A Phase II Trial to Assess TroVax® Plus Chemotherapy in Patients With Malignant Pleural Mesothelioma

NCT01569919 | Unknown Phase 2 DMC

• 2 other identifiers: 2010/VCC/00492010-023230-22
• Study Type: interventional
• Target: 26
• Locations: 1 country
• Sites: 1

Brief Summary

This study is for patients with malignant mesothelioma of the lung lining (called pleura) who are planning to have pemetrexed-cisplatin chemotherapy. We are investigating whether giving a vaccine called TroVax® with pemetrexed-cisplatin chemotherapy is both safe and potentially beneficial in patients with mesothelioma. This vaccine has been used in combination with chemotherapy in other types of cancer and has been shown to be safe. Cancer vaccines work by stimulating the person's immune system to fight the disease, in a similar way to the immune system fighting infection. In laboratory experiments, the vaccine has been shown to stimulate an immune response to a particular protein widely found on mesothelioma cells called 5T4. In patients with mesothelioma it is hoped that the vaccine will stimulate the immune system to attack mesothelioma cells carrying the 5T4 protein. Pemetrexed-cisplatin chemotherapy is currently seen as the best treatment for patients with mesothelioma, and this is why we plan to combine it with the vaccine. It is hoped that the combination of the TroVax® vaccine and chemotherapy is more beneficial than chemotherapy alone. Pemetrexed-cisplatin will be given into a vein in the arm (intravenously) every 3 weeks. The TroVax® vaccine will be given as an injection into the shoulder muscle (intramuscularly) 3 weeks before chemotherapy starts, one week before chemotherapy starts, then every 3 weeks. Each participant will receive 4 chemotherapy and 9 vaccine treatments if they complete the planned trial schedule. We aim to recruit 26 patients into the trial over a two year period. If this study shows that pemetrexed-cisplatin chemotherapy plus the TroVax® vaccine is safe and beneficial in terms of stimulating the immune system, the combination will be tested further in larger clinical trials.

Conditions

Malignant; Pleural; Mesothelioma

Keywords

Phase II; Single arm; Vaccine

Outcome Measures

Primary Outcomes (1)

• Immune response to 5T4 and MVA antigens as measured by intracellular cytokine staining (ICCS)

  To evaluate whether TroVax® is active in the treatment of MPM. This will be assessed by measuring the cellular or humoral anti-5T4 immune responses following treatment with TroVax® given in combination with Pem/Cis.

  34 weeks

Secondary Outcomes (4)

• Safety and tolerability

  34 weeks

• Clinical activity in terms of PFS, ORR and OS

  1 year

• Relationship between immune response and clinical response

  1 year

• Identify potential predictors of treatment benefit

  1 year

Study Arms (1)

TroVax®

EXPERIMENTAL

In this single-arm study, all participants will receive 9 injections of the TroVax® vaccine, plus standard cisplatin and pemetrexed chemotherapy.

Biological: TroVax®; Drug: Pemetrexed; Drug: Cisplatin; Dietary Supplement: Vitamin B12; Dietary Supplement: Folic Acid; Drug: Dexamethasone

Interventions

TroVax® BIOLOGICAL

Dose of 1 x 10\^9 TCID 50/ml, in 1ml, given on day 1 of weeks 1, 3, 6, 9, 12, 15, 18, 21, 24.

TroVax®

Pemetrexed DRUG

500 mg/m\^2 over 10 mins, given on day 3 of weeks 4, 7, 10, 13.

TroVax®

Cisplatin DRUG

75mg/m\^2 over 1 hour, given on day 3 of weeks 4, 7, 10, 13

TroVax®

Vitamin B12 DIETARY_SUPPLEMENT

1000μg intramuscular, Day 2 of weeks 3 and 12

TroVax®

Folic Acid DIETARY_SUPPLEMENT

400μg oral daily from Day 2 of week 3 to Day 2 of week 16

TroVax®

Dexamethasone DRUG

4mg BD, Days 2-6 of weeks 4, 7, 10, 13

TroVax®

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Signed and dated written informed consent obtained from the patient in accordance with the local regulations
• Locally advanced or metastatic, histologically or cytologically proven MPM
• Aged 18 years or over
• WHO performance status 0-1 (Appendix I)
• Life expectancy \> 6months
• Haemoglobin ≥ 12 g/dl, total white cell count ≥ 3 x 10\^9/L, neutrophil count \> 1.5 x 10\^9/L, lymphocyte count ≥1 x 10\^9/L, monocyte count \<0.8 x 10\^9/L platelet count \>100 x 10\^9/L and \<400 x 10\^9/L. Blood transfusion is allowed.
• Adequate renal function: Creatinine ≥ 50 mL/min as measured by EDTA or 60mL/min as measured by the Cockcroft-Gault formula
• Adequate liver function: ALT, AST and bilirubin \< 2 times the upper limit of normal
• At least four weeks from any previous therapy including surgery, or radiotherapy
• Able to comply with the protocol
• Women must be either post-menopausal, or rendered surgically sterile or, if of child-bearing potential, must have a negative pregnancy test prior to trial entry. Two reliable forms of contraception (oral contraception and a barrier method) must be used by all participants while they are being treated with the TroVax® vaccine. Females must continue to use this level of contraception for 3 months following the last trial treatment, and male patients must continue for 1 month.

You may not qualify if:

• Serious infections within the 28 days prior to entry to the trial.
• Prior TroVax® treatment
• Previous chemotherapy for MPM
• Major surgery or radiation therapy completed ≤ 4 weeks prior to enrolment
• Prior radiopharmaceuticals (strontium, samarium) less than 8 weeks prior to enrolment
• Participation in any other clinical trial of a licensed or unlicensed drug within the previous 30 days
• History of prior malignant disease unless patient has been disease-free for at least 3 years or the tumour was a non-melanoma skin cancer or early cervical cancer
• Autoimmune disease including systemic Lupus Erythematosis, Grave's disease, Hashimoto's thyroiditis, multiple sclerosis, insulin dependent diabetes mellitus or systemic (non-joint) manifestations of rheumatoid disease
• Clinical significant cardiac failure or a measured ejection fraction of \<40%
• Other severe acute or chronic medical or psychiatric conditions or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgement of the investigator, would make the patient inappropriate for entry into this study.
• Chronic corticosteroid use unless prescribed as replacement therapy in the case of adrenal insufficiency, or other immunosuppressive agents. Dexamethasone is allowed as part of trial treatment.
• Cerebral metastases
• History of allergic response to previous vaccine vaccinations
• Known allergy to egg proteins
• Known to test positive for HIV or hepatitis B or C

Sponsors & Collaborators

• Wales Cancer Trials Unit: lead
• Velindre NHS Trust: collaborator
• June Hancock Mesothelioma Research Fund: collaborator
• Velindre Cancer Centre Stepping Stones Appeal: collaborator

Study Sites (1)

Velindre Cancer Centre

Cardiff, South Wales, CF14 2TL, United Kingdom

RECRUITING

MeSH Terms

Conditions

Mesothelioma

Interventions

TroVax; Pemetrexed; Cisplatin; Vitamin B 12; Folic Acid; Dexamethasone

Condition Hierarchy (Ancestors)

Adenoma; Neoplasms, Glandular and Epithelial; Neoplasms by Histologic Type; Neoplasms; Neoplasms, Mesothelial

Intervention Hierarchy (Ancestors)

Guanine; Hypoxanthines; Purinones; Purines; Heterocyclic Compounds, 2-Ring; Heterocyclic Compounds, Fused-Ring; Heterocyclic Compounds; Glutamates; Amino Acids, Acidic; Amino Acids; Amino Acids, Peptides, and Proteins; Amino Acids, Dicarboxylic; Chlorine Compounds; Inorganic Chemicals; Nitrogen Compounds; Platinum Compounds; Corrinoids; Tetrapyrroles; Pyrroles; Azoles; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds, 4 or More Rings; Macrocyclic Compounds; Polycyclic Compounds; Pterins; Pteridines; Pregnadienetriols; Pregnadienes; Pregnanes; Steroids; Fused-Ring Compounds; Steroids, Fluorinated

Study Officials

• Jason F Lester, FRCR, MRCP

  Velindre Cancer Centre

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Hayley Clements, BSc

CONTACT

+442920687500; skopos@cardiff.ac.uk

Angela Casbard, MSc

CONTACT

+442920687500; skopos@cardiff.ac.uk

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 28, 2012
• First Posted: April 3, 2012
• Study Start: December 1, 2012
• Primary Completion: June 1, 2014
• Study Completion: December 1, 2014
• Last Updated: March 12, 2013

Record last verified: 2013-03

Locations

GB (1)