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I can judge Iressa's effectiveness on my personal experience. I used the medication after having undergone my intravenous chemotherapy. I started taking Iressa in 2005. My last scan after the chemotherapy and Iressa treatment showed that the cancer stopped growing. I also noticed the improvement in my condition; I started feeling myself much better than before. Each scan thereafter showed slow but still noticeable improvement. I'm still taking Iressa and still showing signs of improvement. Wonderful medication for lung cancer.



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My sister was diagnosed with lungs cancer about four years ago. It was a real shock for the whole family, but we soon recovered from it as we needed to support her and make her struggle with the disease. We have visited many doctors and all of them prescribed strange unconventional drugs, we even tried some of them, but they provided no effect and my sister's condition was growing worse. One day we visited a doctor in Chicago and he advised us to try Iressa as a medication aimed exactly at lungs cancer. He was so enthusiastic about the drug that my sister let me talk her into trying it. Iressa really helped her! She's much better now and she started believing in recovery! Great med, thanks to its inventors.

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Patients with smaller disease without lymph node involvement or distant metastases have a better chance at long-term tumor control than those with larger disease or with lymph node involvement or distant metastases.

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These effects of ZD1839 on p21 WAF1 and p27 Kip1 agree well with those observed on the cell cycle.

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Crizotinib is a cancer medication that interferes with the growth and spread of cancer cells in the body.

An analysis of pooled median progression-free survival in the first-line setting was similar to the overall results.

To reduce your chance of having a skin reaction while using pemetrexed, your doctor will prescribe a corticosteroid medicine (e.

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The effect of ZD1839 was cytostatic, but higher doses increased apoptotic cell death, and in combination with cytotoxic drugs, ZD1839 markedly enhanced apoptotic cell death.

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The elimination half-life of Iressa is approximately 48 hours.

We brought Dad down that weekend to live with my sister.

Erlotinib is the only targeted agent that significantly improves survival and offers symptom relief to patients with advanced NSCLC who have not responded to chemotherapy.

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The relatively low incidence of pancreatic cancer, combined with the assumption that only 23% of new patients would be treated with erlotinib plus gemcitabine and the short duration of treatment, suggested that the use of erlotinib in this setting would have a relatively low budgetary impact.

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Since EGFR expression and phosphorylation were the major determining factors for sensitivity of the cells to gefitinib-induced growth-inhibition, biochemical modulation of EGFR by CPT-11 might be responsible for the synergistic interaction between gefitinib and CPT-11.

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Continuous hyperfractionated accelerated radiotherapy (CHART) administers multiple doses of radiation per day but uses the standard doses.

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Results of a recent trial in patients with anthracycline resistant breast cancer show that the addition of capecitabine to docetaxal significantly prolongs survival ().

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The complexity and the number of tyrosine kinases have greatly increased with the sequencing effort of the Human Genome Project, thus providing more opportunities for drug discovery.

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Unfortunately, lung surgery may be too risky for patients with other lung diseases or serious medical conditions, and because lung cancers tend to occur in smokers over 50, such health problems are likely to be present.

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Lung cancer patients who have acquired gene mutations associated with resistance to tyrosine kinase inhibitors such as Iressa or Tarceva can be identified far more accurately using a new mutation test kit from DxS.

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In the beginning the doctors gave her about a year and said her care is strictly paliative, and that chemo would only extend her life 1 to 3 months.

There were no grade 3 or 4 adverse events recorded during the treatment period, and no patients discontinued erlotinib due to unacceptable toxicity.

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