Maintenance with lanreotide in small-cell lung cancer expressing somatostatine receptors: A multicenter, randomized, phase 3 trial.
Aged
Aged, 80 and over
Female
Gene Expression
Humans
Italy
Lung Neoplasms
/ diagnosis
Maintenance Chemotherapy
Male
Middle Aged
Neoplasm Metastasis
Neoplasm Staging
Peptides, Cyclic
/ administration & dosage
Prognosis
Proportional Hazards Models
Receptors, Somatostatin
/ genetics
Small Cell Lung Carcinoma
/ diagnosis
Somatostatin
/ administration & dosage
Treatment Outcome
Lanreotide
Maintenance
Small-cell lung cancer
Somatostatine analogue
Journal
Lung cancer (Amsterdam, Netherlands)
ISSN: 1872-8332
Titre abrégé: Lung Cancer
Pays: Ireland
ID NLM: 8800805
Informations de publication
Date de publication:
08 2019
08 2019
Historique:
received:
29
04
2019
revised:
06
06
2019
accepted:
11
06
2019
entrez:
20
7
2019
pubmed:
20
7
2019
medline:
23
6
2020
Statut:
ppublish
Résumé
Considering the frequent expression of somatostatine receptors, we designed the G04.2011 trial to investigate the efficacy of the somatostatine analogue lanreotide in maintenance for SCLC patients after response to standard treatment. A multicenter, randomized, phase 3 trial was conducted in SCLC expressing somatostatine receptors at baseline Octreoscan, responding after platinum-based chemotherapy with/without radiotherapy. Patients were randomized 1:1 to receive maintenance lanreotide 120 mg subcutaneously every 28 days, up to 1 year or progression versus observation. Randomization was stratified according to stage (limited/extended, LD/ED). The primary end-point was progression-free survival (PFS). Secondary endpoints were overall survival (OS) and safety. Seventy-one patients were randomly assigned (39 to lanreotide, 32 to observation) in 9 Italian institutions. Median PFS was 3.6 (95% CI 3.2-3.9) with lanreotide versus 2.3 months (95% CI 1.7-2.9) with observation (HR 1.51, 95% CI 0.90-2.50; P = 0.11). Stage was an independent predictor for PFS (HR 3.14, 95% CI 1.77-5.57; P < 0.0001). Median PFS was 7.0 (95% CI <1-13.5) with lanreotide versus 3.8 months (95% CI <1-8.6) with observation in LD (P = 0.21), and 3.0 (95% CI 2.2-3.8) versus 2.2 (95% 1.7-2.7) in ED (P = 0.19). Median OS was 9.5 (95% CI 4.8-14.3) with lanreotide versus 4.7 months (95% CI <1-16.6) with observation (P = 0.47). Treatment-related adverse events occurred in 28% of patients with lanreotide (grade 3 in two patients). Although survival outcomes were not significantly prolonged with lanreotide as a maintenance in SCLC expressing somatostatin receptors after response to standard treatment, lanreotide showed a slight PFS benefit in LD SCLC deserving further investigations.
Identifiants
pubmed: 31319970
pii: S0169-5002(19)30504-5
doi: 10.1016/j.lungcan.2019.06.011
pii:
doi:
Substances chimiques
Peptides, Cyclic
0
Receptors, Somatostatin
0
lanreotide
0G3DE8943Y
Somatostatin
51110-01-1
Types de publication
Clinical Trial, Phase III
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
121-126Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.