Wanted pages
From Glioblastoma Treatments
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List of non-existing pages with the most links to them, excluding pages which only have redirects linking to them. For a list of non-existent pages that have redirects linking to them, see the list of broken redirects.
Showing below up to 50 results in range #51 to #100.
- 3 (awaiting research) (2 links)
- 3 - Under investigation (2 links)
- 5.6 months reported in recent studies using fractionated sessions with Gamma Knife ICON. (2 links)
- 6 out of 14 patients were alive after one year (2 links)
- 8.0 months mOS observed in phase 2 trial for patients receiving treatment dose of 30 mg/m2/day (2 links)
- Based on available data, potentially highly useful in specific dosing schedules (2 links)
- Celebrex (Celecoxib) and Other NSAIDs (2 links)
- Chronotherapy with TMZ could significantly extend survival times, particularly for patients with MGMT methylated tumors. (2 links)
- Chronotherapy with Temozolomide (TMZ) (2 links)
- Combination of Repurposed Drugs plus Temodar (2 links)
- Comparable to standard treatment, specifics depend on individual patient factors. (2 links)
- Data on progression-free survival specifically for SL-701 is under investigation; significant antitumor activity has been noted. (2 links)
- Data varies; traditional radiation therapies offer median OS of around 16-21 months for glioblastoma (2 links)
- Details on progression-free survival (PFS) improvement need further clarification; the trial primarily highlighted improvements in overall survival (2 links)
- Disulfiram (Antabuse) (2 links)
- Early clinical trials show promising results in improving overall survival and progression-free survival in various cancers, including potential benefits for GBM. Ongoing trials will provide more definitive data. (2 links)
- Early studies indicate variable results; ongoing trials, including combinations with PARP inhibitors, aim to determine efficacy (2 links)
- Early trials show median survival times from 56 weeks for recurrent GBM to up to 24.9 months in certain cohorts (2 links)
- Enhancements in progression-free survival noted in combination therapies, ranging from improvement in median progression-free survival times to higher 6-month survival rates (2 links)
- Gamma Knife Radiosurgery (GKRS) for GBM (2 links)
- High-dose PBT showed a median OS of 65.6 months for patients with radiation necrosis, and 26.9 months for patients without radiation necrosis in specific studies (2 links)
- Historical controls indicate median overall survival around 15-17 months for newly diagnosed GBM. (2 links)
- Historical controls suggest a median overall survival of 20-35% at 12 months for similar populations. (2 links)
- Historical mOS for similar patient population using lomustine is 7.2 months (2 links)
- Hyperthermia has shown potential in enhancing the effectiveness of radiation and chemotherapy, improving overall survival and progression-free survival rates in glioblastoma patients. (2 links)
- ICT-107 (Tumor-associated Antigen Vaccine) (2 links)
- Impressive 25.3 months in a study combining vaccine with dose-intense temozolomide. (2 links)
- Improved PFS observed with PBT, specific rates vary by study (2 links)
- Increases observed in specific combination trials, such as Irinotecan with Bevacizumab (2 links)
- Isotretinoin (Accutane) (2 links)
- Lower compared to traditional GBM treatments, with no significant radiation-induced toxicities reported in recent studies. (2 links)
- MN-166 (Ibudilast) (2 links)
- Median overall survival for GBM is typically 15-17 months from diagnosis, or 8 months from recurrence (2 links)
- Median overall survival for GBM typically ranges around 16 months with standard treatment. (2 links)
- Median overall survival with standard treatment ranges around 15-17 months for newly diagnosed GBM (2 links)
- Median progression-free survival with standard treatments is about 6-9 months for GBM (2 links)
- Median survival with standard treatment: 17.4 months (2 links)
- Methadone (D,L-methadone) (2 links)
- Metronomic Low-Dose Temozolomide (TMZ) (2 links)
- Metronomic low-dose TMZ may offer a viable option for patients with recurrent GBM, providing a balance between efficacy and reduced toxicity compared to standard dosing. Further research is ongoing to confirm these benefits. (2 links)
- Not applicable; research has not extensively measured progression-free survival in cancer patients (2 links)
- Not directly specified; historical control data needed for comprehensive comparison (2 links)
- Not directly specified; improvements noted in selected patient analyses (2 links)
- Not directly specified; ongoing studies aim to clarify Carboplatin's impact on survival in recurrent glioma (2 links)
- Not explicitly detailed in recent reviews (2 links)
- Not fully established from available data (2 links)
- Not specifically documented; focus on overall survival improvements (2 links)
- Not specified; however, survival six months after recurrence was used as a primary measure in comparative studies with Avastin (2 links)
- Not specified in the provided context (2 links)
- Optune (Optune Gio® for newer version) (2 links)