Daily Oral Everolimus Activity in Patients With Metastatic Pancreatic Neuroendocrine Tumors After Failure of Cytotoxic Chemotherapy: A Phase II Trial

Author:

Yao James C.1,Lombard-Bohas Catherine1,Baudin Eric1,Kvols Larry K.1,Rougier Philippe1,Ruszniewski Philippe1,Hoosen Sakina1,St. Peter Jessica1,Haas Tomas1,Lebwohl David1,Van Cutsem Eric1,Kulke Matthew H.1,Hobday Timothy J.1,O'Dorisio Thomas M.1,Shah Manisha H.1,Cadiot Guillaume1,Luppi Gabriele1,Posey James A.1,Wiedenmann Bertram1

Affiliation:

1. From the University of Texas M. D. Anderson Cancer Center, Houston, TX; H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL; Novartis Oncology, Florham Park, NJ; Dana-Farber Cancer Institute, Boston, MA; Mayo Clinic, Rochester, MN; University of Iowa, Iowa City, IA; Ohio State University Comprehensive Cancer Center, Columbus, OH; University of Alabama at Birmingham, Birmingham, AL; H. E. Herriot, Hospices Civils de Lyon, Lyon; Institut Gustave Roussy, Villejuif; Hôpital Ambroise Paré, Boulogne...

Abstract

PurposeNo established treatment exists for pancreatic neuroendocrine tumor (NET) progression after failure of chemotherapy. Everolimus (RAD001), an oral inhibitor of mammalian target of rapamycin, in combination with octreotide has demonstrated encouraging antitumor activity in patients with NETs.Patients and MethodsThis open-label, phase II study assessed the clinical activity of everolimus in patients with metastatic pancreatic NETs who experienced progression on or after chemotherapy. Patients were stratified by prior octreotide therapy (stratum 1: everolimus 10 mg/d, n = 115; stratum 2: everolimus 10 mg/d plus octreotide long-acting release [LAR], n = 45). Tumor assessments (using Response Evaluation Criteria in Solid Tumors) were performed every 3 months. Chromogranin A (CgA) and neuron-specific enolase (NSE) were assessed monthly if elevated at baseline. Trough concentrations of everolimus and octreotide were assessed.ResultsBy central radiology review, in stratum 1, there were 11 partial responses (9.6%), 78 patients (67.8%) with stable disease (SD), and 16 patients (13.9%) with progressive disease; median progression-free survival (PFS) was 9.7 months. In stratum 2, there were two partial responses (4.4%), 36 patients (80%) with SD, and no patients with progressive disease; median PFS was 16.7 months. Patients with an early CgA or NSE response had a longer PFS compared with patients without an early response. Coadministration of octreotide LAR and everolimus did not impact exposure to either drug. Most adverse events were mild to moderate and were consistent with those previously seen with everolimus.ConclusionDaily everolimus, with or without concomitant octreotide LAR, demonstrates antitumor activity as measured by objective response rate and PFS and is well tolerated in patients with advanced pancreatic NETs after failure of prior systemic chemotherapy.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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