Adjuvant Nivolumab Treatment in Stage II (IIA, IIB, IIC) High-risk Melanoma

NCT ID: NCT04309409

Last Updated: 2024-05-23

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 374 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-07-01
• Study Completion Date: 2028-01-31

Brief Summary

Stage II patients with primary surgical treatment of cuMM are often at risk for recurrence of their disease. This risk may be reduced by adjuvant systemic treatment. Due to toxicities of adjuvant therapies the aim is to identify patients at high risk for relapse and to administer adjuvant treatment only to these patients. Thus an optimal balance between insufficient treatment vs. overtreatment has to be found.

To define these patients a prognostic biomarker test will be used in addition to conventional AJCC staging. AJCC staging takes into account several prognostic factors. However, to subdivide stage II melanoma patients into having a low or high risk for relapse further methods are needed.

This clinical trial will evaluate whether adjuvant nivolumab treatment will improve relapse-free survival (RFS) in patients with stage II high-risk melanoma as compared to observation only. The randomized approach of this trial offers the most objective method with the least influence of bias. Since patients with stage II melanoma are usually not receiving adjuvant treatment, no patient will be undertreated in case of randomization into observational arm.

Detailed Description

The NivoMela trial is a randomized, controlled, prospective, multi-center national phase III trial with biomarker-based risk stratification.

Stage II melanoma patients having undergone surgery of the malignant melanoma will be screened using the MelaGenix GEP score to identify patients at high risk for relapse. It is expected, that 61% of screened patients will belong to this group.

Patients with a risk score of > 0.0 (HR 1.48, 1.11-1.98) corresponding to high risk of relapse will be randomized at a ratio of 2:1 to receive either nivolumab as adjuvant treatment (arm A) or observation only (arm B).

Stratification factors for randomization are:

1. Tumor stage: IIA versus IIB versus IIC

2. Gender: Female versus Male

3. Site of primary tumor: extremities versus trunk versus head &neck

All screened patients with a risk score of ≤ 0.0 who are not eligible for randomization will be followed for RFS, DMFS and OS for at least 5 years according to German Follow-up guidelines (Arm C).

Various factors that could potentially predict clinical response and incidence of AEs to treatment with nivolumab will be investigated in peripheral blood and tumor specimen taken at baseline. Data from these investigations will be evaluated for associations with clinical efficacy (eg, ORR, PFS, OS) and safety/toxicity (AE). The samples may also be used for exploratory analyses to assess biomarkers associated with melanoma and/or with immunotherapy treatment.

Conditions

Malignant Melanoma Stage II

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Nivolumab (Arm A)

Patients with a risk score of > 0.0 corresponding to high risk of relapse (randomized):

Nivolumab will be applied at a flat dose of 480 mg given as 60-minute iv infusion every 4 weeks for 12 doses over 1 year. Afterwards these patients will receive intense clinical follow up according German Follow up guidelines.

Group Type: EXPERIMENTAL

Nivolumab

Intervention Type: DRUG

480 mg nivolumab fixed dose given as 60-minute iv infusion every 4 weeks for 12 doses over 1 year

Observation, High Risk (Arm B)

Patients with a risk score of > 0.0 corresponding to high risk of relapse (randomized):

Control group (observation only). These patients will receive intense clinical follow up but no further specific therapy according German Follow up guidelines.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Observation, Low Risk (Arm C)

Patients with a risk score of ≤ 0.0 corresponding to low risk of relapse who are not eligible for randomization:

These patients will receive intense clinical follow up but no further specific therapy according German Follow up guidelines. Documentation of clinical outcome of these patients.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Nivolumab

480 mg nivolumab fixed dose given as 60-minute iv infusion every 4 weeks for 12 doses over 1 year

Intervention Type: DRUG

Other Intervention Names

Opdivo

Eligibility Criteria

Inclusion Criteria

1. Histologically confirmed diagnosis of stage II (AJCCv8) melanoma arising from a primary cutaneous site after surgery therapy

2. Sentinel node biopsy (SNB) without detection of melanoma deposits

3. Randomization not later than 12 weeks after SNB procedure

4. Tumor tissue from primary tumor must be provided for biomarker analyses. In order to be randomized, a subject must be classified by MelaGenix risk analysis.

5. Men and women at the age of 18 to 80 years

6. Signed written, informed consent

7. Patients must be willing and able to comply with scheduled visits, treatment schedule, laboratory testing, and other requirements of the study

8. Minimum life expectancy of five years excluding their melanoma diagnosis

9. ECOG performance status of 0-1

10. Screening laboratory values must meet the following criteria and should be obtained within 14 days prior to randomization:

• White blood cells (WBC) ≥ 2000/μL
• Neutrophils ≥ 1500/μL
• Platelets ≥ 100 x103/μL
• Hemoglobin ≥ 9.0 g/dL
• Serum creatinine ≤ 1.5xUL
• Creatinine clearance (CrCl) ≥ 40mL/min (using the Cockcroft-Gault formula)
• AST / ALT ≤ 3 x ULN
• Total Bilirubin ≤ 1.5 x ULN (except subjects with Gilbert Syndrome, who may have total bilirubin < 3.0 mg/dL)

11. Negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of HCG) for women of childbearing potential (WOCBP) within 72 hours prior to registration.

Women will be considered to be of childbearing potential unless surgically sterilized (hysterectomy, bilateral tubal ligation, or bilateral oophorectomy), or being post-menopausal for at least 24 months or being amenorrheic for > 12 months and follicle-stimulating hormone (FSH) levels ≥ 40 IU/L.

12. WOCBP and male patients with partners of childbearing potential must agree to always use a highly effective form of contraception according to CTFG during the course of this study and for at least 5 months after last dose of study medication (in Arm A only).

Exclusion Criteria

1. History of primary uveal or mucosal melanoma

2. No access to sufficient tumor tissue of primary tumor

3. SNB procedure > 12 weeks before randomization

4. Prior active malignancy within the previous 3 years except for locally curable cancers that have been apparently cured, such as: basal or squamous cell skin cancer, superficial bladder cancer or carcinoma in situ of the prostate, cervix, or breast. Exception: Participants with a history of non-ulcerated cutaneous/acral primary melanoma <1 mm in depth with no nodal involvement are allowed in this trial.

5. Prior or planned therapy with Interferon alpha, CTLA4 or PD-1 / PD L1 antibodies

6. Use of any investigational or non-registered product (drug or vaccine) other than the study treatment

7. Administration of live vaccines within 4 weeks before start of study therapy

8. Any immunosuppressive therapy given within the past 30 days

9. Active psychiatric or addictive disorders that may compromise his/her ability to give informed consent or to comply with the trial procedures

10. Active immune deficiencies or significant autoimmune disease

11. Serious cardiac, gastrointestinal, hepatic or pulmonary disease which would reduce life expectancy to less than five years

12. Serious intercurrent illness, requiring hospitalization

13. Other serious illnesses, e.g., serious infections requiring antibiotics or bleeding disorders

14. The patient is known to be positive for Human Immunodeficiency Virus (HIV) or other active chronic infections (HBV, HCV) or has another confirmed or suspected immunosuppressive or immunodeficient condition

15. Any serious or uncontrolled medical disorder that, in the opinion of the investigator, may increase the risk associated with study participation or study drug administration, impair the ability of the subject to receive protocol therapy, or interfere with the interpretation of study results.

16. Hypersensitivity to the active substance or to any of the excipients

17. Participation in another clinical study within the 30 days before registration

18. For female patients: Pregnancy or breast-feeding

19. For WOCBP and male patients with partners of childbearing potential: Refusal or inability to use effective means of contraception

20. Lack of availability for clinical follow-up assessments

21. Legal incapacity or limited legal capacity

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital, Essen

OTHER

Sponsor Role: lead

Responsible Party

Prof. Dr. med. Dirk Schadendorf

Director of the Department of Dermatology and the West German Tumour Centre at the University Hospital

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Dirk Schadendorf, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Essen

Locations

Universitätsklinikum Würzburg - Klinik für Dermatologie, Venerologie und Allergologie

Würzburg, Bavaria, Germany

Universitätsmedizin Rostock -Klinik und Poliklinik für Dermatologie und Venerologie

Rostock, Mecklenburg-Vorpommern, Germany

Universitätsklinikum Augsburg, Campus Süd

Augsburg, , Germany

St. Josef-Hospital - Dermatologische Studienambulanz

Bochum, , Germany

Klinikum Dortmund gGmbH - Dermatologie

Dortmund, , Germany

Universitätsklinik Carl Gustav Carus der Technischen Universität Dresden - Klinik und Poliklinik für Dermatologie

Dresden, , Germany

HELIOS Klinikum Erfurt

Erfurt, , Germany

University Hospital Essen, Department of Dermatology, Skin Cancer Center

Essen, , Germany

Universitätsklinikum Freiburg - Klinik für Dermatologie und Venerologie

Freiburg im Breisgau, , Germany

Universitätsklinikum Gießen und Marburg GmbH - Klinik für Dermatologie und Allergologie

Giessen, , Germany

Universitätsklinikum Hamburg-Eppendorf - Hauttumorzentrum

Hamburg, , Germany

Universitätsklinikum Schleswig-Holstein, Campus Kiel - Dermatologie

Kiel, , Germany

Universitätsklinikum Leipzig - Klinik u. Poliklinik f. Dermatologie, Venerologie u. Allergologie

Leipzig, , Germany

Universitätsklinikum Mannheim - Klinik f. Dermatologie, Venerologie u. Allergologie

Mannheim, , Germany

Klinikum der Universität München - Klinik und Poliklinik für Dermatologie und Allergologie

München, , Germany

Universitätsklinikum Münster - Zentrale Studienkoordination für innovative Dermatologie (ZID)

Münster, , Germany

Fachklinik Hornheide - Internistische Onkologie

Münster, , Germany

Klinikum Nürnberg Nord - Hautklinik

Nuremberg, , Germany

Harzklinikum Dorothea Christiane Erxleben - Klinik für Dermatologie & Allergologie

Quedlinburg, , Germany

Universitätsklinikum Tübingen - Dermatoonkologie

Tübingen, , Germany

Countries

Germany

Other Identifiers

CA209-7DL

Identifier Type: -

Identifier Source: org_study_id