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Duration of Anti-PD-1 Therapy in Metastatic Melanoma

Phase 3
Recruiting
Conditions
Unresectable/Metastatic Melanoma
Interventions
Drug: Continuous PD-1 inhibitor therapy
Drug: Intermittent PD-1 inhibitor therapy
Registration Number
NCT02821013
Lead Sponsor
Canadian Cancer Trials Group
Brief Summary

The purpose of this study is to compare the effects on patients with metastatic melanoma of taking a government approved and paid-for PD-1 inhibitor intermittently, with taking the same type of agent continuously. Researchers want to see if the two ways of giving this type of treatment work equally well in extending the life of patients with melanoma, or not.

Detailed Description

The standard or usual treatment for this disease is to receive treatment with a class of agents known as PD-1 inhibitors, or also with the names anti-PD-1 therapy, immunotherapy and checkpoint inhibitors. PD-1 inhibitors turn on the immune system, so that it can fight the cancer cells in the body. Clinical trials have shown that PD-1 inhibitors (such as pembrolizumab and nivolumab) can shrink tumours and extend the life of patients with melanoma.

To-date, PD-1 inhibitors have been given to patients with melanoma continuously (non-stop), for as long as they remain beneficial, for up to a total duration of 2 years. The 2 year duration was chosen because doctors thought it was reasonable, and has been adopted as the standard or usual duration because it was shown to work in clinical trials. However, some recent observations suggest that PD-1 inhibitors may work just as well if they are given for a shorter time and/or in an intermittent schedule. Intermittent means to take breaks from receiving the drug when, and for as long as, the melanoma is better.

The investigators doing this study are interested to find out whether patients with melanoma live as long when the PD-1 inhibitors are given continuously (non-stop) or in an intermittent schedule (taking breaks). If the two ways of giving the treatment were to be shown to be just as good, benefits of an intermittent schedule may include less clinic visits and side effects, better quality of life, and less cost over time for the Health Care System. However, this is not known at present.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
614
Inclusion Criteria
  • Histologically confirmed melanoma that is unresectable / metastatic (stage III or stage IV).

  • Eligible to receive treatment with a government approved and publically-funded PD-1 inhibitor, according to the guidance / indications described in the Product Monograph / Provincial Formulary.

  • Patients must have evidence of unresectable / metastatic disease, that is considered evaluable by the investigator and can be followed, but measurable disease is not mandatory.

  • Patients with brain metastases are allowed, provided they are stable according to the following definitions:

    1. Without evidence of progression for at least four weeks prior to randomization and have no evidence of new or enlarging brain metastases.
    2. Treated with surgery and without evidence of progression prior to randomization and have no evidence of new or enlarging brain metastases.
    3. Treated with stereotactic radiosurgery and without evidence of progression prior to randomization and have no evidence of new or enlarging brain metastases.
  • Patient is able (i.e. sufficiently fluent) and willing to complete the quality of life and health utility questionnaires in either English or French. The baseline assessment must be completed within required timelines, prior to randomization. Inability (lack of comprehension in English or French, or other equivalent reason such as cognitive issues or lack of competency) to complete the questionnaires will not make the patient ineligible for the study. However, ability but unwillingness to complete the questionnaires will make the patient ineligible.

  • Patient consent must be appropriately obtained in accordance with applicable local and regulatory requirements. Each patient must sign a consent form prior to enrollment in the trial to document their willingness to participate.

  • Patients must be accessible for treatment and follow-up. Investigators must assure themselves the patients randomized on this trial will be available for complete documentation of the treatment, adverse events, and follow-up.

  • Patients must be randomized prior to the start of, or within 16 weeks from, the initiation of PD-1 inhibitor treatment. For patients who are being randomized before the start of treatment, the PD-1 inhibitor should be started within 5 working days after randomization. Patients who initiate treatment with combination anti-PD-1 and anti-CTLA-4 therapies who experience toxicity may be randomized at the time prior to starting single-agent PD-1 inhibitor. Repeat imaging must be done within 50 days prior to randomization to ensure the patient has no evidence of disease progression

Exclusion Criteria
  • Patients not willing to stop anti-PD-1 therapy, if randomized to the intermittent arm.
  • Patients with any contraindications to PD-1 inhibitors, as described in the Product Monograph or Provincial Formulary, and/or not eligible to receive anti-PD-1 therapy.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Arm 2: Continuous PD-1 Inhibitor therapyContinuous PD-1 inhibitor therapyAny PD-1 inhibitor that is commercially available, government approved and publicly funded. Dose as recommended by the manufacturer.
Arm 1: Intermittent PD-1 Inhibitor therapyIntermittent PD-1 inhibitor therapyAny PD-1 inhibitor that is commercially available, government approved and publicly funded. Dose as recommended by the manufacturer.
Primary Outcome Measures
NameTimeMethod
Overall survival7 years
Secondary Outcome Measures
NameTimeMethod
Progression-free survival using RECIST 1.1 / Immune-Related RECIST (irRECIST)7 years
Response rate using RECIST 1.1 / Immune-Related RECIST (irRECIST)7 years
Economic evaluation consisting of both healthcare utilization and health utilities measured by the EQ-5D questionnaire7 years
Duration of response using RECIST 1.1 / Immune-Related RECIST (irRECIST)7 years
Quality of Life measured by EORTC QLQ-C307 years
Number and severity of adverse events using CTCAE v 4.07 years

Trial Locations

Locations (31)

Ottawa Hospital Research Institute

🇨🇦

Ottawa, Ontario, Canada

Health Sciences North

🇨🇦

Sudbury, Ontario, Canada

London Health Sciences Centre Research Inc.

🇨🇦

London, Ontario, Canada

Mildura Base Public Hospital

🇦🇺

Victoria, Mildura, Australia

Coffs Habour Health Campus - NCCI

🇦🇺

Coffs Harbour, New South Wales, Australia

Riverina Cancer Care Centre Wagga Wagga

🇦🇺

Wagga Wagga, New South Wales, Australia

Calvary Mater Newcastle Hospital

🇦🇺

Waratah, New South Wales, Australia

Westmead Hospital

🇦🇺

Westmead, New South Wales, Australia

Sunshine Coast University Hospital

🇦🇺

Birtinya, Queensland, Australia

Cairns Hospital

🇦🇺

Cairns, Queensland, Australia

Gold Coast University Hospital

🇦🇺

Southport, Queensland, Australia

The Queen Elizabeth Hospital

🇦🇺

Woodville, South A., Australia

Monash Medical Centre

🇦🇺

Clayton, Victoria, Australia

Alfred Hospital

🇦🇺

Melbourne, Victoria, Australia

Royal Brisbane and Womens Hospital

🇦🇺

Herston, Australia

Cross Cancer Institute

🇨🇦

Edmonton, Alberta, Canada

BCCA - Surrey

🇨🇦

Surrey, British Columbia, Canada

BCCA - Vancouver

🇨🇦

Vancouver, British Columbia, Canada

BCCA - Victoria

🇨🇦

Victoria, British Columbia, Canada

Horizon Health Network

🇨🇦

Fredericton, New Brunswick, Canada

Royal Victoria Regional Health Centre

🇨🇦

Barrie, Ontario, Canada

Juravinski Cancer Centre at Hamilton Health Sciences

🇨🇦

Hamilton, Ontario, Canada

Kingston Health Sciences Centre

🇨🇦

Kingston, Ontario, Canada

Grand River Regional Cancer Centre

🇨🇦

Kitchener, Ontario, Canada

Trillium Health Partners - Credit Valley Hospital

🇨🇦

Mississauga, Ontario, Canada

Lakeridge Health Oshawa

🇨🇦

Oshawa, Ontario, Canada

Odette Cancer Centre

🇨🇦

Toronto, Ontario, Canada

University Health Network

🇨🇦

Toronto, Ontario, Canada

The Research Institute of the McGill University

🇨🇦

Montreal, Quebec, Canada

Allan Blair Cancer Centre

🇨🇦

Regina, Saskatchewan, Canada

Saskatoon Cancer Centre

🇨🇦

Saskatoon, Saskatchewan, Canada

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