Ep. Armour et al., HYPERTHERMIC ENHANCEMENT OF HIGH-DOSE-RATE IRRADIATION IN 9L GLIOSARCOMA CELLS, International journal of radiation oncology, biology, physics, 28(1), 1994, pp. 171-177
Citations number
26
Categorie Soggetti
Oncology,"Radiology,Nuclear Medicine & Medical Imaging
Purpose: Long duration-mild temperature hyperthermia has previously be
en shown to be an effective potentiator of low-dose-rate irradiation.
An in vitro investigation was initiated to determine if 41 degrees C h
yperthermia could be useful in sensitizing high-dose-rate (HDR) brachy
therapy. Experiments were designed to determine the optimal length of
heat treatments to be applied with a twice daily 5 Gy times five fract
ion high-dose-rate protocol. Methods and Materials: Rat 9L gliosarcoma
cells growing exponentially in flasks were exposed to X-irradiation a
nd 41 degrees C hyperthermia. Irradiation was applied in 5 Gy fraction
s two times per day to a total dose of 25 Gy. Hyperthermia consisted o
f combinations of 1 or 4 hr beatings before and/or after each of the r
adiation exposures. In addition, a set of cells was heated continuousl
y at 41 degrees C starting 6 hr before the first fraction and continui
ng to 4 hr after the 5th fraction. Cell survival was assayed by colony
formation. Results: Sensitization of high-dose-rate increased linearl
y with increasing length of 41 degrees C heating over the entire range
of heat exposures applied. Maximum sensitization was produced by cont
inuous heating for 58 hr throughout the entire radiation course. Heati
ng for 4 hr before fractions two through five produced less sensitizat
ion to these later fractions than was expected if each heat-radiation
fraction had acted independent of the other fractions. Conclusion: Con
tinuous 41 degrees C heating eliminated split dose sparing during high
-dose-rate. The apparent development of thermotolerance during the cou
rse of heat and high-dose-rate resulted in reduced sensitization in th
e later fractions when 4 hr pre- and/or post-heat were applied. This t
olerance was overcome if heat was applied continuously between radiati
on fractions. The clinical relevance of these in vitro data is that 41
degrees C hyperthermia should be applied for as long as is possible d
uring this type of high-dose-rate protocol. This combined hyperthermia
-high-dose-rate treatment may enhance the efficacy of interstitial irr
adiation in situations such as boost irradiation of high grade glioma.