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Related Concept Videos

Treatment Resistent Cancers02:56

Treatment Resistent Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
Treatment Resistant Cancers02:56

Treatment Resistant Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
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.
The Tumor Microenvironment02:17

The Tumor Microenvironment

Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
Tumor Progression02:07

Tumor Progression

Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Tumor Progression02:07

Tumor Progression

Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...

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Related Experiment Video

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Modeling Brain Tumors In Vivo Using Electroporation-Based Delivery of Plasmid DNA Representing Patient Mutation Signatures
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Published on: June 23, 2023

Lecture: fotemustine in brain tumors.

A Silvani1, P Gaviani, E Lamperti

  • 1Neuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 11 Via Celoria, 20133 Milan, Italy. silvani.a@istituto-besta.it

Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|October 12, 2011
PubMed
Summary

Fotemustine (FTMS), a nitrosourea, shows promise for recurrent malignant glioma. New schedules and combination therapies, like with bevacizumab, are being explored to manage side effects and improve outcomes.

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Area of Science:

  • Oncology
  • Neuro-oncology
  • Pharmacology

Background:

  • Fotemustine (FTMS) is a third-generation nitrosourea with preclinical efficacy against human tumor cell lines.
  • Conventional FTMS schedules (induction + maintenance) show 20-52% progression-free survival in recurrent malignant glioma after temozolomide.
  • Myelosuppression, particularly thrombocytopenia and leukopenia, is a significant toxicity in temozolomide-pretreated patients.

Discussion:

  • Hematological toxicities associated with conventional FTMS schedules have prompted the investigation of low-dose regimens.
  • Alternative dosing strategies are being explored to mitigate side effects while maintaining therapeutic benefit.
  • Combining FTMS with novel agents like bevacizumab is a recent development in treating recurrent glioblastoma multiforme.

Key Insights:

  • Fotemustine demonstrates potential in treating recurrent malignant gliomas, especially glioblastoma multiforme.
  • Managing hematological toxicities is crucial for optimizing FTMS treatment in heavily pretreated patients.
  • Combination therapy with bevacizumab represents a promising avenue for enhancing treatment efficacy.

Outlook:

  • Further research into optimized FTMS dosing and scheduling is warranted.
  • Investigating novel combinations with anti-angiogenic agents like bevacizumab may improve outcomes for recurrent glioblastoma.
  • Long-term efficacy and safety data for modified FTMS regimens and combination therapies are needed.