Détails sur le projet
Description
DESCRIPTION: (adapted from the investigator's abstract) A new
initiative in brachytherapy first proposed under the auspices of this
grant, involves pulsed as opposed to continuous low dose irradiation
using a computer controlled remote afterloader. A single Ir-192 source
steps under computer control through the catheters of an implant or
applicator with dwell times in each position determined to produce an
optimized dose distribution. This results in several advantages:
improved dose optimization, greatly improved radiation safety since no
source preparation is involved, only one source to replace, and no
variation in overall treatment time between patients. A commercial
company has produced a machine based on this principle which is in use
worldwide and hundreds of patients have already been treated
successfully, using pulse lengths and frequencies that the applicants
suggested.
To date, the emphasis has been on demonstrating the equivalence of pulsed
(PDR) to continuous low dose rate (CLDR). However, the applicants
suggest that appropriate PDR regimens will allow an increase in the
differential between effects on tumors relative to late-responding
normal tissues. Specifically, there is strong evidence that late-
responding tissues repair sublethal damage more slowly than early
responding tissues, including tumors. The basic hypothesis upon which
this proposal is based is that a difference in repair half-times (T1/2)
between early and late responding tissues can be exploited to improve
the therapeutic ratio in brachytherapy in the same way as differences
in the alpha/beta ratios are exploited in external beam radiotherapy.
To exploit this difference in repair times, the optimal PDR regimen
would not consist of equal doses per pulse but would use larger doses
in the first and last pulses and less in the intermediate pulses. The
applicants refer to the process of designing these improved schemes as
temporal optimization. This potentially increased differential between
systems with different rates of repair can be modeled in vitro using well
characterized cell lines with different rates of repair to test the
hypothesis that temporal optimization of PDR spare cells with a long
T1/2 more than cells with a short T1/2. Measurements of cell survival
ratios will be made using an automated cellular imaging system, allowing
ratios in cellular survival of factors of 2 to 5 to be identified.
While cells cultured in vitro cannot mimic all the complexities of
tissues in vivo, they can demonstrate a specific principle - as indeed
they did for the initial concept of pulse brachytherapy. Temporal
optimization of PDR has potential applications in interstitial implants
in, for example, head and neck or prostate cancers, as well as in the
endocavitary treatment of carcinoma of the cervix.
Statut | Terminé |
---|---|
Date de début/de fin réelle | 3/1/85 → 7/31/00 |
Financement
- National Cancer Institute
Keywords
- Radiación
- Investigación sobre el cáncer
Empreinte numérique
Explorer les sujets de recherche abordés dans ce projet. Ces étiquettes sont créées en fonction des prix/bourses sous-jacents. Ensemble, ils forment une empreinte numérique unique.