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S. Fine

Researcher at University of Toronto

Publications -  26
Citations -  1624

S. Fine is an academic researcher from University of Toronto. The author has contributed to research in topics: Chemotherapy & Combination chemotherapy. The author has an hindex of 17, co-authored 26 publications receiving 1600 citations. Previous affiliations of S. Fine include Credit Valley Hospital.

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A randomized trial of two dose levels of cyclophosphamide, methotrexate, and fluorouracil chemotherapy for patients with metastatic breast cancer.

TL;DR: This trial suggests that better palliation is achieved by using full-dose chemotherapy, and patients experienced more vomiting, myelosuppression, conjunctivitis, and alopecia when receiving higher doses of chemotherapy.
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Increased thromboembolic complications with concurrent tamoxifen and chemotherapy in a randomized trial of adjuvant therapy for women with breast cancer. National Cancer Institute of Canada Clinical Trials Group Breast Cancer Site Group.

TL;DR: Thromboembolism related to the addition of CMF chemotherapy to tamoxifen as adjuvant therapy in this group of women represents a relatively common and serious complication that may outweigh any benefits offered by this additional therapy.
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A randomized study of oral nutritional support versus ad lib nutritional intake during chemotherapy for advanced colorectal and non-small-cell lung cancer.

TL;DR: A multivariate prognostic factor analysis demonstrated that for lung cancer, the percent of weight loss, serum albumin concentration, and presence of liver metastases were significant and independent prognostic variables for survival duration and for colorectal cancer, serumalbumin, alkaline phosphatase, lactic dehydrogenase levels, and percent targeted caloric intake were significant independent predictors of survival duration.
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The Combination of p53 Mutation and neu/erbB-2 Amplification Is Associated With Poor Survival in Node-Negative Breast Cancer

TL;DR: Evaluation of tumors for p53 mutations may be beneficial to identify women at higher risk of disease recurrence and death when the tumor has neu/erbB-2 amplification, but in the absence of neu/, the presence of p53 mutation may not provide additional independent prognostic information.