B. Szczepek et al., RISK OF LATE RECURRENCE AND OR 2ND LUNG-CANCER AFTER TREATMENT OF PATIENTS WITH SMALL-CELL LUNG-CANCER (SCLC), Lung cancer, 11(1-2), 1994, pp. 93-104
The aim of this study was to illustrate some difficulties in distingui
shing late recurrence of small cell lung cancer (SCLC), from second pr
imary lung cancer. Three-hundred fourteen SCLC patients were observed
at the Institute of Tuberculosis and Chest Diseases in Warsaw, during
the period 1976-1985. All patients were treated with chemotherapy and
125 were also treated with radiotherapy on the tumour and mediastinum.
Nineteen patients (6%) survived 3 years. This group consisted of eigh
t females (9%) and 11 males (5%). In all of them a complete remission
was obtained. In six patients from this group no progression of lung c
ancer was observed. Four of them are still living, 7.9-16.2 years afte
r the start of treatment. Two patients died of heart infarct. In the r
emaining 13 patients, progression of SCLC or development of new cancer
was noted in the course of observation. In seven of them, histologica
l proof of the character of progression was obtained. In four cases no
n-small cell lung cancer (NSCLC) was diagnosed after 3-11 years of obs
ervation. In one of them SCLC metastases in the liver were unexpectedl
y found in the autopsy, although adenocarcinoma in the lung diagnosed
during bronchoscopy was also confirmed in the autopsy. In three cases
SCLC was diagnosed. In one case, 2.7 years from the beginning of treat
ment, only SCLC metastases were found during laparoscopy. SCLC was fou
nd in two other cases after a 7-year cancer-free period. In one of tho
se patients, a new lesion was found in the other lung while the second
patient developed a new lesion exactly in the place of the former can
cer. In six other patients no histological proof of the character of p
rogression was obtained. Two of the six are still. living, 8.2 and 15.
1 years later. In the first of these two, a new lesion developed very
early in the course of treatment in the same place as the primary tumo
ur and it was regarded as the progression of SCLC. In the second patie
nt, who probably had NSCLC the lesion developed in the contralateral l
ung after 12.5 years of remission and disappeared after radiotherapy.
Four patients died of cancer after 3.2-6.4 years of observation. The c
umulative risk of a second primary lung cancer after a 3-year survival
period oscillated in our SCLC patients between 4% and 6% for every pa
tient/year of observation. It was concluded that prognosis in SCLC pat
ients is still doubtful, nevertheless, some patients made a complete r
ecovery.