Avelumab in Patients With Gestational Trophoblastic Tumors With Resistance to Single-Agent Chemotherapy: Cohort A of the TROPHIMMUN Phase II Trial.
Adult
Antibiotics, Antineoplastic
/ therapeutic use
Antibodies, Monoclonal, Humanized
/ adverse effects
Antimetabolites, Antineoplastic
/ therapeutic use
Antineoplastic Agents, Immunological
/ adverse effects
Chorionic Gonadotropin
/ blood
Dactinomycin
/ therapeutic use
Drug Resistance, Neoplasm
Fatigue
/ chemically induced
Female
Follow-Up Studies
Gestational Trophoblastic Disease
/ blood
Humans
Injection Site Reaction
/ etiology
Methotrexate
/ therapeutic use
Middle Aged
Nausea
/ chemically induced
Pregnancy
Retreatment
Vomiting
/ chemically induced
Young Adult
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333
Informations de publication
Date de publication:
20 09 2020
20 09 2020
Historique:
pubmed:
28
7
2020
medline:
3
3
2021
entrez:
28
7
2020
Statut:
ppublish
Résumé
Women with gestational trophoblastic tumors (GTT) resistant to single-agent chemotherapy receive alternative chemotherapy regimens, which, although effective, cause considerable toxicity. All GTT subtypes express programmed death-ligand 1 (PD-L1), and natural killer (NK) cells are involved in trophoblast immunosurveillance. Avelumab (anti-PD-L1) induces NK cell-mediated cytotoxicity. The TROPHIMMUN trial assessed avelumab in women with chemotherapy-resistant GTT. In this phase II multicenter trial (ClinicalTrials.gov identifier: NCT03135769), women with GTT who experienced disease progression after single-agent chemotherapy received avelumab 10 mg/kg intravenously every 2 weeks until human chorionic gonadotropin (hCG) normalization, followed by 3 consolidation cycles. Rate of hCG normalization was the primary endpoint (2-step Simon design). Between December 2016 and September 2018, 15 patients were treated. Median age was 34 years; disease stage was I or III in 53.3% and 46.7% of women, respectively; and International Federation of Gynecology and Obstetrics (FIGO) score was 0-4 in 33.3%, 5-6 in 46.7%, and ≥ 7 in 20% of patients. Prior treatment included methotrexate (100%) and actinomycin D (7%). Median follow-up was 25 months, and median number of avelumab cycles was 8 (range, 2-11). Grade 1-2 treatment-related adverse events occurred in 93% of patients, most commonly (≥ 25%) fatigue (33.3%), nausea/vomiting (33.3%), and infusion-related reaction (26.7%). One patient had grade 3 uterine bleeding (treatment unrelated). Eight patients (53.3%) had hCG normalization after a median of 9 avelumab cycles; none subsequently relapsed. Probability of normalization was not associated with disease stage, FIGO score, or baseline hCG. One patient subsequently had a healthy pregnancy. In avelumab-resistant patients (46.7%), hCG was normalized with actinomycin D (42.3%) or combination chemotherapy/surgery (57.1%). In patients with single-agent chemotherapy-resistant GTT, avelumab had a favorable safety profile and cured approximately 50% of patients. Avelumab could be a new therapeutic option, particularly in patients who would otherwise receive combination chemotherapy.
Identifiants
pubmed: 32716740
doi: 10.1200/JCO.20.00803
pmc: PMC7499607
doi:
Substances chimiques
Antibiotics, Antineoplastic
0
Antibodies, Monoclonal, Humanized
0
Antimetabolites, Antineoplastic
0
Antineoplastic Agents, Immunological
0
Chorionic Gonadotropin
0
Dactinomycin
1CC1JFE158
avelumab
KXG2PJ551I
Methotrexate
YL5FZ2Y5U1
Banques de données
ClinicalTrials.gov
['NCT03135769']
Types de publication
Clinical Trial, Phase II
Journal Article
Multicenter Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
3129-3137Commentaires et corrections
Type : CommentIn
Type : CommentIn
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