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Journal of Contemporary Brachytherapy
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1/2021
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Original paper

Impact of pre-brachytherapy magnetic resonance imaging on dose-volume histogram of locally advanced cervical cancer patients treated with radiotherapy including high-dose-rate brachytherapy

Keiko Nemoto Murofushi
1
,
Toshiki Ishida
1
,
Keiichiro Baba
1
,
Kenji Kawakita
1
,
Tsukasa Saida Sasaki
1
,
Toshiyuki Okumura
1
,
Toyomi Sato
1
,
Hideyuki Sakurai
1

1.
Department of Radiation Oncology and Proton Medical Research Center, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan
J Contemp Brachytherapy 2021; 13, 1: 32–38
Online publish date: 2021/02/18
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Purpose

For early-stage cervical cancer patients, radical radiotherapy with intracavitary brachytherapy (ICBT) delivering the prescribed dose to point A using Manchester planning methods could achieve a local control (LC) rate of 80-90% [1,2]. However, the LC remains disappointing in cases with bulky and extensive tumors, as ICBT does not administer an adequate dose to the whole tumor [3,4]. In such complex cases, both interstitial brachytherapy (ISBT) and combined intracavitary brachytherapy with interstitial techniques (IC/ISBT) can provide irregularly shaped dose distributions, resulting in an improved LC [5,6,7,8]. Even though, characteristics of tumors, which most likely are to benefit from ICBT vs. ISBT or IC/ISBT remain unclear, and no study has described these before, the appropriate type of brachytherapy could be selected according to tumor characteristics in pre-brachytherapy magnetic resonance imaging (MRI). In our previous study, high-dose-rate (HDR) brachytherapy selection based on pre-brachytherapy MRI findings has achieved an LC rate of up to 90% among patients with locally advanced cervical cancer [9,10]. Furthermore, LC among patients treated with unsuitable brachytherapy, i.e., brachytherapy other than that selected based on pre-brachytherapy MRI findings, was worse than that among patients treated with appropriate brachytherapy (p < 0.01) [10]. However, dose-volume-histogram (DVH) data for the patients treated with ICBT was lacking, as ICBT was performed based on two-dimensional treatment planning. In this study, all types of brachytherapy were planned based on computed tomography (CT); thus, this study aimed to analyze the DVH parameters of three-dimensional ICBT vs. ISBT or IC/ISBT to confirm the appropriate suitability of HDR brachytherapy selection according to pre-brachytherapy MRI findings.

Material and methods

Eligible patients

Between June 2017 and April 2019, 63 patients with locally advanced cervical cancer received definitive HDR brachytherapy. We included patients as per the following criteria: 1) both of pre-treatment and pre-brachytherapy MRI were performed, 2) type of brachytherapy selected according to pre-brachytherapy MRI findings, 3) the Eastern Cooperative Oncology Group performance status of 0-1, 4) no history of pelvic irradiation. Finally, this retrospective study evaluated data of 61 patients. The study’s protocol was approved by our institutional ethics committee.

MRI examinations

Pre-brachytherapy MRIs were obtained within 7 days before patients’ first HDR brachytherapy. Hyoscine butylbromide (Buscopan®; Sanofi, France) was injected intramuscularly to all patients to reduce motion artifact by bowel peristalsis. Pre-treatment and pre-brachytherapy MRI examinations were performed with a 3T system (Ingenia, Philips Medical Systems, Best, The Netherlands), with a phased-array body coil of 32 channels. The field of view was 28 cm, with at least a 256 × 256 matrix. The slice thickness was 3 mm, with a 0.3-mm intersection gap. Sagittal T2-weighted images were perpendicular to the uterine long axis with TR/TE 1400/110 msec, axial T2-weighted images were perpendicular to the uterine short axis with TR/TE 6746/110 msec, and a 24-echo train length was obtained in all cases.

Selection of brachytherapy type

Our previous studies mention more details about selection of brachytherapy type [9,10]. The residual tumor was defined as the high T2WI area on the pre-brachytherapy MRI. IC/ISBT or ISBT were selected for cases with vaginal invasion, bulky asymmetrical tumors, and bulky barrel-shaped tumors based on pre-brachytherapy MRI scans (Figure 1). Vaginal invasion was defined as present in cases with vaginal invasion thicker than 5 mm (* in Figure 1A). Bulky asymmetrical tumors were defined as a tumor defined by two criteria: distance between cervical canal and distal tumor edge (** in Figure 1B) was larger than 2 cm, and [distance between cervical canal and distal tumor edge, **] minus [contralateral tumor distance, †] (Figure 1B) was 1 cm or larger. Bulky barrel-shaped tumors were defined as invading the uterine fundus or with a width of ≥ 5 cm at 3 cm above the external os (‡ in Figure 1C) [10]. ICBT was selected for patients without these findings. The above-mentioned tumor classifications were established by both diagnostic radiologist and a radiation oncologist.

Radiotherapy and brachytherapy protocol

Treatment schedules were divided into two groups, based on the tumor response and extension of the tumor (Figure 2). Good response was defined by tumor shrinkage and/or parametrium invasion mollified after whole-pelvis external beam radiation therapy (EBRT) in the gynecological examination. Poor response was described as an unchanged or grown tumor. Extensive tumor was defined as the tumor, for which further reduction was desired since a prescribed dose could not be administered to high-risk clinical target volume (HR-CTV), even by IC/ISBT or ISBT. In the group 1, a total EQD2 of 60-70 Gy was administered to D90 for HR-CTV, and 70-80 Gy was delivered in group 2. All patients underwent EBRT and HDR brachytherapy. EBRT was administered using a three-dimensional conformal technique with a linear accelerator (Clinac IX; Varian Medical System, Palo Alto, CA, USA) and a 10-MV photon beam. For the International Federation of Gynecology and Obstetrics (FIGO) stage IB-III cervical cancer patients, whole-pelvis (WP)-EBRT was initially administered at a dose of 30 Gy in 15 fractions using four-field technique; an additional dose of 20 Gy in 10 fractions was applied with EBRT, with a 3-cm midline block (MB) and anterior-posterior/posterior-anterior technique. For stage IVA, a dose of 40 Gy in 20 fractions with WP-EBRT, and an additional dose of 10 Gy in 5 fractions with MB were delivered. For the patients with poor response and/or extensive tumors, a dose of 40-50 Gy in 20-25 fractions with WP-EBRT and an additional dose of 0-10 Gy in 0-5 fractions with MB were administered. In cases where a pelvic lymph node had the shortest diameter of ≥ 1 cm, an EBRT boost dose of 6-10 Gy was applied in 3-5 fractions. Brachytherapy was performed using iridium-192 (192Ir) remote after-loading system (MicroSelectron HDRTM; Nucletron, Veenendaal, The Netherlands), and the first HDR brachytherapy treatment was performed within 7 days after midline block insertion. Brachytherapy schedule was decided based on FIGO stage, tumor response, and extension of the tumor as shown in Figure 2. ICBT was administered once per week, at a dose prescribed to D90 for HR-CTV of 20-24 Gy in 4 fractions (Figure 3A). IC/ISBT was used to deliver a dose of 20-24 Gy in 4 fractions (prescribed as D90 to HR-CTV) once per week using tandem-ovoid applicators and 1-3 transvaginal needles (Figure 3B). During ISBT, Martinez universal perineal interstitial template was used to deliver a dose of 14-30 Gy in 2-5 fractions on 1-3 consecutive days (prescribed as D90 to HR-CTV) (Figure 3C). CT-based brachytherapy planning was performed using Oncentra version 4.0 (Nucletron) and a bright speed excel CT scanner (General Electric Healthcare, Chicago, IL, USA). Image acquisition was performed with tube voltage of 140 kVp, rotation time of 1.0 s, detector configuration of 4 × 0.5 mm, pitch of 0.75, a slice thickness of 2.5 mm, display field-of-view of 450 mm, and standard reconstruction kernel. The dose was calculated using the Oncentra system without applying a heterogeneity correction according to the American Association of Physicists in Medicine Task Group 43 protocol [11]. In the guidelines reported by the Groupe Européen de Curiethérapie and the European Society for Radiotherapy and Oncology (GEC-ESTRO), HR-CTV includes residual tumor at the time of brachytherapy, whole cervix, and adjacent residual pathologic tissue [12]. In this study, the HR-CTV included the macroscopic residual tumor with high signal intensities on T2-weighted images (T2WI) in the pre-brachytherapy MRI, the tumor extension recognized by gynecologic examination, and the entire cervix. An image diagnostician defined the macroscopic residual tumor detected in the pre-brachytherapy MRI, and a radiation oncologist finally defined HR-CTV based on the findings of a gynecologic examination.

Chemotherapy

The indications for concurrent chemoradiotherapy (CCRT) were as follow: 1) FIGO stage IIB or higher, 2) cervical tumor size of 4.0 cm or more, and 3) positive pelvic and/or para-aortic lymph nodes. During the radiotherapy period, patients generally received a weekly regimen of cisplatin (40 mg/m2). CCRT was not performed for patients with insufficient renal function or for those, who were ≥ 75 years old. Ultimately, seven patients received radiotherapy alone and 54 patients received CCRT.

Statistical analysis

For the dose summation of brachytherapy plus EBRT before the insertion of MB, the equivalent dose in 2 Gy fractions (EQD2) was calculated, based on the linear-quadratic model [13]. The tumor dose was calculated using an α/β ratio of 10 Gy. For calculating the dose-volume parameters of organ at risk (OAR) (i.e., D2.0cc), the α/β ratio was assumed to be 3 Gy. The relative proportion was defined using the following formula: Categorical variables were described as frequency and percentages, and continuous variables were defined using mean, median, and interquartile range (IQR) values. To compare dose of whole-pelvic irradiation, DVH data, and relative proportion of HR-CTV and OARs between ICBT and ISBT plans, means for continuous variables were compared using Student’s t-test if the data were normally distributed; otherwise, Mann-Whitney test was applied. The normality of data was assessed with Kolmogorov-Smirnov test. Statistical significance was defined as p < 0.05. All statistical analyses were performed using SPSS Base System software program version 24.0.0.0 (SPSS, Chicago, IL, USA) and SAS software version 9.4 (SAS Institute, Cary, NC, USA). Although, the analyses were not adjusted for multiple comparisons, and given the potential for type I error, our findings should be interpreted as exploratory and descriptive.

Results

Patients’ and tumor characteristics are presented in Table 1. The median tumor size at pre-brachytherapy MRIs was 38 mm (range, 0-79 mm). In the pre-brachytherapy MRI, 13 patients had a tumor with severe vaginal invasion, 15 presented with an asymmetrical tumor, and 4 had a bulky barrel-shaped tumor. Four patients had an asymmetrical tumor with severe vaginal invasion, and 2 had an asymmetrical tumor with a bulky barrel-shape. Finally, 26 patients (43%) were treated with IC/ISBT (6 patients, 10%) or ISBT (20 patients, 33%). The remaining 35 patients (57%) received ICBT. Group 1 with good tumor response included 35 patients treated with ICBT, and 15 patients treated with IC/ISBT or ISBT. Group 2 with poor tumor response and/or extensive tumor included 0 and 11 patients, respectively. The median dose of whole-pelvis EBRT for IC/ISBT or ISBT-treated patients (40 Gy) was significantly higher than that for ICBT-treated patients (30 Gy, p < 0.01).
Table 2 shows volume of HR-CTV and DVH parameters. The median EQD2 of HR-CTV D90 was 70.8 Gy (IQR, 66.8-73.5 Gy) for all patients. The EQD2 of HR-CTV D90 was significantly higher (p < 0.01) in the IC/ISBT- or ISBT-treated patients than in the ICBT-treated patients, although the median volume of HR-CTV was more than doubled. Figure 4 indicates the relationship between volume of HR-CTV and HR-CTV D90. In the patients treated with ICBT, the median EQD2 of HR-CTV D90 was 70 Gy (IQR, 67.3-72.2 Gy) and 66.7 (range, 65.0-68.8) for the volume of HR-CTV ≤ 30 cc and HR-CTV > 30 cc, respectively (p = 0.76). In only one patient treated with IS/ICBT, the HR-CTV volume was 30 cc or smaller. There were no significant differences in the EQD2 of D2cc to the bladder or sigmoid colon between IC/ISBT- or ISBT- and ICBT-treated patients (p = 0.90, p = 0.08, respectively). However, the EQD2 of D2cc to the rectum of IC/ISBT- or ISBT-treated patients was significantly higher than that of ICBT-treated patients (p < 0.01). Moreover, no patients received doses to the OARs in excess of doses recommended by the American Brachytherapy Society (ABS) (bladder, 90 Gy; sigmoid and rectum, 75 Gy) [14]. The relative proportions of HR-CTV and OARs are demonstrated in Figure 5. In the ICBT-treated patients, the relative proportion of HR-CTV was higher than that of IC/ISBT- or ISBT-treated patients (p < 0.01); however, the median relative proportion exceeded 100% in both treatment groups. The relative proportions of bladder and rectum in the IC/ISBT- or ISBT-treated patients were significantly lower than those in the ICBT-treated patients (p < 0.01, p ≤ 0.01, respectively).

Discussion

For cervical cancer patients, dose delivered to HR-CTV was considered as a surrogate marker for local control [5,15]. in this study, the median EQD2 of HR-CTV D90 (70.8 Gy, IQR, 66.8-73.5 Gy) was much lower than that recommended by the Groupe Européen de Curie­thérapie, the European Society for Radiotherapy and Oncology (GEC-ESTRO), and the ABS [14,16]. However, a Japanese protocol with a lower dose over a shorter treatment time has demonstrated comparable outcomes of concurrent chemoradiotherapy delivering an EQD2 of 62-65 Gy to point A comparing with that demonstrated in studies from the United States and European countries [17]. In fact, Murakami et al. have shown that in the Japanese protocol, the dose of 60 Gy or greater for HR-CTV D90 resulted in 3-year LC at 97.3% [15]. Also, Ohno et al. reported 5-year LC rate of 96% for FIGO stage IB-IVA cervical cancer patients and in 90% of them, greater than 60 Gy was delivered to HR-CTV D90 [18]. In this study, the dose of 60 Gy or greater can be administered to HR-CTV D90 for both treatment groups. Therefore, it was estimated that more than 90% of LC might be obtained for the patients with severe vaginal invasion, bulky parametrial extension, or bulky tumor.
Most patients treated with IC/ISBT or ISBT, received a dose of 40 Gy or more with WP-EBRT, because this treatment schedule was applied for the patients with FIGO stage IVA, poor response, and/or extensive tumor. Furthermore, the total EQD2 delivered to the patients treated with IS/ICBT or ISBT was higher than that in the ICBT group; however, there was no significant difference in the EQD2 of D2cc to the bladder between two treatment groups, and no patients exceeded the ABS recommended dose [14]. This was probably due to a higher relative proportion of bladder in the patients treated with ICBT. The EQD2 of D2cc to the rectum in the patients treated with IS/ICBT or ISBT (median, 64.3 Gy, IQR, 59.4-65.5 Gy) was significantly higher than that in patients treated with ICBT (median, 56.8 Gy, IQR, 53.3-58.8 Gy). It had been reported that for patients treated with ICBT or IS/ICBT, mean EQD2 of D2cc to the rectum was 61.8-66.3 Gy [5,19], and EQD2 of D2cc for a 10% probability for overall rectum grade 2 or more morbidity was 69.5 Gy [20]. In this study, the EQD2 of D2cc to the rectum in the patients treated with IS/ICBT or ISBT was not considered extreme high, and all cases remained within the doses recommended by the ABS [14]. The reasons for such a significant difference might be higher doses with WP-EBRT and total EQD2 administering to most patients treated with IC/ISBT or ISBT as well as severe vaginal invasion required to include the entire vagina in HR-CTV for 13 patients (50%), regardless of a lower relative proportion of rectum in the ICBT patients.
Previous studies have shown that IS/ICBT was performed in 4% to 65% of patients with locally advanced cervical cancer, where it was able to deliver adequate dose to the entire tumor [5,18,19]. The MRI-guided brachytherapy in locally advanced cervical cancer (retroEMBRACE and EMBRACE I) studies had divided participating institutions into IC and IS/IC groups, according to technique of brachytherapy. The IS/IC group included centers performing IS/ICBT consistently in > 20% of patients. In the retroEMBRACE study, LC improved by 10% in patients with CTV ≥ 30 cc in the IS/IC group [5]. The EBRACE I study has shown that IS/ICBT was performed in 91% of patients with parametrium involvement [19]. Jastaniyah et al. reported that IS/ICBT was frequently used in patients with large tumor, tumor with poor response or tumor involvement to distal parametrium, or pelvic wall in MRI at the time of brachytherapy [20]. While the criteria for selecting IS/ICBT technique were continuing to discuss in these studies, IS/ICBT was typically performed in patients with large tumors and extensive parametrial and/or vaginal involvement [5,18,20,21]. However, IS/ICBT or ISBT might not be performed for all these tumors in facilities, where IS/ICBT or ISBT were not routinely performed. In a questionnaire-based survey regarding image-guided adaptive brachytherapy, limited number of staff and time were major impediments for performing image-guided adaptive brachytherapy [22]. Under these circumstances, in order to secure the staff and time in advance by selecting appropriate type of brachytherapy before starting the procedure, may lead to more frequently performed IS/ICBT or ISBT, resulting in an improved LC. It was more desirable that an appropriate brachytherapy could be selected according to the findings from pre-treatment MRI. Although Palhares et al. reported that large tumor at pre-treatment MRI (not pre-brachytherapy MRI) could predict to deliver inadequate dose to HR-CTV by using ICBT [23], in a previous study, 46-57% of patients with pre-treatment MRI-evaluated severe vaginal invasion, asymmetrical tumor, or bulky primary tumor received IS/ICBT or ISBT, which were selected according to the findings of pre-brachytherapy MRI; tumor characteristics in pre-treatment MRI were not prognostic factors for LC [10]. Thus, pre-brachytherapy MRI was suitable to select an appropriate brachytherapy method rather than pre-treatment MRI.
Recent studies [5,19,20,21,23] demonstrated that tumor characteristics were most likely to benefit from ISBT or IC/ISBT in pre-treatment, pre-brachytherapy MRI, or MRI at the time of brachytherapy; however, type of brachytherapy was not selected according to their criteria before their first brachytherapy. In this study, IS/ICBT or ISBT selected according to the findings in pre-brachytherapy MRI were performed in 26 patients (43%), and HR-CTV with a mean volume of 62.7 cc (IQR, 46.5-79.7 cc) was administered as the adequate dose (median D90 of 73.7 Gy, IQR, 70.9-75.1 Gy). Among the patients treated with ICBT, there was no significant difference in EQD2 of HR-CTV D90 between HR-CTV volume of ≤ 30 cc and > 30 cc (p = 0.76), and ICBT could administer the adequate dose to the tumor, which had no extensive involvement and was larger than 30 cc, while providing tolerable doses to the OARs. Therefore, our selection criteria according to pre-brachytherapy MRI findings were effective in selecting suitable candidates for HDR brachytherapy, and might lead to LC improvement also at facilities, where IS/ICBT or ISBT are not routinely performed. This study’s limitations include its single-center retrospective design. Further prospective multicenter studies are needed to evaluate the suitability of selection criteria based on pre-brachytherapy MRI.

Conclusions

Pre-brachytherapy MRI may help to select suitable candidates for HDR brachytherapy and deliver the recommended doses to tumor and OARs, in particular, in cases with large tumors, severe vaginal invasion, asymmetrical tumors, and/or corpus invasion.

Acknowledgements

This research was supported by the University of Tsukuba. Statistical analysis was supported by Makoto Saito, MS.

Disclosure

The authors report no conflict of interest.

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Copyright: © 2021 Termedia Sp. z o. o. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
 
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