orabase and Skin-Neoplasms

orabase has been researched along with Skin-Neoplasms* in 4 studies

Reviews

1 review(s) available for orabase and Skin-Neoplasms

ArticleYear
Using wound bed preparation to heal a malignant fungating wound: a single case study.
    Journal of wound care, 2007, Volume: 16, Issue:9

    Full healing was achieved within eight weeks in a malignant fungating wound using the principles of the TIME paradigm. This concept appears to provide a structured and systematic approach for managing such non-healing wounds.

    Topics: Adult; Bandages, Hydrocolloid; Breast Neoplasms; Carboxymethylcellulose Sodium; Clinical Protocols; Drug Combinations; Exudates and Transudates; Female; Gelatin; Humans; Humidity; Infection Control; Inflammation; Metronidazole; Nursing Assessment; Odorants; Palliative Care; Patient Selection; Pectins; Polyenes; Referral and Consultation; Skin Care; Skin Neoplasms; Wound Healing; Wound Infection

2007

Trials

1 trial(s) available for orabase and Skin-Neoplasms

ArticleYear
Combined Vaccination with NY-ESO-1 Protein, Poly-ICLC, and Montanide Improves Humoral and Cellular Immune Responses in Patients with High-Risk Melanoma.
    Cancer immunology research, 2020, Volume: 8, Issue:1

    Given its ability to induce both humoral and cellular immune responses, NY-ESO-1 has been considered a suitable antigen for a cancer vaccine. Despite promising results from early-phase clinical studies in patients with melanoma, NY-ESO-1 vaccine immunotherapy has not been widely investigated in larger trials; consequently, many questions remain as to the optimal vaccine formulation, predictive biomarkers, and sequencing and timing of vaccines in melanoma treatment. We conducted an adjuvant phase I/II clinical trial in high-risk resected melanoma to optimize the delivery of poly-ICLC, a TLR-3/MDA-5 agonist, as a component of vaccine formulation. A phase I dose-escalation part was undertaken to identify the MTD of poly-ICLC administered in combination with NY-ESO-1 and montanide. This was followed by a randomized phase II part investigating the MTD of poly-ICLC with NY-ESO-1 with or without montanide. The vaccine regimens were generally well tolerated, with no treatment-related grade 3/4 adverse events. Both regimens induced integrated NY-ESO-1-specific CD4

    Topics: Adjuvants, Immunologic; Aged; Antigens, Neoplasm; Cancer Vaccines; Carboxymethylcellulose Sodium; CD4-Positive T-Lymphocytes; CD8-Positive T-Lymphocytes; Cross-Priming; Female; Humans; Immunity, Cellular; Immunity, Humoral; Interferon Inducers; Male; Mannitol; Melanoma; Membrane Proteins; Middle Aged; Oleic Acids; Patient Safety; Poly I-C; Polylysine; Skin Neoplasms; Treatment Outcome

2020

Other Studies

2 other study(ies) available for orabase and Skin-Neoplasms

ArticleYear
Bioengineered carboxymethyl cellulose-doxorubicin prodrug hydrogels for topical chemotherapy of melanoma skin cancer.
    Carbohydrate polymers, 2018, Sep-01, Volume: 195

    Melanoma is the most aggressive type of skin cancer with high rates of mortality. Despite encouraging advances demonstrated by anticancer drug carriers in recent years, developing ideal drug delivery systems to target tumor microenvironment by overcoming physiological barriers and chemotherapy side effects still remain intimidating challenges. Herein, we designed and developed a novel carbohydrate-based prodrug composed of carboxymethylcellulose (CMC) polymer bioconjugated with anticancer drug doxorubicin hydrochloride (DOX) by covalent amide bonds and crosslinked with citric acid for producing advanced hydrogels. The results demonstrated the effect of CMC hydrogel network structure with distinct degree of substitution of carboxymethyl groups of the cellulose backbone regarding to the process of bioconjugation and on tailoring the DOX release kinetics in vitro and the cytotoxicity towards melanoma cancer cells in vitro. To this end, an innovative platform was developed based on polysaccharide-drug hydrogels offering promising perspectives for skin disease applications associated with topical chemotherapy of melanoma.

    Topics: Antineoplastic Agents; Carboxymethylcellulose Sodium; Cell Line, Tumor; Citric Acid; Cross-Linking Reagents; Doxorubicin; Drug Liberation; HEK293 Cells; Humans; Hydrogels; Melanoma; Prodrugs; Skin Neoplasms

2018
A highly reproducible bolus immobilization technique for the treatment of scalp malignancies.
    Medical dosimetry : official journal of the American Association of Medical Dosimetrists, 2008,Spring, Volume: 33, Issue:1

    Radiation treatment of scalp malignancies can be a challenge due to the multiple curved surfaces to which homogenous dose must be delivered. The most readily available techniques utilize linear accelerator-based technique of opposed lateral electron field abutting opposed lateral photon field with central blocking. Bolus material is used to achieve adequate skin dose. Although plans to add bolus material often occur in the virtual setting during treatment planning, the practical aspects of reproducibly maintain the bolus material along curved surfaces during the day-to-day patient setup can be a challenge. We present a case of a patient with squamous cell carcinoma of the scalp with neck node involvement treated with surgery followed by adjuvant radiotherapy. We demonstrate a unique immobilization technique that maintains the bolus material on the aquaplast mesh adherent to the patient's scalp as well as the neck. TomoTherapy with daily megavoltage computed tomography (CT) scan was utilized to verify the daily bolus position. We were able to maintain a 95% reproducibility rate. This technique reliably maintains the bolus material on the desired locations with minimum adjustments and manipulation by the therapist and is a technique that can be universally adaptable for conventional radiotherapy or intensity modulated radiation therapy (IMRT) techniques.

    Topics: Carboxymethylcellulose Sodium; Carcinoma, Squamous Cell; Head and Neck Neoplasms; Humans; Immobilization; Male; Middle Aged; Radiotherapy Dosage; Reproducibility of Results; Scalp; Sensitivity and Specificity; Skin Neoplasms

2008