Canadian Profiling and Targeted Agent Utilization Trial (CAPTUR)

Sponsor

Canadian Cancer Trials Group (Other)

Overall Status

Recruiting

CT.gov ID

NCT03297606

Collaborator

AstraZeneca (Industry), Bristol-Myers Squibb (Industry), Hoffmann-La Roche (Industry), Pfizer (Industry)

720

Enrollment

Locations

Arms

71.8

Anticipated Duration (Months)

Patients Per Site

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Cancer drugs which target the effects of abnormal gene changes are called 'targeted therapies'. This study, called PM.1 or CAPTUR, will include some targeted therapies that are currently available. The purpose of this study is to find out what are the effects on a patient and their cancer when they are given a targeted therapy drug that is specific to an abnormal gene change in their cancer.

Condition or Disease	Intervention/Treatment	Phase
Lymphoma, Non-Hodgkin Multiple Myeloma Advanced Solid Tumors	Drug: Olaparib Drug: Dasatinib Drug: Nivolumab plus Ipilimumab Drug: Axitinib Drug: Bosutinib Drug: Crizotinib Drug: Palbociclib Drug: Sunitinib Drug: Temsirolimus Drug: Erlotinib Drug: Trastuzumab plus Pertuzumab Drug: Vemurafenib plus Cobimetinib Drug: Vismodegib	Phase 2

Detailed Description

Recent advances in laboratory technology have enabled the identification of changes in the genetic makeup of tumors that might be responsible for their malignant behavior such as uncontrolled growth and spread. Some of these changes can be 'druggable', i.e. there may be cancer medicines that can specifically act on the tumour's genetic abnormality. Several cancer centers and programs have initiated this type of molecular profiling across Canada, with the goal to identify 'druggable' changes in tumors to find matching therapy for patients. These include initiatives in British Columbia, Ontario and Quebec. The CAnadian Profiling and Targeted agent Utilization tRial (CAPTUR) will test the activity of a list of commercially available targeted agents in patients who have undergone tumor profiling and have 'druggable' changes identified in their cancers.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

720 participants

Allocation:

Non-Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Canadian Profiling and Targeted Agent Utilization Trial (CAPTUR): A Phase II Basket Trial

Actual Study Start Date :

Oct 6, 2017

Anticipated Primary Completion Date :

Sep 30, 2022

Anticipated Study Completion Date :

Sep 30, 2023

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Group 1 VEGFR1, VEGFR2, VEGFR3	Drug: Axitinib 5mg orally twice daily
Experimental: Group 2 BCR-ABL, SRC	Drug: Bosutinib 500mg orally once daily
Experimental: Group 3 ALK, ROS1, MET	Drug: Crizotinib 250mg orally twice daily
Experimental: Group 4 KIT, PDGFRA, PDGFRB, ABL1	Drug: Dasatinib 100mg administered orally once daily
Experimental: Group 5 EGFR	Drug: Erlotinib 150mg orally, once daily
Experimental: Group 6 high mutation burden, POLE, POLD1	Drug: Nivolumab plus Ipilimumab Combination Phase - 3mg/kg nivolumab administered as an intravenous infusion over 30 minutes every 3 weeks for the first 4 doses in combination with ipilmumab 1mg/kg administered intravenously over 30 minutes, followed by the single-agent phase. Single-Agent Phase - 480mg nivolumab administered as an intravenous infusion over 30 minutes every 4 weeks.
Experimental: Group 7 BRCA1, BRCA2, mutations in HRD	Drug: Olaparib 300mg taken twice daily
Experimental: Group 8 CDKN2A, CDK4, CCND1, SMARCA4	Drug: Palbociclib 125mg orally once daily for 21 consecutive days followed by 7 days off treatment to comprise a complete cycle of 28 days
Experimental: Group 9 CSF1R, PDGFRA, PDGFRB,VEGFR1, VEGFR2, VEGFR3, KIT, FLT3, RET, FGFR1, FGFR2, FGFR3, VHL	Drug: Sunitinib 50mg orally once daily on a schedule of 4 weeks on treatment followed by 2 weeks off
Experimental: Group 10 AKT1, AKT2, AKT3, FBXW7, FLCN, mTOR, NF1, NF2, NTRK3, PIK3CA, PIK3R1, PTEN, RHEB, STK11, TSC1, TSC2	Drug: Temsirolimus 25mg infused over a 30-60 minute period once a week
Experimental: Group 11 ERBB2	Drug: Trastuzumab plus Pertuzumab Trastuzumab = 3-weekly dose schedule. The recommended initial loading dose is 8mg/kg administered as a 90-minute infusion followed by 3-weekly maintenance dose of 6mg/kg administered as 90-minute infusion. Pertuzumab = 840mg administered as a 60-minute intravenous infusion, followed every 3 weeks thereafter by a dose of 420mg administered over a period of 30-60 minutes.
Experimental: Group 12 BRAFV600	Drug: Vemurafenib plus Cobimetinib Vemurafenib = 960 mg orally every 12 hours. Cobimetinib = 60 mg orally once daily for 21 days, followed by 7 days of rest
Experimental: Group 13 PTCH1, SMO	Drug: Vismodegib 150mg taken orally, once daily

Outcome Measures

Primary Outcome Measures

Objective response rate defined as the number of patients with complete response or partial response [4 years]
over the total number of patients in a given cohort.

Secondary Outcome Measures

Number and severity of adverse events grade >3, or of lesser grade resulting in discontinuation, delay or reduction in dose of study drug [4 years]
measured by CTCAE
Progression-free survival by disease-appropriate objective criteria [4 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria: (screening step - non-drug specific)

Adult (≥ 18 yrs) patient with a histologically-proven incurable metastatic solid tumour (excluding primary brain tumours), multiple myeloma or B cell non-Hodgkin lymphoma (excluding CLL, SLL and HCL), for whom there is no standard treatment known to prolong life, or who has refused such treatment.
ECOG performance status 0-2.
Patients must have normal organ function as follows:
Absolute neutrophil count: ≥ 1.5 x 10^{9/L for solid tumours; ≥ 1.0 x 10}9/L for neurologic malignancies
Platelets ≥ 75 x 10^{9/L (or ≥ 50 x 10}9/L if bone marrow involvement by myeloma or lymphoma).
Total bilirubin ≤ 1.5 x UNL.
AST (SGOT)/ALT (SGPT) ≤ 2.5 x institutional upper limit of normal value unless liver metastases are present in which case they must be < 5 x ULN;
Serum creatinine ≤ 1.5 x UNL or calculated or measured creatinine clearance ≥ 50mg/min/1.73µ^2
Patients must have measurable disease
Results must be available from tumour genomic or protein expression testing (if used to identify genetic variants), from one of the initiatives / groups listed in protocol Appendix VII. The test may have been performed on the primary tumour or a metastatic deposit (including bone marrow), or blood, in a diagnostic or research laboratory and must reveal a potentially actionable variant.
Patient consent (Main Study Consent for the screening step) must be appropriately obtained in accordance with applicable local and regulatory requirements. Each patient must sign a consent form prior to the screening step to document their willingness to participate
Patients must be accessible for treatment and follow-up. Patients registered on this trial must be treated and followed at the participating centre or a CCTG IND site. This implies there must be reasonable geographical limits (for example: 1 ½ hour's driving distance) placed on patients being considered for this trial.
Women/men of childbearing potential must have agreed to use a highly effective contraceptive method.

Exclusion Criteria: (screening step - non-drug specific)

Patients with prior or concurrent malignancy whose natural history or treatment has the potential to interfere with the safety or efficacy assessment of the investigational regimen.
Patients with ongoing toxicity ≥ CTCAE grade 2, other than peripheral neuropathy or asymptomatic, corrected biochemical toxicities (e.g. hypothyroidism corrected by thyroid replacement), related to prior anti-tumour treatment. Patients with ongoing peripheral neuropathy of ≥ CTCAE grade 3 will be excluded.
Patients concurrently receiving any other anti-cancer therapy (cytotoxic, biologic, radiation, or hormonal other than for replacement) except for medications that are prescribed for supportive care but may potentially have an anti-cancer effect (e.g. megestrol acetate, bisphosphonates) or ongoing castration-intent therapy for prostate cancer. These medications must have been started ≥ one month prior to enrollment on this study. Patients may be on warfarin, low molecular weight heparin or direct factor Xa inhibitors, unless such therapies are prohibited by drug-specific ineligibility criteria.
Patients with known active progressive brain metastases. Patients with previously treated brain metastases are eligible, provided that the patient has not experienced a seizure or had a clinically significant change in neurological status within one month prior to screening. All patients with previously treated brain metastases must be stable (clinically and radiologically) for at least one month after completion of treatment and either off steroid treatment or only taking physiological doses of steroids prior to the screening step.
Patients with clinically significant pre-existing cardiac conditions, including uncontrolled or symptomatic angina, uncontrolled atrial or ventricular arrhythmias, or symptomatic congestive heart failure.
Patients with known left ventricular ejection fraction (LVEF) < 40%.
Patients with stroke (including TIA) or acute myocardial infarction within three months prior to the screening step.
Patients with acute gastrointestinal bleeding within one month prior to the screening step.
Patients with any other clinically significant medical condition which, in the opinion of the treating physician, makes it undesirable for the patient to participate in the study or which could jeopardize compliance with study requirements including, but not limited to: ongoing or active infection, significant uncontrolled hypertension, or severe psychiatric illness/social situations.
Lactating and nursing women
Patients who do not meet drug-specific eligibility requirements for the drug selected by the treating physician.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Cross Cancer Institute	Edmonton	Alberta	Canada	T6G 1Z2
2	BCCA - Cancer Centre for the Southern Interior	Kelowna	British Columbia	Canada	V1Y 5L3
3	BCCA - Vancouver Cancer Centre	Vancouver	British Columbia	Canada	V5Z 4E6
4	Kingston Health Sciences Centre	Kingston	Ontario	Canada	K7L 2V7
5	London Regional Cancer Program	London	Ontario	Canada	N6A 5W9
6	Ottawa Hospital Research Institute	Ottawa	Ontario	Canada	K1H 8L6
7	University Health Network	Toronto	Ontario	Canada	M5G 2M9
8	The Jewish General Hospital	Montreal	Quebec	Canada	H3T 1E2
9	Allan Blair Cancer Centre	Regina	Saskatchewan	Canada	S4T 7T1
10	Saskatoon Cancer Centre	Saskatoon	Saskatchewan	Canada	S7N 4H4

Sponsors and Collaborators

Canadian Cancer Trials Group
AstraZeneca
Bristol-Myers Squibb
Hoffmann-La Roche
Pfizer

Investigators

Study Chair: Lillian Siu, Univ. Health Network-OCI/Princess Margaret Hospital, Toronto, ON Canada
Study Chair: Daniel J Renouf, BCCA - Vancouver Cancer Centre, Vancouver BC, Canada