MEKRT: MEK Inhibitor and Thoracic Radiotherapy Trial

Sponsor

Sally Falk (Other)

Overall Status

Completed

CT.gov ID

NCT01146756

Collaborator

AstraZeneca (Industry), University of Manchester (Other)

Enrollment

Location

Arm

80.2

Actual Duration (Months)

0.3

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Two thirds of non small cell lung cancer patients present with locally advanced tumours (stage III) or metastatic disease (stage IV) and radiotherapy plays a major role in their treatment. Treatment (radiotherapy and chemotherapy) can be given with curative intent to selected patients with locally advanced, stage III disease. Patients with stage III tumours associated with a pleural effusion, and patients who present with advanced, metastatic disease (stage IV) are treated palliatively with no prospect of cure. In the latter, radiotherapy (RT) is offered with the aim of improving symptoms, achieving tumour control and optimising quality of life. It is generally believed that a plateau has been reached for combination of chemotherapy with radiotherapy lung cancer. There is a strong rationale for combining molecular targeted agents with irradiation. AZD6244 is a potent, selective, uncompetitive inhibitor of MEK that has been tested in early phase clinical trials either alone or in combination with chemotherapy in a variety of cancers including lung cancer. Preclinical studies have shown that AZD6244 enhances the effect of radiation. AZD6244 has not yet been combined with radiotherapy in clinical trials. In this study, a maximum of 18 patients will be allocated to one of 3 doses of AZD6244 in combination with a standard dose of RT in a Phase 1 dose escalation/ de-escalation design to determine the recommended dose for Phase 2 trials (RP2D). An expanded cohort of 15 patients will be treated at the RP2D to obtain additional safety and preliminary response data. Patients will undergo 3 FLT positron emission tomogram (PET) scans, the first scan before treatment, second scan during AZD6244 treatment and third scan during RT. All patients will also have tissue/blood samples collected for biomarkers. Biomarkers and FLTPET imaging will be examined to obtain information that may predict for response, resistance or toxicity to radiation and AZD6244.

Condition or Disease	Intervention/Treatment	Phase
Non Small Cell Lung Cancer	Drug: AZD6244	Phase 1

Detailed Description

As above

Study Design

Study Type:

Interventional

Actual Enrollment :

21 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Phase I Trial of the MEK Inhibitor AZD6244 in Combination With Thoracic Radiotherapy in Non-small Cell Lung Cancer

Actual Study Start Date :

Jun 4, 2010

Actual Primary Completion Date :

Feb 8, 2017

Actual Study Completion Date :

Feb 8, 2017

Arms and Interventions

Arm	Intervention/Treatment
Experimental: AZD6244 & Thoracic Radiotherapy AZD6244 in combination with thoracic radiotherapy (RT)- the aim is to determine the recommended phase II dose (RP2D).	Drug: AZD6244 MEK inhibitor AZD6244 (Selumentinib) in combination with thoracic radiotherapy Other Names: Selumetinib

Arm

Intervention/Treatment

Experimental: AZD6244 & Thoracic Radiotherapy

AZD6244 in combination with thoracic radiotherapy (RT)- the aim is to determine the recommended phase II dose (RP2D).

Drug: AZD6244

MEK inhibitor AZD6244 (Selumentinib) in combination with thoracic radiotherapy

Other Names:

Selumetinib

Outcome Measures

Primary Outcome Measures

To determine the recommended phase II dose (RP2D) of AZD6244 in combination with thoracic radiotherapy (RT) [18 months]
Recommended Phase II Dose (RP2D) - The RP2D will be the dose level at which < 2/6 patients experience dose limiting toxicity (DLT) during thoracic radiotherapy and for 12 weeks after completion of thoracic radiotherapy during the dose escalation phase. The RP2D will be further evaluated for safety in the expanded cohort.

Secondary Outcome Measures

Secondary objectives : Safety profile of AZD6244 in combination with thoracic RT Dose delivery of AZD6244 in combination with thoracic RT Response to AZD6244 in combination with thoracic RT [12 months]
Safety profile of AZD6244 in combination with thoracic RT. Dose delivery of AZD6244 in combination with thoracic RT. Response to AZD6244 in combination with thoracic RT

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Histologically or cytologically confirmed NSCLC either inoperable, stage III NSCLC or stage IV NSCLC with dominant chest symptoms.
Patient age ≥18
Willingness and able to comply with treatment, tests and attend the required follow-up
Prior chemotherapy is permitted provided the interval between day 8 of the last cycle of chemotherapy and day 1 of AZD6244 dosing is ≥2 weeks
No prior radiotherapy or investigational agents
Life expectancy estimated to be greater than 3 months
Performance status(ECOG) 0 or 1
MRC dyspnoea score <3
Patient considered able to tolerate radical radiotherapy
FEV1 >40% of predicted and DLCO (transfer factor for carbon monoxide) >40% of predicted
Disease which can be encompassed within a radical radiotherapy treatment volume(V20 ≤35% and maximum cord dose 48Gy) on the radiotherapy planning scan
Left ventricular ejection fraction >50% on baseline echocardiogram
Adequate renal function - defined by GFR >50 ml/min (calculated Cockcroft and Gault) or by isotope GFR.
Adequate bone marrow reserve: white cell count >3 x 109/l, absolute neutrophil count

1.5 x 109/l, haemoglobin >10.0 g/dl and platelet count >100 x 109/l (Blood transfusion permitted to achieve Hb >10g/dl)

AST/ALT < 2.5 ULN and bilirubin <1.5 ULN
Group D (expanded cohort) only: diameter of the primary tumour should be > 2 cm

Exclusion Criteria:

Mixed non-small cell and small cell tumours
Other previous or current malignant disease likely to interfere with protocol treatment or comparisons
Lack of recovery from prior chemotherapy toxicity to grade ≤2 except alopecia d)Refractory nausea and vomiting, chronic gastrointestinal diseases (eg, inflammatory bowel disease), or significant bowel resection that would preclude adequate absorption of AZD6244
Presence of clinically significant fluid accumulations in third spaces which cannot be adequately controlled by drainage or other procedures prior to inclusion in the study.
History / evidence of active bleeding diatheses
History of unstable diabetes
History of interstitial pneumonitis
Arterial hypertension defined as SBP≥ 160 or DBP ≥100 (antihypertensive medication to achieve these parameters are permissible)
Myocardial infarction, or unstable or uncontrolled angina, congestive heart failure (NYHA > class II) within 1 year of enrollment
Active infection on day of enrollment
Uncontrolled hypercalcemia >3.0 or symptomatic
History of hypersensitivity to active or inactive excipients of AZD6244
Recent major surgery within 4 weeks prior to entry into the study (excluding the placement of vascular access) which would prevent administration of study treatment
Known and symptomatic brain metastases. Brain imaging is not mandatory if patient is asymptomatic.
Clinical judgement by the investigator that the patient should not participate in the study
Patients of reproductive potential who are unable to comply with effective contraception if sexually active during the study and for a period of at least 90 days (men) or 6 months after treatment (women)
Women who are breastfeeding