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We began analyzing https://link.springer.com/article/10.1007/BF00180817, but it redirected us to https://link.springer.com/article/10.1007/BF00180817. The analysis below is for the second page.

Title[redir]:
A phase II trial of a differentiating agent (tRA) with cisplatin-VP 16 chemotherapy in advanced non-small cell lung cancer | Investigational New Drugs
Description:
The prognosis for advanced non-small cell lung cancer remains poor. Response to chemotherapy is infrequent and overall survival is low. Trans-retinoic acid (tRA), a differentiating agent whose mechanism of action is thought to be different from conventional chemotherapy has activity in preclinical models and low but definite activity in the clinical setting. Its use has been hampered by decrease in bioavailability during continuous administration. We used an interrupted dosing schedule with a drug holiday for tRA that has since been confirmed to restore blood levels in combination with chemotherapy (Cisplatin-VP 16) in 20 patients with stage IIIB and IV non-small cell lung cancer. Ten patients had partial responses among 19 evaluable pts (53%; 95% confidence interval 30–75%) and 4 had minor responses. Neutropenia was the most common acute toxicity-grade 3/4 neutropenia occurring in 90% of patients at some point in the treatment course. Median survival was 25.5 weeks. This regimen of trans-retinoic acid given with drug holiday and chemotherapy has significant activity in advanced non-small cell lung cancer, is fairly well tolerated and is worthy of confirmation in a larger, multi-institutional setting.

Matching Content Categories {πŸ“š}

  • Health & Fitness
  • Telecommunications
  • Education

Content Management System {πŸ“}

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 {πŸ“ˆ}

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.
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How Does Doi.org Make Money? {πŸ’Έ}

We can't figure out the monetization strategy.

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 earning cash quietly, but we haven't detected the monetization method.

Keywords {πŸ”}

cancer, google, scholar, cell, lung, acid, nonsmall, chemotherapy, alltransretinoic, advanced, article, phase, treatment, combination, patients, trial, clin, oncol, thiruvengadam, atiba, drug, acute, privacy, cookies, content, tra, activity, therapy, cisretinoic, promyelocytic, data, journal, publish, search, azawi, holiday, access, study, metastatic, treat, squamous, interferon, haematol, leukemia, letter, natl, inst, analysis, information, log,

Topics {βœ’οΈ}

month download article/chapter multi-institutional setting trans-retinoic acid administered trans-retinoic acid bioavailability related subjects squamous cell carcinoma privacy choices/manage cookies squamous cell cancers cisplatin-vp 16 chemotherapy trans-retinoic acid trans-retinoic acid phase ii toxicity phase ii trial 13-cis-retinoic acid effective combination therapy full article pdf increased pth-rp trans-retinoicoid acid va medical center clinical setting acute promyelocytic leukaemia dose-limiting toxicity lung cancer acute promyelocytic leukemia warrell rp jr miller wh jr plasma drug concentrations european economic area restore blood levels von hoff dd bone marrow transplantation 27 mg/m2/day o'dwyer pj phase ii study multicenter data evaluation interferon alfa-2a conditions privacy policy interrupted dosing schedule interferon alpha-2a pediat hematol/oncol 15 accepting optional cookies transretinoic acid treatment check access instant access cisplatin-vp 16 main content log journal finder publish combination therapy article investigational retinoid β€œresistance”

Questions {❓}

  • Is second-line systemic chemotherapy beneficial in patients with non-small cell lung cancer (NSCLC)?

Schema {πŸ—ΊοΈ}

WebPage:
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         headline:A phase II trial of a differentiating agent (tRA) with cisplatin-VP 16 chemotherapy in advanced non-small cell lung cancer
         description:The prognosis for advanced non-small cell lung cancer remains poor. Response to chemotherapy is infrequent and overall survival is low. Trans-retinoic acid (tRA), a differentiating agent whose mechanism of action is thought to be different from conventional chemotherapy has activity in preclinical models and low but definite activity in the clinical setting. Its use has been hampered by decrease in bioavailability during continuous administration. We used an interrupted dosing schedule with a drug holiday for tRA that has since been confirmed to restore blood levels in combination with chemotherapy (Cisplatin-VP 16) in 20 patients with stage IIIB and IV non-small cell lung cancer. Ten patients had partial responses among 19 evaluable pts (53%; 95% confidence interval 30–75%) and 4 had minor responses. Neutropenia was the most common acute toxicity-grade 3/4 neutropenia occurring in 90% of patients at some point in the treatment course. Median survival was 25.5 weeks. This regimen of trans-retinoic acid given with drug holiday and chemotherapy has significant activity in advanced non-small cell lung cancer, is fairly well tolerated and is worthy of confirmation in a larger, multi-institutional setting.
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      headline:A phase II trial of a differentiating agent (tRA) with cisplatin-VP 16 chemotherapy in advanced non-small cell lung cancer
      description:The prognosis for advanced non-small cell lung cancer remains poor. Response to chemotherapy is infrequent and overall survival is low. Trans-retinoic acid (tRA), a differentiating agent whose mechanism of action is thought to be different from conventional chemotherapy has activity in preclinical models and low but definite activity in the clinical setting. Its use has been hampered by decrease in bioavailability during continuous administration. We used an interrupted dosing schedule with a drug holiday for tRA that has since been confirmed to restore blood levels in combination with chemotherapy (Cisplatin-VP 16) in 20 patients with stage IIIB and IV non-small cell lung cancer. Ten patients had partial responses among 19 evaluable pts (53%; 95% confidence interval 30–75%) and 4 had minor responses. Neutropenia was the most common acute toxicity-grade 3/4 neutropenia occurring in 90% of patients at some point in the treatment course. Median survival was 25.5 weeks. This regimen of trans-retinoic acid given with drug holiday and chemotherapy has significant activity in advanced non-small cell lung cancer, is fairly well tolerated and is worthy of confirmation in a larger, multi-institutional setting.
      datePublished:
      dateModified:
      pageStart:395
      pageEnd:401
      sameAs:https://doi.org/10.1007/BF00180817
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         lung cancer
         retinoic acid
         cisplatin
         etoposide
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         name:Department of Medicine, VA Medical Center and University of California, Irvine
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               name:Department of Radiation Oncology, VA Medical Center, Long Beach, USA
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