Intravesical Radiofrequency-Induced Chemohyperthermia for Carcinoma in Situ of the Urinary Bladder: A Retrospective Multicentre Study
Abstract
Objective:
To examine the effect of intravesical radiofrequency-induced chemohyperthermia (RF-CHT) in carcinoma in-situ (CIS) patients overall and split according to previously received therapy.
Methods:
CIS patients that underwent an induction and maintenance phase of≥6 RF-CHT instillations, and had either pathology or cystoscopy plus cytology available at 6 months of follow-up were retrospectively included. Complete response (CR), recurrences, cystectomy-free rate, overall survival (OS), and adverse events were evaluated. Analysis was performed for overall, bacillus Calmette-Guérin (BCG)-unresponsive, other BCG-treated, and treatment naïve patients.
Results:
Patients (n = 150) had a mean of 17.5, 9.2, or 0 previous BCG instillations in the BCG-unresponsive (n = 50), other BCG-treated (n = 46, missing n = 4), and treatment naïve groups (n = 47, missing n = 3), respectively. After 6 months, a CR of 46.0%, 71.7%, and 83.0% was found (p < 0.001). Subsequent 2-year recurrence rates were 17.4%, 27.3%, and 12.8%, respectively. The overall cystectomy-free rate and OS at mean follow-up (35.8 months) were 78.5% and 78.0%, respectively. These were 71.4% vs. 84.1% vs. 86.7% (cystectomy-free rate, p = 0.006) and 76.0% vs. 69.6% vs. 87.2% (OS, p = 0.06) for BCG-unresponsive vs. other BCG-treated vs. treatment naïve patients. Progression to muscle-invasive disease was seen in 13.3% of patients. Patients stopped induction or maintenance RF-CHT instillations due to adverse events in respectively 13.4% and 17.8%.
Conclusions:
Intravesical RF-CHT showed good results in both treatment naïve and BCG-treated CIS patients, avoiding the need for cystectomy in 78.5% of cases for at least 3 years with a modest risk of progression. Thus, RF-CHT proves an alternative to cystectomy in selected high-risk patients.
INTRODUCTION
Urothelial cell carcinoma in-situ (CIS) of the urinary bladder is a relatively uncommon finding in patients with non-muscle-invasive bladder cancer (NMIBC), with less than 10% of cases having associated CIS [1]. However, due to the high number of patients with bladder cancer and its high recurrence rate, urothelial CIS is still associated with a significant prevalence [2, 3]. Urothelial CIS is a non-papillary high-grade form of NMIBC. Unlike most intraepithelial carcinomas in other organs, CIS of the urinary tract is – with a hazard ratio of 1.46 – at high risk of progression to muscle-invasive disease (MIBC), with a subsequent risk of metastasis and mortality [4, 5]. Without treatment, over 50% of patients progress to MIBC [6].
To prevent progression to MIBC and facilitate bladder preservation in patients with CIS, an intensive intravesical management is advised by the urological guidelines [7, 8]. The current gold standard for CIS consists of full dose bacillus Calmette-Guérin (BCG) immunotherapy in a 3-year induction plus maintenance scheme according to the SWOG protocol [9, 10]. This results in a complete response (CR) rate of 70–75% after 3 months [11]. However, a significant number of patients eventually prove to be BCG-unresponsive or intolerant [12–15]. Two potential issues with BCG are the adverse events associated with this viable, although weakened, mycobacterium, and the fact that availability of BCG is dependent on growth of the mycobacterium under highly controlled circumstances which can be achieved by a limited number of manufacturers, making BCG susceptible to scarcity.
Alternative bladder-sparing therapies to replace BCG immunotherapy are being investigated [16]. An effective option is to combine intravesical chemotherapy with mild hyperthermia of the bladder mucosa [17, 18]. A recent randomized clinical trial evaluated the efficacy of intravesical radiofrequency-induced chemohyperthermia (RF-CHT) vs. BCG immunotherapy in intermediate-high risk NMIBC patients, showing a 2-year recurrence free survival (RFS) rate of 81.8% and 64.8%, respectively, and a progression rate of <2% in both groups [19]. However, this study included only 43 CIS patients who all were BCG-naïve. A previous exploratory retrospective study of RF-CHT efficacy in 49 CIS patients, of which 15 were BCG-naïve, showed a 3-months CR rate of 92% which remained 51% after 2 years [20]. Nonetheless, evidence on RF-CHT efficacy in CIS patients is limited, specifically in those who have been previously treated with BCG. In these patients, RF-CHT might be considered prior to radical cystectomy provided that its efficacy is sufficient [21].
We aimed to examine the effect of intravesical RF-CHT in CIS patients who were either treatment naïve, or who were previously treated with or unresponsive to BCG immunotherapy.
PATIENTS AND METHODS
Patient selection
Patients with histologically proven CIS, with or without coexisting papillary Ta/T1 NMIBC tumor(s), who had been treated with RF-CHT using mitomycin C (MMC) were retrospectively collected from six international centres between January 2000 and December 2016. Of these, those who had received≥6 RF-CHT instillations and had either pathology or the combination of cytology and cystoscopy results available at 6 months (range 5–9 months) of follow-up were eligible for the efficacy analysis. Efficacy analysis was additionally performed separately for treatment naïve patients, for patients that were BCG-unresponsive, and for the remaining BCG-treated group, i.e. patients who were BCG-intolerant or did not meet the definition of BCG-unresponsive disease due to late disease recurrence or due to an inadequate BCG regimen. Treatment naïve patients generally had received RF-CHT due to unavailability of BCG, or within a previous different study protocol. BCG-unresponsive disease was defined as a persistence or recurrence of CIS after an adequate BCG regimen was initiated, or relapse of CIS within 6 months of their last intravesical treatment with BCG despite an initial complete response to BCG [16, 22]. An adequate BCG regimen was defined as at least 2 courses of BCG where the first course (induction) must have included at least 5 out of 6 weekly treatments and the second course may have included a re-induction (5 out of 6 treatments) or maintenance of at least 2 out of 3 treatments.
For evaluation of treatment tolerability all patients who had received any RF-CHT instillations were used.
Due to the retrospective nature, no approval of any ethical committee was needed.
Outcomes
The primary endpoint was CR after 6 months since start of RF-CHT, defined as absence of CIS, papillary high-grade (HG) tumor, stage T1 tumor, or extra-vesical evidence of urothelial carcinoma. To be considered a complete responder, a patient had to have a negative result as proven by histopathologic examination or by cystoscopy and urine cytology. Exceptions to this definition included patients with only upper tract involvement, or patients with a Ta-low grade (TaLG) recurrence only since this was regarded as having a clinical benefit from therapy. These patients were evaluated as responders.
As secondary end-points, both the 2-year recurrence rate and recurrence free survival (RFS) after CR, as confirmed by pathology or cytology plus cystoscopy, were evaluated. Additionally, progression rate, overall survival (OS), cystectomy-free survival, and treatment tolerability were assessed at final follow-up. Progression was defined as development of MIBC with or without lymph node or distant metastasis at final follow-up. Treatment tolerability was evaluated by assessment of the drop-out rate due to adverse event which could include spasms, urgency or frequency between or during sessions, or allergic reactions to the instilled drug.
To investigate whether additional RF-CHT instillations were of value in treatment of CIS, we also evaluated CR rates after further maintenance RF-CHT instillations with its associated 2-year recurrence rate.
Treatment
Radiofrequency-induced chemohyperthermia was given using the Synergo® SB-TS 101 system [18]. This system consists of a 915 MHz intravesical microwave applicator located in a specifically designed catheter that delivers mild hyperthermia (40.5 to 44°C) to the bladder wall via direct non-ionizing irradiation. Temperatures were monitored by two urethral and three mucosal thermocouples integrated in the 20 French catheter. To avoid urethral overheating and disintegration of the chemotherapeutic agent, the solution was continuously recirculated and cooled. Typically, MMC was used in a dose of 40 mg/50 ml. The instilled solution was replaced by a fresh identical solution after 30 min (a total of 80 mg MMC in 1 h). Patients were treated weekly for 4 to 8 weeks depending on the planned induction schedule, which was followed by maintenance instillations (one instillation every 4–8 weeks). Schedules slightly differed per centre.
Analyses
For demographics, means with standard deviations (SD) or standard error of the mean (SEM) were calculated for continuous variables. For dichotomous variables, percentages were determined.
Complete response was assessed and additionally compared between BCG-unresponsive, other BCG-treated, and treatment naïve patients using the chi-square test. Absolute recurrence rates were assessed. Kaplan-Meier analysis with Mantel-Cox log rank tests was used for the recurrence-free, overall and cystectomy-free survival evaluation. Additionally, relative survival was determined, defined as the ratio of overall survival of the patients by the survival of a similar general Dutch population matched on age, sex and calendar year and can be used as an approximation of cancer-specific survival.
Analyses were performed using SPSS software, version 22, with a two-sided p < 0.05 considered statistically significant. For the relative survival analysis, SAS version 9.4 (SAS Institute Inc., Cary, NC, USA) was used.
RESULTS
Patients
In total, 270 CIS patients treated with RF-CHT were identified. Of these, 236 patients had received≥6 RF-CHT instillations, whereas pathology or cystoscopy and cytology results at 6 months of follow-up were available in 150 patients. Exclusion of the 86 patients was solely based on this criterion. Patient demographics of the included group of patients (n = 150) – which were used for the efficacy analysis – are depicted in Table 1, and were similar to the total group of patients who had received≥6 RF-CHT instillations. Mean age was 69.4 years, with a male-to-female ratio of 4.6 to 1. Patients received an average of 9.1 previous BCG-instillations and were treated with a mean of 8.2 RF-CHT instillations at CR assessment, with a dose of twice 40 mg (n = 119, 79.3%) or, less frequently, twice 20 mg MMC (n = 31, 20.7%). Of all 150 patients, 76.7% had recurrent CIS with or without concomitant papillary tumor as a worst stage in their history, whereas the other 23.3% of patients had primary CIS.
Table 1
Demographics
| Overall CIS | BCG-unresponsive CIS | Other BCG-treated CIS | Treatment naïve CIS | |
| n | 150 | 50 | 46 missing n = 4 | 47 missing n = 3 |
| Sex | ||||
| Male n (%) | 123 (82.0) | 38 (76.0) | 39 (84.8) | 40 (85.1) |
| Female n (%) | 27 (18.0) | 12 (24.0) | 7 (15.2) | 7 (14.9) |
| Mean age at start of RF-CHT y (SD) | 69.4 (9.52) | 69.4 (9.84) | 72.2 (9.00) | 67.2 (9.08) |
| General history n (%) | ||||
| BPH | 25 (16.7) | 7 (14.0) | 9 (19.6) | 9 (19.1) |
| Prostate cancer | 14 (9.3) | 4 (8.0) | 7 (15.2) | 3 (6.4) |
| Urethral stricture | 4 (2.6) | 0 (0.0) | 2 (4.3) | 2 (4.3) |
| Bladder diverticulum | 2 (1.3) | 1 (2.0) | 1 (2.2) | 0 (0.0) |
| Worst stage in NMIBC history† n (%) | ||||
| Ta | 11 (7.3) | 3 (6.0) | 4 (8.7) | 4 (8.5) |
| T1 | 24 (16.0) | 4 (8.0) | 7 (15.2) | 13 (27.7) |
| CIS | 63 (42.0) | 28 (56.0) | 14 (30.4) | 18 (38.3) |
| Ta + CIS | 20 (13.3) | 8 (16.0) | 8 (17.4) | 2 (4.3) |
| T1 + CIS | 32 (21.3) | 7 (14.0) | 13 (28.3) | 10 (21.3) |
| Worst grade in NMIBC history† n (%) | ||||
| G1 | 7 (4.7) | 3 (6.0) | 1 (2.2) | 3 (6.4) |
| G2 | 8 (5.3) | 2 (4.0) | 1 (2.2) | 4 (8.5) |
| G3 | 135 (90.0) | 45 (90.0) | 44 (95.7) | 40 (85.1) |
| Pathology before start of RF-CHT n (%) | ||||
| CIS only | 89 (59.3) | 39 (78.0) | 20 (43.5) | 27 (57.4) |
| CIS + TaLG | 7 (4.7) | 1 (2.0) | 3 (6.5) | 2 (4.3) |
| CIS + TaHG | 20 (13.3) | 6 (12.0) | 10 (21.7) | 3 (6.4) |
| CIS + T1LG | 1 (0.7) | 1 (2.0) | 0 (0.0) | 0 (0.0) |
| CIS + T1HG | 33 (22.0) | 3 (6.0) | 13 (28.3) | 15 (31.9) |
| BCG instillations before RF-CHT mean (SEM)* | 9.1 (0.76) | 17.5 (0.94) | 9.2 (0.98) | N/A N/A |
| TURBTs before RF-CHT mean (SEM) | 2.3 (0.10) | 2.6 (0.15) | 2.4 (0.16) | 2.1 (0.16) |
| RF-CHT instillations at CR evaluation mean (SEM)‡ * | 8.2 (0.13) | 7.6 (0.15) | 8.8 (0.20) | 8.0 (0.28) |
BCG, bacille Calmette-Guérin; BPH, benign prostate hypertrophia; CIS, carcinoma in-situ; CR, complete response; HG, high grade; LG, low grade; N/A, not applicable; NMIBC, non-muscle invasive bladder cancer; RF-CHT, radiofrequency-induced chemohyperthermia; SD, standard deviation; SEM, standard error of the mean; TURBT, trans-urethral resection of bladder tumor or biopsies.
[i] * Values differ significantly between each group.
[ii] †Excluding the pathology stage or grade for which RF-CHT was started.
[iii] ‡Calculation for 6-months CR evaluation (range 5–9 months). For CR evaluation after additional maintenance RF-CHT instillations, the mean amount of instillations was 10.3 (SEM 0.20), 9.8 (SEM 0.27), 10.0 (0.25), and 11.0 (SEM 0.43), respectively, and did not differ significantly between groups.
The mean time of follow-up for the overall group (n = 150), BCG-unresponsive patients (n = 50), other BCG-treated patients (n = 46, missing n = 4), and treatment naïve patients (n = 47, missing n = 3) was 35.8 months, 27.5 months, 38.5 months, and 40.6 months, respectively.
Efficacy
CR after 6 months was 66.2% (Table 2). For BCG-unresponsive patients the CR was 46.0%, which differed significantly from other BCG-treated and treatment naïve CIS patients (71.7% and 83.0% respectively, p < 0.001). In patients with a CR, the subsequent recurrence rate and RFS after 2 years of follow-up were 18.8% and 74.5% for the overall group and did not differ significantly between any of the groups (Table 2, Fig. 1). CR rate increased with an increased number of RF-CHT instillations from 66.2% to 77.1% for the overall group after respectively a mean amount of 8.2 and 10.3 instillations. For BCG-unresponsive patients, CR rate increased from 46.0% to 57.6% after a mean amount of 7.6 and 9.8 instillations, respectively (Table 3). Patients treated with a dose of 40 mg had a trend towards higher CR rates compared with a dose of 20 mg, although not significant (69.5% vs. 51.6%, p = 0.06).
Fig. 1.
Recurrence-free survival after RF-CHT split by treatment history. No significant difference between BCG-unresponsive, other BCG-treated, and treatment naïve CIS patients was observed, p = 0.08. BCG, bacillus Calmette-Guérin; CIS, carcinoma in situ; CR, complete response; RF-CHT, radiofrequency-induced chemohyperthermia.
Table 2
Complete response rates at 6 months from start of RF-CHT with corresponding 2-year recurrence rates and recurrence free survival
| Overall CIS | BCG-unresponsive CIS | Other BCG-treated CIS | Treatment naïve CIS | |
| n | 143 (missing n = 7) | 50 | 46 (missing n = 4) | 47 (missing n = 3) |
| CR at 6 months from start RF-CHT n (%) | 96 (66.2) | 23 (46.0)* | 33 (71.7)* | 39 (83.0)* |
| 2-year recurrence rate n (% of patients with CR) | 18 (18.8) | 4 (17.4) | 9 (27.3) | 5 (12.8) |
| 2-year RFS cumulative surviving proportion in % | 74.5 | 68.9 | 68.6 | 83.6 |
BCG, bacille Calmette-Guérin; CIS, carcinoma in-situ; CR, complete response; RF-CHT, radiofrequency-induced chemohyperthermia; RFS, recurrence free survival.
[i] *significant difference between BCG-unresponsive, other BCG-treated, and treatment naïve CIS patients, p < 0.001.
Table 3
Complete response rates after additional maintenance instillations with corresponding 2-year recurrence rates and recurrence free survival
| Overall CIS | BCG-unresponsive CIS | Other BCG-treated CIS | Treatment naïve CIS | |
| n† | 131 | 33 | 57 | 41 |
| CR after additional maintenance instillations‡ n (%) | 101 (77.1) | 19 (57.6)* | 45 (78.9)* | 37 (90.2)* |
| 2-year recurrence rate n (% of patients with CR) | 20 (19.4) | 5 (26.3) | 10 (22.2) | 5 (13.5) |
| 2-year RFS cumulative surviving proportion in % | 75.2 | 59.9 | 73.7 | 82.8 |
BCG, bacille Calmette-Guérin; CIS, carcinoma in-situ; CR, complete response; RF-CHT, radiofrequency-induced chemohyperthermia; RFS, recurrence free survival.
[i] †The n differs with the CR assessment at 6 months calculation due to missing data on CR in the different groups.
[ii] ‡On average, an additional amount of two RF-CHT instillations had been received as compared to the CR assessment at 6 months from start of RF-CHT. Patient group was not identical to the CR group at 6 months.
[iii] *significant difference between BCG-unresponsive, other BCG-treated, and treatment naïve CIS patients, p = 0.002.
In 13.3% of patients, progression to MIBC with or without lymph node or distant metastasis at final follow-up was seen, consisting of 16.0% in BCG-unresponsive, 13.0% in other BCG-treated, and 10.6% in treatment naïve CIS patients (p = 0.74).
The bladder preservation rate at final follow-up was 78.5% with a mean cystectomy-free time of 99.9 months (95% -CI 86.7–113.1). For BCG-unresponsive patients these were 71.4% and 45.2 months (95% -CI 35.7–54.7), respectively, and differed significantly between BCG-unresponsive and both other BCG-treated and treatment naïve patients (p = 0.006, Fig. 2, Table 4).
Fig. 2.
Cystectomy-free survival split by treatment history. A significant difference between BCG-unresponsive, other BCG-treated, and treatment naïve CIS patients was observed, p = 0.006. BCG, bacillus Calmette-Guérin; CIS, carcinoma in situ; RF-CHT, radiofrequency-induced chemohyperthermia.
Table 4
Bladder preservation and overall survival rate
| Overall | BCG- | Other BCG- | Treatment naïve | |
| CIS† | unresponsive CIS‡ | treated CIS§ | CIS¶ | |
| n | 144 (missing n = 6) | 49 (missing n = 1) | 44 (missing n = 6) | 45 (missing n = 5) |
| Bladder preservation rate n (%) | 113 (78.5) | 35 (71.4)* | 37 (84.1)* | 39 (86.7)* |
| n | 150 | 50 | 46 (missing n = 4) | 47 (missing n = 3) |
| Overall survival n (%) | 117 (78.0) | 38 (76.0) | 32 (69.6)** | 41 (87.2)** |
BCG, bacille Calmette-Guérin; CIS, carcinoma in-situ; RF-CHT, radiofrequency-induced chemohyperthermia; SEM, standard error of the mean.
[i] †mean follow-up of 35.8 months, SEM 2.18.
[ii] ‡mean follow-up of 27.5 months, SEM 3.01.
[iii] §mean follow-up of 38.5 months, SEM 3.67.
[iv] ¶mean follow-up of 40.6 months, SEM 4.47.
[v] *significant difference between BCG-unresponsive and both other BCG-treated and treatment naïve CIS patients, p = 0.006.
[vi] **trend towards a significant difference between other BCG-treated and treatment naïve CIS patients, p = 0.06.
Patients had an overall survival of 78.0% at final follow-up (Table 4). The mean survival time was 89.5 months (95% -CI 74.7–104.8). For BCG-unresponsive patients these were 76.0% and 79.7 months (95% -CI 65.2–94.3), respectively (Fig. 3). No statistical difference between the groups was found, although a trend towards a significant difference between other BCG-treated and treatment naïve patients was observed (p = 0.06). The relative survival, acting as an approximation of the cancer-specific survival, was 89% after 3 years and 84% after 5 years of follow-up, although 95% confidence intervals overlapped substantially between the actually observed overall survival and the relative survival. For Dutch patients only, relative survival was 82% after 3 years and 86% after 5 years of follow-up (Fig. 4).
Fig. 3.
Observed overall survival split by treatment history. A trend towards a significant difference between other BCG-treated and treatment naïve CIS patients was observed, p = 0.06. BCG, bacillus Calmette-Guérin; CIS, carcinoma in situ; RF-CHT, radiofrequency-induced chemohyperthermia.
Fig. 4.
Survival relative to a matched general Dutch population. Survival for a) all patients (n = 150), and b) Dutch patients only (n = 58). Vertical bars represent 95% confidence intervals. RF-CHT, radiofrequency-induced chemohyperthermia.
If CIS patients who had at least six RF-CHT instillations were used for the efficacy analysis (n = 236), thus abandoning the more strict inclusion criterion of either pathology or cystoscopy plus cytology availability at follow-up, progression rate, cystectomy-free rate, and overall survival rate did not substantially differ from the group analyzed above. This analysis thus confirms that our data are consistent also within a broader inclusion of patients and unlikely subject to significant selection bias.
Treatment tolerability
In total, 13.4% and 17.8% of patients receiving any amount of RF-CHT instillations eventually had to stop either induction or maintenance RF-CHT instillations due to adverse events. Pooled for both induction and maintenance, these adverse events consisted of pain or spasms during an instillation in 7.8%, allergy in 8.2%, and frequency or urge between instillations in 7.5% of total patients.
DISCUSSION
CIS is at risk for progression to muscle-invasive disease. In cases not responding or intolerant to BCG immunotherapy, urological guidelines advise a radical cystectomy. Due to its associated morbidity and mortality, alternatives to radical cystectomy are desired in CIS patients who no longer respond to or tolerate BCG instillations. Indeed, even in BCG naïve intermediate to high-risk NMIBC, such an alternative might be of value in light of BCG toxicity and availability.
We found that with intravesical RF-CHT, a complete response rate of 66.2% with subsequent recurrences in 18.8% after 2 years can be achieved in CIS patients. A higher amount of RF-CHT instillations further improved these figures. More interestingly, a bladder preservation rate of 78.5% after a mean follow-up of about 3 years with a 13.3% rate of disease progression was found. Also for BCG-unresponsive patients – who are at the highest risk of progression – a promising bladder preservation rate of 71.4% and a disease progression rate of 16.0% was found. Thus, RF-CHT might prove to be an option in patients who are at high risk of progression and unwilling or unable to undergo a radical cystectomy.
Although the current gold standard for CIS, i.e. BCG immunotherapy, has proven to be effective in high-risk NMIBC, a substantial amount of patients recur, progress, or appear intolerant for BCG [12–15]. For these patients, several alternative options to radical cystectomy are being investigated. Electromotive drug administration, in which uptake of MMC is enhanced by electrical facilitation of osmosis, has shown promising results combined with BCG vs. BCG alone, but has yet only been described in BCG-naïve T1 patients after transurethral resection and not in BCG-unresponsive CIS patients [23]. Other options under research include photodynamic therapy which uses photo-activation of a cytotoxic agent targeted to tumor cells, chemotherapeutic agents other than the typically administered drugs like mitomycin C and epirubicin [24–28], or combinations of chemotherapeutic drugs (NCT02202772). None have yet shown sufficient efficacy to replace BCG. In future trials, a specific interest in using cytokines (NCT02773849), PD-(L)1 inhibitors (NCT02844816, NCT02625961), and device-assisted therapies (e.g. RF-CHT, NCT03335059) is seen. To date, the most promising results in NMIBC have been achieved using RF-CHT [18, 19, 29].
This study demonstrates that RF-CHT might be a useful treatment option for patients unfit or unwilling to undergo a radical cystectomy. Apart from the good CR rate and subsequent low recurrence rate, the progression rate for overall and, in particular, BCG-unresponsive CIS patients of 13.3% and 16.0% after up to nearly 36 months compares favorable to progression rates in similar high-risk groups as reported by the CUETO group [13, 14]. Most interestingly, however, is the accomplished cystectomy-free rate of 78.5%. In this group of high-risk patients, AUA and EAU guidelines advise a radical cystectomy in all patients fit enough for major surgery [7, 8]. Thus, an important finding of this alternative treatment option is the potential avoidance, or at least delay, of a cystectomy in a majority of these patients.
In addition, we found an overall absolute survival of about 71% at 5 years of follow-up (Fig. 3). The relative survival after 5 years is about 53% for all stage bladder cancer [30] and 88% for NMIBC only[source: Netherlands Cancer Registry] in Dutch bladder cancer patients. For Europe in general, the relative survival is about 68% and 88% for all stage disease and NMIBC only, respectively [31]. In this light, the relative 5-year survival of 84% in our high-risk patient cohort seemed relatively good.
Of interest is the trend towards a lower OS in other BCG-treated patients vs. treatment naïve patients. This possibly is explained by the BCG-intolerant patients in this group, who might have been more frail or might have stopped BCG more often due to comorbidity.
Although BCG-unresponsive patients had significantly worse CR (46.0%, p < 0.001) and cystectomy-free rates (71.4%, p = 0.006), OS did not differ significantly compared with the other groups. Moreover, the CR, RFS, and cystectomy-free rates still seem higher compared with other conservative therapeutic options [32] and fulfill the minimum criterion of a 30% RFS at 18 to 24 months as defined by the Food and Drug Administration and AUA for BCG-unresponsive high risk NMIBC [21]. These results reflect a substantial gain in this patient group.
One study which has previously evaluated RF-CHT in CIS patients, showed better 3-months CR rates of 92% with 49% having a recurrence and 13% undergoing a cystectomy at a mean follow-up of 27 months [20]. However, this patient group was somewhat smaller (n = 49) and consisted of fewer BCG-treated patients (n = 34) of which only 17 were BCG-refractory. Another study on RF-CHT evaluated a group of patients of whom 83% had CIS, and 80% of patients were previously treated with BCG, without further information on BCG-response. After 8 weeks, a CR rate in CIS patients of 80% was found [33]. A similar rate was observed in a recent randomized controlled trial comparing BCG-naïve patients treated with BCG vs. RF-CHT [19]. Although CR and RFS rates found in this study are lower, we have evaluated patients who likely were at higher risk for recurrence or progression considering two-thirds were BCG-failures or intolerant, possibly explaining the different CR rates. Moreover, the CR-rate was evaluated at 6 months in our study instead of at≤3 months of follow-up. To our best knowledge, no additional studies have investigated RF-CHT effect in CIS patients.
Compared to BCG alone, our reported CR rates at 6 months after RF-CHT and the associated recurrence rates are at the better end of the literature-reported range after BCG in treatment naïve CIS patients, with the CR rate ranging from 65–77% at 3–5 months and recurrence rates varying up to 30% [34, 35].
In considering RF-CHT as an alternative to surgery, one should take the risks of potential under-treatment with RF-CHT vs. the impact on quality of life after radical cystectomy into account [28]. The significant morbidity and mortality associated with a radical cystectomy combined with its functional consequences is for many patients the main reason to opt for conservative management. However, 13% and 18% of the studied patients eventually had to stop either induction or maintenance RF-CHT instillations due to adverse events, consisting of pain, urgency, frequency and allergic reactions. In comparison to BCG, RF-CHT seems to have a similar quantity of AEs, although the type of AEs differ [19].
Due to the retrospective nature, some limitations to this study exist. The collected data was highly heterogeneous due to randomly missing values and different standards of treatment and follow-up between the participating centres. Despite missing values, the different groups had comparable demographic data. To overcome different disease management per centre, strict definitions were applied to improve reliability and assess results objectively. As a downside, a substantial proportion of the selected patients needed to be excluded from analysis inducing risk of selection bias. Moreover, by setting pathology or combined cystoscopy plus cytology availability as a precondition to analysis, a bias towards higher tumor rates or non-response was created: if solely a cystoscopy or cytology only – showing a negative result – was performed, the patient was excluded from analysis even though it is likely that no significant tumor (i.e.>TaLG) was present. If, on the other hand, a positive result with solely cystoscopy or cytology was found, additional evaluation was performed and the patient – who had a higher likelihood of tumor presence – was included. Therefore, the results presented in this paper might depict a worst-case scenario.
In addition, either pathology or the combination of cystoscopy and cytology was also used to assess the 2-year recurrence rate. Since specificity for cytology and cystoscopy is higher than its sensitivity, the amount of false negative cases is limited whereas the amount of false positive cases might be high [36, 37]. Again, this might have resulted in a higher amount of observed recurrences than the actual amount of recurrences, although most recurrences in our study were pathology-confirmed (17/18). Lastly, since this study was non-randomized, a selection bias with confounding by indication to treat may be present even though analysis of all patients with≥6 RF-CHT instillations did not yield substantially different results.
CONCLUSIONS
Intravesical radiofrequency-induced chemohyperthermia showed good results in CIS patients – even if BCG-unresponsive – and avoided radical cystectomy in 78.5% of cases for at least 3 years with a modest risk of progression. Thus, RF-CHT might prove to be an alternative to cystectomy in selected patients, even in this cohort at high risk of disease progression. Consequently, further comparison of RF-CHT with other techniques of chemohyperthermia and with different bladder-sparing approaches is of great interest.
ACKNOWLEDGMENTS
Conflict of interest
B Ayres has received non-financial support from Medical Enterprises Ltd. and speaker fees from Kyowa Kirin and Olympus. R Issa reports grants from Medical Enterprises Ltd., outside the submitted work. JA Witjes and G Lüdecke are advisors for Medical Enterprises Ltd. and JA Witjes additionally for Spectrum, Taris, and BioCanCell; without any financial disclosure or conflict of interest on this manuscript. FJP van Valenberg, A Kajtazovic, G Canepa, J Kilb, KKH Aben, O Nativ, and S Madaan have no financial disclosures or conflicts of interest to report.
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