Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 15 de 15
Filter
1.
BMC Pulm Med ; 15: 92, 2015 Aug 19.
Article in English | MEDLINE | ID: mdl-26285574

ABSTRACT

BACKGROUND: The FinnishIPF registry is a prospective, longitudinal national registry study on the epidemiology of idiopathic pulmonary fibrosis (IPF). It was designed to describe the characteristics, management and prognosis of prevalent and incident IPF patients. The study was initiated in 2012. METHODS: We present here results limited to five university hospitals. Patients with IPF were screened from hospital registries using ICD-10 diagnosis codes J84.1 and J84.9. All patients who gave informed consent were included and evaluated using novel diagnostic criteria. Point prevalence on the 31(st) of December in 2012 was calculated using the reported population in each university hospital city as the denominator. RESULTS: Patients with ICD-10 codes J84.1 and J84.9 yielded a heterogeneous group - on the basis of patient records assessed by pulmonologists only 20-30 % of the cases were IPF. After clinical, radiological and histological re-evaluation 111 of 123 (90 %) of patients fulfilled the clinical criteria of IPF. The estimated prevalence of IPF was 8.6 cases/100 000. 60.4 % were men. Forty four percent of the patients were never-smokers. At diagnosis, the patients' mean age was 73.5 years and mean FVC was 80.4 % and DLCO 57.3 % of predicted. CONCLUSIONS: Our results suggest that hospital registries are inaccurate for epidemiological studies unless patients are carefully re-evaluated. IPF is diagnosed in Finland at a stage when lung function is still quite well preserved. Smoking in patients with IPF was less common than in previous reports.


Subject(s)
Idiopathic Pulmonary Fibrosis/diagnosis , Medical Records , Registries , Aged , Data Accuracy , Female , Finland/epidemiology , Follow-Up Studies , Hospitals, University , Humans , Idiopathic Pulmonary Fibrosis/epidemiology , Incidence , Male , Prevalence , Prognosis , Prospective Studies , Tomography, X-Ray Computed
2.
Eur Respir J ; 29(1): 78-84, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17050560

ABSTRACT

The objective of the present study is to determine the feasibility of chest computed tomography (CT) in screening for lung cancer among asbestos-exposed workers. In total, 633 workers were included in the present study and were examined with chest radiography and high-resolution CT (HRCT). A total of 180 current and ex-smokers (cessation within the previous 10 yrs) were also screened with spiral CT. Noncalcified lung nodules were considered positive findings. The incidental CT findings not related to asbestos exposure were registered and further examined when needed. Noncalcified lung nodules were detected in 86 workers. Five histologically confirmed lung cancers were found. Only one of the five cancers was also detected by plain chest radiography and three were from the group of patients with a pre-estimated lower cancer probability. Two lung cancers were stage Ia and were radically operated. In total, 277 individuals presented 343 incidental findings of which 46 required further examination. Four of these were regarded as clinically important. In conclusion, computed tomography and high-resolution computed tomography proved to be superior to plain radiography in detecting lung cancer in asbestos-exposed workers with many confounding chest findings. The numerous incidental findings are a major concern for future screenings, which should be considered for asbestos-exposed ex-smokers and current smokers.


Subject(s)
Asbestos/adverse effects , Lung Diseases/diagnostic imaging , Occupational Diseases/diagnostic imaging , Occupational Exposure/adverse effects , Pleural Diseases/diagnostic imaging , Tomography, X-Ray Computed , Aged , Aged, 80 and over , Cross-Sectional Studies , Feasibility Studies , Female , Finland , Humans , Incidental Findings , Lung Diseases/etiology , Male , Mass Screening , Middle Aged , Occupational Diseases/etiology , Pleural Diseases/etiology , Smoking/adverse effects
3.
Respir Med ; 95(5): 387-92, 2001 May.
Article in English | MEDLINE | ID: mdl-11392580

ABSTRACT

The aim of the study was to investigate which features predict favourable response to omeprazole therapy in asthmatics with gastro-oesophageal reflux (GER). The study population consisted of 52 outpatient asthmatics with GER who had completed an intervention where they were randomized to receive omeprazole 40 mg once a day or placebo for 8 weeks. After a 2-week washout period the patients were crossed over. Asthma symptoms were found to be relieved > or = 20% in 18 (35%) patients who were thus regarded as responders. A logistic regression analysis was performed in order to identify which features separate the responders from the non-responders. More responders were found among the patients whose body mass index (BMI) was higher (P = 0.02) or whose distal esophageal reflux was more severe [total time (%) pH < 4 (P = 0.01) or time (%) pH < 4 in upright position (P = 0.04)]. Adding other predictors to the total time (%) pH < 4, which was the most significant predictor for response in multi-variate analysis, did not further increase the prediction for favourable outcome. It is concluded that severe distal oesophageal reflux and obesity predict amelioration in asthma symptoms after 8-week omeprazole treatment in asthmatics with GER. Adding more than one predictor does not seem to further increase prediction for favourable asthma response.


Subject(s)
Anti-Ulcer Agents/therapeutic use , Asthma/complications , Gastroesophageal Reflux/drug therapy , Omeprazole/therapeutic use , Adult , Aged , Asthma/drug therapy , Body Mass Index , Confidence Intervals , Cross-Over Studies , Double-Blind Method , Female , Gastroesophageal Reflux/complications , Humans , Hydrogen-Ion Concentration , Logistic Models , Male , Middle Aged , Multivariate Analysis , Odds Ratio , Severity of Illness Index , Treatment Outcome
4.
Eur Respir J ; 16(4): 633-8, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11106204

ABSTRACT

Gastro-oesophageal reflux (GOR) is an important cause of chronic cough. There has been a lack of placebo-controlled trials treating GOR related chronic cough with antireflux therapy. The aim of this study was to determine the efficacy of omeprazole on GOR related chronic cough. After excluding other common causes of cough, oesophageal pH monitoring was performed on 48 patients with chronic cough. Twenty-nine patients found to have GOR were randomized in a double-blind fashion to receive omeprazole 40 mg o.d. or placebo for 8 weeks. After a 2-week washout period, patients were crossed over to the other treatment. Symptoms were recorded daily in a diary. Twenty-one patients completed both treatment periods. Cough (p=0.02) and gastric symptoms (p=0.003) improved significantly during the omeprazole treatment in twelve patients who received placebo during the first and omeprazole during the second 8-week period. In nine patients who received omeprazole during the first 8-week period, amelioration in cough reached statistical significance only after cessation of omeprazole. Gastric symptoms also remained minor during placebo in these nine patients. Omeprazole 40 mg o.d. seems to improve chronic cough in patients with gastrooesophageal reflux and the effect of omeprazole in ameliorating both cough and reflux symptoms continues after treatment ceases.


Subject(s)
Anti-Ulcer Agents/therapeutic use , Cough/drug therapy , Gastroesophageal Reflux/drug therapy , Omeprazole/therapeutic use , Adult , Aged , Cough/etiology , Cross-Over Studies , Double-Blind Method , Female , Gastroesophageal Reflux/complications , Humans , Hydrogen-Ion Concentration , Male , Middle Aged , Statistics, Nonparametric , Treatment Outcome
5.
Cancer ; 89(11 Suppl): 2387-91, 2000 Dec 01.
Article in English | MEDLINE | ID: mdl-11147616

ABSTRACT

BACKGROUND: The prognosis of lung carcinoma patients is better when the diagnosis is made early, the disease is localized, and radical surgery is possible. Screening for lung carcinoma with mass radiography or sputum cytology should contribute to a more favorable prognosis. To the author's knowledge to date, large-scale screening studies have shown improved survival but no reduction in mortality. METHODS: The histologic tumor type, disease stage, treatment, and survival rates were studied in 93 men who were found to have lung carcinoma during a single chest X-ray screening of > 33,000 smoking men ages 50-69 years and in 239 men of the same age range whose lung carcinoma was detected either through symptomatic presentation or through chest X-ray obtained for other purposes. RESULTS: The histologic distribution was similar in the two groups but screening detected more early stage tumors that more often were resectable (37% vs. 19%). The 5-year survival rate for the patients detected by screening was 19% and that of the other patients was 10%, with a relative risk 0.65 (95% confidence interval, 0.50-0.84). CONCLUSIONS: The results of the current study demonstrate that chest X-ray screening might improve the prognosis of patients with lung carcinoma. However, these results are subject to many factors that were only partially controlled and should be interpreted cautiously.


Subject(s)
Lung Neoplasms/diagnostic imaging , Lung Neoplasms/mortality , Aged , Finland/epidemiology , Humans , Lung Neoplasms/pathology , Lung Neoplasms/prevention & control , Male , Mass Chest X-Ray , Middle Aged , Neoplasm Staging , Prevalence , Prognosis , Randomized Controlled Trials as Topic
6.
Chest ; 116(5): 1257-64, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10559084

ABSTRACT

STUDY OBJECTIVES: To investigate the prevalence of gastroesophageal reflux (GER) among patients with asthma and to determine the effect of omeprazole on the outcome of asthma in patients with GER. DESIGN: A double-blind, placebo-controlled crossover study. SETTING: Asthmatic patients who attended the pulmonary outpatient clinic of Turku University Central Hospital, Finland. PATIENTS: One hundred seven asthmatic patients. INTERVENTIONS: The patients who were found to have GER in ambulatory esophageal pH monitoring were randomized to receive either omeprazole, 40 mg qd, or placebo for 8 weeks. After a 2-week washout period, the patients were crossed over to the other treatment. Spirometry was performed at baseline and immediately after both treatment periods. Peak expiratory values, use of sympathomimetics, and pulmonary and gastric symptoms were recorded daily in a diary. RESULTS: Pathologic GER was found in 53% of the asthmatic patients. One third of these patients had no typical reflux symptoms. Daytime pulmonary symptoms did not improve significantly (p = 0.14), but a reduction in nighttime asthma symptoms (p = 0.04) was found during omeprazole treatment. In the patients with intrinsic asthma, there was a decline in [corrected] FEV(1) values (p = 0.049). Based on symptom scores, 35% of the patients were regarded as responders to 8-week omeprazole treatment. The reflux (time [percent] of pH < 4) was found to be more severe (p = 0. 002) in the responders. CONCLUSIONS: There is a high prevalence of GER in the asthmatic population. This reflux is often clinically "silent." After an 8-week omeprazole treatment, there was a reduction in nocturnal asthma symptoms, whereas daytime asthma outcome did not improve. There seems to be a subgroup of asthma patients who benefit from excessive antireflux therapy.


Subject(s)
Anti-Ulcer Agents/therapeutic use , Asthma/physiopathology , Gastroesophageal Reflux/drug therapy , Omeprazole/therapeutic use , Adult , Aged , Asthma/complications , Asthma/epidemiology , Circadian Rhythm , Cross-Over Studies , Double-Blind Method , Esophagus/metabolism , Female , Finland/epidemiology , Gastroesophageal Reflux/complications , Gastroesophageal Reflux/epidemiology , Hospitals, University , Humans , Hydrogen-Ion Concentration , Male , Middle Aged , Outpatient Clinics, Hospital , Outpatients , Prevalence , Respiratory Function Tests , Treatment Outcome
7.
Chest ; 114(3): 723-30, 1998 Sep.
Article in English | MEDLINE | ID: mdl-9743157

ABSTRACT

STUDY OBJECTIVES: The aim of this study was to determine the role of complement components in pleural effusion measured with novel markers of complement activation, to assess which pathway of activation is predominant in different diseases, and to find out whether the analysis of complement components and their activation products could help in diagnostic procedure differentiating the etiologies of pleural effusion. PATIENTS: The study population consisted of 71 patients who had pleural effusion secondary to tuberculosis (n=23), rheumatic disease (n=10), or malignancy (n=38). MEASUREMENTS: Complement components and their activation products, including the soluble terminal complex SC5b-9, were measured in plasma and pleural fluid. RESULTS: In all patients with rheumatic pleurisy, pleural fluid SC5b-9 was higher than 2 AU/mL and in all patients with malignant pleural fluid it was lower than 2 AU/mL. The mean level of SC5b-9 in rheumatic pleural effusion was also significantly higher than in tuberculosis. In addition, the concentrations of pleural fluid C3 and C4 were significantly lower and the ratio C4d/C4 was significantly higher in rheumatic compared with tuberculous or malignant pleurisy. In plasma, both SC5b-9 and C1s-C1r-C1INH-complexes were significantly higher in rheumatic subjects than in other patients. In stepwise multinominal logistic regression analyses, the most significant predictors for rheumatic pleural fluid were high pleural fluid SC5b-9 and low C4. CONCLUSIONS: These observations indicate that the complement cascade is activated through both the classic and the alternative pathways in rheumatic pleurisy. Determinations of SC5b-9 and C4d/C4 in pleural fluid were the best variables differentiating rheumatic, tuberculous, and malignant effusions.


Subject(s)
Complement Activation , Complement System Proteins/analysis , Pleural Effusion/immunology , Adult , Aged , Aged, 80 and over , Arthritis, Rheumatoid/complications , Complement C1/analysis , Complement C3/analysis , Complement C4/analysis , Complement Factor B/analysis , Complement Membrane Attack Complex , Female , Glycoproteins/analysis , Humans , Male , Middle Aged , Pleural Effusion/blood , Pleural Effusion/etiology , Pleural Effusion, Malignant/blood , Pleural Effusion, Malignant/immunology , Tuberculosis, Pleural/complications
8.
Chest ; 114(6): 1514-8, 1998 Dec.
Article in English | MEDLINE | ID: mdl-9872181

ABSTRACT

BACKGROUND: The prognosis of patients with lung cancer is better when the diagnosis is made early; the disease is localized, and radical surgery is possible. Screening for lung cancer with mass radiography or sputum cytology should contribute to a more favorable prognosis. Large-scale screening studies have improved the survival rates for lung cancer but have yielded no reduction in mortality rates. METHODS: The histologic types, stages, treatments, and survival rates were studied in 93 men who were found to have lung cancer in a single chest radiograph screening of more than 33,000 men who smoked and were 50 to 69 years old ("screened cases"), and in 239 men of the same age range whose lung cancer was detected through ordinary health care system ("other cases") during the screening period. RESULTS: The distribution of the histology was similar in the two groups, but screening detected more instances of early-stage disease that were resectable more often than in the other group (37 vs 19%). The 5-year survival rate for men in the screened cases was 19%, and that of men in the other cases was 10% (relative risk, 0.65; 95% confidence interval [CI], 0.50 to 0.84). The survival rate of men in the screened cases remained significantly higher than that of men in the other cases even after adjustments for age, smoking status, histology, stage of the disease, and resectability of the disease (relative risk, 0.74; 95% CI, 0.55 to 1.00). CONCLUSIONS: According to this study, chest radiograph screening might improve the prognosis of lung cancer. Our results are, however, subject to many factors that were only partially controlled for, and they should be interpreted cautiously.


Subject(s)
Lung Neoplasms/diagnostic imaging , Lung Neoplasms/mortality , Adenocarcinoma/diagnostic imaging , Adenocarcinoma/mortality , Aged , Carcinoma, Small Cell/diagnostic imaging , Carcinoma, Small Cell/mortality , Carcinoma, Squamous Cell/diagnostic imaging , Carcinoma, Squamous Cell/mortality , Humans , Male , Mass Screening , Middle Aged , Prognosis , Radiography , Survival Analysis
9.
Clin Drug Investig ; 16(2): 101-10, 1998.
Article in English | MEDLINE | ID: mdl-18370527

ABSTRACT

OBJECTIVE: The clinical efficacy, tolerability and acceptability of a new multidose powder inhaler (MDPI) [Easyhaler((R)), Orion Pharma, Finland] containing a high dose (500 microg/dose) of beclomethasone dipropionate (BDP) were compared with those of BDP metered dose inhaler administered with a large volume spacer (MDI-spacer). PATIENTS AND STUDY DESIGN: Recruited patients were adult asthmatics currently receiving 800 to 1000 microg/day of inhaled corticosteroid. The dose of BDP during the study was 1000 mg/day. The study was an open, randomised, parallel-group multicentre study and included a 2-week run-in period followed by a 12-week treatment period. RESULTS: 74 patients were randomised to both groups. During the run-in period the mean morning peak expiratory flow (PEF) was 489 and 478 L/min in the MDPI and MDI-spacer groups, respectively. During the last 2 weeks of the study the morning PEF was 485 L/min in the MDPI group and 477 L/min in the MDI-spacer group. Asthma symptom scores and use of rescue medication were low in both groups. The median dose of histamine required to decrease forced expiratory volume in 1 second (FEV(1)) by 15% was 1.05mg in the MDPI group and 0.64mg in the MDI-spacer group. The most frequent adverse events were hoarseness and sore throat. Mean serum cortisol levels were not affected in either treatment group. Patients' personal opinion regarding acceptability of the devices clearly favoured the MDPI. CONCLUSION: In conclusion, the novel powder inhaler was well tolerated and at least equally effective compared with the conventional MDI-spacer combination in the treatment of asthma with BDP. However, in everyday use the patients clearly favoured the powder inhaler.

10.
Lung Cancer ; 16(1): 75-80, 1996 Dec.
Article in English | MEDLINE | ID: mdl-9017586

ABSTRACT

The efficacy and safety of toremifene-ifosfamide as a first-line chemotherapy in non-small cell lung cancer were assessed. Sixteen patients were treated with oral toremifene (420 mg on days 1-4 and 240 mg on day 5) followed by ifosfamide infusion 5 g/m2 on day 5 every 3 weeks 1-6 times. Toremifene at the doses used did not enhance the effect or toxicity of ifosfamide in previously untreated non-small cell lung cancer patients.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Carcinoma, Non-Small-Cell Lung/drug therapy , Lung Neoplasms/drug therapy , Aged , Drug Administration Schedule , Drug Resistance, Multiple , Female , Humans , Ifosfamide/administration & dosage , Male , Middle Aged , Prospective Studies , Toremifene/administration & dosage , Treatment Outcome
11.
J Natl Cancer Inst ; 88(21): 1560-70, 1996 Nov 06.
Article in English | MEDLINE | ID: mdl-8901854

ABSTRACT

BACKGROUND: Experimental and epidemiologic investigations suggest that alpha-tocopherol (the most prevalent chemical form of vitamin E found in vegetable oils, seeds, grains, nuts, and other foods) and beta-carotene (a plant pigment and major precursor of vitamin A found in many yellow, orange, and dark-green, leafy vegetables and some fruit) might reduce the risk of cancer, particularly lung cancer. The initial findings of the Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study (ATBC Study) indicated, however, that lung cancer incidence was increased among participants who received beta-carotene as a supplement. Similar results were recently reported by the Beta-Carotene and Retinol Efficacy Trial (CARET), which tested a combination of beta-carotene and vitamin A. PURPOSE: We examined the effects of alpha-tocopherol and beta-carotene supplementation on the incidence of lung cancer across subgroups of participants in the ATBC Study defined by base-line characteristics (e.g., age, number of cigarettes smoked, dietary or serum vitamin status, and alcohol consumption), by study compliance, and in relation to clinical factors, such as disease stage and histologic type. Our primary purpose was to determine whether the pattern of intervention effects across subgroups could facilitate further interpretation of the main ATBC Study results and shed light on potential mechanisms of action and relevance to other populations. METHODS: A total of 29,133 men aged 50-69 years who smoked five or more cigarettes daily were randomly assigned to receive alpha-tocopherol (50 mg), beta-carotene (20 mg), alpha-tocopherol and beta-carotene, or a placebo daily for 5-8 years (median, 6.1 years). Data regarding smoking and other risk factors for lung cancer and dietary factors were obtained at study entry, along with measurements of serum levels of alpha-tocopherol and beta-carotene. Incident cases of lung cancer (n = 894) were identified through the Finnish Cancer Registry and death certificates. Each lung cancer diagnosis was independently confirmed, and histology or cytology was available for 94% of the cases. Intervention effects were evaluated by use of survival analysis and proportional hazards models. All P values were derived from two-sided statistical tests. RESULTS: No overall effect was observed for lung cancer from alpha-tocopherol supplementation (relative risk [RR] = 0.99; 95% confidence interval [CI] = 0.87-1.13; P = .86, logrank test). beta-Carotene supplementation was associated with increased lung cancer risk (RR = 1.16; 95% CI = 1.02-1.33; P = .02, logrank test). The beta-carotene effect appeared stronger, but not substantially different, in participants who smoked at least 20 cigarettes daily (RR = 1.25; 95% CI = 1.07-1.46) compared with those who smoked five to 19 cigarettes daily (RR = 0.97; 95% CI = 0.76-1.23) and in those with a higher alcohol intake (> or = 11 g of ethanol/day [just under one drink per day]; RR = 1.35; 95% CI = 1.01-1.81) compared with those with a lower intake (RR = 1.03; 95% CI = 0.85-1.24). CONCLUSIONS: Supplementation with alpha-tocopherol or beta-carotene does not prevent lung cancer in older men who smoke. beta-Carotene supplementation at pharmacologic levels may modestly increase lung cancer incidence in cigarette smokers, and this effect may be associated with heavier smoking and higher alcohol intake. IMPLICATIONS: While the most direct way to reduce lung cancer risk is not to smoke tobacco, smokers should avoid high-dose beta-carotene supplementation.


Subject(s)
Antioxidants/therapeutic use , Lung Neoplasms/prevention & control , Vitamin E/therapeutic use , beta Carotene/therapeutic use , Age Factors , Aged , Alcohol Drinking/adverse effects , Anticarcinogenic Agents/therapeutic use , Carcinogens/adverse effects , Food, Fortified , Humans , Incidence , Lung Neoplasms/blood , Lung Neoplasms/etiology , Lung Neoplasms/mortality , Male , Middle Aged , Multivariate Analysis , Patient Compliance , Proportional Hazards Models , Risk , Risk Factors , Smoking/adverse effects , Vitamin E/blood , beta Carotene/blood
12.
Acta Oncol ; 34(1): 117-21, 1995.
Article in English | MEDLINE | ID: mdl-7865226

ABSTRACT

Pleurodesis with doxycycline (100 mg and 600 mg) and Corynebacterium parvum (1 mg and 7 mg) were compared in 41 patients with malignant effusion. To evaluate the mechanisms, pleural fluid pH, leukocytes, granulocytes, interleukin-6 (IL-6) and serum IL-6, as well as C-reactive protein (CRP) were measured before and on 2 consecutive days after treatment. Corynebacterium parvum produced a greater acute-phase response measured with fever, serum CRP and IL-6 than doxycycline. However, no change in pleural fluid IL-6 was demonstrated. Among the 35 assessed patients, 26 had objective response, similar in all four treatment groups. Side-effects were more common with Corynebacterium parvum. Based on this preliminary study we conclude that doxycycline, even in low doses, is a highly effective and well tolerated agent for palliative treatment of malignant pleural effusion. As the responses were similar despite different inflammatory reactions, the two agents probably induce pleural obliteration through different mechanisms.


Subject(s)
Doxycycline/administration & dosage , Pleural Effusion, Malignant/therapy , Pleurodesis , Propionibacterium acnes , Acute-Phase Reaction , Aged , Female , Humans , Hydrogen-Ion Concentration , Lactates/metabolism , Lactic Acid , Male , Middle Aged , Pleural Effusion, Malignant/etiology , Pleural Effusion, Malignant/physiopathology , Retrospective Studies , Treatment Outcome
13.
Article in English | MEDLINE | ID: mdl-1488251

ABSTRACT

An analysis of 33 patients with histologically confirmed intrathoracic tuberculous lymphadenopathy was made. Tuberculosis could have been diagnosed without mediastinoscopy only in 3 patients: 2 had positive bronchial cultures and 1 simultaneous cervical lymph node tuberculosis. Bacteriological confirmation is conclusive, but seldom possible. Mediastinoscopy provides the best method to obtain tissue samples, and consequently, it is still necessary in the diagnosis of intrathoracic tuberculous lymphadenitis.


Subject(s)
Mediastinoscopy , Tuberculosis, Pulmonary/diagnosis , Adolescent , Adult , Aged , Bronchoscopy , Diagnosis, Differential , Female , Humans , Male , Middle Aged , Tuberculosis, Lymph Node/diagnosis , Tuberculosis, Lymph Node/therapy , Tuberculosis, Pulmonary/physiopathology , Tuberculosis, Pulmonary/therapy
14.
Acta Oncol ; 31(7): 761-5, 1992.
Article in English | MEDLINE | ID: mdl-1335738

ABSTRACT

Sixty-eight patients with limited small cell lung cancer were treated between April 1988 and October 1990 with combination carboplatin 450 mg/m2 i.v. on day 1 and etoposide 100 mg/m2 i.v. on days 1-3 (CarE) for two courses, followed by thoracic radiotherapy (TRT) 50 Gy, and then vincristine 1 mg/m2, doxorubicin 50 mg/m2 and cyclophosphamide 750 mg/m2 on day one (VAC) for four courses. Prophylactic cranial irradiation (30 Gy) was given to patients with CR after completion of chemotherapy. Sixty patients (89%) achieved an objective response (40% complete responses). The median time to progression was 8.5 months and median survival time 12.1 months. Predicted one- and two-year survival was 50% and 12% respectively. Myelosuppression was the main toxicity, with WHO grade 3 and 4 leukopenia occurring in 32% of VAC courses. There were 5 (7%) treatment-related deaths, all of them during VAC. We conclude that the present combination is active in terms of response rate, but it did not demonstrate any superiority in survival. The frequency of haematological toxicity was substantial during VAC courses.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Carcinoma, Small Cell/diagnostic imaging , Carcinoma, Small Cell/drug therapy , Lung Neoplasms/diagnostic imaging , Lung Neoplasms/drug therapy , Adolescent , Aged , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Bone Marrow/drug effects , Carboplatin/administration & dosage , Carcinoma, Small Cell/mortality , Combined Modality Therapy , Cyclophosphamide/administration & dosage , Dactinomycin/administration & dosage , Etoposide/administration & dosage , Female , Humans , Leukopenia/chemically induced , Lung Neoplasms/mortality , Male , Middle Aged , Radiography , Time Factors , Treatment Outcome , Vincristine/administration & dosage
15.
Postgrad Med J ; 66(778): 647-9, 1990 Aug.
Article in English | MEDLINE | ID: mdl-2217032

ABSTRACT

An 88 year old woman with bacteriologically confirmed pulmonary tuberculosis was first treated with isoniazid, rifampicin and pyrazinamide. Two weeks later she developed pulmonary infiltrates with fever. A drug-induced reaction was suspected but the reaction recurred three times until isoniazid was identified as the cause. The reaction became worse each time, finally being nearly fatal.


Subject(s)
Fever/chemically induced , Isoniazid/adverse effects , Pulmonary Fibrosis/chemically induced , Aged , Aged, 80 and over , Bacterial Infections/diagnosis , Diagnosis, Differential , Drug Hypersensitivity/diagnosis , Female , Humans
SELECTION OF CITATIONS
SEARCH DETAIL
...