Table 1.
Process steps | ||||
---|---|---|---|---|
Tumor coverage aim | ||||
PTV | 90% isodose to cover 98% of PTV | |||
Tumor dose prescribed to the ICRU reference point initially selected to achieve | ||||
Lung | EQD2mean 18.2 Gy | |||
Prescribed tumor dose reduced by 10%, and further if needed to meet the following limits | ||||
Heart | D100% <45 Gy, D67% <53 Gy, D33% <60 Gy | |||
Spinal cord | D0.1cc ≤ 47 Gy | |||
Brachial plexus | D30% ≤60 Gy, D0.1cc ≤65 Gy | |||
Esophagus | Dose to 1 cm3=65 Gy | Dose to 1 cm3=68 Gy | Dose to 1 cm3=71 Gy | Dose to 1 cm3 ≤63 Gy∗ |
Limit for | Group 1: cohort 1 | Group 1: cohort 2 | Group 1: cohort 3 | Group 2 |
Abbreviations: EQD2mean = equivalent dose in 2-Gy fractions averaged across lung, excluding gross tumor volume (GTV); ICRU = International Commission on Radiation Units and Measurements; PTV = planning target volume.
Prescribed tumor dose finally limited to 63-73 Gy, patients being ineligible for the trial if this causes lung V20Gy (the volume of lung excluding GTV receiving more than 20 Gy) or EQD2mean to exceed 35% or 19.3 Gy, respectively.
This dose level increased to 65 Gy, and then 68 Gy as safety data became available from group 1.