TY - JOUR
T1 - Peptide Receptor Radionuclide Therapy or Everolimus in Metastatic Neuroendocrine Tumors
T2 - The SeqEveRIV Study, a National Study from the French Group of Endocrine Tumors and Endocan–RENATEN Network
AU - Fosse, Aurelien
AU - Hadoux, Julien
AU - Girot, Paul
AU - Beron, Amandine
AU - Afchain, Pauline
AU - Cottereau, Anne Segolene
AU - Baudin, Eric
AU - Dierickx, Lawrence O.
AU - Lecomte, Thierry
AU - Perrier, Marine
AU - Lepage, Come
AU - Bouhier-Leporrier, Karine
AU - Goichot, Bernard
AU - Lachachi, Boumediene
AU - Walter, Thomas
AU - Durand, Alice
N1 - Publisher Copyright:
COPYRIGHT © 2024 by the Society of Nuclear Medicine and Molecular Imaging.
PY - 2024/9/1
Y1 - 2024/9/1
N2 - Everolimus and peptide receptor radionuclide therapy (PRRT, 177Lu-DOTATATE) are 2 treatments recommended in guidelines for gastroenteropancreatic metastatic neuroendocrine tumors. However, the best treatment sequence remains unknown. Methods: We designed a retrospective multicenter study that included patients from the national prospective database of the Groupe d’Étude des Tumeurs Endocrines who had been treated using everolimus and PRRT between April 2004 and October 2022. The primary aim was to compare the 2 treatments (everolimus and PRRT) in terms of efficacy and safety, and the secondary aim was to evaluate the sequences (PRRT followed by everolimus or everolimus followed by PRRT) based on overall progression-free survival (PFS) (PFS during first treatment + PFS during second treatment) in patients with metastatic neuroendocrine tumors. Results: Both treatments were used for 84 patients. The objective response rate and median PFS were 5 (6.0%) and 16.1 mo (95% CI, 11.5–20.7 mo), respectively, under everolimus and 19 (22.6%) and 24.5 mo (95% CI, 17.7–31.3 mo), respectively, for PRRT. The safety profile was also better for PRRT. Median overall PFS was 43.2 mo (95% CI, 33.7–52.7 mo) for the everolimus–PRRT sequence and 30.6 mo (95% CI, 17.8–43.4 mo) for the PRRT–everolimus sequence (hazard ratio, 0.69; 95% CI, 0.39–1.24; P 5 0.22). Conclusion: PRRT was more effective and less toxic than everolimus. Overall PFS was similar between the 2 sequences, suggesting case-by-case discussion if the patient is eligible for both treatments, but PRRT should be used first when an objective response is needed or in frail populations.
AB - Everolimus and peptide receptor radionuclide therapy (PRRT, 177Lu-DOTATATE) are 2 treatments recommended in guidelines for gastroenteropancreatic metastatic neuroendocrine tumors. However, the best treatment sequence remains unknown. Methods: We designed a retrospective multicenter study that included patients from the national prospective database of the Groupe d’Étude des Tumeurs Endocrines who had been treated using everolimus and PRRT between April 2004 and October 2022. The primary aim was to compare the 2 treatments (everolimus and PRRT) in terms of efficacy and safety, and the secondary aim was to evaluate the sequences (PRRT followed by everolimus or everolimus followed by PRRT) based on overall progression-free survival (PFS) (PFS during first treatment + PFS during second treatment) in patients with metastatic neuroendocrine tumors. Results: Both treatments were used for 84 patients. The objective response rate and median PFS were 5 (6.0%) and 16.1 mo (95% CI, 11.5–20.7 mo), respectively, under everolimus and 19 (22.6%) and 24.5 mo (95% CI, 17.7–31.3 mo), respectively, for PRRT. The safety profile was also better for PRRT. Median overall PFS was 43.2 mo (95% CI, 33.7–52.7 mo) for the everolimus–PRRT sequence and 30.6 mo (95% CI, 17.8–43.4 mo) for the PRRT–everolimus sequence (hazard ratio, 0.69; 95% CI, 0.39–1.24; P 5 0.22). Conclusion: PRRT was more effective and less toxic than everolimus. Overall PFS was similar between the 2 sequences, suggesting case-by-case discussion if the patient is eligible for both treatments, but PRRT should be used first when an objective response is needed or in frail populations.
KW - everolimus
KW - metastatic
KW - neuroendocrine tumors
KW - peptide receptor radionuclide therapy
KW - sequence
UR - http://www.scopus.com/inward/record.url?scp=85203259176&partnerID=8YFLogxK
U2 - 10.2967/jnumed.123.267363
DO - 10.2967/jnumed.123.267363
M3 - Article
C2 - 39089810
AN - SCOPUS:85203259176
SN - 0161-5505
VL - 65
SP - 1416
EP - 1422
JO - Journal of Nuclear Medicine
JF - Journal of Nuclear Medicine
IS - 9
ER -