallone@womenagainstlungcancer.eu
{"title":"Lung cancer patient needs in different countries.","authors":"Stefania Vallone, Ingeborg Beunders, Ewelina Szmytke","doi":"10.2217/lmt-2017-0005","DOIUrl":"https://doi.org/10.2217/lmt-2017-0005","url":null,"abstract":"Association For The Fight Against Lung Cancer in Poland, Gdansk, Poland Lung Cancer Europe (LuCE), Bern, Switzerland MAS, MBA, Focus patient Ltd, Baden, Austria *Author for correspondence: Tel.: +39 0119 026 980; stefania.vallone@womenagainstlungcancer.eu","PeriodicalId":43551,"journal":{"name":"Lung Cancer Management","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2017-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/lmt-2017-0005","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36864625","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}
Pub Date : 2017-07-01Epub Date: 2017-07-14DOI: 10.2217/lmt-2017-0007
Silvia Novello
Silvia Novello speaks to Roshaine Wijayatunga, Managing Commissioning Editor: Silvia Novello is a Full Professor of Medical Oncology in the Oncology Department at San Luigi Hospital in Orbassano, Italy, part of the University of Turin. She earned her medical degree and completed the postgraduate training in respiratory medicine and medical oncology at the University of Turin and partially at the Institut Gustave Roussy in France. Currently, she is head of the Thoracic Oncology Unit at the San Luigi Hospital, Orbassano (Turin), where she also tutors medical students and postgraduate students in respiratory medicine and medical oncology. Novello's research interests include thoracic malignancies, primary prevention, gender differences in lung cancer, basic and clinical applied research on lung cancer, including pharmacogenomics. She is involved in many European and national controlled clinical trials evaluating new approaches in diagnosis and lung cancer therapy. From July 2012 until 2016, Novello has been a Member of the Board of Directors of the International Association for the Study of Lung Cancer and since October 2016 Member of the Board of Directors of the Italian Association of Medical Oncology and member of other several scientific societies including the American Society of Clinical Oncology and the European Society of Medical Oncology. Currently, she is the President of Women Against Lung Cancer in Europe, a nonprofit European Association founded in 2006 in Turin, Italy, part of the scientific Committee of Lung cancer Europe and also a member of the Scientific Committee of Bonnie J Addario Lung Cancer Foundation and Member of the Scientific Committee of Investigación sobre Cáncer de Pulmón en Mujeres. She is the author or co-author of over 100 publications in peer-reviewed journals.
Silvia Novello是意大利奥尔巴萨诺圣路易吉医院肿瘤科的医学肿瘤学全职教授,该医院隶属于都灵大学。她获得了医学学位,并在都灵大学和法国古斯塔夫·鲁西研究所完成了呼吸医学和肿瘤医学的研究生培训。目前,她是都灵奥尔巴萨诺圣路易吉医院胸部肿瘤科的主任,她还在那里指导医科学生和呼吸医学和肿瘤医学研究生。Novello的研究兴趣包括胸部恶性肿瘤、初级预防、肺癌的性别差异、肺癌的基础和临床应用研究,包括药物基因组学。她参与了许多欧洲和国家对照临床试验,评估诊断和肺癌治疗的新方法。从2012年7月到2016年,Novello一直是国际肺癌研究协会的董事会成员,自2016年10月以来,他是意大利肿瘤医学协会的董事会成员和其他几个科学学会的成员,包括美国临床肿瘤学会和欧洲肿瘤医学学会。目前,她是欧洲妇女抗肺癌协会(Women Against Lung Cancer in Europe,一家于2006年在意大利都灵成立的非营利性欧洲协会)的主席,也是欧洲肺癌科学委员会的一部分,也是Bonnie J Addario肺癌基金会科学委员会的成员和Investigación sobre Cáncer de Pulmón en Mujeres科学委员会的成员。她在同行评议的期刊上发表了100多篇论文。
{"title":"Interview: developing therapies for lung cancer.","authors":"Silvia Novello","doi":"10.2217/lmt-2017-0007","DOIUrl":"https://doi.org/10.2217/lmt-2017-0007","url":null,"abstract":"<p><p><b>Silvia Novello speaks to Roshaine Wijayatunga, Managing Commissioning Editor:</b> Silvia Novello is a Full Professor of Medical Oncology in the Oncology Department at San Luigi Hospital in Orbassano, Italy, part of the University of Turin. She earned her medical degree and completed the postgraduate training in respiratory medicine and medical oncology at the University of Turin and partially at the Institut Gustave Roussy in France. Currently, she is head of the Thoracic Oncology Unit at the San Luigi Hospital, Orbassano (Turin), where she also tutors medical students and postgraduate students in respiratory medicine and medical oncology. Novello's research interests include thoracic malignancies, primary prevention, gender differences in lung cancer, basic and clinical applied research on lung cancer, including pharmacogenomics. She is involved in many European and national controlled clinical trials evaluating new approaches in diagnosis and lung cancer therapy. From July 2012 until 2016, Novello has been a Member of the Board of Directors of the International Association for the Study of Lung Cancer and since October 2016 Member of the Board of Directors of the Italian Association of Medical Oncology and member of other several scientific societies including the American Society of Clinical Oncology and the European Society of Medical Oncology. Currently, she is the President of Women Against Lung Cancer in Europe, a nonprofit European Association founded in 2006 in Turin, Italy, part of the scientific Committee of Lung cancer Europe and also a member of the Scientific Committee of Bonnie J Addario Lung Cancer Foundation and Member of the Scientific Committee of Investigación sobre Cáncer de Pulmón en Mujeres. She is the author or co-author of over 100 publications in peer-reviewed journals.</p>","PeriodicalId":43551,"journal":{"name":"Lung Cancer Management","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2017-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/lmt-2017-0007","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36864626","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}
Pub Date : 2016-12-01Epub Date: 2016-11-03DOI: 10.2217/lmt-2016-0013
Surein Arulananda, Gareth Rivalland, Thomas John
Immune checkpoint inhibition has been proven to be highly efficacious in NSCLC and associated with durable responses in a limited number of patients. Chemotherapy and targeted therapies, which have also expanded rapidly in this field lead to high response rates and improved survival although inevitably resistance occurs and hence treatment failure. There is increasing evidence showing that chemotherapy and targeted therapy interplay with the immune system including exerting effects on tumor cells and the host immune cells. Naturally combining both of these treatment modalities to induce cytotoxic effects on tumor cells to release tumor antigens and priming of the immune system should in turn lead to enhanced anticancer activity. This review will explore some of the preclinical rationale and clinical trial data we have to date on combining various systemic therapies with immunotherapies.
{"title":"Combination approaches in NSCLC involving immune checkpoint inhibitors.","authors":"Surein Arulananda, Gareth Rivalland, Thomas John","doi":"10.2217/lmt-2016-0013","DOIUrl":"https://doi.org/10.2217/lmt-2016-0013","url":null,"abstract":"<p><p>Immune checkpoint inhibition has been proven to be highly efficacious in NSCLC and associated with durable responses in a limited number of patients. Chemotherapy and targeted therapies, which have also expanded rapidly in this field lead to high response rates and improved survival although inevitably resistance occurs and hence treatment failure. There is increasing evidence showing that chemotherapy and targeted therapy interplay with the immune system including exerting effects on tumor cells and the host immune cells. Naturally combining both of these treatment modalities to induce cytotoxic effects on tumor cells to release tumor antigens and priming of the immune system should in turn lead to enhanced anticancer activity. This review will explore some of the preclinical rationale and clinical trial data we have to date on combining various systemic therapies with immunotherapies.</p>","PeriodicalId":43551,"journal":{"name":"Lung Cancer Management","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2016-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/lmt-2016-0013","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36854072","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}
Pub Date : 2016-12-01Epub Date: 2017-06-05DOI: 10.2217/lmt-2017-0002
Roshaine A-M Wijayatunga
*Author for correspondence: r.wijayatunga@futuremedicine.com We have come to the final issue of volume 5 of Lung Cancer Management and would like to thank all the authors and reviewers, along with our editorial and production teams (both internal and external) for their contribution in making volume 5 another great one! We certainly value their hard work, dedication and cooperation throughout this year. The journal has been well supported by our knowledgeable and helpful Editorial Advisory Board, headed by our Editor-in-Chief David J Sugarbaker, Baylor College of Medicine, USA. Their time and effort, be it in an ambassadorial, advisory or authorship role, on behalf of Lung Cancer Management, are very much appreciated and valued, and we extend a big thank you to them all. As with all the past volumes of Lung Cancer Management, the standard of content published in volume 5 has been very high – having been assessed using our rigorous peer review and revisions process. We have published a wide range of article types in volume 5, from the shorter opinion and discussion-based editorial and commentary articles, case reports and original research, as well as the longer reviewer articles, covering a variety of subject areas including, neurotrophic tyrosine kinase gene fusions, oligometastatic lung cancer, advanced NSCLC, immunotherapy, symptom burden, liquid biopsy, immune checkpoint inhibitors and surgery. Many articles proved to be popular with our readers through this year and some of the most read articles so far include: ● Review: Nintedanib in advanced NSCLC: management of adverse events (by Lemmens) [1];
{"title":"Foreword: message from the Editor.","authors":"Roshaine A-M Wijayatunga","doi":"10.2217/lmt-2017-0002","DOIUrl":"10.2217/lmt-2017-0002","url":null,"abstract":"*Author for correspondence: r.wijayatunga@futuremedicine.com We have come to the final issue of volume 5 of Lung Cancer Management and would like to thank all the authors and reviewers, along with our editorial and production teams (both internal and external) for their contribution in making volume 5 another great one! We certainly value their hard work, dedication and cooperation throughout this year. The journal has been well supported by our knowledgeable and helpful Editorial Advisory Board, headed by our Editor-in-Chief David J Sugarbaker, Baylor College of Medicine, USA. Their time and effort, be it in an ambassadorial, advisory or authorship role, on behalf of Lung Cancer Management, are very much appreciated and valued, and we extend a big thank you to them all. As with all the past volumes of Lung Cancer Management, the standard of content published in volume 5 has been very high – having been assessed using our rigorous peer review and revisions process. We have published a wide range of article types in volume 5, from the shorter opinion and discussion-based editorial and commentary articles, case reports and original research, as well as the longer reviewer articles, covering a variety of subject areas including, neurotrophic tyrosine kinase gene fusions, oligometastatic lung cancer, advanced NSCLC, immunotherapy, symptom burden, liquid biopsy, immune checkpoint inhibitors and surgery. Many articles proved to be popular with our readers through this year and some of the most read articles so far include: ● Review: Nintedanib in advanced NSCLC: management of adverse events (by Lemmens) [1];","PeriodicalId":43551,"journal":{"name":"Lung Cancer Management","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2016-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/lmt-2017-0002","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36854069","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}
Pub Date : 2016-12-01Epub Date: 2017-03-06DOI: 10.2217/lmt-2017-0001
Vassiliki A Papadimitrakopoulou
Vassiliki A Papadimitrakopoulou speaks to Roshaine Wijayatunga, Managing Commissioning Editor: Dr Papadimitrakopoulou is the Jay and Lori Eisenberg Distinguished Professor of Medicine and Chief of the section of Thoracic Medical Oncology in the Department of Thoracic/Head and Neck Medical Oncology at the University of Texas/MD Anderson Cancer Center. Her areas of expertise include design and development of novel therapeutic clinical trials for lung and head and neck neoplasms, personalized genomics-driven lung cancer therapy and translational research and cancer chemoprevention. Her extensive experience in design, development and implementation of translational research in the context of multidisciplinary research teams has led to research funding from National Cancer Institute (NCI), American Society of Clinical Oncology (ASCO) and Department of Defense (DOD) both independently and as a member of a research team in the Head and Neck SPORE program. Currently, she serves as the principal investigator and leads numerous clinical and translational research projects with a focus on the development of biomarker-based targeted therapy to overcome therapeutic resistance in advanced disease and immunotherapy. Most notably, she has led the multidisciplinary clinical and translational research infrastructure dedicated to the treatment of metastatic refractory NSCLC as part of the BATTLE-2 program, designed and developed the first-in-the-world comprehensive genomics-driven umbrella approach in Squamous Lung Cancer, the Lung Master protocol, jointly sponsored by NCI-Cancer Therapy Evaluation Program (CTEP) and Foundation for the National Institutes of Health (FNIH)/industry, aiming at bringing personalized medicine to patients with this disease. She is the Co-PI of an R01 award focusing on the role of KRAS mutations and targeting in lung cancer. She is the lead author or coauthor of over 150 published articles, book chapters and reviews, and numerous abstracts involving cancer therapeutics, prevention and translational research and she has received several awards including the ASCO Young Investigator and Career Development Award. On this R01 application, she will serve as Co-PI, working closely with Roy Herbst (Yale Cancer Center) and Don Gibbons (UT/MD Anderson Cancer Center), building on the recently completed BATTLE-2 program, and capitalizing on both laboratory findings supporting MEK targeted therapy and clinical effectiveness of immunotherapy and their combinations in addressing KRAS mutated lung cancer.
Vassiliki A Papadimitrakopoulou博士是Jay和Lori Eisenberg杰出医学教授,也是德克萨斯大学/MD安德森癌症中心胸/头颈肿瘤内科胸内科肿瘤科主任。她的专业领域包括设计和开发肺和头颈部肿瘤的新型治疗性临床试验,个性化基因组学驱动的肺癌治疗和转化研究以及癌症化学预防。她在多学科研究团队中设计、开发和实施转化研究方面的丰富经验,使她获得了美国国家癌症研究所(NCI)、美国临床肿瘤学会(ASCO)和国防部(DOD)的研究资助,无论是作为头颈部孢子项目研究团队的成员,还是作为独立研究团队的成员。目前,她担任首席研究员并领导许多临床和转化研究项目,重点是开发基于生物标志物的靶向治疗,以克服晚期疾病和免疫治疗的治疗耐药性。最值得注意的是,她领导了多学科临床和转化研究基础设施,致力于转移性难治性非小细胞肺癌的治疗,作为BATTLE-2项目的一部分,设计和开发了世界上第一个全面的基因组学驱动的鳞状肺癌伞形方法,肺主方案,由nci癌症治疗评估项目(CTEP)和美国国立卫生研究院基金会(FNIH)/行业联合赞助。旨在为患有这种疾病的患者提供个性化医疗。她是R01奖的共同负责人,专注于KRAS突变和靶向在肺癌中的作用。她是150多篇已发表的文章、书籍章节和评论的主要作者或合著者,以及涉及癌症治疗、预防和转化研究的众多摘要,并获得了包括ASCO青年研究员和职业发展奖在内的多个奖项。在这项R01申请中,她将担任联合负责人,与Roy Herbst(耶鲁癌症中心)和Don Gibbons (UT/MD Anderson癌症中心)密切合作,以最近完成的BATTLE-2项目为基础,利用支持MEK靶向治疗和免疫治疗及其联合治疗KRAS突变肺癌的临床有效性的实验室发现。
{"title":"AURA3 trial: does Tagrisso (osimertinib) have the potential to become the new standard of care for second-line treatment of patients with <i>EGFR</i> T790M mutation-positive locally advanced or metastatic NSCLC.","authors":"Vassiliki A Papadimitrakopoulou","doi":"10.2217/lmt-2017-0001","DOIUrl":"https://doi.org/10.2217/lmt-2017-0001","url":null,"abstract":"<p><p><b>Vassiliki A Papadimitrakopoulou speaks to Roshaine Wijayatunga, Managing Commissioning Editor:</b> Dr Papadimitrakopoulou is the Jay and Lori Eisenberg Distinguished Professor of Medicine and Chief of the section of Thoracic Medical Oncology in the Department of Thoracic/Head and Neck Medical Oncology at the University of Texas/MD Anderson Cancer Center. Her areas of expertise include design and development of novel therapeutic clinical trials for lung and head and neck neoplasms, personalized genomics-driven lung cancer therapy and translational research and cancer chemoprevention. Her extensive experience in design, development and implementation of translational research in the context of multidisciplinary research teams has led to research funding from National Cancer Institute (NCI), American Society of Clinical Oncology (ASCO) and Department of Defense (DOD) both independently and as a member of a research team in the Head and Neck SPORE program. Currently, she serves as the principal investigator and leads numerous clinical and translational research projects with a focus on the development of biomarker-based targeted therapy to overcome therapeutic resistance in advanced disease and immunotherapy. Most notably, she has led the multidisciplinary clinical and translational research infrastructure dedicated to the treatment of metastatic refractory NSCLC as part of the BATTLE-2 program, designed and developed the first-in-the-world comprehensive genomics-driven umbrella approach in Squamous Lung Cancer, the Lung Master protocol, jointly sponsored by NCI-Cancer Therapy Evaluation Program (CTEP) and Foundation for the National Institutes of Health (FNIH)/industry, aiming at bringing personalized medicine to patients with this disease. She is the Co-PI of an R01 award focusing on the role of <i>KRAS</i> mutations and targeting in lung cancer. She is the lead author or coauthor of over 150 published articles, book chapters and reviews, and numerous abstracts involving cancer therapeutics, prevention and translational research and she has received several awards including the ASCO Young Investigator and Career Development Award. On this R01 application, she will serve as Co-PI, working closely with Roy Herbst (Yale Cancer Center) and Don Gibbons (UT/MD Anderson Cancer Center), building on the recently completed BATTLE-2 program, and capitalizing on both laboratory findings supporting MEK targeted therapy and clinical effectiveness of immunotherapy and their combinations in addressing <i>KRAS</i> mutated lung cancer.</p>","PeriodicalId":43551,"journal":{"name":"Lung Cancer Management","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2016-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2217/lmt-2017-0001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36864621","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}