Abstract

Mycobacterium bovis bacillus Calmette–Guerin (BCG) remains at the forefront of immunotherapy for treating bladder cancer patients. However, the incidence of recurrence and progression to invasive cancer is commonly observed. There are no established effective intravesical therapies available for patients, whose tumors recur following BCG treatment, representing an important unmet clinical need. In addition, there are very limited options for patients who do not respond to or tolerate chemotherapy due to toxicities, resulting in poor overall treatment outcomes. Within this context, nanotechnology is an emergent and promising tool for: (1) controlling drug release for extended time frames, (2) combination therapies due to the ability to encapsulate multiple drugs simultaneously, (3) reducing systemic side effects, (4) increasing bioavailability, (5) and increasing the viability of various routes of administration. Moreover, bladder cancer is often characterized by high mutation rates and over expression of tumor antigens on the tumor cell surface. Therapeutic targeting of these biomolecules may be improved by nanotechnology strategies. In this mini-review, we discuss how nanotechnology can help overcome current obstacles in bladder cancer treatment, and how nanotechnology can facilitate combination chemotherapeutic and BCG immunotherapies for the treatment of non-muscle invasive urothelial bladder cancer.

Highlights

  • Bladder cancer (BC) is the second most common malignancy of the urinary tract, the fourth most common cancer in men with a yearly incidence rate of 330, 380 cases, and the 11th most common among women with a yearly incidence rate of 99,413

  • This review focuses on currently available BC therapies and describes nanotechnology tools to enhance therapeutic effects and overcome side effects, emphasizing its use to improve Bacillus Calmette-Guérin (BCG) immunotherapy

  • It is estimated that 20% of patients with high-risk non-muscle-invasive bladder cancers (NMIBC) treated with BCG will progress to muscle invasion or suffer from NMIBC recurrence within 5 years (Rübben et al, 1988)

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Summary

INTRODUCTION

Bladder cancer (BC) is the second most common malignancy of the urinary tract, the fourth most common cancer in men with a yearly incidence rate of 330, 380 cases, and the 11th most common among women with a yearly incidence rate of 99,413. Nano-BCG and Human Bladder Cancer architectural and cytological atypia and include papillary urothelial neoplasm or low malignant potential (Cheng et al, 2012). Trimodal treatment with simultaneous delivery of chemotherapy and radiotherapy has emerged as an effective bladder sparing treatment with similar survival rates compared to RC (Arcangeli et al, 2015). None of these local therapies have shown to be more effective for BC control than early RC (Ahn et al, 2014)

BLADDER CANCER TREATMENTS
CHEMOTHERAPY OPTIMIZATION USING NANOTECHNOLOGY FOR BLADDER CANCER THERAPY
FUNCTIONALIZATION OF NANOPARTICLES TO OPTIMIZE BLADDER CANCER THERAPY
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Findings
To develop a novel
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