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European Journal of Cardio-Thoracic Surgery, Vol 2, 433-437, Copyright © 1988 by European Association for Cardio-thoracic Surgery
F Eckersberger, E Moritz and E Wolner
One hundred and fifty-nine thoracotomies were performed in 122 patients
with pulmonary metastases. The patients' ages ranged from 2 to 76 years,
and 13 patients were younger than 18 years. The primary tumour was
carcinoma in 83 cases, sarcoma in 29 cases and melanoma in 10 cases. The
primary tumour in children was osteogenic sarcoma (6 patients), Ewing's
sarcoma (2 patients) and Wilms' tumour (2 patients). With a minimum
follow-up of 2 years, an actuarial 5-year survival rate of 38% was observed
for carcinoma and 28% for sarcoma. Four of the children survived
disease-free for 3 years or more after pulmonary metastasectomy. The
primary tumour in these cases was osteogenic sarcoma and Ewing's sarcoma. A
statistically significant difference in survival was found between the
groups of carcinoma and sarcoma, but the prognosis for melanoma patients
was markedly worse. In carcinoma patients the main prognostic factor was
the duration of the disease- free interval. The actuarial postthoracotomy
survival in patients with osteogenic sarcomas was 31% at 5 years, and 18%
at 5 years in soft- tissue sarcomas. The size of the lesions, activity and
disease-free interval correlated with survival in the osteogenic sarcoma
group, and the number of lesions in the soft-tissue sarcoma group. An
aggressive surgical approach towards pulmonary metastatic disease thus
appears to be justified.
ARTICLES
Results and prognostic factors after resection of pulmonary metastases
II. Department of Surgery, University of Vienna, Austria.
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