In 1988, we reported a Phase II study of mitomycin, ifosfamide and cis
platin (MIG) in inoperable non-small cell lung cancer. The overall obj
ective response rate was 56% in 66 evaluable cases. An improvement in
performance status was observed in responding patients and toxicity wa
s acceptable. Consequently we then embarked upon two major, multicentr
e randomised trials to test this regimen in cases with localised disea
se (MIC 1 - chemotherapy plus radical radiotherapy versus radical radi
otherapy alone) and advanced disease (MIC 2 - chemotherapy plus pallia
tive care versus palliative care alone). These trials are still in pro
gress with targets of 500 and 300 randomised cases, respectively. The
present interim analysis is based on 317 cases randomised in MIC 1 and
193 in MIC 2. The overall response rate (CR + PR) in the MIC 1 trial
is 52% with 10% CRs and in the MIC 2 trial is 42% with 5% CRs. Formal
symptomatic assessments are monitored in both trials and the present i
nterim analysis indicates symptom improvement in cases randomised to c
hemotherapy, including patients who fail to achieve an objective PR or
CR. Other Phase II studies employing MIC are also reviewed.