Category:Other Chemotherapy and Cancer Drugs: Difference between revisions

From Glioblastoma Treatments
Jump to navigationJump to search
No edit summary
No edit summary
 
(10 intermediate revisions by the same user not shown)
Line 1: Line 1:
Category:Other Chemotherapy and Cancer DrugsThis category encompasses a range of chemotherapy and cancer drugs used in the treatment of glioblastoma and other high-grade gliomas. These treatments are integral to multimodal cancer therapy approaches, combining traditional chemotherapy agents with newer, targeted drugs to improve patient outcomes.List of TreatmentsHere we provide an overview of various chemotherapy and cancer drugs categorized under "Other Chemotherapy and Cancer Drugs." These treatments have been utilized in clinical trials and have shown varying degrees of efficacy in the management of glioblastoma multiforme (GBM) and other malignancies.{{#ask: [[Category:Other Chemotherapy and Cancer Drugs]] |?Has treatment name |?Has clinical trial phase |?Has common side effects |?Has OS with |?Has usefulness_rating |format=table |limit=50 }}
== Other Chemotherapy and Cancer Drugs ==
Includes various chemotherapy and cancer drugs used in treatment.
 
{{#ask: [[Category:Other Chemotherapy and Cancer Drugs]]
| ?Has treatment name=Drug Name
| ?Has OS without=Overall Survival without PBT
| ?Has OS with=Overall Survival with PBT
| ?Has PFS without=Progression-Free Survival without PBT
| ?Has PFS with=Progression-Free Survival with PBT
| ?Has Usefulness Rating=Usefulness Rating
| ?Has Toxicity Level=toxicity level
| ?Has Toxicity Explanation=Toxicity Explanation
| format=table
| limit=50
}}
 
<comments />
 
[[Belongs to Grouping::Standard Treatments]]
[[Category:TreatmentCategory]]

Latest revision as of 17:02, 17 November 2024

Other Chemotherapy and Cancer Drugs

Includes various chemotherapy and cancer drugs used in treatment.

 Drug NameOverall Survival without PBTOverall Survival with PBTProgression-Free Survival without PBTProgression-Free Survival with PBTUsefulness Ratingtoxicity levelToxicity Explanation
BCNU (Carmustine) and Gliadel (Carmustine Wafers)BCNU (Carmustine) and Gliadel (Carmustine Wafers)Not specifiedGliadel: 13.9 months median survival; Combination with TMZ: Median survival ranges from 17 to 20.7 monthsNot specifiedNot specified44The combination of BCNU and Gliadel Wafers in treatment for glioblastoma is assigned a toxicity level of 4, this is relatively high on a scale of 1 to 5. This means that the treatment has serious side effects which may include low blood counts, pulmonary problems, infections, and seizures. Despite these side effects, the improvement in survival rates may make this treatment an important option for many patients. However, managing these side effects could potentially be challenging and may significantly impact the quality of life. It's important to discuss these risks and potential benefits with your healthcare provider.
Bevacizumab (Avastin)Bevacizumab (Avastin)Not specifiedAVAglio trial: 16.8 months; RTOG trial: 15.7 monthsNot specifiedNot specified43Bevacizumab has an intermediate level of toxicity. Although it is a powerful medication against glioblastoma, it can have serious side effects including high blood pressure (hypertension), presence of excess proteins in the urine (proteinuria), and bleeding (hemorrhage). These side effects can impact your general health and daily activities. Therefore, this treatment needs regular monitoring by your health care provider and should be used with caution.
CCNU (Lomustine)CCNU (Lomustine)Not specified23 months median survival, with 47% at 2 yearsNot specifiedNot specified44The toxicity level of CCNU is quite high due to several common side effects. Most notably, it can cause hematological toxicity, which means it can damage your blood cells and affect your body's ability to fight infections and clot properly. It can also cause nausea, vomiting, and pulmonary toxicity, which can lead to lung damage. On a scale from 1 to 5, with 5 being the most toxic, CCNU is rated as a 4. However, despite these side effects, the treatment showed promising results in a clinical trial.
Gleevec (Imatinib)Gleevec (Imatinib)Not specifiedNot applicable; studies focusing on PFS-6 as a primary endpointNot specifiedPFS-6 value was 53% in a restricted patient population with overexpression of PDGFR33Gleevec (Imatinib) is at a moderate toxicity level. This is because while it does have side effects such as fluid retention, nausea, muscle cramps, rashes, and fatigue, these are common to most treatments and they vary from patient to patient. Also, it has not been specifically approved for glioma treatment, indicating that it might have unexpected results, slightly increasing the risk factor. However, it has shown some potential benefits in early research, hence the moderate, not high, toxicity rating.
Platinum CompoundsPlatinum CompoundsNot specifiedNot specifiedNot specifiedNot specified34The treatment with Platinum Compounds (Cisplatin) is considered relatively high in toxicity due to potential side effects like kidney damage (Nephrotoxicity), hearing loss (ototoxicity), and nervous system damage (neurotoxicity). It's important for patients to discuss these risks with their healthcare provider before starting therapy. A toxicity level of 4 out of 5 means this treatment carries significant risks, but it may be necessary for managing glioblastoma.
ProcarbazineProcarbazineNot specifiedNot specifiedNot specifiedNot specified34The drug Procarbazine is considered quite toxic. This rating is based on the common side effects like hematological toxicity, which refers to potential harm to your blood cells, nausea, and neurological effects such as headache or dizziness. These side effects are relatively common and could significantly affect your day-to-day life. Remember, all treatments come with potential risks, and it's important to discuss these with your doctor.
Loading comments...

Standard Treatments

Pages in category "Other Chemotherapy and Cancer Drugs"

The following 6 pages are in this category, out of 6 total.