J Cancer 2018; 9(9):1635-1641. doi:10.7150/jca.23974 This issue
Department of Radiation Oncology, Xijing Hospital, The Fourth Military Medical University, 17 Changle Western Road, Xi'an 710032, China
* These authors contributed equally.
Purpose: To report the efficacy and late side effects(LSEs) of CT-based image-guided brachytherapy for the treatment of cervical cancer.
Materials: Between 2008 and 2014, 100 patients with FIGO stage IIB-IVA cervical carcinoma were analyzed. The patients received pelvic irradiation (45-50 Gy in 25 fractions) with concurrent chemotherapy, whereas the mean prescribed EBRT dose, including initial and boost doses to positive lymph nodes, ranged from 54 to 64 Gy. Afterwards, intracavitary(IC) or combined intracavitary/interstitial(IC/IS) brachytherapy was performed using a CT-based procedure with prescribed doses of 6 or 8 Gy in 3-7 fractions.
Results: The median follow-up time was 46 months. The 5-year local control, distant metastasis-free survival, and overall survival rates were 88.9%, 81.8%, 77.9%, respectively. IC/IS brachytherapy improved the HR-CTV D90 compared with IC (p<0.01). Seven patients (7.0%) had grade 2 bladder LSEs and none had grade 3/4 bladder LSEs. There was no significant relationship between bladder LSEs and the dose-volume histogram (p>0.05 for all). Thirty-seven patients (37%) had grade 2 rectal LSEs, 3(3%) had grade 3 rectal LSE. The rectum D1cc, D2cc, and D5cc values were significantly higher in patients with grades 2/3 rectal toxicity than in those with grades 0/1 (p<0.05 for all). There was no grade 2 and above small bowel LSEs.
Conclusions: CT-based brachytherapy planning can achieve excellent local control with acceptable morbidity. HR-CTV D90 can increase in the IC/IS group compared with the IC group. The D1cc, D2cc, and D5cc all showed excellent predictive values for rectal LSEs.
Keywords: cervical cancer, dose-volume histogram, brachytherapy, late side effects, computed tomography
A combination of external beam radiotherapy (EBRT), concurrent cisplatin-based chemotherapy, and brachytherapy is the standard treatment for locally advanced cervical cancer. Brachytherapy provides a high dose of radiation to the area of disease while sparing the surrounding normal structures. Accordingly, prospective trials that compared 2D and 3D brachytherapy have shown that the latter method exhibits improvements in both toxicity and local control rates[2, 3]. The Groupe Européen de Curiethérapie (GEC) and the European Society for Radiotherapy and Oncology (ESTRO) jointly published guidelines for magnetic resonance imaging (MRI)-based planning of intracavitary (IC) brachytherapy in cervical cancer. They recommended reporting dose-volume histogram (DVH) parameters for OARs in small volumes such as D0.1cc (the minimal dose evaluated in the most exposed 0.1 cc of the organ) and D2cc [4, 5].
It is reported that MRI is more reliable than computed tomography (CT) for demarcating the tumor and tumor-involved parametrium in patients with cervical cancer. However, MRI equipment is either located too remotely or is entirely unavailable to some radiation oncology clinics. The adoption of MR-guided brachytherapy in developing countries still has many difficult in access and expense. Since CT simulators are increasing availability in Radiation oncology departments, CT brachytherapy planning has been showed in many studies to be feasible since 2007[7-9].
CT-based brachytherapy optimizes treatment by enabling physicians to decrease the dose to critical organs such as the bladder and bowel, while it can also prescribe the dose to point A or to the high-risk clinical target volume (HR-CTV). This allows for dose escalation to the tumor while maintaining safe doses to the OARs. Since most of the consensus regarding 3D brachytherapy has been achieved based on MRI, analyze the relationship between brachytherapy DVH parameters and clinical outcomes using CT-based planning should be more explored with sufficient follow-up periods.
In this study, we analyzed the CT-guided brachytherapy in a large cohort of patients with locally advanced cervical cancer to investigate clinical outcomes, toxicities, and dosimetric finding of this method.
Between January 2008 and December 2014, all primary cervical cancer patients treated with curative intent at our center and received CT-based brachytherapy with new plan for every time were included in this study. All patients on this study had no-metastatic disease and staged according to International Federation of Gynecology and Obstetrics (FIGO) classification. The study was approved by the local Institutional Review Board. Prior to RT, all patients underwent a pelvic examination, chest radiography, and pelvic MRI with/without CT.
The EBRT was performed using 3D conformal radiation and the entire pelvic irradiation dose was 45-50 Gy in 25 fractions with concurrent cisplatin (40 mg/m2 per week), whereas the mean prescribed EBRT dose, including initial and boost doses to positive lymph nodes, ranged from 54 to 64 Gy. After patients had completed 36-40 Gy in 18-20 fractions, they underwent MRI to evaluate the therapy's effect unless they were not suitable, in which case CT with contrast was performed instead.
After completing EBRT, IC, interstitial (IS), or combined IC/IS brachytherapy was performed using a CT-based procedure. The prescribed doses were 6 or 8 Gy in 4-7 fractions (doses ranged from 24 Gy/3 fractions to 42 Gy/6 fractions) once or twice a week. The brachytherapy applicator was inserted under surface anesthesia. Patients were treated with a high-dose-rate iridium-192 source according to a treatment planning system (Nucletron Systems, Veenendaal, The Netherlands). Proper preparation of the bowel and bladder was conducted before CT-based. On the day before brachytherapy, a soaking solution with folium sennae was ingested to completely empty sigmoid and rectum. On the treatment day, 100-120 mL saline was instilled into the empty bladder before the CT scan and BT implementation. The CT-compatible Nucletron Standard tandem-ovoid applicator was inserted and the vagina was packed with gauze to fix the applicator and to increase the distance between the radiation source and the rectum and bladder. IS needles were used in patients with large tumors and poor responses to EBRT. The pelvic transverse images were acquired using a CT simulator (Philips Medical Systems, Cleveland, USA) and transferred to a treatment planning system. The slice thickness of the CT scan was 3 mm, the upper border was crista iliaca while the lower border was at a level 3 cm below the ischial tuberosity. Based on the CT-standardized contour report, reference MRI image, and Gynecological GEC ESTRO working group recommendations[4, 11], the HR-CTV, intermediate-risk clinical target volume (IR-CTV), and OARs (intestine, rectum, sigmoid, and bladder) were contoured via CT. The HR-CTV included the entire cervix and the macroscopic extent of the tumor at brachytherapy plus any residual tissue in the parametria. The IR-CTV encompassed either the tumor extension at diagnosis or a 1 cm margin around the HR-CTV. The outer walls of the OARs were delineated according to the GEC-ESTRO protocol. The rectum was contoured from the anorectal junction to the rectosigmoid flexure. The sigmoid colon delineation commenced at the rectosigmoid and ended 2 cm above the uterus (unless the descending colon started below this level, in which case the sigmoid colon was delineated cranially up to the transition into descending colon). Small bowel loops lying in the vicinity of the uterus were delineated. The plan for the HR-CTV was calculated by using the treatment planning system and then implemented using the Nucletron system.
The doses delivered to the organs at risk were evaluated using the DVH parameters D0.1cc, D1cc, D2cc, and D5cc, representing the minimum dose calculated at the most irradiated 0.1, 1, 2, and 5 cc volumes, respectively. All doses reported here are based on the total (EBRT plus brachytherapy) and were converted into the biologically equivalent dose in 2 Gy fractions (EQD2). EQD2 used the linear quadratic model with α/β=10 Gy for the tumor and α/β=3 Gy for the OARs.
Patients were reviewed at 1 and 3 months after treatment for the resolution of acute side effects. Subsequently, they received follow-up at 3-6 month intervals by a radiation oncologist and gynecologist. A pelvic examination, ultrasound, CT or MRI, were performed at every visit. Complete response was determined on pelvic examination and imaging results. If abnormalities were found, biopsies were acquired as appropriate. The treating physician according to Radiation Therapy Oncology Group criteria graded acute or late toxicities and the highest grade was recorded. Any intervention required by the patient owing to toxicity was also recorded.
Clinical outcome after radiotherapy ±chemotherapy and image-guided adaptive brachytherapy. (a) Local control, Distant metastasis-free survival and overall survival for all 100 patients. (b) Distant metastasis-free survival for stage IIB, IIIB, IVA. (c) Overall survival for FIGO stages IIB, IIIB, IVA.
Statistical analysis was conducted using SPSS 18.0 (SPSS, Chicago, IL, USA). Treatment failures were sorted according to the site(s) of first tumoral relapse and were defined as local (cervix, vagina, parametria), pelvic node and distant metastases. Time intervals for local control rate (LC) and distant metastasis-free survival (DFS) and overall rate (OS) were calculated from the date of completion of radiotherapy to the date of event or the last time follow-up. LC, DFS and OS all were calculated using the Kaplan-Meier method. The measurement data, including DVH parameters, were compared by analysis of variance (ANOVA) or t-test, whereas categorical data (such as the LSE grade) were compared by using the chi-square test.
Between 2008 and 2014, 100 patients with FIGO stage IIB-IVA cervical carcinoma were analyzed. The patient and tumor characteristics were shown in Table 1. The median follow-up was 46 months (range: 3-107 months). The tumor diameters in 51 patients (51%) were larger than 5 cm. The tumors in all patients were of squamous cell carcinoma histology (Table 1).
Patient and tumor characteristics (N=100)
|Age at primary diagnosis (years)||Median: 49 (range: 30-73)|
|Tumor diameter (cm)||Mean: 4.7 (4.7±1.8)|
|Tumor stage (FIGO stage*)|
|Squamous carcinoma||100 (100%)|
|Combined intracavitary/interstitial||52 (52%)|
|Overall treatment time (days)|
|Follow-up period (months)||Median: 46 (range: 3-107)|
*FIGO: International Federation of Gynecology and Obstetrics
Pelvic recurrence discovered in 10 patients. Moreover, 17 patients experienced distant metastasis and 22 died (the 5-year LC, DFS and OS were 88.9%, 81.8%, 77.9%, respectively) (Figure 1a).
The 5-year LC rates were 100% for patients with stage IIB, 84.2% for those with stage IIIB, and 100% for those with stage IVA disease. The 5-year DMFS rates were 86.3% for patients with stage IIB, 81.8% for those with stage IIIB, and 66.7% for those with stage IVA (Figure 1b). The 5-year OS rates were 86.3% for patients with stage IIB, 77.8% for those with stage IIIB, and 50% for those with stage IVA disease (Figure 1c).
The mean (±standard deviation) D90 values for the HR-CTV and point A were 84.8±11.6 Gy and 74.3±12.9 Gy, respectively.
Combined IC/IS brachytherapy was used in 52% of the patients. Patient related characteristics of the IC and IC/IS groups were summarized in Table 2. Patients related factors including the age, FIGO-stage, D2cc for organ at risk (OAR), and treatment time were equally distributed within the two groups. There were no significant differences in D2cc for small bowel, bladder and rectum between the two groups (p=0.47, 0.34, 0.20, respectively). Univariate analysis showed no different between bladder and rectum late morbidity of the two groups.
The D90 dose were 89.29±10.9 and 79.96±10.45 for IC/IS and IC group, respectively (p<0.01). LC in the IC/IS group was 91.6% at 4-year compared to 86.3% at 4-year in the IC group. Though Local control was about 5% higher in the IC/IS group compared with the IC group, this difference was not significant (p=0.45).
Clinical parameters and treatment outcomes between IC and IC/IS group
|Characteristic||IC group(n=48)||IC/IS group(n=52)||p-value|
|Diameter of the tumor (cm)|
|Tumor stage (FIGO stage)|
|D2cc for OAR|
|Small bowel D2cc||61.23±7.45||60.14±7.56||0.47|
|Rectum D 2cc||73.55±6.54||71.84±6.69||0.20|
|Overall treatment time (days)|
Thirty-seven patients (37%) were found to have grade 2 rectal LSEs, 3 (3%) had grade 3, and none had grade 4. The most common events reported in patients with grade 1 LSE were slight diarrhea and abdominal pain. Patients with grade 2 LSEs experienced similar symptoms as well as intermittent bloody stool. Most patients with grade 2 LSEs were treated with mesalazine. All events reported in patients with grade 3 LSEs were continuous bloody stool requiring transfusion of red cells. None of the patients had fistulas. The mean D0.1cc, D1cc, D2cc, and D5cc doses to the rectum in all patients were 83.5±9.2, 75.9±7.3, 72.6±6.6, and 67.4±6.2Gy, respectively. The D1cc, D2cc, and D5cc values were significantly higher in patients with grade 2/3 rectal toxicity than in those with grade 0/1 (p=0.03, p=0.02, and 0.02, respectively), while the D0.1cc value was not significantly different (p=0.05). The mean D2cc to the rectum in patients with grade 2/3 rectal LSEs was 74.5±5.6 Gy. The estimated probability of grade ≥2 rectal LSEs according to the dose-volumetric parameters are shown in Figure 2.
The estimated probability of grade ≥2 rectal LSE according to the dose-volumetric parameters (D0.1cc, D1cc, D2cc, and D5cc).
The patient characteristics that we investigated, including age, tumor diameter, overall treatment time, IC vs IC/IS, and fraction schedule, showed no significant association with the occurrence of rectal LSEs (Table 3). The median interval from the time of completion of radiotherapy to the onset of rectal LSEs was 11 months (range: 1-45 months) and the median last duration was 12 months (range: 1-33 months).
Seven patients (7.0%) had grade 2 bladder LSEs, while none had grade 3/4 LSEs. The median interval from the time of radiotherapy completion to the onset of bladder LSEs was 12 months (range: 3-17 months). The median last duration was 6.6 months (range: 1-17 months). The mean D0.1cc, D1cc, D2cc, and D5cc values for all the patients with bladder LSEs were 83.7±10.2, 76.1±8.7, 72.8±8.1, and 66.7±6.9 Gy, respectively. There was no significant relationship between LSEs and the DVH (p=0.307, 0.248, 0.227, and 0.181, respectively).
Relationship between rectal late side effects and clinical parameters
|Characteristic||Grade 0-1||Grade 2-3||p-value|
|Diameter of the tumor (cm)|
|Overall treatment time (days)|
In our study, we limited the dose to the small bowel to below 64 Gy in all patients. The mean D0.1cc, D1cc, D2cc, and D5cc values to the small bowel were 67.4±11.5, 62.44±8.4, 60.66±7.5, and 57.3±5.5 Gy, respectively. At baseline, none of the patients reported chronic small bowel morbidity. Moreover, 80 patients (80%) reported no small bowel morbidity at any time during the follow-up period (grade 0), while 20 patients (20%) had grade 1 LSEs. The most common events reported were slight diarrhea and discontinuous abdominal pain.
Several studies have compared dose distributions between conventional radiography-based planning and 3D treatment planning using CT or MRI. All have shown that 3D optimizations can improve tumor target dose coverage while maintaining a safe dose to the OARs[11-17]. Although MRI provides a better delineation of the tumor and involved parametria, it is not readily available to many institutions. CT is the most commonly utilized imaging modality for 3D planning of brachytherapy in developing countries. In a study which compares the consensus of CT contours based CT and MRI based brachytherapy, it shows the large volume on CT for all 3 case and there is no significant different in D2cc OAR or D90 between CT and MRI. Our study showed with long follow up excellent local control and OS for CT-guided brachytherapy planning using the GEC-ESTRO guidelines for delineation. Moreover, late toxicity was low following adequate bowel and bladder preparation as well as proper plan optimization.
Our study showed excellent clinical outcomes in terms of 5-year LC, DMFS, and OS. The clinical local control rates comparable to those in previous studies of CT or MRI-based brachytherapy. Wang et al. also showed excellent clinical outcomes following CT-based brachytherapy planning for cervical cancer patients. With median follow-up of 15 months, 2 of 20 patients experienced local failure and 1 showed internal iliac nodal metastasis. A recent study by Agnieszka et al. investigated 216 cervical cancer patients who underwent CT-based brachytherapy. The 5-year OS and disease-free survival rates were 66.4% and 58.5%, respectively. In 2007, Pötter et al. reported 145 Austrian patients treated with MRI-based image-guided high-dose-rate brachytherapy using a tandem-ring applicator, where they achieved a local control rate of 88% for the true pelvis at 3 years, as well as an OS rate of 68%. Ribeiro et al. investigated 170 patients who underwent MRI or CT-based brachytherapy, and found a 5-year OS rate of 65% and a local control rate of 81%.
In our study, only 10 patients experienced local recurrence, this may be because 52% of our patients underwent IC/IS treatment. The introduction of IC/IS applicators has made possible dose distributions with higher conformity, especially for eccentric cervical tumors. In our study, we implemented IC/IS treatment for patients with persistent or eccentric tumors. The mean D90 was significantly higher in the IC/IS group compared to the IC-only group. Though Local control was about 5% higher in the IC/IS group compared with the IC group, the difference was not significant (p = 0.52). However, this difference was not significant (p=0.52), this maybe because the small size of patients. Additionally, there were no increases in grade 2/3 rectal LSEs when IS needles were used. These findings were consistent with previous study which found combined IC/IS brachytherapy enabled tumor-specific dose escalation and resulted in significantly better local control in large tumors, without increased treatment-related late morbidities. For the recurrent cervical cancer, cisplatin and paclitaxel may be the acceptable chemotherapy regimens.
In our study, 37% and 3% of the patients experienced grade 2 and grade 3 rectal LSEs, respectively. There were no grade 4 LSEs. Additionally, the D0.1cc, D1cc, D2cc, and D5cc doses to the rectum were shown to be predictive of LSEs, as was reported in a previous study. In our investigation, the D2cc to the rectum in most patients was limited to 75 Gy, which was in accordance with the recommendation of the Gynecological GEC-ESTRO working group. The mean rectal D2cc was 72.6±6.6 Gy. The rectal toxicity rates were comparable to those in previous CT or MRI-guided brachytherapy studies (Table 4)[9, 19, 25, 26]. However, Beant et al reported a gastrointestinal or genitourinary LSE rate of only 0.9% for grade 3 or above at 2 years. This may be because the use of intensity-modulated radiotherapy in their series decreased the incidence of long-term toxicity. Our study also suggested that the D5cc may be another powerful factor in predicting rectal LSEs, which was consistent to previous finding.
Comparison of late toxicity rates among studies using computed tomography or magnetic resonance imaging planning for brachytherapy
|Study||Patients (n)||Follow-up (years)||CT or MRI guided||Grade 3 bladder toxicity (%)||Grade 3 rectal toxicity (%)|
|Tan et al.||28||3||MRI||0||11|
|Pötter et al.||189||3||MRI||2.9||6.1|
|Vicky et al.||95||3||MRI||2||11|
|Ribeiro et al.||170||3||MRI or CT||6||5|
|Agnieszka et al.||216||4||CT||3.3||6|
In our study, we limited all the bladder D2cc values to under 78 Gy since the bladder has a higher tolerance to radiation, and the mean D2cc to the bladder was 72.8±8.1 Gy. Only 7 patients experienced grade 2 bladder LSEs, while none experienced grade 3 or above LSEs. Petra et al. investigated 141 cervical cancer patients for bladder side effects, and observed a significant dose effect for all DVH parameters as related to grade 2 complications. We found no significant relationship between bladder LSE and DVH, this may have been attributable to the lower incidence of LSE grades ≥2 in our study.
To date, there are few reports on dose-volume effect relationships for the small bowel. Petit et al. found that small bowel D0.1cc, and D2cc were not predictive of late small bowel morbidity. In our study, the mean D2cc to the small bowel was 60.66±7.5 Gy, there were no grade 2 and above LSEs. However, because we limited the dose to the small bowel to <64 Gy in all patients, the highest-tolerated dose for the small bowel is still unclear. Furthermore, the dose-effect relationships are yet to be established for the sigmoid.
The advantage of this study was the large cohort size as well as the long follow-up times that produced mature results. To our knowledge, there are relatively few studies that have investigated the relationship between DVH parameters and efficacy, as well as late toxicities to OARs, using CT-based brachytherapy. A limitation of this study, however, is its retrospective nature.
CT-based brachytherapy for the treatment of locally advanced cervical cancer results in high local control rates and excellent OS. The DVH parameters can predict the incidence and grades of LSEs. There was no grade 3 bladder LSEs when the mean D2cc was 72.8 Gy. The mean rectal D2cc in our patients with grade 2/3 rectal LSE was 74.5±5.6 Gy. Moreover, a mean D2cc of 60.6 Gy to the small bowel was deemed safe.
This work is supported by the grants from National Natural Science Foundation of China (No. 81272346).
The authors have declared that no competing interest exists.
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Corresponding author: Li-Chun Wei and Mei Shi, Department of Radiation Oncology, Xijing Hospital, The Fourth Military Medical, University, 17 Changle Western Road, 710032, China. Tel +86-29-8477 5425; Fax +86-29-8477 5425; Email: weilichunedu.cn (LCW) and mshifmmucom (MS)