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1.
Ann Oncol ; 12(9): 1259-64, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11697837

ABSTRACT

BACKGROUND: Docetaxel and gemcitabine are active against breast cancer. The purpose of this phase II study was to evaluate the efficacy and safety of monthly docetaxel combined with weekly gemcitabine in patients with chemotherapy-pretreated metastatic breast cancer. PATIENTS AND METHODS: Thirty-nine patients were enrolled, of whom thirty had received prior chemotherapy in the adjuvant setting, seven for metastatic disease, and two for both, including prior anthracycline in 33 patients. Treatment was gemcitabine 800 mg/m2 days 1, 8, 15 and docetaxel 100 mg/M2 on day 1, with cycles repeated every four weeks. RESULTS: Response rate was 79% (95% confidence interval (CI): 63%-91%), with 2 complete and 29 partial responses. Twenty-five of the responders remained progression-free for more than six months. Median survival was 24.5 months. Delivered dose intensity of gemcitabine was lower than expected (63% of planned). The predominant hematologic toxicity was grade 4 neutropenia in 36 patients, complicated by fever in three patients. With the exception of asthenia, severe non-hematological toxicities were infrequent. CONCLUSIONS: Monthly docetaxel, combined with weekly gemcitabine, has significant but manageable hematologic toxicity. Despite frequent dose adjustments, this doublet is very active in metastatic breast cancer, producing a high proportion of durable responses associated with favorable survival.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Breast Neoplasms/drug therapy , Deoxycytidine/analogs & derivatives , Paclitaxel/analogs & derivatives , Taxoids , Adult , Aged , Aged, 80 and over , Breast Neoplasms/pathology , Chemotherapy, Adjuvant , Deoxycytidine/administration & dosage , Docetaxel , Female , Humans , Infusions, Intravenous , Middle Aged , Neoplasm Metastasis , Neutropenia/chemically induced , Paclitaxel/administration & dosage , Survival Analysis , Treatment Outcome , Gemcitabine
2.
Am J Occup Ther ; 53(6): 561-5, 1999.
Article in English | MEDLINE | ID: mdl-10578433

ABSTRACT

This article describes the Village AIDS Day Treatment Program, a program for people living with HIV/AIDS that provides health care by using a full range of interdependent services. Opened in 1988, this program was the first of its kind in the country. It has provided leadership in developing a model of care that addresses the full spectrum of health care--promotion, prevention, maintenance, and treatment. Along with describing the program and its services, this article includes the program's history and its influencing philosophies.


Subject(s)
Acquired Immunodeficiency Syndrome/therapy , Delivery of Health Care/organization & administration , Health Promotion , Patient Care Team/organization & administration , Delivery of Health Care/standards , Health Promotion/standards , Humans , Interprofessional Relations , Patient Care Team/standards , Preventive Health Services
4.
Am J Occup Ther ; 44(3): 234-7, 1990 Mar.
Article in English | MEDLINE | ID: mdl-2316611

ABSTRACT

This paper describes the Village Nursing Home's day treatment program for persons with AIDS, with an emphasis on the role of occupational therapy and the outcomes of occupational therapy interventions. The clients' demographics are included, and a general program philosophy of clients' empowerment is discussed. The health promotion framework and the use of holistic modalities address the spiritual aspect of the individual and how occupational therapy and spirituality might interconnect.


Subject(s)
Acquired Immunodeficiency Syndrome/rehabilitation , Day Care, Medical/organization & administration , Occupational Therapy , Acquired Immunodeficiency Syndrome/psychology , Holistic Health , Humans , Male , Motivation , New York City , Patient Care Planning , Power, Psychological , Self Care , Social Support
7.
J Rheumatol ; 13(2): 440-1, 1986 Apr.
Article in English | MEDLINE | ID: mdl-3487652

ABSTRACT

A 61-year-old patient with rheumatoid arthritis receiving treatment with methotrexate developed bone marrow hypoplasia after treatment with trimethoprim-sulfamethoxazole. The bone marrow recovered after stopping methotrexate.


Subject(s)
Bone Marrow Diseases/chemically induced , Methotrexate/adverse effects , Sulfamethoxazole/adverse effects , Trimethoprim/adverse effects , Arthritis, Rheumatoid/complications , Arthritis, Rheumatoid/drug therapy , Drug Combinations/adverse effects , Drug Combinations/therapeutic use , Drug Interactions , Female , Humans , Methotrexate/therapeutic use , Middle Aged , Sulfamethoxazole/therapeutic use , Trimethoprim/therapeutic use , Trimethoprim, Sulfamethoxazole Drug Combination
8.
R I Med J (1976) ; 69(3): 123-6, 1986 Mar.
Article in English | MEDLINE | ID: mdl-3457425
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