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1.
Int J Radiat Oncol Biol Phys ; 33(5): 1009-17, 1995 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-7493827

RESUMO

PURPOSE: Preirradiation hormonal cytoreduction of prostate cancer has been proven to reduce exposure of normal structures by decreasing the size of the target volume. Dose-volume histogram (DVH) analysis, however, does not always appear to demonstrate a strong positive benefit with the use of neoadjuvant hormone therapy. This study analyzes various other factors influencing dose to normal organs, which may determine the success or failure of neoadjuvant hormonal therapy in achieving its goals. METHODS AND MATERIALS: Patients with bulky clinical Stage C adenocarcinoma of the prostate were given 3 months of hormone treatment consisting of oral Flutamide and monthly Zoladex injections prior to irradiation. Computerized tomography (CT) scans of the pelvis were obtained both prior to and following hormonal treatment. Treatment plans were generated by three-dimensional (3D) conformal treatment planning. The change in the volume of the prostate was assessed along with the percentage of prescribed dose delivered to the rectum and bladder. Various factors such as prostate size, bladder/rectum size, and organ shape were studied. Both dose-volume histograms (DVH) and dose-surface area histograms (DSH) were used for analysis. RESULTS: Six of seven patients had reduction in the size of their prostates. The mean volumes of the prostate before and after hormonal manipulation were 129.1 +/- 32.9 standard deviation (SD) cm3 and 73.0 +/- 29.5 SD cm3, respectively (p = 0.0059). The volume of rectum receiving 80% of the prescribed dose was reduced in five of seven patients from a mean of 83.2 to 59.9 cm3 (p = 0.045). The volume of bladder receiving 80% of the prescribed dose was also reduced in five out of seven patients from a mean of 74.5 to 40.2 cm3 (p = 0.098). Correlation between the size of the prostate and volume of rectum and bladder treated was not always consistent: greater reduction in prostate size did not necessarily result in large decreases in dose to bladder or rectum. The total size of the bladder and rectum were found to be important factors in normal tissue radiation exposure; the benefits of hormone therapy may be lost if the bladder and rectum are allowed to decrease in size. Also, the bladder may be prone to sagging into the pelvis of some patients following hormone therapy, resulting in a less optimal therapeutic ratio. CONCLUSION: Reduction in prostate size by neoadjuvant hormonal manipulation does decrease the amount of normal tissue irradiated in most patients. However, the correlation between the reduction in prostate size and amount of rectum or bladder treated is not linear if other variables are not controlled. Factors such as the shape of the organs, as well as the distensible nature of the bladder and rectum, play major roles in dose to normal tissues. These facts may mask the benefits of cytoreduction and could be obstacles in realizing consistent benefits from preirradiation hormonal treatment in the clinical setting if they are ignored.


Assuntos
Adenocarcinoma/tratamento farmacológico , Adenocarcinoma/radioterapia , Antineoplásicos Hormonais/uso terapêutico , Flutamida/uso terapêutico , Gosserrelina/uso terapêutico , Neoplasias da Próstata/tratamento farmacológico , Neoplasias da Próstata/radioterapia , Reto , Bexiga Urinária , Adenocarcinoma/patologia , Quimioterapia Adjuvante , Humanos , Masculino , Próstata/efeitos dos fármacos , Próstata/patologia , Neoplasias da Próstata/patologia , Dosagem Radioterapêutica , Reto/patologia , Estudos Retrospectivos , Bexiga Urinária/patologia
2.
Am J Med Genet ; 17(4): 723-30, 1984 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-6539070

RESUMO

A newborn infant was found to have multiple congenital anomalies including bilateral cleft of lip and palate, intrauterine growth retardation, microcephaly, tetralogy of Fallot, ambiguous external genitalia, and presence of male and female internal genitalia. Chromosome analysis showed a tandem duplication of part of the short arm of chromosome 1, resulting in a dup(1p31----35). The karyotype designation is 46,XY,dir dup(pter----31::p35----p31::p31----qter). The exact nature of the chromosome anomaly was clarified with use of several banding methods.


Assuntos
Anormalidades Múltiplas/genética , Aberrações Cromossômicas , Cromossomos Humanos 1-3/ultraestrutura , Disgenesia Gonadal/genética , Bandeamento Cromossômico , Fissura Palatina/genética , Feminino , Retardo do Crescimento Fetal/genética , Cardiopatias Congênitas/genética , Humanos , Recém-Nascido , Cariotipagem , Microcefalia/genética , Gravidez , Síndrome
4.
Obstet Gynecol ; 38(5): 739-42, 1971 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-5114224

RESUMO

PIP: This study of 16 patients compares treatment for adenomatous or atypical hyperplasia with one of three schedules of oral progestational drugs. Treatment of endometrial hyperplasia with megestrol, 80 mg daily for 6 weeks, was not satisfactory with the first 5 patients. Treatment was then prolonged to 9 weeks and 4 additional patients so treated. Another 7 patients were treated with medroxyprogesterone acetate (Provera), 80 mg daily for 6 weeks. All medication was given orally. Patients ranged from 36 to 60 years of age with parity from 0 to 10. Endometrial biopsies were done at intervals. All but 1 had a complete remission under therapy. This patient's endometrium progressed from atypica to carcinoma in situ. At hysterectomy glandular hyperplasia with focal carcinoma in situ in the endometrium, adenomyosis, and cellular leiomyomas were found. Remissions persisted only in 5, the longest period being 4 years. Hysterectomy was required in 6. None developed invasive carcinoma. Patients are mildly symptomatic. It is thought that continuous progestational treatment for indefinite periods may be necessary if hysterectomy is to be avoided.^ieng


Assuntos
Hiperplasia Endometrial/tratamento farmacológico , Progestinas/uso terapêutico , Adulto , Carcinoma/etiologia , Hiperplasia Endometrial/complicações , Hiperplasia Endometrial/cirurgia , Feminino , Humanos , Histerectomia , Pessoa de Meia-Idade , Neoplasias Ovarianas/etiologia , Paridade
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