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Related Concept Videos

Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against specific...
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against specific...
Modified-Release Drug Delivery Systems: Site-Targeted01:24

Modified-Release Drug Delivery Systems: Site-Targeted

Site-targeted drug delivery systems enhance therapeutic efficacy while minimizing systemic toxicity and treatment costs. Unlike conventional methods, these systems ensure precise drug delivery, improving bioavailability and reducing side effects. Targeted drug delivery is classified into three levels. First-order targeting directs drugs to the capillary beds of specific organs or tissues. Second-order targets specific cell types, such as tumor cells, using receptor-mediated interactions.
Tumor Immunotherapy01:27

Tumor Immunotherapy

Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
Chemotherapy-Induced Nausea and Vomiting: 5-HT3 Receptor Antagonists01:27

Chemotherapy-Induced Nausea and Vomiting: 5-HT3 Receptor Antagonists

5-HT3 receptor antagonists, such as dolasetron, granisetron (Kytril), ondansetron (Zofran), and palonosetron (Axoli), are crucial in managing chemotherapy-induced nausea and vomiting (CINV) and postoperative nausea. These drugs selectively block 5-HT3 receptors in the visceral vagal and spinal afferent nerves, chemoreceptor trigger zone, and the vomiting center. They have a rapid onset of action and can be given as a single dose before chemotherapy. Ondansetron and granisetron, in particular,...
Urinary Tract Calculi VI: Surgical Management01:25

Urinary Tract Calculi VI: Surgical Management

Procedures for Kidney StonesMedical intervention is necessary when kidney stones or renal calculi are too large to pass spontaneously (typically greater than 5 millimeters) when stones are accompanied by symptomatic infection (such as fever or pyelonephritis), when they impair kidney function, or when they cause persistent symptoms like severe pain, nausea, or urinary retention. Additionally, patients with only one kidney or those who cannot be treated with medical management also require...

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Related Experiment Video

Updated: May 19, 2026

An Orthotopic Bladder Cancer Model for Gene Delivery Studies
07:48

An Orthotopic Bladder Cancer Model for Gene Delivery Studies

Published on: December 1, 2013

Targeted agents in second-line bladder cancer therapy.

Holger Gerullis1, Thomas Otto, Thorsten H Ecke

  • 1Department of Urology, Lukas Hospital, Neuss, Germany. holger.gerullis@gmx.net

Anti-Cancer Drugs
|August 24, 2012
PubMed
Summary

Targeted therapies show limited success in second-line urothelial cancer treatment after platinum failure. This review examines clinical trials of targeted agents for advanced urothelial carcinoma, offering insights for palliative care options.

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Induction of Invasive Transitional Cell Bladder Carcinoma in Immune Intact Human MUC1 Transgenic Mice: A Model for Immunotherapy Development

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An Orthotopic Bladder Cancer Model for Gene Delivery Studies
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Induction of Invasive Transitional Cell Bladder Carcinoma in Immune Intact Human MUC1 Transgenic Mice: A Model for Immunotherapy Development
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Induction of Invasive Transitional Cell Bladder Carcinoma in Immune Intact Human MUC1 Transgenic Mice: A Model for Immunotherapy Development

Published on: October 30, 2013

Area of Science:

  • Oncology
  • Urothelial Carcinoma Research
  • Clinical Trials

Background:

  • Metastatic urothelial cancer treatment landscape is evolving.
  • Limited options exist in the second-line setting post-platinum therapy.
  • Targeted therapies have shown less efficacy in urothelial cancer compared to other malignancies.

Purpose of the Study:

  • To review clinical studies of targeted agents in second-line treatment for metastatic urothelial carcinoma.
  • To highlight the oncologic outcomes of targeted therapies in this setting.
  • To provide an overview of potential alternative treatment strategies.

Main Methods:

  • Systematic review of clinical trials.
  • Focus on targeted agents investigated in the second-line setting.
  • Analysis of phase II trials for advanced transitional carcinoma of the urothelium.

Main Results:

  • Many targeted drugs investigated as single agents showed unconvincing oncologic outcomes.
  • Vinflunine is a recently approved standard in Europe for second-line treatment.
  • Further well-designed clinical trials may offer alternatives for patients.

Conclusions:

  • Targeted therapy has not yet met expectations in urothelial cancer.
  • The efficacy of single-agent targeted therapies requires further investigation.
  • Clinical trials remain crucial for identifying effective second-line treatments for metastatic urothelial cancer.