Non-muscle invasive

Table of Contents

What Is Non-Muscle Invasive Bladder Cancer?

Non-Muscle Invasive Bladder Cancer (NMIBC) refers to bladder cancers that are confined to the inner layers of the bladder wall and have not spread to the muscle layer. These cancers account for approximately 75% of newly diagnosed bladder cancer cases.

Types of NMIBC

  • Ta tumors: Limited to the inner lining (epithelium).
  • T1 tumors: Invade connective tissue but not muscle.
  • Carcinoma in situ (CIS): Flat, high-grade, non-invasive cancer.

Common Symptoms

  • Blood in the urine (hematuria)
  • Frequent or urgent urination
  • Burning or pain during urination
  • Pelvic discomfort

Contact us if you experience any of these symptoms.

Diagnosis

NMIBC is diagnosed using the following methods:

  • Urinalysis and urine cytology
  • Cystoscopy (bladder examination using a camera)
  • Transurethral Resection of Bladder Tumor (TURBT)
  • Imaging (e.g., CT urogram)

Treatment Options

1. TURBT

Endoscopic removal of visible tumors from the bladder lining.

2. Intravesical Therapy

Drugs delivered directly into the bladder:

  • BCG therapy: First-line treatment for high-risk NMIBC.
  • Intravesical chemotherapy: Used for low to intermediate-risk cases.
Intravesical Therapies for NMIBC

Intravesical Therapies for Non-Muscle Invasive Bladder Cancer (NMIBC)

Summary of Therapies
Therapy Type Indications Key Side Effects Key Considerations
BCG Immunotherapy High-risk NMIBC (CIS, high-grade Ta/T1) Dysuria, frequency, hematuria, fever, fatigue, rare sepsis Gold standard; requires induction + maintenance; shortages common
Mitomycin C (MMC) Chemotherapy Intermediate- to high-risk; post-TURBT Chemical cystitis, rash, bladder irritation Often used post-TURBT (within 24 hrs); some use for maintenance
Gemcitabine Chemotherapy BCG-unresponsive or intermediate-risk NMIBC Mild bladder symptoms (dysuria, frequency) Good safety profile; increasing use in BCG failure or shortage
Gemcitabine + Docetaxel Chemotherapy (Combo) BCG-unresponsive or relapsing disease Mild urinary symptoms, rare systemic effects Effective salvage regimen; growing role in BCG-unresponsive cases
Adstiladrin (nadofaragene firadenovec) Gene Therapy BCG-unresponsive CIS ± Ta/T1 Fatigue, urgency, dysuria, hematuria FDA-approved gene therapy; instilled every 3 months; IFNα gene-based
Anktiva (N-803) Immunotherapy BCG-unresponsive CIS ± papillary tumors (with BCG) Fatigue, flu-like symptoms, urinary urgency FDA-approved with BCG; IL-15 superagonist; promising results in BCG-unresponsive disease
UGN-102 (mitomycin gel) Chemotherapy Low-grade intermediate-risk NMIBC Urinary frequency, dysuria, hematuria, bladder spasms Thermo-sensitive gel; prolongs drug contact time; promising in low-grade tumors
TAR-200 (gemcitabine implant) Chemotherapy delivery system BCG-unresponsive NMIBC Urinary tract irritation, dysuria, urinary retention Implant releasing gemcitabine over weeks; alternative delivery approach

3. Surveillance

Regular cystoscopy, urine tests, and imaging to monitor for recurrence.

Risk CategoryCystoscopyUrine CytologyImaging (Upper Tract)Other Notes
Low-RiskEvery 3 months for 6–12 months, then annuallyOptionalOnly if indicated (e.g., hematuria)May stop after 5 years if no recurrence
Intermediate-RiskEvery 3 months for 2 years, every 6 months to 5 years, then annuallyAt each visitEvery 1–2 years or as neededConsider single-dose intravesical chemo post-TURBT
High-RiskEvery 3 months for 2 years, every 6 months until year 5, then annuallyAt each visitAnnually (CT urogram or ultrasound + cytology)Consider repeat TURBT, BCG maintenance, or early cystectomy
Additional Notes:
– Post-TURBT: Consider early cystoscopy at 4–6 weeks for high-grade tumors.
– BCG patients: May require bladder mapping if cytology remains abnormal.
– Urine biomarkers: Optional and should not replace cystoscopy.

Risk of Recurrence and Progression in NMIBC

Risk Group1-Year Recurrence Risk5-Year Recurrence Risk1-Year Progression Risk5-Year Progression RiskCommon Characteristics
Low Risk15%31%<1%~1%Small, single, low-grade Ta tumor, no CIS
Intermediate Risk24–38%38–62%1–5%6–17%Multiple or recurrent low-grade tumors, no CIS
High Risk~61%~78%~17%>45%High-grade T1, CIS, large/multiple tumors
Notes:
– Risk estimates based on EORTC tables, commonly used for counseling and treatment planning.
– CIS (Carcinoma in Situ) significantly increases risk of progression.
– Recurrent tumors may carry a higher risk even if initially low-grade.

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Whether you’re seeking expert care for a urological condition or looking for a second opinion, we’re here to support you every step of the way. Reach out to schedule an appointment, ask questions, or learn more about personalized, minimally invasive treatment options tailored to your needs.