BioMed Research International

BioMed Research International / 2018 / Article

Research Article | Open Access

Volume 2018 |Article ID 9153496 | 8 pages | https://doi.org/10.1155/2018/9153496

Radiotherapy for Adult Medulloblastoma: Evaluation of Helical Tomotherapy, Volumetric Intensity Modulated Arc Therapy, and Three-Dimensional Conformal Radiotherapy and the Results of Helical Tomotherapy Therapy

Academic Editor: Pasquale De Bonis
Received18 Oct 2017
Revised30 Jan 2018
Accepted19 Feb 2018
Published21 Mar 2018

Abstract

Introduction. All adult medulloblastoma (AMB) patients should be treated with craniospinal irradiation (CSI) postoperatively. Because of the long irradiation range, multiple radiation fields must be designed for conventional radiotherapy technology. CSI can be completed in only one session with helical tomotherapy (HT). We evaluated the dose of HT, volumetric intensity modulated arc therapy (VMAT), and three-dimensional conformal radiotherapy (3D-CRT) of AMB and the results of 5 cases of AMB treated with HT. Methods. Complete craniospinal and posterior cranial fossa irradiation with HT, VMAT, and 3D-CRT and dose evaluation were performed. And results of 5 cases of AMB treated with HT were evaluated. Results. A large volume of tissue was exposed to low dose radiation in the organs at risk (OAR), while a small volume was exposed to high dose radiation with HT. The conformity and uniformity of the targets were good with HT and VMAT, and the volume of targets exposed to high dose with VMAT was larger than that of HT. The uniformity of 3D-CRT was also good, but the dose conformity was poor. The main toxicity was hematologic toxicity, without 4th-degree bone marrow suppression. There was 3rd-degree inhibition in the white blood cells, hemoglobin, and platelets. The three female patients suffered menstrual disorders during the course of radiation. Two female patients with heavy menstruation suffered 3rd-degree anemia inhibition, and 2 patients suffered amenorrhea after radiotherapy. Although menstrual cycle was normal, the third patient was not pregnant. Conclusion. CSI with HT is convenient for clinical practice, and the side effects are mild. With good conformity and uniformity, VMAT can also be used for selection in CSI. For poor conformity, 3D-CRT should not be the priority selection for CSI. In female patients, the ovaries should be protected.

1. Introduction

Medulloblastoma (MB), which can spread through the cerebrospinal fluid, is a malignant primitive neuroectodermal tumor that originates from the posterior cranial fossa (PCF). A total of 80% of medulloblastoma patients are diagnosed when they are younger than 15 years of age (median age, 5 years) [1]. The incidence of adult medulloblastoma (AMB) is approximately 0.5/100000 [2, 3], accounting for 0.4–1% of adult nervous system tumors [4]. Surgery is the first treatment choice for nonmetastatic MB, and all patients should be treated with craniospinal irradiation (CSI) postoperatively. Because of the long irradiation range, multiple radiation fields must be designed for conventional radiotherapy technology. It is difficult to abut adjacent radiation fields. CSI can be completed in only one session with helical tomotherapy (HT) [58], which is convenient for clinical practice.

This study retrospectively analyzed the treatment results of 5 cases of AMB treated with HT at Zhejiang Cancer Hospital. After that we completed the volumetric intensity modulated arc therapy (VMAT) and three-dimensional conformal radiotherapy (3D-CRT) plan retrospectively and evaluated the dose of HT, VMAT, and 3D-CRT.

2. Methods

2.1. General Information

Five AMB patients (18 years of age and older) who were confirmed by pathology and treated with HT from June 2015 to October 2016 at Zhejiang Cancer Center were enrolled in the study. The Chang staging system [9] was used to evaluate the patients. Acute toxicity was evaluated with Common Toxicity Criteria (CTC) V4.0, and the last follow-up time was in January 2018. Patients were immobilized by the head, neck, and shoulder, and they wore body thermoplastic masks. CT-simulation equipment was used (i.e., Philips Brilliance CT or GE Light Speed), and the scanning range was from the top of the head to the ossa sedentarium. The simulation images were transmitted to an Accuray CT Planning Station Hi-Art Version 5.1.0 workstation, RayStation 4.0V, and Pinnacle Version 9.2 workstation.

2.2. Target Definition and Prescription Dose

The brain, spinal cord, PCF, and organs at risk (OAR) were contoured on the simulation CT images layer by layer. The brain and spinal cord were PTV1 (planning target volume, PTV), while the PCF was PTV2. The doses for PTV1 and PTV2 were 30.6–36 Gy/17–20 F and 50.4–54 Gy/28–30 F, respectively.

2.3. Planning

All five patients adopted HT plan; VMAT (RayStation 4.0V) and 3D-CRT (Pinnacle Version 9.2) plan were retrospectively designed for dose evaluation. VMAT consisted of 4 parts: the superior part (brain and upper cervical spinal cord) adopted double therapeutic arc (182–178 degrees and 178–182 degrees); the remaining 3 parts (the spinal cord was derived from the lower cervical part, the thoracic, the lumbar spine, and sac) adopted single therapeutic arc (182–178 degree). 3D-CRT plan consisted of 3 abutting plans: the superior part consisted of 90-degree radiation beam and 270-degree radiation beam (lower bound at C2-3); the median and inferior parts consisted of 0-degree radiation beam, 130–140-degree radiation beam, and 220–230-degree radiation beam (beam angle was slightly different among individual patients).

2.4. Image Registration and Plan Execution
2.4.1. Image Registration

Before each plan was executed, the head, neck, and body were scanned separately with megavoltage computed tomography (MVCT). The MVCT images were compared with the corresponding planning images, and then the “superior inferior,” “left right,” “anterior posterior,” and “rotation” movement values of the treatment bed were determined. The mean values of the above head, neck, and body directions were confirmed.

2.4.2. Planning Execution

After completing the image registration, the treatment bed was moved, and the plan was executed.

2.5. Plan Evaluation

The dose uniformity was evaluated using the dose homogeneity index (DHI). DHI = /. was the irradiation dose that 5% PTV received, and was the irradiation dose that 95% PTV received [10]. A DHI value close to 1 suggested better dose uniformity, and dose conformity was evaluated with the conformity index (CI). . is the volume of the target covered by the prescription dose. is the volume of the target, and is the tissue volume, including the target covered by the prescription dose [11]. A CI close to 1 suggested better conformity. As the prescription doses differed among the 5 patients, the irradiation dose of the OAR was expressed by the percent prescription dose of the percent volume.

2.6. Statistical Analysis

Statistical analysis was performed with the Statistical Package for Social Sciences (SPSS, Chicago, IL) software package, version 18.0, for Windows. Single factor analysis of variance was performed. And, in this study, a two-tailed value < 0.05 was considered statistically significant.

3. Results

3.1. General Data

The general characteristics of the patients and radiotherapy-related parameters are showed in Table 1. Patient 1 received CSI after a second operation, and the PTV 2 for him was the tumor bed. There was residual tumor in the posterior fossa and intramedullary metastasis in patient 2, who needed morphine for lumbar pain and abandoned treatment after 7 fractions of radiotherapy. The T stage could not be judged for patient 3, who underwent surgery at another hospital and received 2 cycles of etoposide plus carboplatin chemotherapy after radiotherapy. Patient 5 received 4 cycles of temozolomide plus cisplatin chemotherapy after radiotherapy.


CategoryPatients
Patient 1Patient 2Patient 3Patient 4Patient 5

General characteristics
 GenderMaleMaleFemaleFemaleFemale
 Age (year)3025281823
 Tumor locationCerebellopontine angle areaFourth cerebral ventricleCerebellumCerebellar vermisCerebellar vermis
 Neurological examinationNegativeNegative-NegativeNegative
 Tumor size (cm)3.0 × 3.12.4 × 3.6-3.5 × 4.32.8 × 3.0
 Histological featuresGroup 4Group 4-Group 4Group 4
 Extension of tumorCerebellumThird ventricle of cerebrum-Fourth cerebral ventricleFourth cerebral ventricle
 The amount of surgical removal (cm)3.0 × 3.0 × 2.04.0 × 6.0 × 3.0-4.5 × 4.5 × 3.03.5 × 3.5 × 3.0
 MRI
  Brain MRI/tumor residualYes/noYes/yesYes/noYes/noYes/no
  Spinal cord MRI/metastasisYes/noYes/yesNo/-No/-No/-
  Posttreatment MRI/progressive diseaseYes/no-#Yes/noYes/noYes/no
Radiotherapy-related parameters
 TM stageT2M0T4M3TXMXT2MXT3aMX
 Prescription dose (Gy/F)
  PTV130.6/1735/2030.6/1736/2036/20
  PTV219.8/1118/1023.4/1318/1018/10
 Interruption/causeYes/
bone suppression
Yes/
vacation, pain
Yes/
machine
breakdown
Yes/
bone suppression
No/-
 Interruption time (day)45230

: the patient underwent surgery at another hospital in Shanghai City, and the pathology data cannot be obtained, and the histological characteristics of the patient cannot be furtherly determined; : the patient abandoned treatment after 7 fractions of radiotherapy and had no MRI reexamination. And the patient died in July 2017.
3.2. Dosimetry Results

HT took the longest CSI beam-on time. VMAT took the second place, and 3D-CRT took the shortest time. The dose uniformity and conformity of HT and VMAT were good. The target volume exposed to high dose () in VMAT was larger than that of HT, and 3D-CRT took the highest . The dose uniformity of 3D-CRT was also good, but the dose conformity was poor. The target dosimetry results were showed in Tables 3 and 4, and the isodose diagram was showed in Figure 1. For HT, and of the OAR were high, and most of OAR was 100%. of lens decreased to 0. The remaining of OAR decreased rapidly, and partially decreased to 0. Most of OAR decreased to 0. The dose characteristic of VMAT was similar to that of HT. The dose gradient of HT and VMAT dropped rapidly, while the dose gradient of 3D-CRT dropped slowly. The dosimetry results of OAR were shown in Table 5.

3.3. Treatment Toxicity

All patients suffered from headache, dizziness, nausea, and vomiting, which could be relieved with hormones and mannitol. 5-HT3 receptor antagonists were used for patients 1 and 4. Treatment toxicity and clinical treatment are showed in Table 2. The 4 patients who completed the treatment suffered 2nd-degree hair loss after radiotherapy, and their hair eventually returned to normal. During radiotherapy, the main toxicity was hematologic toxicity. There was no 4th-degree bone marrow suppression, but there was a 3rd-degree inhibition of leukocyte and hemoglobin in 2 cases, 3rd-degree platelet inhibition in 1 case, and 2nd-degree neutrophils inhibition in 2 cases. There were menstrual disorders in 3 female patients during the treatment, and 2 patients with heavy menstrual volume suffered 3rd-degree hemoglobin inhibition.


CategoryPatients
Patient 1Patient 2Patient 3#Patient 4Patient 5

Acute toxicity grade
 Leukocyte31023
 Neutrophils20012
 Hemoglobin00033
 Platelet31020
 Hair loss20222
Clinical treatmentIL-11, G-CSF,
Anti-infection, platelet transfusion
Pain
management
-IL-11, G-CSFG-CSF, EPO

: no blood samples reexamined after 3 weeks of radiotherapy; G-CSF: recombinant human granulocyte colony stimulating factor; EPO: erythropoietin; IL-11: interleukin-11.

CategoryPatient
Patient 1Patient 2Patient 3Patient 4Patient 5
HTVMAT3D-CRTHTVMAT3D-CRTHTVMAT3D-CRTHTVMAT3D-CRTHTVMAT3D-CRT

Time6823267472832667676333726053336661033087
99.2298.8198.9599.8399.0299.6797.6999.9299.9399.4599.4999.4599.8098.6597.58
016.0063.844.0920.6238.870.370.503.090.018.473.310.392.2851.36
32.3233.8235.0237.8339.0639.1233.0532.6633.1237.5538.9239.1438.2238.6242.07
29.3828.8029.0435.4233.2834.0827.1430.3730.0834.8435.3034.8035.5133.7030.14
31.5431.9232.9336.6136.7137.2732.1831.7131.7536.7137.5937.1636.8137.2938.45
DHI1.051.081.131.041.091.091.081.051.071.031.061.071.041.061.10
CI0.870.830.680.850.870.660.860.870.680.850.850.680.920.880.74

Time: beam-on time (second); : % prescription dose delivered to percent volume; : irradiation dose delivered to 1% volume, representing the maximum dose; : irradiation dose delivered to 99% volume, representing the minimum dose; : average irradiation dose.

ParametersCategory
Mean (SD)P value
Overall
P value
P value among groups
HTVMAT3D-CRTHT versus
VMAT
HT versus
3D-CRT
VMAT versus
3D-CRT

Time660.20 (52.17)329.60 (3.51)73.20 (8.41)0.000.000.000.00
99.20 (0.88)99.18 (0.52)99.12 (0.93)0.990.970.870.90
0.97 (1.75)9.57 (8.66)32.09 (27.81)0.030.440.010.06
35.79 (2.86)36.62 (3.11)37.69 (3.58)0.650.690.370.60
32.46 (3.92)32.29 (2.64)31.63 (2.62)0.910.930.680.74
34.77 (2.67)35.04 (2.97)35.51 (2.97)0.920.880.690.80
DHI1.05 (0.02)1.07 (0.02)1.09 (0.02)0.020.150.010.09
CI0.87 (0.03)0.86 (0.02)0.69 (0.03)0.000.570.000.00

Time: beam-on time (second); : % prescription dose delivered to percent volume; : irradiation dose delivered to 1% volume, representing the maximum dose; : irradiation dose delivered to 99% volume, representing the minimum dose; : average irradiation dose.

OARCategory

Left lens
 Tomo4.75 (0.88)3.67 (0.57)100 (0)69.90 (36.35)0 (0)0 (0)0 (0)0 (0)0 (0)
 VMAT4.72 (0.50)4.31 (0.50)100 (0)100 (0)0 (0)0 (0)0 (0)0 (0)0 (0)
 3D-CRT3.34 (0.94)2.92 (0.92)93.49 (10.66)34.19 (44.71)0 (0)0 (0)0 (0)0 (0)0 (0)
 Tomo4.86 (0.97)3.83 (0.64)100 (0)78.17 (34.88)0 (0)0 (0)0 (0)0 (0)0 (0)
Right lens
 VMAT4.92 (0.59)4.22 (0.49)100 (0)100 (0)0 (0)0 (0)0 (0)0 (0)0 (0)
 3D-CRT3.79 (1.18)3.11 (0.99)99.50 (1.12)51.10 (47.55)0 (0)0 (0)0 (0)0 (0)0 (0)
 Tomo23.75 (3.93)11.60 (2.39)100 (0)96.80 (4.47)75.64 (9.52)53.21 (9.37)37.32 (9.72)22.05 (9.06)0.03 (0.08)
Left eye ball
 VMAT15.19 (2.49)7.21 (1.30)100 (0)99.99 (0.02)45.10 (18.34)16.52 (10.00)4.95 (3.80)0.65 (0.67)0 (0)
 3D-CRT28.58 (7.32)7.58 (1.79)98.42 (2.24)69.77 (22.76)31.89 (10.41)22.63 (9.06)16.30 (7.55)11.91 (6.85)4.42 (3.74)
 Tomo24.79 (3.40)12.09 (2.09)100 (0)97.62 (3.37)73.99 (6.30)56.33 (8.13)40.18 (8.49)25.16 (7.93)0.29 (0.58)
Right eye ball
 VMAT17.72 (3.59)8.85 (3.26)100 (0)100 (0)50.21 (13.79)20.26 (6.20)7.84 (3.77)1.10 (1.56)0 (0)
 3D-CRT33.66 (3.30)10.17 (2.87)98.54 (1.13)75.66 (17.78)41.62 (12.74)32.40 (10.80)26.53 (9.87)21.22 (10.22)11.67 (6.31)
 Tomo11.09 (2.55)4.09 (0.72)98.06 (4.35)56.32 (15.37)8.63 (4.63)1.96 (1.92)0.51 (0.63)0.20 (0.19)0.01 (0.01)
Left lung
 VMAT12.10 (2.20)3.80 (4.59)92.88 (3.70)45.74 (5.01)9.05 (2.74)2.10 (1.00)0.64 (0.50)0.21 (0.21)0 (0.01)
 3D-CRT14.56 (2.53)4.42 (0.90)72.37 (12.45)42.73 (11.34)26.87 (10.26)8.91 (5.09)1.73 (1.64)0.44 (0.49)0.02 (0.04)
 Tomo13.41 (3.20)4.31 (0.83)98.25 (3.81)56.84 (14.69)12.01 (6.10)3.63 (3.03)1.31 (1.35)0.48 (0.54)0.01 (0.01)
Right lung
 VMAT14.46 (2.72)4.08 (0.71)91.63 (7.84)49.67 (8.58)11.22 (4.20)3.62 (1.57)1.34 (0.80)0.51 (0.42)0.02 (0.03)
 3D-CRT17.18 (3.56)5.27 (1.18)77.95 (12.97)48.95 (11.38)33.89 (9.40)14.93 (6.10)4.77 (3.65)1.62 (1.83)0.03 (0.08)
 Tomo11.18 (2.64)5.45 (0.90)100 (0)91.07 (8.18)21.44 (15.88)3.95 (6.94)1.62 (2.38)0.24 (0.54)0 (0)
Heart
 VMAT14.44 (6.53)6.85 (3.0)100 (0)86.22 (12.99)38.56 (33.63)16.88 (26.68)8.15 (16.49)4.19 (9.36)0.28 (0.64)
 3D-CRT17.03 (3.64)5.40 (1.07)73.36 (8.98)47.40 (11.08)36.08 (10.64)21.59 (13.29)8.07 (6.87)0.67 (1.04)0 (0)
 Tomo9.24 (1.66)3.97 (0.91)95.78 (9.33)58.35 (21.37)7.07 (4.04)0.66 (0.76)0.05 (0.10)0 (0.01)0 (0)
Liver
 VMAT12.75 (2.68)4.42 (0.95)87.83 (9.23)53.87 (13.51)18.38 (10.56)4.96 (4.09)1.22 (1.23)0.47 (0.70)0 (0)
 3D-CRT17.07 (2.78)5.01 (1.08)69.19 (13.03)45.24 (11.78)31.54 (9.79)16.95 (7.54)4.89 (2.73)0.97 (0.68)0 (0)
 Tomo8.16 (1.62)4.96 (0.53)100 (0)93.96 (5.04)9.22 (7.29)0.09 (0.14)0 (0)0 (0)0 (0)
Stomach
 VMAT14.60 (4.55)7.19 (2.56)96.95 (6.80)85.28 (19.45)53.20 (31.90)18.75 (19.52)4.88 (5.70)1.20 (1.83)0 (0)
 3D-CRT17.54 (5.30)6.43 (2.62)81.30 (17.83)57.95 (21.38)44.47 (17.91)20.90 (14.30)7.06 (6.97)4.10 (5.51)0 (0)
 Tomo11.25 (2.39)6.52 (1.30)100 (0.01)99.28 (1.60)39.70 (23.27)4.91 (4.20)0.21 (0.31)0 (0)0 (0)
Left kidney
 VMAT7.62 (4.82)3.61 (2.09)92.09 (9.99)36.37 (36.44)9.26 (19.08)1.81 (3.49)0.24 (0.46)0 (0)0 (0)
 3D-CRT14.45 (6.42)3.33 (1.27)70.35 (16.60)19.05 (14.56)12.44 (13.79)9.02 (11.44)3.49 (4.87)1.51 (2.14)0 (0)
 Tomo9.43 (1.46)6.15 (0.78)100 (0)99.82 (0.40)29.92 (9.91)0.61 (1.08)0 (0)0 (0)0 (0)
Right kidney
 VMAT5.93 (2.22)3.50 (1.75)92.61 (9.53)39.47 (35.46)6.17 (13.55)0 (0)0 (0)0 (0)0 (0)
 3D-CRT13.48 (3.78)4.21 (0.56)78.08 (17.11)35.52 (8.48)25.11 (8.49)10.41 (7.29)1.34 (2.24)0.34 (0.76)0 (0)

: % prescription dose delivered to percent volume.
3.4. Follow-Up Results

At the time of follow-up, 4 patients had survived, while patient 2 who abandoned radiotherapy died in July 2017. Among the 3 cases of menstrual disorders, the 2 patients who suffered 3rd-degree hemoglobin inhibition had amenorrhea, and the third patient was in a normal menstrual cycle and not pregnant.

4. Discussion

The Chang staging was widely used in MB [9, 12, 13]. Craniospinal MRI and CSF examination were helpful in determining whether the tumor was locally residual or intraspinal infiltration, and then the TM stage could be accurately judged [9, 14]. The M stage could be judged only in 2 patients who underwent craniospinal MRI. Residual tumor in the PCF and intraspinal tumor infiltration were showed on the MRI of one patient. Craniospinal MRI and CSF examinations should be completed before CSI; otherwise the tumor stage and patient prognosis cannot be evaluated properly.

Before CSI irradiation, the therapeutic outcomes of MB were poor. In 1953, Paterson and Farr [15] reported using the CSI technique to treat patients with MB, and the 3-year OS was 65%. Then, the CSI technique established its status in the treatment of MB. The target range of CSI is long enough that one radiation field cannot cover the target. Abutting radiation fields is inevitable in two-dimensional radiotherapy, 3D-CRT, intensity modulated radiotherapy (IMRT), and VMAT [16, 17]. Field abutment is difficult and may result in cold or hot dose spots. The dose of cold spot resulted in low dose at the target, which is one cause of tumor recurrence. A hot spot dose can lead to serious complications, and radiation myelopathy has been reported in the literature [13].

HT is a new revolutionary technology that can complete CSI in one session, and the abutment between irradiation fields is avoided. Compared with 3DCRT and IMRT, HT can provide better dose uniformity and conformity in CSI plan [7, 8]. In this study, data in Table 3 showed that of HT, VMAT, and 3D-CRT was close to 100%, and the lowest value is 97.58% of patient 5 with 3D-CRT. The maximum with HT was 4.09%, and the remaining values fluctuated between 0 and 0.39%. The minimum with VMAT was 0.5%, and the remaining values fluctuated between 2.28% and 20.62%. The two smaller values were 3.09% and 3.31% in VMAT, and the remaining values fluctuated between 38.87% and 63.84%. The difference in between HT and 3D-CRT reached statistical difference, while that between VMAT and 3D-CRT nearly reached statistical difference. These results indicated that the target volume covered with high dose was minimum with HT, the maximum value with 3D-CRT, and the value of VMAT was between HT and 3D-CRT. was obviously different in individuals. The difference could be associated with individual body shape and thickness.

There was overall statistical difference in DHI and CI among HT, VMAT, and 3D-CRT. In this study, data showed that with HT the DHI values were close to 1, and the CI values fluctuated between 0.85 and 0.92, which was similar to that reported in the literature [8, 18]. Dose uniformity and conformity are good for the HT plan, which can provide ideal dose distribution. The DHI values of VMAT and 3D-CRT were also close to 1, and the maximum value was 1.13 with 3D-CRT. It was indicated that the uniformity was also good with VMAT and 3D-CRT. The CI values of VMAT fluctuated between 0.83 and 0.88. The CI values of VMAT of patient 2 and patient 3 were slightly higher than that of HT. It was indicated that the conformity of VMAT was also good. The CI value of 3D-CRT fluctuated between 0.66 and 0.74; therefore the conformity of 3D-CRT was poor.

There was statistical difference in time among HT, VMAT, and 3D-CRT. The beam-on time of HT was the longest, and the time fluctuated between 605 and 682 seconds, which was similar to that reported in the literature [19]. The beam-on time of VMAT which fluctuated between 326 and 330 seconds was relatively long. The beam-on time of 3D-CRT which fluctuated between 66 and 87 seconds was the shortest. Before the application of CSI, image registration also took a relatively long time, but the HT plan could be completed in one setup. Image registration before treatment is conducive to the accurate implementation of the treatment. Conventional radiation technology application requires a number of setups, and treatment technicians need journeys to and from treatment room and control room to complete the radiation field abutment, which is also time-consuming. The beam-on and image registration time of HT treatment is relatively long, while the beam-on time of conventional technique is short. However, the conventional technique needs several times setup, and the application of abutting fields requires a relatively long time. Study showed that the procedures from setup to the completion of CSI required about 45 minutes in HT, and other techniques required similar time [19].

The OAR volume exposed to high doses decreased in the HT plan, while the OAR volume exposed to low doses increased. It was a major drawback of HT [7, 8]. Table 4 showed that and of OAR were high, reaching 100% in some cases with HT. The dose of OAR dropped rapidly from , and some rapidly fell to 0, similar to the results reported in the literature [8]. Although the volume of lung exposed to low dose was large, no patients developed symptomatic acute radiation pneumonitis [20]. The effect of large volume exposed to low dose needs to be confirmed in a long-term follow-up.

As showed in Table 5, and of OAR were also high with VMAT, and dose dropped rapidly. of lens was lowest with 3D-CRT. of the other OAR was the highest with 3D-CRT. At left lung, right lung, heart, liver, stomach, left kidney, and right kidney dose fall of 3D-CRT was slower than that of VMAT and HT. This is because of fixed radiation beams with 3D-CRT. Irradiation dose was low in organs away from the beam path, while the irradiation dose was high in organs that were in the beam path. Compared with HT and VMAT, there was poor conformity, small dose gradient, and slow dose fall in 3D-CRT. Sharma et al. [8] reported that the exposed dose to lung with 3D-CRT was lower than that with HT, but our result was contrary. This situation may be caused by the three radiation beams that irradiated relatively a lot of volume of lung with our 3D-CRT plan.

Ovaries are sensitive to radiation. Up to 50% of ovarian follicles can be destroyed by 2 Gy irradiation [21]. The ovaries are inevitably irradiated in CSI, and the irradiation can result in infertility caused by ovarian function damage. Ovary transplantation was used before the start of CSI. After the transplantation, the irradiation dose exposed to ovary reduced significantly, and ovarian function could be preserved [22]. There have also been reports of reduced ovarian doses and that ovarian function could be preserved with the use of proton irradiation [23]. Three female patients in this study were treated with CSI, without ovary protection. Menstrual disorders occurred in the 3 female patients during the treatment, and 2 patients whose menstrual volume increased significantly suffered 3rd-degree hemoglobin inhibition. At the time of follow-up, patient 3 had normal menstruation but was not pregnant. Patients 4 and 5 had amenorrhea. In this group, the irradiation dose to which the ovaries of the 3 female patients were exposed could not be evaluated. However, from the dose results of the other OAR, we could infer that a large ovarian tissue volume was exposed to low doses. Ovarian function could be significantly affected by CSI irradiation. To preserve ovarian function, ovary transplantation should be performed before CSI treatment. Ovary protection should be strengthened in the process of CSI planning.

The incidence of AMB is low, and the use of HT in the treatment of AMB has been reported less frequently. This small sample in a retrospective study showed that the application of CSI with HT is convenient for clinical practice, and the side effects are mild. Attention should be paid to the protection of the ovary function in female patients in CSI. For good dose uniformity and conformity, VMAT can also be the treatment selection for CSI. Meanwhile the target volume exposed to high dose () with VMAT was higher than that of HT, and HT is more convenient for clinical practice. The uniformity is also good with 3D-CRT, but the conformity is poor. So 3D-CRT should not be the priority selection for CSI. Because of small sample size, incomplete data of the patients, nonuniform radiation dose, and short follow-up time, the long-term effect of HT treatment about AMB should be confirmed by larger sample size and longer follow-up times.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.

Acknowledgments

This work was supported by the Medical and Health Science and Technology Plan Project of Zhejiang Province [2016KYA041, Natural Science Foundation of Zhejiang Province [LY16H160037, and National Natural Science Foundation of China [81672971.

References

  1. R. J. Packer, P. Cogen, G. Vezina, and L. B. Rorke, “Medulloblastoma: Clinical and biologic aspects,” Neuro-Oncology, vol. 1, no. 3, pp. 232–250, 1999. View at: Publisher Site | Google Scholar
  2. M. T. Giordana, P. Schiffer, M. Lanotte, P. Girardi, and A. Chio, “Epidemiology of adult medulloblastoma,” International Journal of Cancer, vol. 80, no. 5, pp. 689–692, 1999. View at: Publisher Site | Google Scholar
  3. P. J. Frost, N. J. Laperriere, C. S. Wong, M. F. Milosevic, W. J. S. Simpson, and M. Pintilie, “Medulloblastoma in adults,” International Journal of Radiation Oncology Biology Physics, vol. 32, no. 4, pp. 951–957, 1995. View at: Publisher Site | Google Scholar
  4. C. F. Lynch, M. N. Hart, and M. P. Jones, “Medulloblastoma: A population-based study of 532 cases,” Journal of Neuropathology & Experimental Neurology, vol. 50, no. 2, pp. 134–144, 1991. View at: Publisher Site | Google Scholar
  5. G. Bauman, S. Yartsev, T. Coad, B. Fisher, and T. Kron, “Helical tomotherapy for craniospinal radiation,” British Journal of Radiology, vol. 78, no. 930, pp. 548–552, 2005. View at: Publisher Site | Google Scholar
  6. B. Qu, L. Du, and Y. Huang, “Clinical analysis of intracranial germinoma's craniospinal irradiation using helical tomotherapy,” Chinese Journal of Cancer Research, vol. 26, pp. 247–254, 2014. View at: Google Scholar
  7. A. Bandurska-Luque, T. Piotrowski, A. Skrobała, A. Ryczkowski, K. Adamska, and J. Kaźmierska, “Prospective study on dosimetric comparison of helical tomotherapy and 3DCRT for craniospinal irradiation - A single institution experience,” Reports of Practical Oncology and Radiotherapy, vol. 20, no. 2, pp. 145–152, 2015. View at: Publisher Site | Google Scholar
  8. S. D. Sharma, T. Gupta, R. Jalali, Z. Master, R. D. Phurailatpam, and R. Sarin, “High-precision radiotherapy for craniospinal irradiation: Evaluation of three-dimensional conformal radiotherapy, intensity-modulated radiation therapy and helical TomoTherapy,” British Journal of Radiology, vol. 82, no. 984, pp. 1000–1009, 2009. View at: Publisher Site | Google Scholar
  9. C. H. Chang, E. M. Housepian, and C. Herbert Jr., “An operative staging system and a megavoltage radiotherapeutic technic for cerebellar medulloblastomas.,” Radiology, vol. 93, no. 6, pp. 1351–1359, 1969. View at: Publisher Site | Google Scholar
  10. X. Wang, X. Zhang, L. Dong et al., “Effectiveness of noncoplanar IMRT planning using a parallelized multiresolution beam angle optimization method for paranasal sinus carcinoma,” International Journal of Radiation Oncology Biology Physics, vol. 63, no. 2, pp. 594–601, 2005. View at: Publisher Site | Google Scholar
  11. I. Paddick, “A simple scoring ratio to index the conformity of radiosurgical treatment plans,” Journal of Neurosurgery, vol. 93, supplement 3, pp. 219–222, 2000. View at: Google Scholar
  12. A. A. Brandes, E. Franceschi, A. Tosoni, V. Blatt, and M. Ermani, “Long-term results of a prospective study on the treatment of medulloblastoma in adults,” Cancer, vol. 110, no. 9, pp. 2035–2041, 2007. View at: Publisher Site | Google Scholar
  13. N. Zhang, T. Ouyang, H. Kang, W. Long, B. Thomas, and S. Zhu, “Adult medulloblastoma: clinical characters, prognostic factors, outcomes and patterns of relapse,” Journal of Neuro-Oncology, vol. 124, no. 2, pp. 255–264, 2015. View at: Publisher Site | Google Scholar
  14. C. Chargari, L. Feuvret, A. Levy et al., “Reappraisal of clinical outcome in adult medulloblastomas with emphasis on patterns of relapse,” British Journal of Neurosurgery, vol. 24, no. 4, pp. 460–467, 2010. View at: Publisher Site | Google Scholar
  15. E. Paterson and R. F. Farr, “Cerebellar medulloblastoma: Treatment by irradiation of the whole central nervous system,” Acta Radiologica, vol. 39, no. 4, pp. 323–336, 1953. View at: Publisher Site | Google Scholar
  16. R. B. Hawkins, “A simple method of radiation treatment of craniospinal fields with patient supine,” International Journal of Radiation Oncology • Biology • Physics, vol. 49, no. 1, pp. 261–264, 2001. View at: Publisher Site | Google Scholar
  17. M. T. Studenski, X. Shen, Y. Yu et al., “Intensity-modulated radiation therapy and volumetric-modulated arc therapy for adult craniospinal irradiation-A comparison with traditional techniques,” Medical Dosimetry, vol. 38, no. 1, pp. 48–54, 2013. View at: Publisher Site | Google Scholar
  18. Xu. Yj, Hu. ZH, P. Huang et al., Application of TomoDirect for craniospinal irradiation. Chin J Radiol Med Prot, vol. 35, 2015.
  19. W. Parker, M. Brodeur, D. Roberge, and C. Freeman, “Standard and Nonstandard Craniospinal Radiotherapy Using Helical TomoTherapy,” International Journal of Radiation Oncology Biology Physics, vol. 77, no. 3, pp. 926–931, 2010. View at: Publisher Site | Google Scholar
  20. J. Peñagarícano, E. Moros, P. Corry, R. Saylors, and V. Ratanatharathorn, “Pediatric Craniospinal Axis Irradiation With Helical Tomotherapy: Patient Outcome and Lack of Acute Pulmonary Toxicity,” International Journal of Radiation Oncology • Biology • Physics, vol. 75, no. 4, pp. 1155–1161, 2009. View at: Publisher Site | Google Scholar
  21. W. H. B. Wallace, A. B. Thomson, and T. W. Kelsey, “The radiosensitivity of the human oocyte,” Human Reproduction, vol. 18, no. 1, pp. 117–121, 2003. View at: Publisher Site | Google Scholar
  22. F.-T. Kung, H.-C. Chen, C.-C. Huang, J. T. Ho, and B.-H. Cheng, “Preservation of ovarian germinal follicles by temporary laparoscopic ovarian transposition in teenaged girls undergoing craniospinal irradiation for radiosensitive central nervous system tumors,” Taiwanese Journal of Obstetrics and Gynecology, vol. 47, no. 3, pp. 300–304, 2008. View at: Publisher Site | Google Scholar
  23. A. Pérez-Andújar, W. D. Newhauser, P. J. Taddei, A. Mahajan, and R. M. Howell, “The predicted relative risk of premature ovarian failure for three radiotherapy modalities in a girl receiving craniospinal irradiation,” Physics in Medicine and Biology, vol. 58, no. 10, pp. 3107–3123, 2013. View at: Publisher Site | Google Scholar

Copyright © 2018 Sun Zong-wen et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


More related articles

1425 Views | 426 Downloads | 7 Citations
 PDF  Download Citation  Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

We are committed to sharing findings related to COVID-19 as quickly and safely as possible. Any author submitting a COVID-19 paper should notify us at help@hindawi.com to ensure their research is fast-tracked and made available on a preprint server as soon as possible. We will be providing unlimited waivers of publication charges for accepted articles related to COVID-19. Sign up here as a reviewer to help fast-track new submissions.