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Influence of Hyaluronic Acid on Bacillus Calmette-Guérin Local Side Effects

Pilot Study of Influence of Hyaluronic Acid (HA) on Bacillus Calmette-Guérin (BCG) Local Side Effects

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02207608
Enrollment
30
Registered
2014-08-04
Start date
2011-09-30
Completion date
2012-08-31
Last updated
2015-05-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Poisoning by BCG Vaccine

Keywords

BCG, hyaluronic acid, non-muscle invasive bladder cancer, non bacterial cystitis

Brief summary

The purpose of this study is to evaluate a possible role of intravesical Hyaluronic Acid in reducing local toxicity of Bacillus Calmette Guerin (BCG) used to treat bladder urothelial cell carcinoma.

Detailed description

Bacillus Calmette-Guérin (BCG) is considered the most effective treatment to increase disease-free interval and reduce progression of non-muscle invasive bladder cancer (NMIBC) \[1\]. Although considered safe, BCG can produce both local and systemic side effects leading to treatment discontinuation or interruption. The most common local side-effects of BCG intravesical instillations include cystitis, characterized by irritative voiding symptoms and hematuria, which occur in approximately 75% of all patients. More rarely, serious local adverse events as a result of BCG infection, such as symptomatic granulomatous prostatitis and epididymo-orchitis, might occur and require permanent discontinuation of BCG treatment. Systemic side-effects include flu-like symptoms, such as general malaise and fever, occuring in approximately 40% of patients. A high persistent fever might be related to BCG infection or sepsis. Local and systemic side-effects might lead to discontinue intravesical BCG treatment in approximately 20% of patients \[2\]. Up to 54% of the patients undergoing intravesical therapy with chemotherapeutic agents to treat superficial bladder tumours can be affected by nonbacterial cystitis \[3\]. Several solutions have been proposed to reduce the occurrence of side effects from BCG with the aim to limit BCG discontinuation and the concomitant discomfort during endovesical treatment. Some Authors have proposed to avoid BCG administration in case of TUR within previous 2 weeks, traumatic catheterization, macroscopic hematuria, urethral stenosis, active tuberculosis, prior Bacillus Calmette-Guérin sepsis, immuno-suppression or urinary tract infection \[4\]. Other procedures include the prophylactic administration of isoniazid \[5\] or ofloxacin \[6,7\] or usually involve BCG dose reductions \[8\]. In common practice antimicrobials, anticholinergics, anaesthetics and analgesics are often used to relieve patients' symptoms. Glycosaminoglycan (GAG) substitution therapy is an emerging treatment of Bladder Pain Syndrome/Interstitial Cystitis (BPS/IC) and response rates between 30% and 80% have been described with intravesical administration of various GAGs (hyaluronic acid, pentosan polysulfate, heparin, chondroitin sulfate, and dimethyl sulfoxide) \[9,10\]. Few papers report the results of GAG substitution therapy in the treatment of radiation and chemical cystitis \[9,10\]. To our knowledge, to date, only two papers have described GAG use in the treatment of BCG local side effects; this papers show very good results, with significant reduction of lower urinary tract symptoms after intravesical administration of HA \[11,12\]. Aim of the present randomized pilot study was to evaluate if the sequential administration of HA and BCG could be safe in prevention of early recurrence and progression of bladder tumor, and safe in reduction of local side-effects in patients with high risk NMIBC.

Interventions

DRUGHyaluronic Acid

Add hyaluronic acid to BCG Treatment

DRUGBCG (Immucist®)

Usual BCG treatment

Sponsors

University of Rome Tor Vergata
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Histologically proven non-muscle invasive bladder cancer; * Indication to intravesical instillation of BCG according to EAU guidelines; * Age \> 18 years; * Willingness, to participate to the study; * Written informed consent.

Exclusion criteria

* Previous or ongoing BCG or different intravesical instillations; * Urinary tract infections (UTI) or other known pathologies of the lower urinary tract; * Indication for a radical cystectomy; * Severe systemic disorders, including neurological pathologies, kidney, liver or heart failure; * Contraindications to BCG use.

Design outcomes

Primary

MeasureTime frameDescription
Visual Analogue Scale for PainBefore and after six weeks of treatment (end of induction course)1 to 10 scale (1 minimum pain perceivable; 10 unbearable pain, as perceived by the patient)

Participant flow

Participants by arm

ArmCount
BCG Alone (Immucist®)
Group A receive BCG (Immucist® 81 mg, Sanofi-Aventis Group) alone BCG (Immucist®)
14
Hyaluronic Acid
Group B receive BCG and HA 40 mg (Cystistat, Mylan, Pittsburgh, PA, U.S.A.). Hyaluronic Acid BCG (Immucist®)
15
Total29

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyAdverse Event10

Baseline characteristics

CharacteristicBCG Alone (Immucist®)TotalHyaluronic Acid
Age, Continuous66 years67 years68 years
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
0 Participants0 Participants0 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
14 Participants29 Participants15 Participants
Region of Enrollment
Italy
14 participants29 participants15 participants
Sex: Female, Male
Female
3 Participants7 Participants4 Participants
Sex: Female, Male
Male
11 Participants22 Participants11 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
1 / 150 / 15
serious
Total, serious adverse events
0 / 150 / 15

Outcome results

Primary

Visual Analogue Scale for Pain

1 to 10 scale (1 minimum pain perceivable; 10 unbearable pain, as perceived by the patient)

Time frame: Before and after six weeks of treatment (end of induction course)

ArmMeasureGroupValue (MEAN)Dispersion
BCG Alone (Immucist®)Visual Analogue Scale for PainData Before treatment4.5 units on a scaleStandard Deviation 2
BCG Alone (Immucist®)Visual Analogue Scale for PainData after treatment5.8 units on a scaleStandard Deviation 1
Hyaluronic AcidVisual Analogue Scale for PainData after treatment4.2 units on a scaleStandard Deviation 1.6
Hyaluronic AcidVisual Analogue Scale for PainData Before treatment4.9 units on a scaleStandard Deviation 1.8

Source: ClinicalTrials.gov · Data processed: Mar 19, 2026