Differences between late-responding (slowly proliferating) normal tiss
ues and early-responding (rapidly proliferating) normal tissues and tu
mor cells and the event of tumor cell repopulation occurring during tr
eatment have essentially led to the development of altered fractionati
on schemes. Altered fractionation regimens mainly refer to schedules u
tilising two or more (small lose) fractions per day for part of or for
the entire treatment course. It must be underlined that a true standa
rd or conventional fractionation regimen does not exist: no schedule i
s universally recognised as the standard of reference to be compared w
ith. However, continental European and U.S, conventional regimens are
the considered control arm with which the new experimental regimens ha
ve to be compared. For this reason they are generally recognised as th
e standards. The basic rationale for hyperfractionated or accelerated
regimens respectively lies in the possibility (a) to deliver higher to
tal doses reducing late-responding normal tissue damage, (b) to delive
r total doses in a reduced overall treatment time to defeat tumor clon
ogen repopulation. Multiple fractions per day should not be delivered
with interfraction intervals smaller than 6 hours. Clinical results of
phase III and limited but convincing phase III randomised trials sugg
est that a therapeutic benefit can be achieved with new altered regime
ns.