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Mini Oral - NETs and endocrine tumours

1161MO - Lanreotide autogel (LAN) and temozolomide (TMZ) combination therapy in progressive thoracic neuroendocrine tumours (TNETs): ATLANT study results

Date

18 Sep 2020

Session

Mini Oral - NETs and endocrine tumours

Topics

Tumour Site

Neuroendocrine Neoplasms

Presenters

Piero Ferolla

Citation

Annals of Oncology (2020) 31 (suppl_4): S711-S724. 10.1016/annonc/annonc281

Authors

P. Ferolla1, A. Berruti2, F. Spada3, M.P. Brizzi4, T. Ibrahim5, A. Colao6, A. Faggiano7, R. Marconcini8, V. Vaccaro9, D. Giuffrida10, S. Ghizzoni11, A. Houchard12, N. Fazio2

Author affiliations

  • 1 Multidisciplinary Net Group, Umbria Regional Cancer Network, 06126 - Perugia/IT
  • 2 Department Of Medical And Surgical Specialties, Radiological Sciences, And Publi, Azienda Ospedaliera Spedali Civili di Brescia, 25123 - Brescia/IT
  • 3 Medical Oncology, European Institute of Oncology, IRCCS, IEO, 20141 - Milan/IT
  • 4 Gic Colorectal Cancers, A.O.U. San Luigi Gonzaga, 10043 - Orbassano/IT
  • 5 Tumori Rari E Testa-collo Dept., IRCCS Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori - I.R.S.T, 47014 - Meldola/IT
  • 6 Department Of Clinical Medicine And Surgery, Endocrinology Unit, Università Federico II di Napoli, Naples/IT
  • 7 Dipartimento Di Medicina Sperimentale, Università Sapienza di Roma, Rome/IT
  • 8 A.o.u. Pisana, Santa Chiara Hospital, Pisa/IT
  • 9 Regina Elena National Cancer Institute, IRCCS, Rome/IT
  • 10 ., Istituto Oncologico del Mediterraneo, Viagrande/IT
  • 11 Medical Scientific Liaison, Ipsen, Milan/IT
  • 12 Statistics, Ipsen, Boulogne-Billancourt/FR

Resources

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Abstract 1161MO

Background

LAN and TMZ are among the main therapies recommended for progressive TNETs but prospective data are lacking. We present safety and efficacy outcomes of this combination in progressive TNETs.

Methods

ATLANT was a 12-month, phase II, multicentre, single-arm, open-label study. Eligible patients had unresectable, locally advanced or metastatic, well-differentiated TNETs (bronchial or thymic, typical or atypical carcinoid) with baseline radiological progression (RECIST v1.1) in the previous 12 months. Patients received subcutaneous LAN 120 mg and oral TMZ 250 mg/day over 5 days, every 28 days. Primary endpoint: disease control rate (DCR) at 9 months (RECIST v1.1 complete response, partial response or stable disease [clinically relevant: ≥30%, unacceptable: ≤10%]). Data were analysed using exact binomial proportion tests for one-way tables.

Results

Patients (N=40; 60% male) had a mean (SD) age of 64.9 (11.8) years. The primary tumour site was: lung, 90%; thymus, 10% (typical, 20.0%; atypical, 52.5%; carcinoid, 27.5%). Mitotic count (mitoses/2 mm2): <2: 30%; ≥2–<10: 42.5%; ≥10: 2.5%; not done: 25%. Ki-67 expression (N=20): <4%: 10%; 4–<25%: 80%; ≥25%: 10%. TNM staging: primary tumour TX: 5.1%, T0: 46.2%, T1: 7.7%, T2: 12.8%, T3: 10.3%, T4: 17.9%; regional lymph node N0: 56.4%, N1: 2.6%, N2: 23.1%, N3: 17.9%; distant metastasis M0: 5.1%, M1: 94.9%. Locally assessed DCR at 9 months (ITT population; N=40) was 35.0% (95% CI: 20.63; 51.68) (significantly higher than 10% p<0.0001 but not superior to 30% p=0.297). Median progression-free survival was 37.1 (95% CI: 24.1; 52.9) weeks. In total, 97.5% of patients had treatment-emergent adverse events (TEAEs; >90% of TEAEs were Grade 1/2), 9 (22.5%) patients had serious TEAEs (of which 2 were treatment related), 2 TEAEs led to withdrawal of study treatment, and 2 led to death. The observed TEAEs were in line with the known individual drug profiles, and there were no new or unexpected AEs. Most common TEAEs included nausea (52.5%), vomiting (32.5%) and diarrhoea (30.0%).

Conclusions

These results suggest that the LAN and TMZ combination was generally well tolerated and could be an effective regimen for managing progressive TNETs.

Clinical trial identification

NCT02698410; EudraCT: 2014-005579-10.

Editorial acknowledgement

Cara Valvona, PhD, on behalf of Watermeadow Medical, an Ashfield company, provided medical writing support, which was funded by the study sponsor in accordance with Good Publication Practice guidelines.

Legal entity responsible for the study

Ipsen.

Funding

Ipsen.

Disclosure

P. Ferolla: Advisory/Consultancy, Speaker Bureau/Expert testimony: Ipsen; Advisory/Consultancy, Speaker Bureau/Expert testimony: Novartis; Advisory/Consultancy, Speaker Bureau/Expert testimony: Merck Serono. A. Berruti: Honoraria (self), Advisory/Consultancy: Ipsen; Honoraria (self), Advisory/Consultancy: Novartis; Honoraria (self), Advisory/Consultancy: Pfizer. F. Spada: Honoraria (self), Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses: Ipsen; Advisory/Consultancy, Speaker Bureau/Expert testimony: AAA; Advisory/Consultancy, Speaker Bureau/Expert testimony: Novartis; Advisory/Consultancy, Speaker Bureau/Expert testimony: Merck. M.P. Brizzi: Advisory/Consultancy: Ipsen; Advisory/Consultancy: Novartis; Advisory/Consultancy: Celgene. T. Ibrahim: Advisory/Consultancy: Eisai; Research grant/Funding (institution): Novartis. A. Colao: Advisory/Consultancy, Speaker Bureau/Expert testimony, Research grant/Funding (self): Novartis; Advisory/Consultancy, Speaker Bureau/Expert testimony: Ipsen. A. Faggiano: Advisory/Consultancy, Research grant/Funding (institution): Ipsen; Advisory/Consultancy, Research grant/Funding (institution): Novartis. D. Giuffrida: Advisory/Consultancy: AstraZeneca; Advisory/Consultancy: Celgene; Advisory/Consultancy: Ipsen; Speaker Bureau/Expert testimony: Pfizer; Travel/Accommodation/Expenses: Novartis; Travel/Accommodation/Expenses: Roche. S. Ghizzoni: Full/Part-time employment: Ipsen. A. Houchard: Full/Part-time employment: Ipsen. N. Fazio: Honoraria (self), Advisory/Consultancy, Research grant/Funding (institution): Novartis; Honoraria (self), Advisory/Consultancy, Research grant/Funding (institution): Ipsen; Honoraria (self), Advisory/Consultancy: Pfizer; Honoraria (self), Advisory/Consultancy, Research grant/Funding (institution): Merck Serono; Honoraria (self), Advisory/Consultancy: Advanced Accelerator Applications; Honoraria (self), Advisory/Consultancy, Research grant/Funding (institution): MSD. All other authors have declared no conflicts of interest.

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