Improvement in dose escalation using the process of adaptive radiotherapy combined with three-dimensional conformal or intensity-modulated beams for prostate cancer
Aa. Martinez et al., Improvement in dose escalation using the process of adaptive radiotherapy combined with three-dimensional conformal or intensity-modulated beams for prostate cancer, INT J RAD O, 50(5), 2001, pp. 1226-1234
Citations number
42
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Onconogenesis & Cancer Research
Journal title
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS
Purpose: Advances in technology allow the creation of complex treatment pla
ns with tightly conforming doses. However, variations in positioning of the
organ/patient with respect to treatment beams necessitate the use of an ap
preciable margin, potentially limiting dose escalation in many patients. To
(1) reduce this margin and (2) test the hypothesis that the achievable lev
el of dose escalation is patient dependent, a patient-specific, confidence-
limited planning target volume (cl-PTV) was constructed using an adaptive r
adiotherapy (ART) process for prostate cancer treatment developed in-house.
The potential dose escalation achievable with this ART process is quantifi
ed for both conformal radiotherapy (CRT) delivery and intensity-modulated r
adiotherapy (IMRT) delivery.
Material and Methods: Patients with organ confined prostate cancer were ent
ered prospectively into an ART process eve ope in-house. This ART process h
as been designed to improve accuracy and precision of dose delivery, conseq
uently enhancing dose escalation. In this process, a cl-PTV is constructed
for each patient in the second week of treatment based upon on-line portal
and CT images acquired during the first week of treatment. The treatment pr
escription dose, defined as the minimum dose to the cl-PTV, is selected bas
ed on predefined dose-volume constraints for rectum/bladder and derived fro
m the pretreatment planning CT image. In addition, the treatment modality (
CRT or IMRT) is determined based on the level of dose escalation achievable
and the risk of inaccurate targeting. The potential for both dose escalati
on and the application of IMRT was evaluated by comparing the prescription
doses delivered using the ART process, with the cl-PTV, to those in the tra
ditional treatment process, with a conventional generic PTV. In addition, t
he distributions of potential geometric target underdosing and normal tissu
e overdosing were also calculated to evaluate the quality of the convention
al treatment plans.
Results: One hundred and fifty patients have been treated with the ART proc
ess. When compared to the treatment dose delivered with the conventional tr
eatment process (generic PTV), an average 5% (2.5-10%) more dose could be d
elivered using the ART process with CRT, and 7.5% (2.5-15%) more dose could
be delivered with IMRT. Of the 150 patients, 70% were treated to a minimum
cl-PTV dose greater than or equal to 77.4 Gy (81.3 Gy ICRU isocenter dose)
. Dosimetric analysis revealed that 81 Gy to the cl-PTV (or 86.7 Gy ICRU) c
ould be prescribed to at least 50% of patients if IMRT was applied using th
e ART process. In contrast, IMRT did not yield an obvious dose escalation g
ain if patients were treated using the generic PTV. Our results also demons
trate that the cl-PTV is significantly smaller than the conventional generi
c PTV for most patients, with a mean volume reduction of 24% (range, 5-43%)
.
Conclusion: These results support our hypothesis that the achievable level
of dose escalation using ART is patient dependent. By using the ART process
to develop a cl-PTV, one can (1) optimize the dose level, (2) increase the
applicability of IMRT, and (3) improve the quality of dose delivery. The A
RT process provides the foundation to identify a suitable option (CRT or IM
RT) for the delivery of a safe treatment and dose escalation. It is now our
standard of practice for prostate cancer treatment. (C) 2001 Elsevier Scie
nce Inc.