Cited by 285Lung Cancer Treatments and MutationsLung Cancer Diagnosis and TreatmentLung Cancer Research Studies

Scientific Advances in Lung Cancer 2015

Open access
Tsao, Anne S., Scagliotti, Giorgio V., Bunn, Paul A., Carbone, David P., Warren, Graham W., Bai, Chunxue, de Koning, Harry J., Yousaf-Khan, A. Uraujh +29 more·2016·Journal of Thoracic Oncology

Abstract

Lung cancer continues to be a major global health problem; the disease is diagnosed in more than 1.6 million new patients each year. However, significant progress is underway in both the prevention and treatment of lung cancer. Lung cancer therapy has now emerged as a "role model" for precision cancer medicine, with several important therapeutic breakthroughs occurring during 2015. These advances have occurred primarily in the immunotherapy field and in treatments directed against tumors harboring specific oncogenic drivers. Our knowledge about molecular mechanisms for oncogene-driven tumors and about resistance to targeted therapies has increased quickly over the past year. As a result, several regulatory approvals of new agents that significantly improve survival and quality of life for patients with lung cancer who have advanced disease have occurred. The International Association for the Study of Lung Cancer has gathered experts in different areas of lung cancer research and management to summarize the most significant scientific advancements related to prevention and therapy of lung cancer during the past year.

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Crossref · 10.1016/j.jtho.2016.03.012

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  • Interactions among reactive non-neoplastic cells, genetically altered tumor cells, and ECM control the majority of stages of tumorigenesis, including clonal evolution, cancer heterogeneity, epithelial-mesenchymal transition, migration, invasion, metastasis, neovascularization, apoptosis, and chemotherapeutic drug resistance.

    “Therefore, on the other side of the argument, interactions in reactive non-neoplastic cells, genetically-altered tumor cells, and ECM control the majority of the stages of tumorigenesis effectively including clonal evolution, cancer heterogeneity, epithelial-mesenchymal-transition (EMT), migration, invasion, development of metastasis, neovascularization, apoptosis and chemotherapeutic drug resist”

    From Tumor microenvironment complexity and therapeutic implications at a glance (2020) · cites this paper as [13]

    The Hirsch section (page unavailable) says that interactions between malignant and neighboring nonmalignant cells create a dynamic tumor microenvironment, and it mentions matrix-remodeling enzymes. It does not say that those interactions control the majority of tumorigenesis stages or establish the claimed list of effects, including clonal evolution, EMT, metastasis, and chemotherapy resistance. (LLM, conf=0.84)

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1 of the 241 references couldn’t be matched to a known paper.

Research works printed but not linked: 17

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Authors
Tsao, A. S., Scagliotti, G. V., Bunn, P. A., Carbone, D. P., Warren, G. W., Bai, C., de Koning, H. J., Yousaf-Khan, A. U., McWilliams, A., Tsao, M. S., Adusumilli, P. S., Rami-Porta, R., Asamura, H., Van Schil, P. E., Darling, G. E., Ramalingam, S. S., Gomez, D. R., Rosenzweig, K. E., Zimmermann, S., Peters, S., Ignatius Ou, S.-H., Reungwetwattana, T., Jänne, P. A., Mok, T. S., Wakelee, H. A., Pirker, R., Mazières, J., Brahmer, J. R., Zhou, Y., Herbst, R. S., Papadimitrakopoulou, V. A., Redman, M. W., Wynes, M. W., Gandara, D. R., Kelly, R. J., Hirsch, F. R., & Pass, H. I.
Affiliations
  • The University of Texas MD Anderson Cancer Center (US)
  • Ospedale San Luigi Gonzaga (IT)
  • University of Colorado Cancer Center (US)
  • The Ohio State University (US)
  • Medical University of South Carolina (US)
  • Fudan University (CN)
  • Erasmus MC (NL)
  • The University of Western Australia (AU)
  • University Health Network (CA)
  • Memorial Sloan Kettering Cancer Center (US)
  • Keio University (JP)
  • University of Toronto (CA)
  • Emory University (US)
  • Icahn School of Medicine at Mount Sinai (US)
  • HFR Freiburg Kantonsspital (CH)
  • University of Lausanne (CH)
  • Mahidol University (TH)
  • Chinese University of Hong Kong (HK)
  • Stanford Medicine (US)
  • Medical University of Vienna (AT)
  • Université Toulouse III - Paul Sabatier (FR)
  • Johns Hopkins University (US)
  • Yale Cancer Center (US)
  • Fred Hutch Cancer Center (US)
  • International Association for the Study of Lung Cancer (US)
  • UC Davis Comprehensive Cancer Center (US)
  • NYU Langone Health (US)
Corresponding author
Hirsch, Fred R.
Venue
Journal of Thoracic Oncology
Publisher
Elsevier BV
Published
2016-05
Volume
11
Issue
5
Pages
613-638
ISSN
1556-0864 (ISSN-L)
OpenAlex
W2310252196
Cited by
284
References
241
Citations by year
2026: 6 · 2025: 10 · 2024: 23 · 2023: 25 · 2022: 30 · 2021: 30 · 2020: 41 · 2019: 34 · 2018: 29 · 2017: 38 · 2016: 18
FWCI
6.88
Type
journal article
Language
en
Open access
Locations
  • Journal of Thoracic Oncology (publishedVersion)
  • PubMed (publishedVersion)
  • Institutional Research Information System University of Turin (University of Turin) (submittedVersion, other-oa)
  • EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
  • IRIS (submittedVersion)
  • SERVAL (Université de Lausanne) (submittedVersion)
Funders
  • Amgen
  • Bristol-Myers Squibb
  • Eli Lilly and Company
  • Pfizer
  • AstraZeneca
  • International Association for the Study of Lung Cancer
  • Teva Pharmaceutical Industries
  • Ariad Pharmaceuticals
  • Celgene
  • Cancer Care Ontario
  • Vertex Pharmaceuticals
  • Les Laboratories Pierre Fabre
  • Clovis Oncology
  • KWF Kankerbestrijding
  • Astellas Pharma
  • Genentech
  • Chugai Pharmaceutical
  • Ignyta
  • Daiichi Sankyo Europe
Topics
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Treatments and Mutations
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Diagnosis and Treatment
  • Health Sciences › Medicine › Oncology › Lung Cancer Research Studies
Keywords
lung cancer, precision oncology, immunotherapy, targeted therapy, oncogenic drivers, lung cancer prevention, regulatory approval
MeSH terms
Humans, Immunotherapy, Lung Neoplasms, Quality of Life, Precision Medicine

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