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Related Concept Videos

Targeted Cancer Therapies02:57

Targeted Cancer Therapies

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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.
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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.
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Combination Therapies and Personalized Medicine02:50

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Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
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Cancer Therapies02:49

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Cancer therapies are various modes of treatment, such as surgery, radiation therapy, and chemotherapy that are administered to cancer patients.
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Crohn's disease is an inflammatory bowel disorder marked by chronic inflammation of the GI tract. Various treatment strategies for Crohn's disease are employed, such as immunomodulatory agents, glucocorticoids, and biologics or anti-TNF therapy. Azathioprine (Imuran), a commonly used immunomodulatory drug for Crohn's disease, is converted in the body to mercaptopurine, which inhibits purine biosynthesis and cell proliferation. Both are utilized in severe cases of Inflammatory Bowel...
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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...
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Safety and feasibility of electrical muscle stimulation in patients undergoing autologous and allogeneic stem cell transplantation or intensive chemotherapy.

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Progression-free survival at 24 months (PFS24) and subsequent outcome for patients with diffuse large B-cell lymphoma (DLBCL) enrolled on randomized clinical trials.

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Related Experiment Video

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Enhancing Tumor Content through Tumor Macrodissection
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[Current therapeutic strategies for diffuse large B‑cell lymphoma].

M Pfreundschuh1

  • 1Deutsche Studiengruppe Hochmaligne Non-Hodgkin-Lymphome (DSHNHL), Klinik für Innere Medizin I, Universität des Saarlandes, 66421, Homburg (Saar), Deutschland. michael.pfreundschuh@uks.eu.

Der Internist
|February 6, 2016
PubMed
Summary

Rituximab significantly improved outcomes for diffuse large B-cell lymphoma (DLBCL) patients. Future therapies targeting specific DLBCL subtypes (GC type, ABC type) promise even better survival rates and reduced side effects.

Keywords:
Diffuse large B‑cell lymphoma, chemotherapyIbrutinibImmunotherapyPrognostic factorsR-CHOP protocol

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Area of Science:

  • Oncology
  • Hematology
  • Immunology

Background:

  • Diffuse large B-cell lymphoma (DLBCL) is the most prevalent form of non-Hodgkin's lymphoma.
  • The addition of rituximab to CHOP chemotherapy (R-CHOP) has dramatically improved patient survival rates.
  • Current treatment strategies often rely on the International Prognostic Index (IPI) for risk stratification.

Purpose of the Study:

  • To review the impact of rituximab on DLBCL treatment outcomes.
  • To explore the significance of gene expression profiling in classifying DLBCL subtypes (GC type vs. ABC type).
  • To identify novel therapeutic targets for improved DLBCL management.

Main Methods:

  • Review of clinical outcomes in DLBCL patients treated with and without rituximab.
  • Analysis of gene expression profiles to differentiate DLBCL subtypes.
  • Identification of molecular targets based on subtype-specific pathogenesis.

Main Results:

  • Rituximab incorporation has led to a substantial decrease in DLBCL mortality compared to the pre-rituximab era.
  • Gene expression profiling distinguishes between germinal center B-cell (GC) and activated B-cell (ABC) types of DLBCL.
  • Understanding these subtypes has revealed critical molecules for DLBCL growth, presenting new therapeutic targets.

Conclusions:

  • Further advancements in DLBCL treatment are expected through targeted therapies based on molecular subtypes.
  • Incorporating novel agents into R-CHOP regimens or substituting existing drugs may further enhance survival and reduce toxicity.
  • Personalized treatment approaches for DLBCL are becoming increasingly feasible.