Abstract:
Objective To evaluate the dosimetric difference of helical tomotherapy plans for nasopharyngeal carcinoma via Ray Station 7 (V6.99) and Tomotheraphy (TOMO) (Hi-Art@V5.1.3) treatment planning systems.
Methods This retrospective analysis involved 15 patients of nasopharyngeal carcinoma who completed the TOMO plan in Sun Yat-sen University Cancer Center from May 2018 to December 2018. Among them, 11 cases were males and 4 cases were females, aged (44.0±17.7) years. Using the same prescription dose requirements and dose constraints in TOMO, the plan was designed on the Ray Station 7 treatment planning system. The dosimetric indexes for plan comparison included the 100% and 95% prescription dose coverage of the target volume (V100, V95), dose covering 1%, 98%, 99% of the volume of the target volume (D1%, D98%, D99%), homogeneity index (HI), conformity index (CI), key dosimetric indexes for organs at risk, planning optimization time and delivery time of treatment plan. Data from the two groups that fit a normal distribution were compared by paired t-test.
Results The V100 of planning target volume of the primary lesion of nasopharyngeal carcinoma (PTVnx) ((97.5±2.1)% vs. (94.9±3.9)%); V100, V95 of planning target volume of the primary lesion invasion (PTV1) ((98.5±1.4)% vs. (99.1±0.9)%, (99.3±0.7)% vs. 100.0%); V100, V95, CI of planning target volume of primary lesion invasion clinical target volume (CTV1) and expanded gross tumor volume of bilateral lymph node lesions (GTVnd) and the lymphatic drainage area where GTVnd is located and the negative lymphatic drainage area that needs preventive radiotherapy (PTV2) ((98.6±1.1)% vs. (98.9±0.9)%, (99.1±0.9)% vs. (99.8±0.2)%, (74.8±5.7)% vs. (79.2±8.3)%); the dose corresponding to the isodose line surrounding the volume of 1 ml in planning organ at risk volume of spinal cord (PRV-SC) (D1 ml) , the relative volume of the volume surrounded by the isodose line corresponding to 40 and 30 Gy in PRV-SC and the volume of PRV-SC (V40 Gy, V30 Gy), the mean dose (Dmean) of planning organ at risk target volume of the spinal cord ((3 750.0±250.0) cGy vs. (3 443.6±309.3) cGy, (0.7±0.7)% vs. (0.1±0.1)%, (52.3±29.1)% vs. (44.6±22.9)%, (2 705.5±535.5) cGy vs. (2 619.4±413.9) cGy); and Dmean of the right temporal lobe ((1 639.5±594.5) cGy vs. (2 150.3±735.6) cGy) showed statistically significant differences between Ray Station 7 and TOMO plans (t=−4.96−6.71, all P<0.05). The V95, D1%, D98%, HI, CI of PTVnx((99.7±0.3)% vs. (99.8±0.2)%, (7 008.5±746.5) cGy vs. (6 996.0±767.0) cGy, (6 628.0±577.0) cGy vs. (6 548.8±577.3) cGy, (6.2±2.7)% vs. (6.3±2.6)%, (59.8±26.1)% vs. (64.0±24.3)%); V100, V95, D99% and D1% of planning target volume for bilateral lymph node lesion (PTVnd) ((98.5±1.5)% vs. (98.1±1.9)% and (98.7±1.2)% vs. (96.6±3.4)%, (99.7±0.3)% vs. 100.0% and 100.0% vs.100.0%, (6 511.0±500.9) cGy vs. (6 487.1±483.5)cGy and (6 496.0±484.0) cGy vs. (6 493.3±466.6) cGy, (6 824.0±571.0) cGy vs. (6 815.7±562.6) cGy and (6 815.0±583.0) cGy vs.(6 807.0±587.5) cGy) of the two groups of plans showed that the difference was not statistically significant (t=−1.51−0.90, all P>0.05). The relative volume of the volume surrounded by the isodose line corresponding to 50 Gy in PRV-SC and the volume of PRV-SC (V50 Gy) ((0.03±0.03)% vs. 0); Dmean of planning organ at risk target volume of brainstem (PRV-BS) ((2 511.0±792.0) cGy vs. (2 397.0±310.6) cGy); D1% and relative volume of the volume surrounded by the isodose line corresponding to 60 Gy in PRV-BS and the volume of PRV-BS (V60 Gy) ((4 880.0±1 600.0) cGy vs. (5 254.6±755.1) cGy, (1.6±1.6)% vs. (3.6±3.6)%); Dmean of the bilateral parotid ((3 986.5±836.5) cGy vs. (3 953.1±425.6) cGy and (4 223.0±708.0) cGy vs. (4 205.1±800.2) cGy); Dmean of the left temporal lobe ((1 891.5±845.5) cGy vs. (2 077.1±573.0) cGy; V60 Gy of the bilateral temporal lobe ((6.7±6.7)% vs. (6.5±6.5)% and (4.0±4.0)% vs. (5.8±5.8)%) of the two groups of plans showed that the differences were not statistically significant (t=−1.29−1.96, all P>0.05). The dosages of two treatment planning systems were within the clinical requirements range. The planning optimization time of Ray Station 7 treatment planning systems for nasopharyngeal carcinoma was significantly faster than that of TOMO treatment planning systems ((3.00±0.58) min vs. (120.00±17.00) min), the difference was statistically significant (t=−52.31, P<0.01), but their delivery times were similar to each other ((611.0±94.2) s vs. (612.2±94.3) s), the difference was not statistically significant (t=−0.03, P>0.05).
Conclusion Statistical analysis of the quality of helical tomotherapy plans for nasopharyngeal carcinoma designed by the two treatment planning systems showed that the differences were not significant, and both can meet clinical dosimetry requirements. Designing a nasopharyngeal carcinoma plan with the Ray Station 7 treatment planning system can significantly save the optimization time.