ICT-107: Difference between revisions
(Created page with "{{TreatmentInfo |drug_name=ICT-107 (Tumor-associated Antigen Vaccine) |FDA_approval=Still in clinical trials; not yet FDA-approved |used_for=Newly diagnosed and recurrent Glioblastoma Multiforme (GBM) |clinical_trial_phase=Phase III |common_side_effects=Reported side effects are minimal, including potential site reactions and flu-like symptoms. Few serious adverse events related to the vaccine have been reported. |OS_without=Median overall survival for GBM typically rang...") |
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The critical insights into the ICT-107 vaccine's efficacy, especially concerning patient-specific factors like HLA-A2 status and MGMT methylation status, underscore the importance of personalized approaches in cancer immunotherapy. Despite the challenges, including funding issues that have impacted the phase III trial, the continued follow-up of patients and the exploration of ICT-107 in combination with other treatments offer hope for advancements in GBM therapy (Frontiers) | The critical insights into the ICT-107 vaccine's efficacy, especially concerning patient-specific factors like HLA-A2 status and MGMT methylation status, underscore the importance of personalized approaches in cancer immunotherapy. Despite the challenges, including funding issues that have impacted the phase III trial, the continued follow-up of patients and the exploration of ICT-107 in combination with other treatments offer hope for advancements in GBM therapy (Frontiers) | ||
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Latest revision as of 10:44, 12 November 2024
Links: https://www.frontiersin.org/articles/10.3389/fonc.2020.00762/full, https://tcr.amegroups.org/article/view/4305/5159, https://clinicaltrials.gov/ct2/show/NCT02546102 recent_text= While earlier trials indicated significant benefits in survival and progression-free survival, particularly for patients with certain biomarkers, recent reflections and analyses suggest a more complex picture. These findings emphasize the need for further research to understand the vaccine's full potential and its place in GBM treatment strategies.
The critical insights into the ICT-107 vaccine's efficacy, especially concerning patient-specific factors like HLA-A2 status and MGMT methylation status, underscore the importance of personalized approaches in cancer immunotherapy. Despite the challenges, including funding issues that have impacted the phase III trial, the continued follow-up of patients and the exploration of ICT-107 in combination with other treatments offer hope for advancements in GBM therapy (Frontiers)
From Ben Williams Book: One disadvantage of the DCVax approach is that it requires that brain tissue be extracted from individual patients in order to make the vaccine. An alternative approach has been used by Dr. Black’s team at Cedars Sinai. Dendritic cells are still drawn from the peripheral blood of individual patients, but instead of tumor tissue lysate being mixed with those cells, a collection of six proteins typical of of GBMs is mixed with the
dendritic cells, creating an immune response to those antigens, with the mixture then returned to the patient via vaccinations. In a phase I trial (158), 20 GBM patients (17 newly diagnosed, 3 with recurrent tumors) received three vaccinations two weeks apart. Median PFS was 16.9 months, and median overall survival was 38 months. At the time of the clinical trial report, six of the patients had shown no sign of tumor recurrence. A later follow-up was reported in a Press release from ImmunoCellular Therapeutics (159), the biotech company sponsoring the vaccine (now called ICT-107). Survival rate at three years was 55%, with 38% of patients showing no evidence of recurrence, The most
recent update of the clinical trial (160), presented at the 2013 meeting of the World Federation of Neuro-oncology, reported that 7 of the original 16 patients in the trial were still alive, with survivals ranging from 60 to 83 months. One additional patient who was still tumor free after five years died from leukemia.
Currently ongoing is a randomized phase II trial, the interim results of which have recently reported by ImmunoCellular Therapeutics (161). Despite the impressive results described above, there was no statistically significant difference in median survival between the vaccine group and those treated with a placebo, although there was a numerical 2-3 month advantage for the vaccine group. However there was a similar difference in progression-free survival, which was statistically significant. The company emphasized that the results were preliminary and that they expected the difference in progression-free survival to translate into differences in overall survival with longer follow-up. However, the results also suggest that median survival and percentage of long-term survivors may be only weakly correlated due to the possibility that only a minority of patients benefit from the treatment, but those who do benefit a great deal.
Updated data from the phase II ICT-107 trial were presented on June 1, 2014 at the annual ASCO meeting (309). An important conclusion to be drawn from the new data is that mainly patients positive for HLA-A2 (a variant of the Human Leukocyte Antigen-A gene) seem to derive significant benefit from the vaccine. HLA are antigen-presenting proteins found at the cell surface. HLA-A2 is the most common variant in North America and Europe according to the press release and this group comprised 62% of patients randomized in this trial. The updated results are presented only for HLA-A2 positive patients, with results further subgrouped according to MGMT methylation status. Survival results in this trial are measured from the time of randomization after chemoradiation, and average time from initial surgery to randomization was 83 days (2.7 months).
For HLA-A2 positive patients with unmethylated MGMT, the ICT-107-vaccinated group had a median 4-month survival advantage compared with the placebo-vaccinated group. The ICT-107 group also had a median 4.5 month advantage in progression-free survival. These advantages in the vaccine-treated group did not reach statistical significance, though that is perhaps due to the small numbers of patients within these subgroups. 21% of ICT-107 treated patients were still alive at the time of the analysis, compared with only 7% of the placebo-treated patients.
Median survival has not yet been reached in the HLA-A2 positive, MGMT methylated group, though in this subgroup, ICT-107 treatment led to a dramatic and statistically significant increase in median progression-free survival: 24.1 months versus 8.5 months in the placebo-treated group. It is likely that this huge improvement in median progression-free survival in this subgroup will translate into significant median overall survival improvement.
Sadly, in June 2017, Immunocellular Therapeutics announced that their phase 3 ICT-107 trial was suspending recruitment due to insufficient funding. In the press release it was stated the company was looking for a partner for collaboration or acquisition of its ICT-107 program, and they were also taking steps to ensure the continued follow up of patients already being treated in the trial.Property "Has original text" (as page type) with input value "One disadvantage of the DCVax approach is that it requires that brain tissue be extracted</br>from individual patients in order to make the vaccine. An alternative approach has been</br>used by Dr. Black’s team at Cedars Sinai. Dendritic cells are still drawn from the</br>peripheral blood of individual patients, but instead of tumor tissue lysate being mixed</br>with those cells, a collection of six proteins typical of of GBMs is mixed with the</br></br>dendritic cells, creating an immune response to those antigens, with the mixture then</br>returned to the patient via vaccinations. In a phase I trial (158), 20 GBM patients (17</br>newly diagnosed, 3 with recurrent tumors) received three vaccinations two weeks apart.</br>Median PFS was 16.9 months, and median overall survival was 38 months. At the time of</br>the clinical trial report, six of the patients had shown no sign of tumor recurrence. A later</br>follow-up was reported in a Press release from ImmunoCellular Therapeutics (159), the</br>biotech company sponsoring the vaccine (now called ICT-107). Survival rate at three</br>years was 55%, with 38% of patients showing no evidence of recurrence, The most</br></br>recent update of the clinical trial (160), presented at the 2013 meeting of the World</br>Federation of Neuro-oncology, reported that 7 of the original 16 patients in the trial were</br>still alive, with survivals ranging from 60 to 83 months. One additional patient who was</br>still tumor free after five years died from leukemia.</br></br>Currently ongoing is a randomized phase II trial, the interim results of which have</br>recently reported by ImmunoCellular Therapeutics (161). Despite the impressive results</br>described above, there was no statistically significant difference in median survival</br>between the vaccine group and those treated with a placebo, although there was a</br>numerical 2-3 month advantage for the vaccine group. However there was a similar</br>difference in progression-free survival, which was statistically significant. The company</br>emphasized that the results were preliminary and that they expected the difference in</br>progression-free survival to translate into differences in overall survival with longer</br>follow-up. However, the results also suggest that median survival and percentage of</br>long-term survivors may be only weakly correlated due to the possibility that only a</br>minority of patients benefit from the treatment, but those who do benefit a great deal.</br></br>Updated data from the phase II ICT-107 trial were presented on June 1, 2014 at the</br>annual ASCO meeting (309). An important conclusion to be drawn from the new data is</br>that mainly patients positive for HLA-A2 (a variant of the Human Leukocyte Antigen-A</br>gene) seem to derive significant benefit from the vaccine. HLA are antigen-presenting</br>proteins found at the cell surface. HLA-A2 is the most common variant in North America</br>and Europe according to the press release and this group comprised 62% of patients</br>randomized in this trial. The updated results are presented only for HLA-A2 positive</br>patients, with results further subgrouped according to MGMT methylation status.</br>Survival results in this trial are measured from the time of randomization after</br>chemoradiation, and average time from initial surgery to randomization was 83 days (2.7</br>months).</br></br>For HLA-A2 positive patients with unmethylated MGMT, the ICT-107-vaccinated group</br>had a median 4-month survival advantage compared with the placebo-vaccinated group.</br>The ICT-107 group also had a median 4.5 month advantage in progression-free survival.</br>These advantages in the vaccine-treated group did not reach statistical significance,</br>though that is perhaps due to the small numbers of patients within these subgroups. 21%</br>of ICT-107 treated patients were still alive at the time of the analysis, compared with only</br>7% of the placebo-treated patients.</br></br>Median survival has not yet been reached in the HLA-A2 positive, MGMT methylated</br>group, though in this subgroup, ICT-107 treatment led to a dramatic and statistically</br>significant increase in median progression-free survival: 24.1 months versus 8.5 months</br>in the placebo-treated group. It is likely that this huge improvement in median</br>progression-free survival in this subgroup will translate into significant median overall</br>survival improvement.</br></br>Sadly, in June 2017, Immunocellular Therapeutics announced that their phase 3 ICT-107</br>trial was suspending recruitment due to insufficient funding. In the press release it was</br>stated the company was looking for a partner for collaboration or acquisition of its</br>ICT-107 program, and they were also taking steps to ensure the continued follow up of</br>patients already being treated in the trial." contains invalid characters or is incomplete and therefore can cause unexpected results during a query or annotation process.
