Efficacy and Safety of Lanreotide Autogel and Temozolomide Combination Therapy in Progressive Thoracic Neuroendocrine Tumors (Carcinoid): Results from the Phase 2 ATLANT Study.

Carcinoid Disease control rate Lanreotide autogel Progression-free survival Temozolomide Therapy Thoracic neuroendocrine tumors

Journal

Neuroendocrinology
ISSN: 1423-0194
Titre abrégé: Neuroendocrinology
Pays: Switzerland
ID NLM: 0035665

Informations de publication

Date de publication:
2023
Historique:
received: 08 02 2022
accepted: 22 08 2022
pubmed: 1 9 2022
medline: 7 3 2023
entrez: 31 8 2022
Statut: ppublish

Résumé

Lanreotide autogel (LAN) and temozolomide (TMZ) are guidelines-recommended monotherapies for thoracic neuroendocrine tumors (carcinoids; T-NETs), but prospective data for both combined and monotherapies are lacking. ATLANT (NCT02698410) evaluated efficacy and safety of LAN/TMZ in progressive T-NETs. ATLANT was a 12-month, Italian, phase 2, single-arm, open-label, multicenter pilot study. Eligible patients had unresectable, locally advanced/metastatic, well-/moderately differentiated T-NETs with radiological progression. Patients received subcutaneous LAN 120 mg every 28 days and oral TMZ 250 mg/day for 5 consecutive days every 28-day cycle. Main endpoints are disease control rate (DCR) at 9 months (primary; investigator-assessed), median progression-free survival (PFS), biomarkers, and safety. The number of patients was 40; 60% were male. Primary tumor site was lung (90%) and thymus (10%). Carcinoid type was typical (20.0%) and atypical (52.5%). DCR at 9 months was 35.0% (95% confidence interval (CI) 20.63-51.68; nonacceptability threshold ≤10%, p < 0.0001; not significantly above clinically relevant threshold ≥30%, p = 0.2968). DCR between 7.5 and 10.5 months (sensitivity analysis) was 45.0% (95% CI: 29.26-61.51) and clinically relevant (p = 0.0320 at ≥30% threshold). Median PFS was 37.1 (95% CI: 24.1-52.9) weeks. No association was observed between biomarker variations (chromogranin A, neuron-specific enolase, somatostatin receptor type-2, Ki-67, 6-O-methylguanine-DNA-methyl-transferase) and DCR or PFS. Most patients (97.5%) had treatment-emergent adverse events (TEAEs); 72.5% had treatment-related TEAEs. TEAEs were mainly grade 1/2. No unanticipated TEAEs were reported. This study showed that the LAN/TMZ combination has promising efficacy in progressive T-NETs, and was well tolerated. Larger studies are warranted to support the clinical benefits of LAN/TMZ in patients with T-NETs.

Identifiants

pubmed: 36044870
pii: 000526811
doi: 10.1159/000526811
doi:

Substances chimiques

Temozolomide YF1K15M17Y
lanreotide 0G3DE8943Y

Banques de données

ClinicalTrials.gov
['NCT02698410']

Types de publication

Multicenter Study Clinical Trial, Phase II Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

332-342

Informations de copyright

© 2022 S. Karger AG, Basel.

Auteurs

Piero Ferolla (P)

Multidisciplinary NET Center, Umbria Regional Cancer Network, Perugia, Italy.

Alfredo Berruti (A)

Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, Medical Oncology, University of Brescia at ASST-Spedali Civili, Brescia, Italy.

Francesca Spada (F)

Division of Gastrointestinal Medical Oncology and Neuroendocrine Tumors, European Institute of Oncology, IRCCS, IEO, Milan, Italy.

Maria Pia Brizzi (MP)

Department of Oncology, Medical Oncology, A.O.U. San Luigi Gonzaga, Turin, Italy.

Toni Ibrahim (T)

Osteoncology and Rare Tumors Center, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST), "Dino Amadori", Meldola, Italy.

Riccardo Marconcini (R)

Department of Oncology 2, A.O.U. Pisana, Santa Chiara Hospital, Pisa, Italy.

Dario Giuffrida (D)

Department of Oncology, Istituto Oncologico del Mediterraneo, Viagrande (Catania), Italy.

Vito Amoroso (V)

Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, Medical Oncology, University of Brescia at ASST-Spedali Civili, Brescia, Italy.

Anna La Salvia (A)

Department of Oncology, Medical Oncology, A.O.U. San Luigi Gonzaga, Turin, Italy.

Vanja Vaccaro (V)

Medical Oncology 1, Regina Elena National Cancer Institute, IRCCS, Rome, Italy.

Antongiulio Faggiano (A)

Endocrinology Unit, Department of Clinical and Molecular Medicine, Sant'Andrea Hospital, Università Sapienza di Roma, Rome, Italy.

Annamaria Colao (A)

Department of Clinical Medicine and Surgery and UNESCO Chair for Health Education and Sustainable Development, Università Federico II di Napoli, Naples, Italy.

Marco Volante (M)

Department of Oncology, University of Turin, Turin, Italy.

Simona Ghizzoni (S)

Ipsen, Assago, Milan, Italy.

Paola Mazzanti (P)

Ipsen, Assago, Milan, Italy.

Aude Houchard (A)

Ipsen, Boulogne-Billancourt, France.

Nicola Fazio (N)

Division of Gastrointestinal Medical Oncology and Neuroendocrine Tumors, European Institute of Oncology, IRCCS, IEO, Milan, Italy.

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Classifications MeSH