Concurrent radiochemotherapy (RCT) is a promising new therapy option in adv
anced non-small cell lung cancer (NSCLC). In randomized trials concomitant
RCT has been shown to be superior compared to radiotherapy alone and to seq
uential radiochemotherapy. In most treatment schedules platinum salts alone
or in combination with etoposide, mitomycin C or vinca-alkaloids have been
used. Up to now altered fractionation schemas-particularly hyperfractionat
ed radiotherapy-have not been demonstrated to be superior to conventional f
ractionation (2 Gy daily up to 56-60 Gy), when employed concurrently to che
motherapy. Nevertheless open questions remain: (1) What is the best chemoth
erapy administered simultaneously to radiotherapy? (2) Might newer drugs (e
.g. taxanes, inhibitors of topoisomerase I and II, gemcitabine) be more eff
ective and reveal fewer side effects compared to platinum salts? (3) Is the
re a role for adjuvant chemotherapy following RCT? (4) What is the most eff
ective radiotherapy schedule in concepts with RCT? (5) What radiation dose
is necessary to optimize local control in RCT? (C) 2001 Elsevier Science Ir
eland Ltd. All rights reserved.