Ignite Creation Date:
2024-05-06 @ 2:08 AM
Last Modification Date:
2024-10-26 @ 11:14 AM
Study NCT ID:
NCT01972347
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
2023-08-30
First Post:
2013-06-17
Brief Title:
Neoadjuvant Dabrafenib Trametinib for AJCC Stage IIIB-C BRAF V600 Mutation Positive Melanoma
Sponsor:
Melanoma Institute Australia
Organization:
Melanoma Institute Australia
Study Overview
Official Title:
An Open Label Single Centre Phase II Pilot Study of Neoadjuvant Dabrafenib Trametinib in Patients With Resectable American Joint Committee on Cancer AJCC Stage IIIB-C BRAF V600 Mutation Positive Melanoma
Status:
ACTIVE_NOT_RECRUITING
Status Verified Date:
2023-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
Neo Combi
Brief Summary:
This is an open label single centre phase II study of neoadjuvant drug treatment with dabrafenib trametinib in patients with resectable American Joint Committee on Cancer AJCC Stage IIIB-C BRAF V600 mutation positive melanoma
The main aim of this study is to find out if giving of a new combined drug treatment to patients with melanoma that has spread to the lymph nodes BEFORE they have surgery will result in improved clinical and pathological response of the melanoma tissue after 12 weeks treatment
The main aim of this study is to find out if giving of a new combined drug treatment to patients with melanoma that has spread to the lymph nodes BEFORE they have surgery will result in improved clinical and pathological response of the melanoma tissue after 12 weeks treatment
Detailed Description:
Neoadjuvant therapy has been demonstrated to improve outcome in the management of patients of multiple different solid tumours The advantage of a neoadjuvant therapy in melanoma is that it provides in vivo assessment of tumour responsiveness to systemic therapy potentially eradicates micrometastatic disease and may improve the surgical result It also provides an opportunity to obtain tumour samples before and after treatment to study variation of response and effects of treatment on tumour characteristics
This pilot study explores pathological response rates Response Evaluation Criteria in Solid Tumors RECIST response rates and biomarkers for a 12-week duration of neoadjuvant therapy with combined MAP kinase inhibition MAPKi with dabrafenib and trametinib and to establish guidelines for an expanded Phase II or III study
The biomarker component of this study will compare pre-treatment PRE with day 4-7 early during treatment biopsies EDT and 12 week lymphadenectomy samples POST The tissue will be interrogated for immunologic proteomic and genetic RNA and DNA features and changes in tissue and blood The baseline PRE specimen will consist of at least two core excisional or incisional biopsies taken prior to commencing combined dabrafenib and trametinib The EDT specimen will consist of at least two core excisional or incisional biopsies taken at days 4-7 very early after commencing combined dabrafenib and trametinib The POST specimen will be the complete lymph node dissection specimen performed after 12 weeks of treatment with combined dabrafenib and trametinib
The EDT specimen provides a unique opportunity to investigate the early changes that occur in a melanoma tumour with MAPK inhibitors that may set up for later resistance or complete response and that may be amenable to therapeutic manipulation For example EDT samples collected on patients treated with single agent BRAF inhibitors showed increased T cell infiltrate that was associated with a better response in the lesion The T cell infiltrate has also been associated with increased expression of melanoma antigens a decrease in immunosuppressive cytokines interleukin IL-6 and IL-8 and an increase in markers of T-cell cytotoxicity Additional studies have shown the expected suppression in pERK and in paired PRE-EDT samples the decreased ERK suppression is associated with a better RECIST response There have been no reports of the effects of BRAF and MEK inhibitors as single agent or in combination on responding melanoma tissue taken more than 15 days after commencement of treatment As the median PFS for the combination of dabrafenib and trametinib is 94 months 95 of the POST samples will be responding and provide an opportunity to 1 compare the responding POST with the EDT sample and the baseline PRE samples prior to treatment to investigate how signalling pathways as determined by RNA gene expression and protein expression alter with time and 2 how the changes in signalling pathways correlate with clinical and pathological response
Study treatment will be continued as adjuvant therapy The goal is to improve the cure rate after surgery through eradication of occult micrometastatic disease Notable successes have been achieved in oncology when highly effective therapies were available for advanced stage disease eg breast cancer Hodgkins and non-Hodgkins lymphoma embryonal tumours osteosarcoma High-risk resected BRAF V600 mutation positive melanoma represents another attractive setting for testing this paradigm since 1 the population is at high risk for relapse and death without further therapy and 2 the BRAFMAP-ERK kinase combination is highly effective in the metastatic setting and can be targeted to the population most likely to benefit The study design will test the efficacy of study treatment in both the neoadjuvant and adjuvant settings for the first time in this patient population
Approximately 168 patients have received combination therapy with dabrafenib and trametinib at the proposed study doses 150 mg BID dabrafenib and 2 mg once daily trametinib with a median follow-up time of 128 months In the dose-escalation phase PFS was longest for the group receiving the highest doses of dabrafenib and trametinib with an acceptable safety profile Based on these data the combination of 150 mg BID of dabrafenib and 20 mg once daily of trametinib has been selected for this study Mature randomized phase 2 trial Part C in Figure 2 above with a median follow up of 141 months showed a higher response rate 76 versus 54 p003 and a longer median PFS 94 months vs 58 months hazard ratio HR 039 p0001 in MAPK inhibitor-naïve patients on the combination of the full dose of dabrafenib and trametinib compared with dabrafenib monotherapy
The duration of therapy 12 months is based upon expert consensus and does not exceed that administered in other pivotal studies of adjuvant treatment in similar populations where treatment ranged from 12 to 60 months In the absence of a reliable biomarker for minimal residual disease empiric dosing for durations much shorter than the predicted median relapse free interval median of 15 months may increase the risk of treatment failure The design does include predictive biomarkers which may allow further refinement of dosing once a phase III study of this design has been completed Safety of continuous dosing of dabrafenib and trametinib for over a year as monotherapies has been established along with preliminary safety of combination dosing for a similar interval Safety precautions will include clear guidelines for management of toxicity including enhanced surveillance for adverse events of special interest along with instructions for dose modification The inclusionexclusion criteria will also serve to minimize participation of those at greatest risk for known or suspected toxicities of the combination therapy
Neoadjuvant studies in patients with macroscopic stage III melanoma have been performed using the immunotherapies interferon and ipilimumab Interferon has no activity in stage IV melanoma yet there was an objective clinical response in 11 of 17 55 patients with stage III melanoma when given neoadjuvantly Furthermore 317 15 had a complete pathological response Clinical responders had significantly greater increases in endotumoral CD11c and CD3 cells and significantly greater decreases in endotumoral CD83 cells compared with nonresponders In contrast ipilimumab confers an overall survival benefit for patients with stage IV melanoma over vaccine or chemotherapy however the objective response rate is low at 11-15 In the neoadjuvant study with macroscopic stage III melanoma pathological responses were not reported however objective clinical responses were observed in 329 10 patients Immune infiltrate cells were noted in most tumours after treatment with ipilimumab and results correlating biomarker changes with response are awaited
In stage IV melanoma patients over 73 of patients who respond to BRAF inhibitors will achieve a RECIST response by the time of the first scan 8 weeks and the median time to best response is 12 weeks in the poorest prognosis patients The progression free survival PFS for the combination is 94 months and 5 of patients have progression as their best RECIST response Therefore 12 weeks was chosen for the period of neoadjuvant combination therapy to optimise tumour shrinkage without compromising patient safety
Surgeons at the Melanoma Institute Australia perform approximately 120 lymphadenectomies each year for patients with palpable lymphadenopathy The sample size of 35 patients is achievable within the anticipated 12 to 18 month recruitment phase Neoadjuvant therapy with combined dabrafenib trametinib for these high-risk melanoma patients with bulky regional stage IIIB-C lymphadenopathy may result in improved rates and duration of local control with reduced surgical morbidity
Pyrexia Sub-Study Combined therapy with dabrafenib and trametinib is associated with pyrexia in over two-thirds of patients There are no identifiable clinical correlates of pyrexia and the mechanism remains unknown Management involves the use of corticosteroids in 25 of cases Further investigations of this drug-associated pyrexia are urgently required particularly for facilitating the use of these drugs in the adjuvant setting The context of this single institution study with its close and uniform patient monitoring provides an ideal opportunity to study drug-induced pyrexia its mechanisms prevention and management and correlation of pyrexia with parent drug and metabolite plasma levels compared with those who do not develop pyrexia
This pilot study explores pathological response rates Response Evaluation Criteria in Solid Tumors RECIST response rates and biomarkers for a 12-week duration of neoadjuvant therapy with combined MAP kinase inhibition MAPKi with dabrafenib and trametinib and to establish guidelines for an expanded Phase II or III study
The biomarker component of this study will compare pre-treatment PRE with day 4-7 early during treatment biopsies EDT and 12 week lymphadenectomy samples POST The tissue will be interrogated for immunologic proteomic and genetic RNA and DNA features and changes in tissue and blood The baseline PRE specimen will consist of at least two core excisional or incisional biopsies taken prior to commencing combined dabrafenib and trametinib The EDT specimen will consist of at least two core excisional or incisional biopsies taken at days 4-7 very early after commencing combined dabrafenib and trametinib The POST specimen will be the complete lymph node dissection specimen performed after 12 weeks of treatment with combined dabrafenib and trametinib
The EDT specimen provides a unique opportunity to investigate the early changes that occur in a melanoma tumour with MAPK inhibitors that may set up for later resistance or complete response and that may be amenable to therapeutic manipulation For example EDT samples collected on patients treated with single agent BRAF inhibitors showed increased T cell infiltrate that was associated with a better response in the lesion The T cell infiltrate has also been associated with increased expression of melanoma antigens a decrease in immunosuppressive cytokines interleukin IL-6 and IL-8 and an increase in markers of T-cell cytotoxicity Additional studies have shown the expected suppression in pERK and in paired PRE-EDT samples the decreased ERK suppression is associated with a better RECIST response There have been no reports of the effects of BRAF and MEK inhibitors as single agent or in combination on responding melanoma tissue taken more than 15 days after commencement of treatment As the median PFS for the combination of dabrafenib and trametinib is 94 months 95 of the POST samples will be responding and provide an opportunity to 1 compare the responding POST with the EDT sample and the baseline PRE samples prior to treatment to investigate how signalling pathways as determined by RNA gene expression and protein expression alter with time and 2 how the changes in signalling pathways correlate with clinical and pathological response
Study treatment will be continued as adjuvant therapy The goal is to improve the cure rate after surgery through eradication of occult micrometastatic disease Notable successes have been achieved in oncology when highly effective therapies were available for advanced stage disease eg breast cancer Hodgkins and non-Hodgkins lymphoma embryonal tumours osteosarcoma High-risk resected BRAF V600 mutation positive melanoma represents another attractive setting for testing this paradigm since 1 the population is at high risk for relapse and death without further therapy and 2 the BRAFMAP-ERK kinase combination is highly effective in the metastatic setting and can be targeted to the population most likely to benefit The study design will test the efficacy of study treatment in both the neoadjuvant and adjuvant settings for the first time in this patient population
Approximately 168 patients have received combination therapy with dabrafenib and trametinib at the proposed study doses 150 mg BID dabrafenib and 2 mg once daily trametinib with a median follow-up time of 128 months In the dose-escalation phase PFS was longest for the group receiving the highest doses of dabrafenib and trametinib with an acceptable safety profile Based on these data the combination of 150 mg BID of dabrafenib and 20 mg once daily of trametinib has been selected for this study Mature randomized phase 2 trial Part C in Figure 2 above with a median follow up of 141 months showed a higher response rate 76 versus 54 p003 and a longer median PFS 94 months vs 58 months hazard ratio HR 039 p0001 in MAPK inhibitor-naïve patients on the combination of the full dose of dabrafenib and trametinib compared with dabrafenib monotherapy
The duration of therapy 12 months is based upon expert consensus and does not exceed that administered in other pivotal studies of adjuvant treatment in similar populations where treatment ranged from 12 to 60 months In the absence of a reliable biomarker for minimal residual disease empiric dosing for durations much shorter than the predicted median relapse free interval median of 15 months may increase the risk of treatment failure The design does include predictive biomarkers which may allow further refinement of dosing once a phase III study of this design has been completed Safety of continuous dosing of dabrafenib and trametinib for over a year as monotherapies has been established along with preliminary safety of combination dosing for a similar interval Safety precautions will include clear guidelines for management of toxicity including enhanced surveillance for adverse events of special interest along with instructions for dose modification The inclusionexclusion criteria will also serve to minimize participation of those at greatest risk for known or suspected toxicities of the combination therapy
Neoadjuvant studies in patients with macroscopic stage III melanoma have been performed using the immunotherapies interferon and ipilimumab Interferon has no activity in stage IV melanoma yet there was an objective clinical response in 11 of 17 55 patients with stage III melanoma when given neoadjuvantly Furthermore 317 15 had a complete pathological response Clinical responders had significantly greater increases in endotumoral CD11c and CD3 cells and significantly greater decreases in endotumoral CD83 cells compared with nonresponders In contrast ipilimumab confers an overall survival benefit for patients with stage IV melanoma over vaccine or chemotherapy however the objective response rate is low at 11-15 In the neoadjuvant study with macroscopic stage III melanoma pathological responses were not reported however objective clinical responses were observed in 329 10 patients Immune infiltrate cells were noted in most tumours after treatment with ipilimumab and results correlating biomarker changes with response are awaited
In stage IV melanoma patients over 73 of patients who respond to BRAF inhibitors will achieve a RECIST response by the time of the first scan 8 weeks and the median time to best response is 12 weeks in the poorest prognosis patients The progression free survival PFS for the combination is 94 months and 5 of patients have progression as their best RECIST response Therefore 12 weeks was chosen for the period of neoadjuvant combination therapy to optimise tumour shrinkage without compromising patient safety
Surgeons at the Melanoma Institute Australia perform approximately 120 lymphadenectomies each year for patients with palpable lymphadenopathy The sample size of 35 patients is achievable within the anticipated 12 to 18 month recruitment phase Neoadjuvant therapy with combined dabrafenib trametinib for these high-risk melanoma patients with bulky regional stage IIIB-C lymphadenopathy may result in improved rates and duration of local control with reduced surgical morbidity
Pyrexia Sub-Study Combined therapy with dabrafenib and trametinib is associated with pyrexia in over two-thirds of patients There are no identifiable clinical correlates of pyrexia and the mechanism remains unknown Management involves the use of corticosteroids in 25 of cases Further investigations of this drug-associated pyrexia are urgently required particularly for facilitating the use of these drugs in the adjuvant setting The context of this single institution study with its close and uniform patient monitoring provides an ideal opportunity to study drug-induced pyrexia its mechanisms prevention and management and correlation of pyrexia with parent drug and metabolite plasma levels compared with those who do not develop pyrexia
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None