TROPHAMET: Avelumab and Methotrexate in in Low-risk Gestational Trophoblastic Neoplasias as First Line Treatment

Sponsor

Hospices Civils de Lyon (Other)

Overall Status

Recruiting

CT.gov ID

NCT04396223

Collaborator

Merck Healthcare KGaA, Darmstadt, Germany, an affiliate of Merck KGaA, Darmstadt, Germany (Industry)

Enrollment

Locations

Arm

76.9

Anticipated Duration (Months)

3.3

Patients Per Site

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Gestational trophoblastic neoplasias (GTN) are characterized by the persistence of elevated hCG titers after complete uterine evacuation of a partial hydatidiform mole (PHM) or a complete hydatidiform mole.

Low-risk GTN patients (FIGO score ≤ 6) are commonly treated with single agent treatment (methotrexate or actinomycin-D) The cure rate, assessed by hCG normalization, is obtained in 65 to 75% of patients with these agents GTN patients with resistance to these treatments are treated with another single agent drug or polychemotherapy regimens, such as EMA-CO or BEP regimen.

Chemotherapy standard regimens are old and toxic for these young lady patients, with potential long term effects detrimental for further maternity and quality of life

There is a strong rational for investigating the anti-PDL1 monoclonal antibody avelumab in chemoresistant GTN patients. Several elements suggest that the normal pregnancy immune tolerance is "hijacked" by GTN cell for proliferating :

Spontaneous regressions of metastastic GTN are regularly observed, thereby the role of immune system for rejecting GTN cells.
Strong and constant overexpression of PDL1 and NK cells has been found in all subtypes and settings of GTN tumors from French reference gestational trophoblastic center.
Complete and durable responses to pembrolizumab were reported in 3 patients with multi-chemoresistant GTN in United Kingdom.
Three cases of hCG normalization with avelumab in 6 patients with chemo-resistant GTN enrolled in TROPHIMMUN cohort A (resistant to a mono-chemotherapy).
Cytotoxicity of avelumab is mediated through antibody dependent cell cytotoxicity (ADCC) by NK cells.

Condition or Disease	Intervention/Treatment	Phase
Gestational Trophoblastic Neoplasias (GTN)	Drug: Avelumab Injection Drug: Methotrexate 1 GM Injection	Phase 1/Phase 2

Study Design

Study Type:

Interventional

Anticipated Enrollment :

26 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

TROPHAMET, a Phase I/II Trial of Avelumab and METhotrexate in Low-risk Gestational TROPHoblastic Neoplasias as First Line Treatment

Actual Study Start Date :

Feb 12, 2020

Anticipated Primary Completion Date :

Jun 12, 2023

Anticipated Study Completion Date :

Jul 12, 2026

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Avelumab combined with methotrexate and folinic acid Avelumab administration at 800 mg every 2 weeks and methotrexate administration at 1mg/kg/day during 4 months ½ (median)	Drug: Avelumab Injection Avelumab administration at 800mg a 1 hour IV infusion once every 14 days during 4 months ½ (median) Drug: Methotrexate 1 GM Injection methotrexate administration at 1mg/kg/day during 4 months ½ (median)

Arm

Intervention/Treatment

Experimental: Avelumab combined with methotrexate and folinic acid

Avelumab administration at 800 mg every 2 weeks and methotrexate administration at 1mg/kg/day during 4 months ½ (median)

Drug: Avelumab Injection

Avelumab administration at 800mg a 1 hour IV infusion once every 14 days during 4 months ½ (median)

Drug: Methotrexate 1 GM Injection

methotrexate administration at 1mg/kg/day during 4 months ½ (median)

Outcome Measures

Primary Outcome Measures

Incidence of Dose limiting toxicities of methotrexate and avelumab combination in low-risk GTN patients as first line. [treatment duration 3 months (median estimation)]
Safety run-in: dose-limiting toxicities (DLT) will be determined during the first 3 months after the start of treatment
Rate of patients with successful normalization of hCG [treatment duration 3 months (median estimation)]
The main endpoint of this study is the rate of patients with successful normalization of hCG allowing for treatment discontinuation (hCG normalization). Patients will continue on treatment until the weekly hCG assays reach the institutional normal threshold, and then for 3 additional cycles, or otherwise will be stopped in the case of resistance, defined as a rise (a > 20% rise between two assays, observed twice on three consecutive weekly assays) or a plateau (a < 10% decrease between two assays observed three times on four consecutive weekly assays) in the hCG level, or unacceptable toxicity and/or death.

Secondary Outcome Measures

Evaluate the safety of methotrexate and avelumab combination administration [during treatment duration (3 months), 1 month after end of treatment and 36 months after end of treatment (median : 8 months 1/2).]
To assess the rate of treatment-emergent adverse events (TEAEs) and treatment-related adverse events (AEs), treatment-related Grade ≥ 3 AEs, and immune-related AEs, according to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events Version 5.0 (CTCAE v5.0)
To assess the efficacy of avelumab and methotrexate in terms of resistance-free survival in low-risk GTN patients as first line setting [during treatment (3 months median), 1 month after the end of treatment and 36 months after the end of treatment]
Resistance rate will be evaluated according to hCG level.
To assess the efficacy of avelumab and methotrexate in terms of resistance-free survival in low-risk GTN patients as first line setting [during treatment (3 months median), 1 month after the end of treatment and 36 months after the end of treatment]
Resistance-free survival will be evaluated according to hCG level.
To assess the efficacy of avelumab and methotrexate in terms of relapse free survival in low-risk GTN patients as first line setting after an initial hCG normalization that enabled study treatment discontinuation [during treatment (3 months median), 1 month after the end of treatment and 36 months after the end of treatment]
Relapse-free survival will be evaluated in the case of relapse requiring treatment resumption after a hCG normalization that enabled study treatment discontinuation
To assess the efficacy of avelumab and methotrexate in terms of overall survival in low-risk GTN patients as first line setting [during treatment (3 months median), 1 month after end of treatment and 36 months after end of treatment]
Overall survival

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

Female

Accepts Healthy Volunteers:

Inclusion Criteria:

- Woman older than 18 years
Low-risk gestational trophoblastic neoplasia according to FIGO score (FIGO score ≤ 6) with indication of methotrexate as first line treatment
Patients with Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
Patients with adequate bone marrow function measured within 28 days prior to administration of study treatment as defined below
Absolute granulocyte count ≥ 1.5 x 10 9 /L
Platelet count ≥ 100 x 10 9 /L
Haemoglobin ≥ 9.0 g/dL (may have been blood transfused)
Patients with adequate renal function:

Calculated creatinine clearance ≥ 30 ml/min according to the Cockcroft-Gault formula (or local institutional standard method)

Patients with adequate hepatic function

*Serum bilirubin ≤ 1.5 x UNL and AST/ALT ≤ 2.5 X UNL (≤ 5 X UNL for patients with liver metastases)

Patients must have a life expectancy ≥ 16 weeks
Confirmation of non-childbearing status for women of childbearing potential.

An evolutive pregnancy can be ruled out in the following cases:

in case of a previous hysterectomy
if serum hCG level ≥ 2 000 IU/L and no intra or extra-uterine gestational sac is detected on pelvic ultrasound
if serum hCG level < 2 000 IU/L on a first measurement and serum hCG increases <100% on a second measurement performed 3 days later.
Highly effective contraception if the risk of conception exists. (Note: The effects of the trial drug on the developing human fetus are unknown; thus, women of childbearing potential must agree to use 2 highly effective contraceptions, defined as methods with a failure rate of less than 1 % per year. Highly effective contraception is required at least 28 days prior, throughout and for at least 12 months after avelumab treatment.
Patients who gave its written informed consent to participate to the study
Patients affiliated to a social insurance regime
Patient is willing and able to comply with the protocol for the duration of the treatment

Exclusion Criteria:

Prior therapy with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or anti- CTLA 4 antibody (including ipilimumab, tremelimumab or any other antibody or drug specifically targeting T-cell costimulation or immune checkpoint pathways).
Illness, incompatible with avelumab, such as congestive heart failure; respiratory distress; liver failure; uncontrolled epilepsy; allergy.
Patients with a known allergic hypersensitivity to methotrexate or any of the other ingredients (sodium chloride, sodium hydroxide, and hydrochloric acid if excipient)
Patients with second primary cancer, except: adequately treated non-melanoma skin cancer, curatively treated in-situ cancer of the cervix, or other solid tumours curatively treated with no evidence of disease for ≥ 5 years.
All subjects with brain metastases, except those meeting the following criteria:
Brain metastases that have been treated locally and are clinically stable for at least 2 weeks prior to enrolment, No ongoing neurological symptoms that are related to the brain localization of the disease (sequelae that are a consequence of the treatment of the brain metastases are acceptable).
Subjects with brain metastases must be either off steroids except a stable or decreasing dose of <10mg daily prednisone (or equivalent).
Patients receiving any systemic chemotherapy, radiotherapy (except for palliative reasons), within 2 weeks from the last dose prior to study treatment (or a longer period depending on the defined characteristics of the agents used). The patient can receive a stable dose of bisphosphonates for bone metastases, before and during the study as long as these were started at least 4 weeks prior to treatment with study drug.
Persistent toxicities (>=CTCAE grade 2) with the exception of alopecia and sensory neuropathy, caused by previous cancer therapy.
Treatment with other investigational agents.
Bowel occlusive syndrome, inflammatory bowel disease, immune colitis, or other gastro-intestinal disorder that does not allow oral medication such as malabsorption.
Stomatitis, ulcers of the oral cavity and known active gastrointestinal ulcer disease
Clinically significant (i.e., active) and severe cardiovascular disease according to investigator opinion such as myocardial infarction (< 6 months prior to enrollment)
Patients with immune pneumonitis, pulmonary fibrosis
Known severe hypersensitivity reactions to monoclonal antibodies, any history of anaphylaxis, or uncontrolled asthma (ie, 3 or more features of partially controlled asthma Global Initiative for Asthma 2011).
Known human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS) related illness.
Active infection requiring systemic therapy.
Positive test for HBV surface antigen and / or confirmatory HCV RNA (if anti-HCV antibody tested positive)
Administration of a live vaccine within 30 days prior to study entry.
Current or prior use of immunosuppressive medication within 7 days prior to start of study treatment.

The following are exceptions to this exclusion criterion:

Intranasal, inhaled, topical steroids, or local steroid injections (eg, intra-articular injection);
Systemic corticosteroids at physiologic doses not to exceed 10 mg/day of prednisone or equivalent;
Steroids as premedication for hypersensitivity reactions (eg, CT scan premedication).
Active autoimmune disease that might deteriorate when receiving an immunostimulatory agents.

Patients with diabetes type I, vitiligo, psoriasis, hypo- or hyperthyroid disease not requiring immunosuppressive treatment are eligible.

Female patients who are pregnant or lactating, or are of childbearing potential and not practicing a medically acceptable method of birth control.
Treatment with oral anticoagulant such Coumadin.
Alcoholism (patient interview, investigator judgment)
Resting ECG with QTc > 470msec on 2 or more time points within a 24 hour period or family history of long QT syndrome. Torsades de Pointes, arrhythmias (including sustained ventricular tachyarrhythmia and ventricular fibrillation, bradycardia defined as <50 bpm), right bundle branch block and left anterior hemiblock (bifascicular block), unstable angina, coronary/peripheral artery bypass graft, symptomatic congestive heart failure (CHF New York Heart Association Class III or IV), cerebrovascular accident, transient ischemic attack or symptomatic pulmonary embolism.
Prior organ transplantation, including allogeneic stem cell transplantation (excluding autologous bone marrow transplant)
Patients under guardianship.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Centre Hospitalier Lyon Sud	Pierre-Bénite	Pierre Bénite	France	69495
2	Institut Bergonié	Bordeaux		France	33000
3	Centre François Baclesse	Caen		France	14000
4	Centre Oscar Lambret	Lille		France	59000
5	Institut Paoli-Calmettes	Marseille		France	13000
6	Centre Antoine Lacassagne	Nice		France	06000
7	Assistance Publique Hôpitaux de Paris	Paris		France
8	Centre Eugène Marquis	Rennes		France	35000