Literature DB >> 33945297

Lenvatinib in Patients With Advanced Grade 1/2 Pancreatic and Gastrointestinal Neuroendocrine Tumors: Results of the Phase II TALENT Trial (GETNE1509).

Jaume Capdevila1, Nicola Fazio2, Carlos Lopez3, Alexandre Teulé4, Juan W Valle5, Salvatore Tafuto6, Ana Custodio7, Nicholas Reed8, Markus Raderer9, Enrique Grande10, Rocio Garcia-Carbonero11, Paula Jimenez-Fonseca12, Jorge Hernando1, Alberto Bongiovanni13, Francesca Spada2, Vicente Alonso14, Lorenzo Antonuzzo15, Andrea Spallanzani16, Alfredo Berruti17, Adelaida La Casta18, Isabel Sevilla19, Patrizia Kump20, Dario Giuffrida21, Xavier Merino1, Lorena Trejo1, Pablo Gajate22, Ignacio Matos1, Angela Lamarca5, Toni Ibrahim13.   

Abstract

PURPOSE: Approved systemic therapies for advanced gastroenteropancreatic neuroendocrine tumors (GEP-NETs) have shown limited capacity to reduce tumor burden and no antitumor activity after progression to targeted agents (TAs). We investigated the efficacy and safety of lenvatinib in patients with previously treated advanced GEP-NETs. PATIENTS AND METHODS: This was a multicenter, single-arm, open-label, phase II trial with two parallel cohorts (ClinicalTrials.gov identifier: NCT02678780) involving 21 institutions in 4 European countries. Eligible patients had histologically confirmed advanced grade 1-2 pancreatic (panNET) or GI (GI-NET) NETs with documented tumor progression after treatment with a TA (panNET) or somatostatin analogs (GI-NET). Patients were treated with lenvatinib 24 mg once daily until disease progression or treatment intolerance. The primary end point was overall response rate by central radiology review. Secondary end points included progression-free survival, overall survival, duration of response, and safety.
RESULTS: Between September 2015 and March 2017, a total of 111 patients were enrolled, with 55 (panNET) and 56 (GI-NET) patients in each cohort. The median follow-up was 23 months. The overall response rate was 29.9% (95% CI, 21.6 to 39.6): 44.2% (panNET) and 16.4% (GI-NET). The median (range) duration of response was 19.9 (8.4-30.8) and 33.9 (10.6-38.3) months in the panNET and GI-NET groups, respectively. The median progression-free survival was 15.7 months (95% CI, 14.1 to 19.5). The most common adverse events were fatigue, hypertension, and diarrhea; 93.7% of patients required dose reductions or interruptions.
CONCLUSION: We report the highest centrally confirmed response reported to date with a multikinase inhibitor in advanced GEP-NETs, with a particularly strong response in the panNET cohort. This study provides novel evidence for the efficacy of lenvatinib in patients with disease progression following treatment with other TAs, suggesting the potential value of lenvatinib in the treatment of advanced GEP-NETs.

Entities:  

Year:  2021        PMID: 33945297     DOI: 10.1200/JCO.20.03368

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  14 in total

Review 1.  Pancreatic Neuroendocrine Tumors: Molecular Mechanisms and Therapeutic Targets.

Authors:  Chandra K Maharjan; Po Hien Ear; Catherine G Tran; James R Howe; Chandrikha Chandrasekharan; Dawn E Quelle
Journal:  Cancers (Basel)       Date:  2021-10-12       Impact factor: 6.639

Review 2.  Systemic Therapy of Advanced Well-differentiated Small Bowel Neuroendocrine Tumors Progressive on Somatostatin Analogues.

Authors:  Parul Agarwal; Amr Mohamed
Journal:  Curr Treat Options Oncol       Date:  2022-08-08

Review 3.  The Landscape and Clinical Application of the Tumor Microenvironment in Gastroenteropancreatic Neuroendocrine Neoplasms.

Authors:  Shuaishuai Xu; Chanqi Ye; Ruyin Chen; Qiong Li; Jian Ruan
Journal:  Cancers (Basel)       Date:  2022-06-13       Impact factor: 6.575

Review 4.  Advances in medical treatment for pancreatic neuroendocrine neoplasms.

Authors:  Yuan-Liang Li; Zi-Xuan Cheng; Fu-Huan Yu; Chao Tian; Huang-Ying Tan
Journal:  World J Gastroenterol       Date:  2022-05-28       Impact factor: 5.374

5.  The Mount Sinai Clinical Pathway for the Diagnosis and Management of Hypercortisolism due to Ectopic ACTH Syndrome.

Authors:  Eva L Alba; Emily A Japp; Gustavo Fernandez-Ranvier; Ketan Badani; Eric Wilck; Munir Ghesani; Andrea Wolf; Edward M Wolin; Virginia Corbett; David Steinmetz; Maria Skamagas; Alice C Levine
Journal:  J Endocr Soc       Date:  2022-05-06

Review 6.  Pharmacotherapeutic Management of Well-Differentiated Neuroendocrine Tumors in Older Patients: Current Status and Potential Therapies.

Authors:  Christiana Crook; Ya-Han Zhang; Daneng Li
Journal:  Drugs Aging       Date:  2022-03-25       Impact factor: 4.271

7.  Everolimus with or without bevacizumab in advanced pNET: CALGB 80701 (Alliance).

Authors:  Matthew H Kulke; Fang-Shu Ou; Donna Niedzwiecki; Lucas Huebner; Pamela Kunz; Hagen F Kennecke; Edward M Wolin; Jennifer A Chan; Eileen M O'Reilly; Jeffrey A Meyerhardt; Alan Venook
Journal:  Endocr Relat Cancer       Date:  2022-05-09       Impact factor: 5.900

8.  Incidence and risk of hypertension with lenvatinib in treatment of solid tumors: An updated systematic review and meta-analysis.

Authors:  Hongxiao Wu; Xiaoyan Ding; Yongchao Zhang; Wei Li; Jinglong Chen
Journal:  J Clin Hypertens (Greenwich)       Date:  2022-05-10       Impact factor: 2.885

Review 9.  Multimodal Management of Grade 1 and 2 Pancreatic Neuroendocrine Tumors.

Authors:  Ugo Marchese; Martin Gaillard; Anna Pellat; Stylianos Tzedakis; Einas Abou Ali; Anthony Dohan; Maxime Barat; Philippe Soyer; David Fuks; Romain Coriat
Journal:  Cancers (Basel)       Date:  2022-01-15       Impact factor: 6.639

Review 10.  Orchestrating Treatment Modalities in Metastatic Pancreatic Neuroendocrine Tumors-Need for a Conductor.

Authors:  Alexander R Siebenhüner; Melanie Langheinrich; Juliane Friemel; Niklaus Schäfer; Dilmurodjon Eshmuminov; Kuno Lehmann
Journal:  Cancers (Basel)       Date:  2022-03-14       Impact factor: 6.639

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