Search Results - "van Echo, D."
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Final report of the phase I/II clinical trial of the E75 (nelipepimut-S) vaccine with booster inoculations to prevent disease recurrence in high-risk breast cancer patients
Published in Annals of oncology (01-09-2014)“…E75 (nelipepimut-S) is a human leukocyte antigen (HLA)-A2/A3-restricted immunogenic peptide derived from the HER2 protein. We have conducted phase I/II…”
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Phase I study of the orally administered butyrate prodrug, tributyrin, in patients with solid tumors
Published in Clinical cancer research (01-03-1998)“…Butyrates have been studied as cancer differentiation agents in vitro and as a treatment for hemoglobinopathies. Tributyrin, a triglyceride with butyrate…”
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Pleurx tunneled catheter in the management of malignant ascites
Published in Journal of vascular and interventional radiology (01-03-2001)“…The authors report their experience with the Pleurx tunneled catheter in patients with end-stage abdominal carcinomatosis and intractable ascites. Ten patients…”
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The use of carboplatin and paclitaxel with daily radiotherapy in patients with locally advanced squamous cell carcinomas of the head and neck
Published in International journal of radiation oncology, biology, physics (01-04-2000)“…Unresectable squamous cell carcinomas of the head and neck (SCCHN) continue to pose a significant therapeutic challenge. This report defines the toxicities,…”
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Interleukin-2 therapy in patients with metastatic malignant melanoma: a phase II study
Published in Journal of clinical oncology (01-10-1990)“…Forty-seven patients with metastatic malignant melanoma were treated with two 5-day cycles of 100,000 U/kg recombinant interleukin-2 (IL-2) intravenously (IV)…”
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Carboplatin (NSC-241-240): an active platinum analog for the treatment of squamous-cell carcinoma of the head and neck
Published in Journal of clinical oncology (01-10-1986)“…Carboplatin (CBDCA, Bristol-Meyers, New York) is a second generation platinum analog. Preclinical and phase I clinical studies have indicated a different…”
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Phase I trial of granulocyte-macrophage colony-stimulating factor plus high-dose cyclophosphamide given every 2 weeks: a Cancer and Leukemia Group B study
Published in JNCI : Journal of the National Cancer Institute (18-08-1993)“…Chemotherapy-induced myelosuppression often limits escalation of cancer chemotherapy doses. Cyclophosphamide, an alkylating agent, is an ideal candidate for…”
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Population pharmacodynamic study of amonafide: a Cancer and Leukemia Group B study
Published in Journal of clinical oncology (01-03-1995)“…To determine if variability in toxicity of amonafide during phase II trials could be correlated with pharmacokinetic variability. Seventy-three patients…”
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A comparison of carboplatin plus methotrexate versus methotrexate alone in patients with recurrent and metastatic head and neck cancer
Published in Journal of clinical oncology (01-09-1989)“…Patients with recurrent and metastatic squamous cell carcinoma of the head and neck (SCCHN) were stratified by performance status, extent of disease, and prior…”
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Hypersensitivity reactions from taxol
Published in Journal of clinical oncology (01-07-1990)“…Taxol is an antitumor agent in clinical trial that has been shown to have activity against advanced ovarian carcinoma and melanoma. Hypersensitivity reactions…”
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A novel pharmacodynamically based approach to dose optimization of carboplatin when used in combination with etoposide
Published in Journal of clinical oncology (01-12-1989)“…Thrombocytopenia, the dose-limiting toxicity of carboplatin, is manageable and predictable with the dosing equation: Dose (mg/m2) = (0.091) (creatinine…”
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Phase I and pharmacokinetic trial of carboplatin in refractory adult leukemia
Published in JNCI : Journal of the National Cancer Institute (16-03-1988)“…Sixteen patients [13 acute nonlymphocytic leukemia (ANLL), 2 acute lymphocytic leukemia, 1 chronic myelogenous leukemia in a blast crisis; median age, 40 yr;…”
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Phase I clinical trial of all-trans-retinoic acid with correlation of its pharmacokinetics and pharmacodynamics
Published in Cancer chemotherapy and pharmacology (1997)“…A phase I trial of all-trans-retinoic acid (ATRA) was conducted to establish the maximum tolerable dose (MTD) of ATRA given once daily to patients with solid…”
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High-dose chemotherapy without autologous bone marrow transplantation in melanoma
Published in Journal of clinical oncology (01-12-1986)“…High-dose chemotherapy with BCNU, melphalan, or both, followed by autologous bone marrow transplantation (ABMT) has been reported to produce response rates in…”
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Predictors of response and survival after concurrent chemotherapy and radiation for locally advanced squamous cell carcinomas of the head and neck
Published in Cancer (01-02-2001)“…BACKGROUND The objective of this study was to determine prognostic factors for response and survival on three consecutive institutional trials utilizing…”
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Pharmacokinetics and dosage reduction of cis-diammine(1,1-cyclobutanedicarboxylato)platinum in patients with impaired renal function
Published in Cancer research (Chicago, Ill.) (01-11-1984)“…cis-Diammine(1,1-cyclobutanedicarboxylato)platinum (CBDCA) is a nonnephrotoxic but myelosuppressive analogue of cisplatin (DDP) with greatly reduced protein…”
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Mitomycin C and vinblastine chemotherapy for advanced breast cancer
Published in Cancer (15-09-1981)“…Mitomycin C, 20 mg/m2 day 1, and vinblastine, 0.15 mg/m2 days 1 and 21, were administered intravenously to 31 patients with refractory previously treated…”
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Prospective validation of a pharmacologically based dosing scheme for the cis-diamminedichloroplatinum(II) analogue diamminecyclobutanedicarboxylatoplatinum
Published in Cancer research (Chicago, Ill.) (01-12-1985)“…We previously correlated both renal function and thrombocytopenia, the dose limiting toxicity of carboplatin, with the plasma pharmacokinetics of carboplatin…”
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Diaziquone Given as a Continuous Infusion Is an Active Agent for Relapsed Adult Acute Nonlymphocytic Leukemia
Published in Blood (01-01-1986)“…Diaziquone given as a bolus has not been effective in patients with relapsed or refractory leukemia. Because of in vitro data suggesting enhancement of…”
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