TY - JOUR
T1 - Radiobiological evaluation of breast cancer radiotherapy accounting for the effects of patient positioning and breathing in dose delivery. A meta analysis
AU - Tzikas, Athanasios
AU - Komisopoulos, Georgios
AU - Ferreira, Brigida Costa
AU - Hyödynmaa, Simo
AU - Axelsson, Sofie
AU - Papanikolaou, Nikos
AU - Lavdas, Eleftherios
AU - Lind, Bengt K.
AU - Mavroidis, Panayiotis
PY - 2013
Y1 - 2013
N2 - In breast cancer radiotherapy, significant discrepancies in dose delivery can contribute to underdosage of the tumor or overdosage of normal tissue, which is potentially related to a reduction of local tumor control and an increase of side effects. To study the impact of these factors in breast cancer radiotherapy, a meta analysis of the clinical data reported by Mavroidis et al. (2002) in Acta Oncol (41:471-85), showing the patient setup and breathing uncertainties characterizing three different irradiation techniques, were employed. The uncertainties in dose delivery are simulated based on fifteen breast cancer patients (5 mastectomized, 5 resected with negative node involvement (R-) and 5 resected with positive node involvement (R+)), who were treated by three different irradiation techniques, respectively. The positioning and breathing effects were taken into consideration in the determination of the real dose distributions delivered to the CTV and lung in each patient. The combined frequency distributions of the positioning and breathing distributions were obtained by convolution. For each patient the effectiveness of the dose distribution applied is calculated by the Poisson and relative seriality models and a set of parameters that describe the dose-response relations of the target and lung. The three representative radiation techniques are compared based on radiobiological measures by using the complication-free tumor control probability, P+ and the biologically effective uniform dose, D concepts. For the Mastectomy case, the average P+ values of the planned and delivered dose distributions are 93.8% for a DCTV of 51.8 Gy and 85.0% for a DCTV of 50.3 Gy, respectively. The respective total control probabilities, PB values are 94.8% and 92.5%, whereas the corresponding total complication probabilities, P1 values are 0.9% and 7.4%. For the R- case, the average P+ values are 89.4% for a DCTV of 48.9 Gy and 88.6% for a DCTV of 49.2 Gy and 85.5% for a DCTV of 49.1 Gy, respectively. The respective PB values are 90.2% and 90.1%, whereas the corresponding P1 values are 4.1% and 4.6%. The combined effects of positioning uncertainties and breathing can introduce a significant deviation between the planned and delivered dose distributions in lung in breast cancer radiotherapy. The positioning and breathing uncertainties do not affect much the dose distribution to the CTV. The simulated delivered dose distributions show larger lung complication probabilities than the treatment plans. This means that in clinical practice the true expected complications are underestimated. Radiation pneumonitis of Grade 1-2 is more frequent and any radiotherapy optimization should use this as a more clinically relevant endpoint.
AB - In breast cancer radiotherapy, significant discrepancies in dose delivery can contribute to underdosage of the tumor or overdosage of normal tissue, which is potentially related to a reduction of local tumor control and an increase of side effects. To study the impact of these factors in breast cancer radiotherapy, a meta analysis of the clinical data reported by Mavroidis et al. (2002) in Acta Oncol (41:471-85), showing the patient setup and breathing uncertainties characterizing three different irradiation techniques, were employed. The uncertainties in dose delivery are simulated based on fifteen breast cancer patients (5 mastectomized, 5 resected with negative node involvement (R-) and 5 resected with positive node involvement (R+)), who were treated by three different irradiation techniques, respectively. The positioning and breathing effects were taken into consideration in the determination of the real dose distributions delivered to the CTV and lung in each patient. The combined frequency distributions of the positioning and breathing distributions were obtained by convolution. For each patient the effectiveness of the dose distribution applied is calculated by the Poisson and relative seriality models and a set of parameters that describe the dose-response relations of the target and lung. The three representative radiation techniques are compared based on radiobiological measures by using the complication-free tumor control probability, P+ and the biologically effective uniform dose, D concepts. For the Mastectomy case, the average P+ values of the planned and delivered dose distributions are 93.8% for a DCTV of 51.8 Gy and 85.0% for a DCTV of 50.3 Gy, respectively. The respective total control probabilities, PB values are 94.8% and 92.5%, whereas the corresponding total complication probabilities, P1 values are 0.9% and 7.4%. For the R- case, the average P+ values are 89.4% for a DCTV of 48.9 Gy and 88.6% for a DCTV of 49.2 Gy and 85.5% for a DCTV of 49.1 Gy, respectively. The respective PB values are 90.2% and 90.1%, whereas the corresponding P1 values are 4.1% and 4.6%. The combined effects of positioning uncertainties and breathing can introduce a significant deviation between the planned and delivered dose distributions in lung in breast cancer radiotherapy. The positioning and breathing uncertainties do not affect much the dose distribution to the CTV. The simulated delivered dose distributions show larger lung complication probabilities than the treatment plans. This means that in clinical practice the true expected complications are underestimated. Radiation pneumonitis of Grade 1-2 is more frequent and any radiotherapy optimization should use this as a more clinically relevant endpoint.
KW - Biologically effective uniform dose
KW - Breast cancer radiotherapy
KW - Breathing
KW - Complication-free tumour control
KW - Dose-response relations
KW - Organ motion
KW - Positioning uncertainty
KW - Radiobiological evaluation
UR - http://www.scopus.com/inward/record.url?scp=84873731152&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84873731152&partnerID=8YFLogxK
U2 - 10.7785/tcrt.2012.500274
DO - 10.7785/tcrt.2012.500274
M3 - Article
C2 - 22775337
AN - SCOPUS:84873731152
SN - 1533-0346
VL - 12
SP - 31
EP - 44
JO - Technology in Cancer Research and Treatment
JF - Technology in Cancer Research and Treatment
IS - 1
ER -