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1.
J Pediatr Surg ; 34(4): 579-82, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10235327

ABSTRACT

PURPOSE: This 25-year population based, single institution review was conducted to investigate the impact of preoperative chemotherapy on surgical and histological staging in patients with Wilms' tumors. RESULTS: Forty-nine patients under the age of 15 years were identified from case notes to have had histologically verified Wilms' tumors over the 25-year period from January 1972 to December 1996. Twenty-six patients were treated initially with preoperative chemotherapy, 23 with immediate surgery. Eleven had treatment randomized within the UKCCSG WT9101 trial (UKWT3), and the remainder received initial treatment according to unit policy. Surgical stages in the two groups (preoperative chemotherapy and immediate surgery) were respectively, stage 1:14(28.5%) and 11 (22.5%), stage II: one (2%) and eight (16.3%), stage III: 11 (22.5%) and four (8.2%). Seven patients had clinical stage IV disease at presentation. Histology results were favorable in 45 patients and unfavorable in four. All patients received chemotherapy during treatment, whereas 25 (51%) also received radiotherapy. No significant difference was evident in the two groups with respect to treatment-related morbidity. Five patients relapsed, three of whom died within the period of review, but a fourth has since died. CONCLUSIONS: This study suggests that the use of preoperative chemotherapy does not put the patient at increased risk of postoperative morbidity or reduced survival. The distribution of surgical stages suggests that limited tumor downstaging may have occurred as a result of preoperative chemotherapy.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Kidney Neoplasms/drug therapy , Kidney Neoplasms/surgery , Wilms Tumor/drug therapy , Wilms Tumor/surgery , Chemotherapy, Adjuvant , Child , Child, Preschool , Female , Humans , Infant , Kidney/pathology , Kidney Neoplasms/mortality , Kidney Neoplasms/pathology , Male , Neoplasm Staging , Randomized Controlled Trials as Topic , Retrospective Studies , Survival Rate , Time Factors , Wilms Tumor/mortality , Wilms Tumor/pathology
6.
J R Soc Med ; 78(9): 715-20, 1985 Sep.
Article in English | MEDLINE | ID: mdl-4045901

ABSTRACT

Minor invasive procedures in children with leukaemia can be very distressing for patients, parents and staff. In Nottingham a combined clinic has been established with an anaesthetist as an integral member of the team. General anaesthesia, usually by inhalation, is frequently employed. From May 1980 to September 1984, 515 anaesthetics were given to 97 patients. Records are kept to allow analysis of the clinic's function. With close personal contact, induction of anaesthesia becomes increasingly a matter of cooperation between patient and anaesthetist, removing much of the fear of these procedures. The development of this service is described and the reasons for its success are discussed.


Subject(s)
Anesthesia, General/psychology , Leukemia/therapy , Adolescent , Anesthesia, General/methods , Child , Child, Preschool , Emotions , Humans , Infant , Infant, Newborn , Patient Care Team , Patient Compliance
7.
Cancer Chemother Pharmacol ; 15(3): 258-62, 1985.
Article in English | MEDLINE | ID: mdl-4053269

ABSTRACT

Twenty children with recurrent or unresponsive tumours (10 Wilms', 3 rhabdomyosarcoma, 4 Ewings's, 1 osteosarcoma, 1 hepatoblastoma, 1 hepatoma) and one untreated patient with renal carcinoma were given ifosfamide as a 24-h infusion (5 mg/m2), with mesna as uroprotective. The number of courses ranged from 1 to 13 (median 3), and the interval between them was 2-3 weeks. Sixteen of these patients had previously received cyclophosphamide. Complete clinical responses were seen in 3 cases (2 Wilms' and 1 Ewing's) and lasted 5, 7, and 9 months. Partial responses were seen in 3 instances, mixed response or stable disease in 4, and progressive disease in 11. Treatment was well tolerated in most patients, with no cystitis or severe myelosuppression, but 2 children developed transient neurological symptoms and 1 became hypertensive. Nausea and vomiting were controlled by high-dose dexamethasone in most children. Plasma ifosfamide levels were estimated by means of gas-liquid chromatography in 10 patients. Peak concentrations ranged from 38 to 125 micrograms/ml (median 80). The elimination half-life, at 2.5-5.2 h (median 3.2) was shorter than previously reported in adults. Future studies should test the possibility that ifosfamide-containing combination chemotherapy may be more effective than the regimens, usually including cyclophosphamide, that are currently used as front-line treatment of embryonal and Ewing's sarcoma.


Subject(s)
Ifosfamide/toxicity , Neoplasms/drug therapy , Adolescent , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Child , Child, Preschool , Drug Evaluation , Female , Humans , Ifosfamide/blood , Ifosfamide/therapeutic use , Kinetics , Male
10.
Br Med J ; 3(5610): 86-91, 1968 Jul 13.
Article in English | MEDLINE | ID: mdl-4232783

ABSTRACT

A study in Jamaica of 60 patients with sickle-cell anaemia over the age of 30 years showed that most of them were in full-time employment. Pains in the bones or joints, leg ulceration, and jaundice were the most frequent types of presentation, but only two patients had a haemoglobin level consistently below 6 g./ 100 ml. Most of the patients were well developed and of average height, and, though the development of secondary sexual characteristics was delayed, there was an average of 2.6 pregnancies per patient. These findings suggest that the course is more benign than has been realized.


Subject(s)
Anemia, Sickle Cell , Adult , Age Factors , Anemia, Sickle Cell/complications , Anemia, Sickle Cell/mortality , Blood Protein Electrophoresis , Body Height , Cardiomegaly/etiology , Eye Manifestations , Female , Fertility , Heart Auscultation , Hemoglobinometry , Hemoglobins, Abnormal/analysis , Humans , Jamaica , Jaundice/etiology , Leg Ulcer/etiology , Male , Middle Aged , Occupational Medicine , Pregnancy , Splenomegaly/etiology
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