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BMC Cancer

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3D-image-guided HDR-brachytherapy versus 2D HDR - brachytherapy after external beam radiotherapy for early T-stage nasopharyngeal carcinoma

Contributed equally
BMC Cancer201414:894

https://doi.org/10.1186/1471-2407-14-894

Received: 27 May 2014

Accepted: 17 November 2014

Published: 29 November 2014

Abstract

Background

Two-dimensional high-dose-rate brachytherapy (2D-HDR-BT) is an effective method of dose escalation for local tumor control in early T-stage nasopharyngeal carcinoma (NPC). Treatment outcomes for 3D-image-guided high-dose-rate brachytherapy (3D-image-guided-HDR-BT) after external beam radiotherapy (ERT) have not been examined in early T-stage NPC patients. The current study was designed to evaluate whether addition of 3D-HDR-BT to ERT showed further improvement in treatment outcomes in patients with early T-stage NPC when compared to 2D-HDR-BT after ERT.

Methods

The current study retrospectively analyzed and compared treatment outcomes for patients with nonmetastatic stage T1-2b NPC treated with 2D-HDR-BT (n =101) or 3D-HDR-BT (n =118) after ERT. Patients in both groups were treated with ERT at a mean dose of 60 Gy and a brachytherapy dose of 12Gy (8 ~ 20Gy), 2.5 ~ 5Gy per fraction under local anesthesia.

Results

Compared to patients treated with 2D-HDR-BT after ERT, patients treated with 3D-HDR-BT after ERT showed improvement in five-year actuarial local control survival rates (p = 0.024), local/regional relapse-free survival rates (p = 0.038), and disease-free survival rates (p = 0.021). Multivariate analysis showed that NPC patients treated with 3D-HDR-BT had improved local control survival (p = 0.042). The incidence rates of acute or chronic complications were similar between two groups.

Conclusions

The current study showed that 3D-image-guided HDR-BT after ERT was an effective treatment modality for patients with stage T1-2 NPC with acceptable complications. The improvement in local tumor control and disease free survival is likely due to improved conformal dose distributions.

Keywords

Nasopharyngeal carcinomaRadiotherapy3D-image-guidedBrachytherapyLocal control

Background

Nasopharyngeal carcinoma (NPC) is a radiosensitive disease, and radiotherapy is the standard therapy for non-disseminated NPC. Previous studies of radiotherapy treatment of NPC have reported good local control and overall survival rates [1, 2]. Teo et al. [3] have proposed a dose-tumor-control relationship above the conventional effective dose levels for early T-stage NPC patients.

Brachytherapy has been used to apply high doses of radiation directly to the primary tumor. Due to the steep nature of the rapid dose fall-off associated with the brachytherapy source, brachytherapy techniques can provide a higher nasopharyngeal tumor dose in comparison to the techniques of external beam therapy. Brachytherapy provides dose escalation for improving local tumor control and overall survival in early T-stage NPC patients [4, 5]. 3-D CT-based high-dose-rate brachytherapy (3D-HDR-BT) is a treatment method developed from 2D-HDR-BT as image-guided brachytherapy. This modern image-adpated 3D-HDR-BT can provide a higher conformal dose and higher precision distributions relative to 2D-HDR-BT. Previous studies have reported that 3D-HDR-BT after ERT treatment was effective in cervical cancer [6], breast cancer [7] and prostate cancer patients [8]. Ren et al. [9] reported 3D-image-guided CT-based HDR-BT achieved excellent local tumor control rate as salvage treatment to primary IMRT for patients with locally persistent NPC disease, especially for those with T1-2 disease at the initial diagnosis. However, no studies reported the use of 3D-HDR-BT after ERT for the treatment of stage I or II NPC.

In the current study, treatment outcomes of early T-stage NPC patients treated with ERT followed by 3D-HDR-BT or 2D-HDR-BT were analyzed retrospectively to evaluate the relative effectiveness of 3D-HDR-BT versus 2D-HDR-BT in NPC patients and to establish guidelines for future studies to determine whether improved conformality is associated with better therapeutic outcomes.

Methods

Patient populations and characteristics

A total of 118 patients with T1-2 stage NPC who were treated with 3D-HDR-BT after ERT at our center between May 2005 and January 2010 were enrolled in Group A. To evaluate the efficacy of this new technique relative to 2D-HDR-BT, 101 patients with T1-2 stage NPC who were treated with 2D-HDR-BT after ERT at our center between February 2003 and January 2005 were included in Group B. Eligible patients were aged 18–70 years with non-metastatic, histologically proven non-keratinising stage I or II nasopharyngeal carcinoma (6th AJCC). All participants had Karnofsky scores of at least 70, and adequate bone marrow, renal, and liver function. When combined, the male: female ratio of Groups A and B was 3:1, which included 162 males and 57 females. Histological examination showed that 97.7% of the patients in Groups A and B had World Health Organization (WHO) Type III disease, three patients had WHO Type I or II disease, and two patients had adenocarcinoma. The study was performed in accordance with the Declaration of Helsinki and was approved by the ethics committee of Sun Yat-Sen University Cancer Center. Written consent was given by the patients for their information to be stored in the hospital database, and we obtained consent to publish figures from the patient involved in this study.

Clinical staging

All patients were diagnosed with biopsy-confirmed primary NPC. The extent of the disease was evaluated by thorough physical examination, direct fiber-optic examination, complete blood count, blood chemistry test, chest X-ray, bone scan, and magnetic resonance imaging (MRI)/computed tomography (CT) scans of the nasopharynx and neck. NPC disease progression was monitored carefully in each patient during the course of the study.

All MRI/CT materials and clinical records were reviewed to minimize heterogeneity in restaging. Two radiologists specializing in head-and-neck cancers evaluated all scans, and any disagreements were resolved by consensus. All patients were restaged according to the American Joint Committee on Cancer Staging System (6th edition) [10]. All patients had nonmetastatic (M0) NPC. The T-stage distribution was determined for all NPC patients in Groups A and B. Group A consisted of 65 patients with stage T1 NPC, 34 patients with stage T2a NPC (nasal cavity tumors), and 19 patients with stage T2b NPC (parapharyngeal space extension). Group B consisted of 42 patients with stage T1 NPC, 41 patients with stage T2a NPC, and 18 patients with stage T2b NPC.

Treatment methods

All patients were treated with definitive intent radiation therapy: the primary nasopharyngeal tumor received a mean dose of 60 Gy (range, 56 Gy to 62 Gy), followed by brachytherapy of 12Gy (8 ~ 20Gy), 2.5 ~ 5Gy per fraction. The external beam radiotherapy techniques have previously been reported [11]. During ERT, patients in both groups were evaluated fiber optically every week to assess tumor response to treatment.

Group A

The 3D-HDR-BT for Group A was delivered after the completion of EBRT. All patients were treated with a high-dose-rate (HDR) afterloading machine (microSelectron, Nucletron, Veenendaal, the Netherlands) using a 192Ir source. For T1-2a patients, a custom designed nasopharyngeal brachytherapy applicators 10-90°tube set (Figure 1a) was positioned under local anesthesia with fiberoptic endoscopic guidance via the inferior meatus to the treatment locations. Patients were immobilized externally by a head-frame. For T2b patients, a ProGuide Needle was used as a nasopharyngeal applicator (microSelectron, Nucletron, nylon tube technique) (Figure 1b). The interstitial portion of the implant consisted of two to four stationary ProGuide Sharp Needles and was placed in the parapharyngeal tissues of the primary lesion. Treatment with 3D-HDR-BT was performed as follows: two to four applicators were placed at treatment positions near the primary lesion under local anesthesia with fiberoptic endoscopic guidance via the inferior meatus and the applicators were then immobilized, their correct position is verified by MRI and the procedure is generally well tolerated CT scanning of the nasopharyngeal region was performed (0.2 cm step and 0.2 cm slice thickness (Figure 2). The primary nasopharynx tumor received 60 Gy of EBRT, the neck region received an accumulated radiation dose of 50 Gy, while the involved areas of the neck received 60–62 Gy. For 3D-BT,the GTV was determined by a radiation oncologist as the macroscopic extent of the persistent disease area, the CTV included the persistent disease area and the nasopharyngeal primary tumor area. For patients with complete response, The GTV do not delineate, the CTV included the nasopharyngeal primary tumor area. All patients received 12Gy (8 ~ 20Gy), 2.5 ~ 5Gy per fraction over the entire implant volume
Figure 1

Two nasopharyngeal applicators. (a) Nasopharyngeal intracavitary brachytherapy applicator custom designed for T1-2a patients. (b) A ProGuide Needle (189.601 ProGuide Needle Set 6 F, sharp) was used as a nasopharyngeal applicator (microSelectron, Nucletron, nylon tube technique) for stage T2b NPC patients.

Figure 2

Two customer designed applicators for nasopharyngeal brachytherapy were immobilized in the supine position.

Following all target volumes defined and the applicators reconstruction, The PLATO PBS was used to calculate the dosimetry for a HDR 192Ir stepping source. The distance between each source step was 2.5 mm, the dose optimization was done step by step manually. This planning strategy enables us to build up the real time isodose distribution in all CT slices to increase accurate delivery of the prescribed dose, the isodose distribution can be calculated and demonstrated in coronal and sagittal planes, see Figure 3.
Figure 3

Axial computed tomography (CT) image of a stage T1-2a NPC patient showing two brachytherapy intracavitary applicators in situ with 2.5 Gy, 2.25 Gy, 1.75 Gy, 1.25 Gy, and 0.75 Gy isodose lines.

Group B

The 2D-HDR-BT for Group B was delivered after the completion of EBRT. The intracavitary brachytherapy applicators were positioned with fiberoptic endoscopic guidance via the inferior meatus to the treatment locations abutting on the posterosuperior wall of the nasopharynx. The patients were then immobilized externally by a head-frame. The separation between the central axis of the applicators ranged from 1.1 - 1.5 cm. The dose was prescribed at a distance of 1 cm from the center of the surface as defined by the sources.

Chemotherapy

Three cycles of adjuvant chemotherapy were given to patients in the concurrent chemoradiotherapy by intravenous infusion of 80 mg/m2 cisplatin on day 1 and 800 mg/m2 per day fluorouracil on days 1–5 (120 h infusion).

Follow-up

All patients were seen and carefully monitored during follow-up with a radiation oncologist after the treatment schedule was completed. Acute and late complications were scored according to the criteria of the Radiation Therapy Oncology Group (RTOG) scoring system during each follow-up visit.

Statistical analyses

The Statistical Package for Social Sciences (SPSS, Version 13.0, Chicago, IL) was used for statistical analyses. Comparisons of patient clinical-pathologic characteristics between Groups A and B were evaluated by the chi-square test. Survival rates were calculated from the radiotherapy start date. Estimates of the actuarial survival rate were determined by Kaplan-Meier estimate [12]. The log-rank test was used to compare survival curves [13]. Multivariate analysis of outcome data was performed using Cox regression analysis [14]. A p value of ≤0.05 was considered statistically significant. End points were defined as follows: local control survival (LCS), time to local recurrence; overall survival (OS), time to death from any cause; disease-free survival (DFS), time to disease recurrence, disease progression, metastasis, or death from disease-related causes; cause-specific survival (CSS), time to death due to disease; local/regional relapse-free survival (LRFS), time to recurrence/progression involving the primary site with or without regional involvement (deaths from local or regional recurrences were included in this definition); and distant metastasis-free survival (DMFS), time to distant metastatic recurrence, with or without prior or concurrent local/regional recurrence.

Results

Between May 2005 and January 2010, a total of 118 patients with stage T1-2 NPC were treated with 3D-HDR-BT after ERT at our center were enrolled. 101 patients with stage T1-2 NPC were treated with 2D-HDR-BT after ERT between February 2003 and January 2005 in Group B. The median follow-up was 57 · 8 months (range 33.9–117 · 0). The two treatment groups were well balanced in terms of baseline demographic and clinical characteristics, and radiotherapy technique (Table 1).
Table 1

Demographic and clinical characteristics of the two patient groups

Variables

Group A

Group B

p-value

 

3D-HDR-BT (n =118)

2D-HDR-BT (n =101)

 

Age (years)

  

0.594

≤ 45

65 (11.9%)

52 (20.8%)

 

> 45

53 (88.1%)

49 (79.2%)

 

Mean

44.6

47.1

 

Median

43

45

 

Range

19 - 80

18 - 73

 

Gender

  

0.100

Male

88 (74.6%)

65 (64.4%)

 

Female

30 (25.4%)

36 (35.6%)

 

Histology

  

0.529

WHO type I/II

2 (1.7%)

3 (3.0%)

 

WHO type III

116 (98.3%)

98 (97.0%)

 

T-stage

  

0.079

T1

65 (55.1%)

42 (41.6%)

 

T2a

34 (28.8%)

41 (40.6%)

 

T2b

19 (16.1%)

18 (17.8%)

 

N-stage

  

0.740

N0-1

85 (72.0%)

74 (73.3%)

 

N2-3

33 (28.0%)

27 (26.7%)

 

Chemotherapy

  

0.740

Given

33 (28.0%)

27 (26.7%)

 

Not given

85 (72.0%)

74 (73.3%)

 

EBRT modality

   

2D-CRT

96 (81.4%)

88 (87.1%)

0.662

3D-CRT

19 (16.1%)

13 (12.9%)

 

IMRT

3 (2.5%)

0 (0%)

 

Abbreviations: 2D-BT, two-dimensional high-dose-rate brachytherapy; 3D-BT, three-dimensional high-dose-rate brachytherapy; WHO: World Health Organization; 2D-CRT = two-dimensional radiotherapy. IMRT = intensity-modulated radiotherapy. 3D-CRT = three-dimensional conformal radiotherapy.

Local and regional control

Local control was defined as no relapsed tumor within 6 months of completion of primary radiotherapy, and local recurrence, which was proven pathologically by biopsy to have local persistence, was failure beyond 6 months. Seven patients in Group B developed local recurrence beyond six months after the completion of the treatment schedule, and none of the patients in Group A developed local recurrence. The five-year actuarial LCS rates for Groups A and B were 100% and 93.1%, respectively (p = 0.024) (Figure 4a). One patient in Group A and one patient in Group B developed regional nodal-involved recurrence. The five-year actuarial LRFS rates in Groups A and B were 99.2% and 92.1% (Figure 4b), respectively; the LRFS curves for the two groups were statistically significant (p = 0.038).
Figure 4

Five-year actuarial survival curves for the 3D-HDR-BT group and the 2D-HDR-BT group. (a) local control survival (LCS); (b) local/regional relapse-free survival (LRFS).

Survival rates

The five-year actuarial OS, DFS, CSS, and DMFS curves between the two groups were determined (Figure 5 a ~ d), and the corresponding rates for Groups A and B were 98.3% and 85.1% (OS, p = 0.063), 97.5% and 86.1% (DFS, p = 0.021), 98.3% and 88.1% (CSS, p = 0.078), as well as 98.3% and 94.1% (DMFS, p = 0.326), respectively. The DFS rates were statistically significant between the two groups. There was a trend toward improvements in other endpoints in Group A, but the difference was not statistically significant between the two groups.
Figure 5

Five-year actuarial survival curves. (a) disease-free survival (DFS); (b) overall survival (OS); (c) cause-specific survival (CSS); and (d) distant metastasis-free survival (DMFS).

Multivariate analyses

All potential prognostic factors, including gender, age (≤45 years; >45 years), T-stage (T1, T2a, T2b), N-stage (0–3) and brachytherapy techniques (the administration of 3D-HDR-BT or 2D-HDR-BT) and EBRT techniques (2D-CRT, 3D-CRT & IMRT) were included in the Cox proportional hazards model by backward elimination of the insignificant explanatory variables. The results of multivariate analyses are summarized in Table 2. The Cox proportional hazards analysis showed that the T category was an unfavorable prognostic variable with regard to LCS, DFS, and LRFS endpoints. Multivariate analysis also showed that the N category was an unfavorable prognostic factor with regard to DFS, OS, CSS, and LRFS. Group A had a lower hazard of LCS than Group B (DFS = 0.232, 95% CI: 0.057 - 0.949, p = 0.042).
Table 2

Summary of multivariate analysis of prognostic factors

 

Factors

B

p-value

Exp (B)

Exp (B) (95% CI)

LCS

T category

2.298

0.005

9.959

1.977 - 50.169

N category

1.460

0.042

0.232

0.057 - 0.949

3D-BT vs. 2D-BT

NS

   

DFS

T category

0.973

0.031

2.647

1.093 - 6.407

N category

2.950

< 0.001

19.113

5.621 - 64.997

3D-BT vs. 2D-BT

NS

   

OS

T category

NS

   

N category

2.625

< 0.001

13.800

4.128 - 46.127

3D-BT vs. 2D-BT

NS

   

LRFS

T category

1.407

0.025

4.083

1.192 - 13.989

 

N category

NS

   
 

3D-BT vs. 2D-BT

NS

   

CSS

T category

NS

   
 

N category

3.106

< 0.001

22.324

6.073 - 82.067

 

3D-BT vs. 2D-BT

NS

   

DMFS

T category

NS

   
 

N category

4.043

< 0.001

57.020

9.307 - 349.347

 

3D-BT vs. 2D-BT

NS

   

Abbreviations: CI, confidence interval; 2D-BT, two-dimensional high-dose-rate brachytherapy; 3D-BT, three-dimensional high-dose-rate brachytherapy; NS, not significant.

Side effects and complications

Toxicity was acceptable for the patients in Groups A and B. Five patients experienced RTOG grade III-IV hematological toxicity; of those patients with N-stage (N2-3) NPC treated with concurrent chemoradiotherapy (DDP 40 mg/m2), three patients experienced grade-III mucositis. Complication rates were similar between Groups A and B when all patients were compared. The most common radiation-related complication was xerostomia. Almost all patients developed xerostomia via large parallel opposed fields. Slight xerocheilia were seen commonly, there was no severe xerocheilia. Total hearing loss, neck fibrosis limiting movement, severe epistaxis requiring blood transfusion, pituitary-endocrine dysfunction, and neurological complications (temporal lobe necrosis and cranial nerve palsy) were not seen in this series. No significant late toxicities were caused by brachytherapy. Complications associated with nasopharyngeal grade-II ulceration/necrosis were observed in three in Group A patients with foul-smelling crust and/or headache, and in two patients in Group B. A total of 19 patients with stage T2b disease experienced small amounts of blood loss in Group A; the average blood loss was approximately 5 cc during the course of the interstitial implantation and removal. All patients were managed with conservative treatment measures and the bleeding was always self-limiting.

Discussion

Carcinoma of the nasopharynx has a propensity to local recurrence, and has always been a challenge to the radiotherapist [1518].With advances in remote-controlled HDR after loading systems and the ease of applicators, the treatment plans can easily be carried out [19].

In the current study, the treatment outcomes of CT-based 3D HDR-BT versus 2D HDR-BT were evaluated in early T-stage NPC patients. CT-based 3D HDR-BT with stepping source provided good coverage of the target volume, and dose distribution optimization. Meanwhile, CT-based 3D treatment planning obtained excellent visualization of the persistent disease and normal structures. A 100% isodose line was selected to cover the entire target as optimally as possible, then manual optimization on each CT slice was done interactively by dragging the 100% isodose line to cover the target volume as conformally as possible in this study. Our experience shows that this CT-based-3D planning approach improved target volume delineation and optimal coverage, and is more accurate and much easier the conventional orthogonal film dosimetry. The follow-up results showed that 3D-HDR BT arm was an effective treatment modality for patients with stage T1-2 NPC with acceptable complications. We speculate the improvement in local tumor control and disease free survival is likely due to improved conformal dose distributions in 3D-HDR BT arms, or may be because of the short follow-up time.

Improved NPC treatment outcomes with 3D-HDR-BT

The results of the current study showed that 3D-HDR-BT after EBRT was more effective in the treatment of T1-2 NPC than 2D-HDR-BT after EBRT, as shown by a statistically significant improvement in LCS and DFS. Conformality can be improved by using the CT-based 3D-HDR-BT treatment plan, and we hypothesized that improvements in LCS and DFS with 3D-HDR-BT were due to the conformal dose distributions [3, 20]. The dose distribution of 3D-HDR-BT can also cover the target for patients whose tumors are associated with the parapharygeal space better.

Retrospective analysis of the two groups showed that five patients with stage T2b disease who developed local recurrence were in the arm of 2D brachytherapy. The role of brachytherapy in patients with stage T2b disease is controversial [9, 21]. Levendag et al. [22] reported that some patients with stage T2b NPC lesions may benefit from dose-escalation by brachytherapy boost when the tumor had regressed to the clinical target volume after EBRT pretreatment. In the current study, when stage T2b NPC patients in Group A were implanted interstitially and the nylon afterloading tubes were placed in the parapharyngeal tissues of the primary tumor site, the 3D-HDR-BT led to enhanced conformal optimization. Local tumor control may be improved by 3D-HDR-BT in patients initially diagnosed with T2b disease, which is in accordance to the report by Rosenblatt E et al. [23] that the addition of an imaging guided brachytherapy boost to external beam radiotherapy significantly improved local tumor control in patients with T1-2 nasopharyngeal carcinoma. None of the Group A patients with stage T2b NPC developed local recurrence, although five Group B patients with stage T2b NPC relapsed.

Unimproved NPC treatment outcomes with 3D-HDR-BT

Despite showing improvements in LCS and DFS, 3D-HDR-BT treatment did not improve the distant control rates of all N category tumors. These results are consistent with a previous study by Leibel SA et al.[24], which showed that nasopharyngeal tumors have a higher probability of micrometastatic dissemination at initial diagnosis, and concluded that the effect of local tumor control on survival cannot be determined without more effective methods to treat disseminated disease.

To determine the effect of local tumor control on distant tumor control, we should detect distant metastases as soon as possible after the initial diagnosis. A study by Chang JT et al.[25] used 18 F-fluorodeoxyglucose positron emission tomography (FDG-PET) and found that 11% of distant metastases in NPC patients were not discovered using the conventional staging workup (CWU). Based on this finding, they suggested that FDG-PET diagnosed stage M NPC disease more accurately and sensitively than CWU. However, the cost of FDG-PET was so high that it was not performed for each patient. Therefore, it was uncertain whether improved local tumor control by 3D-HDR-BT was associated with improved distant tumor control.

Complications

In the current study, the side effects associated with 3D-HDR-BT after EBRT were less severe than some of the toxicity reports associated with conventional dose levels of EBRT alone [26]. Due to the rapid dose fall-off of the radiotherapy source, brachytherapy can deliver a high radiation dose to the parapharyngeal tumor region while delivering a low radiation dose to the pituitary fossa, the optic nerve/chiasm, the temporal lobes, the temporomandibular joint, and the middle ear. Therefore, severe complications were not commonly observed, and the complication rates were similar for the 3D-HDR-BT and 2D-HDR-BT treatment groups. Both 3D-HDR-BT and 2D-HDR-BT treatment modalities can provide highly conformal dose distribution and improved normal tissue sparing. Patients in the 3D-HDR-BT and 2D-HDR-BT groups did not show significant differences in the acute or chronic incidence rates of radiation complications. Mild chronic radiation nasopharyngeal ulceration/necrosis was seen in both groups, which included a foul-smelling crust and/or headache. Many patients experienced xerostomia as a long-term side effect, which may not be due to the brachytherapy. During the long-term follow-up, the only minor complication related to brachytherapy was synechiae of the nasal mucosal linings, which can be treated easily. In future treatment plans, synechiae of the nasal mucosal linings can be reduced using these measures. In the current study, patient mortality was not related to complications.

The interstitial implantation procedure was well tolerated by all stage T2b NPC patients in Group A. Some patients experienced small amounts of blood loss during the course of interstitial implantation. Bleeding was managed with conservative treatment measures and was always self-limiting: no patients required blood transfusions due to excessive bleeding during the course of treatment.

Conclusions

External beam radiation therapy combined with interstitial/intracavitary 3D-image-guided HDR-brachytherapy showed improved local tumor control relative to traditional 2D-HDR-BT with acceptable toxicity levels. The use of 3D-image-guided HDR-BT for stage T2b NPC patients is relatively complex but well tolerated, the administration of interstitial 3D-HDR-BT achieved excellent local control. Improved therapeutic benefits associated 3D-image-guided HDR-BT may be due to enhanced target volume coverage and improved conformality. Prospective, randomized studies should be conducted to further evaluate the therapeutic benefits of 3D-image-guided HDR-brachytherapy for NPC patients.

Notes

Declarations

Acknowledgments

We thank Wei-Jun Ye, Hong-Ying Liu, Yi Ou-Yang, (Department of Radiation Oncology, Sun Yat-sen University Cancer Centre) for contributing patients to the study, assistance with the data management, and logistic support. We thank the Collaborative Innovation Center of Cancer Medicine, Sun Yat-sen University Cancer Centre, for data management, and statistical assistance. We thank our patients and their families for their willingness in this study.

Funding

This work was supported by NSFC Grant Numbers 81172209.

Authors’ Affiliations

(1)
Department of Radiation Oncology, The First Affiliated Hospital, Sun Yat-sen University
(2)
State Key Laboratory of Oncology in Southern China, Department of Radiation Oncology, Cancer Center, Sun Yat-sen University
(3)
Department of Neurosurgery, Binzhou People’s hospital
(4)
Department of Traditional Chinese medicine, The First Affiliated Hospital, Sun Yat-sen University
(5)
Department of Radiation Oncology, the Methodist Hospital

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  27. Pre-publication history

    1. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/14/894/prepub

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This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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