Induction Therapy With Vemurafenib and Cobimetinib to Optimize Nivolumab and Ipilimumab Therapy (COWBOY)

  • STATUS
    Recruiting
  • End date
    Oct 24, 2023
  • participants needed
    200
  • sponsor
    Radboud University
Updated on 24 February 2022

Summary

Rationale

The combination of ipilimumab and nivolumab induces relatively high response rates and promising response depth in late stage melanoma. Nevertheless, it takes time till responses occur and still a significant number of patients do not benefit from treatment, due to rapid progressive disease or resistance to therapy.

In contrast to immunotherapies targeted therapies (BRAF or MEK inhibitors), can induce faster and higher response rates, but often of shorter duration, even when combined.

Initial attempts of combining vemurafenib or dabrafenib + trametinib with ipilimumab failed due to toxicity.

Patients with elevated levels of serum LDH are less likely to respond to immunotherapy compared to patients with normal LDH levels. This does not mean that such patients do not benefit at all from immunotherapy.

This raises the question, whether response rates upon immunotherapy can be improved by upfront reduction of tumor burden and normalization of LDH.

The investigators postulate that induction therapy with combined BRAF+MEK inhibition, and subsequent LDH normalization, can improve response rates to the rates seen in LDH normal patients.

To address this question the investigators have setup a randomized phase 2 trial in metastatic melanoma patients with elevated serum LDH comparing the response rates upon ipilimumab + nivolumab versus ipilimumab + nivolumab preceded by 6 weeks of vemurafenib + cobimetinib induction.

Furthermore, less than half of the patients treated with the combination of ipilimumab and nivolumab received maintenance nivolumab, and approximately 40% of all patients discontinued treatment for toxicity. In 70% of patients responses were ongoing despite discontinuation of treatment due to toxicity. This raises the question, to what extent does maintenance therapy add clinical benefit to an ongoing immune response. Preclinical data indicate even that continuous restimulation of T cells can result in activation induced non-responsiveness (anergy).

Therefore, a secondary objective of this trial will be, to test a response-driven nivolumab scheme

Objectives

Primary Objective To compare efficacy of induction vemurafenib + cobimetinib followed by ipilimumab + nivolumab (Arm A) versus upfront ipilimumab + nivolumab treatment (Arm B).

Secondary Objectives

  • To describe duration of response and overall survival induced by vemurafenib + cobimetinib followed by the combination of ipilimumab + nivolumab (Arm A) as compared to ipilimumab + nivolumab (Arm B)
  • To describe the rate and quality of toxicity observed in the two study arms
  • To describe the rate of ongoing responses upon response-driven flat dose (240mg q2w or 480mg q4w) nivolumab maintenance
  • To determine the immune-activating capacity of induction therapy with vemurafenib + cobimetinib followed by the combination of ipilimumab + nivolumab.
  • To evaluate the changes in systemic immune competence

Study design:

This is a two-arm phase 2 study consisting of 200 BRAFV600E/K mutation-positive late-stage melanoma patients with an elevated baseline LDH level (> ULN, < 3xULN) randomized 1:1 (stratified according to LDH) to receive either vemurafenib + cobimetinib directly followed by ipilimumab + nivolumab (Arm A) or standard first line ipilimumab + nivolumab (Arm B). Subsequently, patients in both arms will receive flat dose (240mg q2w or 480mg q4w) nivolumab maintenance in a response-driven manner.

Study population:

Stage IV, or unresectable stage III, BRAFV600E/K mutation positive melanoma patients, nave for BRAF/MEK, PD-1/PD-L1 or CTLA-4 targeting therapy, 18 years and older.

Intervention

Patients will be randomized 1:1 to receive either 6 weeks vemurafenib 960 mg bid + cobimetinib 60 mg QD 21-day on, 7-day off (21/7) schedule, directly followed by 4 courses of ipilimumab 3mg/kg q3wk + nivolumab 1mg/kg q3wk (Arm A) or first line standard 4 courses of ipilimumab 3mg/kg q3wk + nivolumab 1mg/kg q3wk (Arm B).

Subsequently, patients in both arms will receive nivolumab maintenance flat dose (240mg q2w or 480mg q4w) in a response-driven manner according to their response at week 18.

Main study parameters/endpoints:

Primary Endpoints

Compare the best overall response rate (BORR) according to RECIST 1.1 of both arms at week 18 from start of treatment.

Secondary Endpoints

  • Progression-free survival (PFS) according to RECIST 1.1
  • Overall survival (OS)
  • Percentage of grade 3/4 toxicities according to CTCv4.03
  • Percentage of ongoing response, percentage of patients requiring re-induction, response percentage upon re-induction
  • Changes in tumor-specific T cell responses

Details
Condition Melanoma, Malignant, of Soft Parts
Treatment vemurafenib and cobimetinib
Clinical Study IdentifierNCT02968303
SponsorRadboud University
Last Modified on24 February 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Adults 18 years and older
World Health Organization (WHO) Performance Status 0-2
Histologically or cytologically confirmed Stage IV, or unresectable stage III, BRAF V600E/K mutated melanoma
Measurable disease according to RECIST 1.1
Signed and dated informed consent form
No prior immunotherapy targeting CTLA-4, PD-1 or PD-L1
No prior BRAFi and/ or MEKi therapy
No immunosuppressive medications
Screening laboratory values must meet the following criteria and should be obtained within 10 days prior to randomization
WBC 2.0x109/L, Neutrophils 1.0x109/L, Platelets 100 x109/L, Hemoglobin 5.0 mmol/L
Creatinine 2x ULN or creatinine clearance (CrCl) 40 ml/min
AST, ALT 3.0 x ULN (5 x ULN for patients with liver metastases)
Bilirubin 2.0 x ULN (except subjects with Gilbert Syndrome, who can have total bilirubin < 3.0 mg/dL )
LDH > ULN, < 5.0 x ULN
No symptomatic brain metastases (asysmptomatic brain metastases, accidentally found during screening can be included)
No leptomeningeal metastases
No active autoimmune disease requiring systemic treatment in the past 3 months or a documented history of autoimmune disease, or history of syndrome that required systemic steroids, at daily dose of 10mg prednisone or equivalent, or immunosuppressive medications. (Subjects with vitiligo or resolved childhood asthma/atopy are excluded from this rule (and will not be excluded from this study). Subjects that require intermittent use of bronchodilators or local steroid injections would not be excluded from the study. Subjects with hypothyroidism stable on hormone replacement or Sjorgen's syndrome will not be excluded from the study.)
No evidence of interstitial lung disease or active, non-infectious pneumonitis
No active infection requiring therapy
No known additional malignancy that is progressing or requires active treatment
Women of childbearing potential (WOCBP) must use appropriate method(s) of contraception. WOCBP should use an adequate method to avoid pregnancy for 23 weeks (30 days + the time required for nivolumab to undergo five half-lives) after the last dose of study medication
WOBCP must have a negative serum or urine pregnancy test within 96 hours prior to the start of study treatment and must not be breast feeding
Men must agree to the use of male contraception during the study treatment period and for at least 31 weeks after the last dose of study drug
Currently not participating in a study of an investigational agent or using an investigational device within 4 weeks of the first dose of treatment
No underlying medical conditions that, in the Investigator's opinion, will make the administration of study drug hazardous or obscure the interpretation of toxicity determination or adverse events
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note