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DOI . ORG {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Doi.org Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. Hosting Providers
  14. CDN Services

We began analyzing https://link.springer.com/article/10.1007/s12032-023-02005-w, but it redirected us to https://link.springer.com/article/10.1007/s12032-023-02005-w. The analysis below is for the second page.

Title[redir]:
A review of recent advances in the novel therapeutic targets and immunotherapy for lung cancer | Medical Oncology
Description:
Lung cancer is amongst the most pervasive malignancies having high mortality rates. It is broadly grouped into non-small-cell lung cancer (NSCLC) and small-cell lung cancer (SCLC). The concept of personalized medicine has overshadowed the conventional chemotherapy given to all patients with lung cancer. The targeted therapy is given to a particular population having specific mutations to help in the better management of lung cancer. The targeting pathways for NSCLC include the epidermal growth factor receptor, vascular endothelial growth factor receptor, MET (Mesenchymal epithelial transition factor) oncogene, Kirsten rat sarcoma viral oncogene (KRAS), and anaplastic lymphoma kinase (ALK). SCLC targeting pathway includes Poly (ADP-ribose) polymerases (PARP) inhibitors, checkpoint kinase 1 (CHK 1) pathway, WEE1 pathway, Ataxia Telangiectasia and Rad3-related (ATR)/Ataxia telangiectasia mutated (ATM), and Delta‐like canonical Notch ligand 3 (DLL-Immune checkpoint inhibitors like programmed cell death protein 1 (PD-1)/ programmed death-ligand 1 (PD-L1) inhibitors and Cytotoxic T-lymphocyte-associated antigen-4 (CTLA4) blockade are also utilized in the management of lung cancer. Many of the targeted therapies are still under development and require clinical trials to establish their safety and efficacy. This review summarizes the mechanism of molecular targets and immune-mediated targets, recently approved drugs, and their clinical trials for lung cancer.

Matching Content Categories {📚}

  • Health & Fitness
  • Education
  • Telecommunications

Content Management System {📝}

What CMS is doi.org built with?

Custom-built

No common CMS systems were detected on Doi.org, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of doi.org audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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How Does Doi.org Make Money? {💸}

The income method remains a mystery to us.

While profit motivates many websites, others exist to inspire, entertain, or provide valuable resources. Websites have a variety of goals. And this might be one of them. Doi.org might be plotting its profit, but the way they're doing it isn't detectable yet.

Keywords {🔍}

pubmed, cancer, article, lung, google, scholar, cell, cas, central, nonsmall, small, oncol, clin, inhibitors, immunotherapy, treatment, therapy, targeting, res, med, patients, nonsmallcell, smallcell, targeted, advances, therapeutic, met, mol, targets, nsclc, growth, pathway, pdl, thorac, advanced, rev, mutations, clinical, molecular, transl, wang, yang, nat, inhibition, inhibitor, zhang, review, factor, parp, efficacy,

Topics {✒️}

gov/drugs/resources-information-approved-drugs/fda-approves-nivolumab line-mnsclc-pd-l1-tumor-expression-1 platinum-etoposide versus platinum-etoposide histology-independent ve-basket study her2/erbb2/neu gene mutations month download article/chapter activate anti-tumor immunity targeting pi3k/akt/mtor pathway eml4-alk fusion gene early-stage lung cancer anti-pd-l1/pd-1 immunotherapy anti-pd-1/pd-l1 immunotherapy pd-1/pd-l1 axis inhibitors small-cell lung cancer small-cell lung cancer small-cell lung cancer tead4-driven transcriptional state small-cell lung carcinoma platinum-treated urothelial carcinoma anti–programmed cell death pi3k/akt/mtor pathway high-level met-amplified biomarker-defined disease subsets her2-mutant lung adenocarcinoma reverse-phase protein arrays recently approved drugs anti–programmed death-ligand 1 e2f/rb pathway leads hgf/c-met axis approved lag-3 inhibitor dll-immune checkpoint inhibitors patient-derived models egfr-directed monoclonal antibodies full article pdf pd-l1-selected patients covalent cdk7 inhibitor cdk7 inhibitor ypn-005 cell cycle pathways article khadela nivolumab versus docetaxel lung cancer therapy single-arm cohort van aller gs privacy choices/manage cookies lung cancer risk torres-roman js nat rev cancer anti-proliferative activity molecular-targeted therapy avinash khadela

Questions {❓}

  • Angiogenesis: an organizing principle for drug discovery?
  • Anti-angiogenic tyrosine kinase inhibitors: What is their mechanism of action?
  • Combination immunotherapy strategies in advanced non-small cell lung cancer (NSCLC): does biological rationale meet clinical needs?
  • EGFR-directed monoclonal antibodies in non-small cell lung cancer: how to predict efficacy?
  • Gender and outcomes in non-small cell lung cancer: an old prognostic variable comes back for targeted therapy and immunotherapy?
  • Trastuzumab in the treatment of advanced non–small-cell lung cancer: is there a role?

Schema {🗺️}

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         headline:A review of recent advances in the novel therapeutic targets and immunotherapy for lung cancer
         description:Lung cancer is amongst the most pervasive malignancies having high mortality rates. It is broadly grouped into non-small-cell lung cancer (NSCLC) and small-cell lung cancer (SCLC). The concept of personalized medicine has overshadowed the conventional chemotherapy given to all patients with lung cancer. The targeted therapy is given to a particular population having specific mutations to help in the better management of lung cancer. The targeting pathways for NSCLC include the epidermal growth factor receptor, vascular endothelial growth factor receptor, MET (Mesenchymal epithelial transition factor) oncogene, Kirsten rat sarcoma viral oncogene (KRAS), and anaplastic lymphoma kinase (ALK). SCLC targeting pathway includes Poly (ADP-ribose) polymerases (PARP) inhibitors, checkpoint kinase 1 (CHK 1) pathway, WEE1 pathway, Ataxia Telangiectasia and Rad3-related (ATR)/Ataxia telangiectasia mutated (ATM), and Delta‐like canonical Notch ligand 3 (DLL-Immune checkpoint inhibitors like programmed cell death protein 1 (PD-1)/ programmed death-ligand 1 (PD-L1) inhibitors and Cytotoxic T-lymphocyte-associated antigen-4 (CTLA4) blockade are also utilized in the management of lung cancer. Many of the targeted therapies are still under development and require clinical trials to establish their safety and efficacy. This review summarizes the mechanism of molecular targets and immune-mediated targets, recently approved drugs, and their clinical trials for lung cancer.
         datePublished:2023-04-18T00:00:00Z
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      headline:A review of recent advances in the novel therapeutic targets and immunotherapy for lung cancer
      description:Lung cancer is amongst the most pervasive malignancies having high mortality rates. It is broadly grouped into non-small-cell lung cancer (NSCLC) and small-cell lung cancer (SCLC). The concept of personalized medicine has overshadowed the conventional chemotherapy given to all patients with lung cancer. The targeted therapy is given to a particular population having specific mutations to help in the better management of lung cancer. The targeting pathways for NSCLC include the epidermal growth factor receptor, vascular endothelial growth factor receptor, MET (Mesenchymal epithelial transition factor) oncogene, Kirsten rat sarcoma viral oncogene (KRAS), and anaplastic lymphoma kinase (ALK). SCLC targeting pathway includes Poly (ADP-ribose) polymerases (PARP) inhibitors, checkpoint kinase 1 (CHK 1) pathway, WEE1 pathway, Ataxia Telangiectasia and Rad3-related (ATR)/Ataxia telangiectasia mutated (ATM), and Delta‐like canonical Notch ligand 3 (DLL-Immune checkpoint inhibitors like programmed cell death protein 1 (PD-1)/ programmed death-ligand 1 (PD-L1) inhibitors and Cytotoxic T-lymphocyte-associated antigen-4 (CTLA4) blockade are also utilized in the management of lung cancer. Many of the targeted therapies are still under development and require clinical trials to establish their safety and efficacy. This review summarizes the mechanism of molecular targets and immune-mediated targets, recently approved drugs, and their clinical trials for lung cancer.
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External Links {🔗}(492)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

Emails and Hosting {✉️}

Mail Servers:

  • mx.zoho.eu
  • mx2.zoho.eu
  • mx3.zoho.eu

Name Servers:

  • josh.ns.cloudflare.com
  • zita.ns.cloudflare.com

CDN Services {📦}

  • Crossref

4.82s.