Temozolomide in grade III neuroendocrine neoplasms (G3 NENs): A multicenter retrospective review.

Author:

Chan David1,Bergsland Emily K.2,Chan Jennifer A.3,Gadgil Rujuta3,Halfdanarson Thorvardur Ragnar4,Hornbacker Kathleen5,Kelly Virginia6,Kunz Pamela L.7,McGarrah Patrick Walsh4,Raj Nitya Prabhakar6,Reidy Diane Lauren6,Thawer Alia1,Whitman Julia2,Wu Linda8,Singh Simron1

Affiliation:

1. Sunnybrook Odette Cancer Centre, Toronto, ON, Canada;

2. University of California - San Francisco, San Francisco, CA;

3. Dana-Farber Cancer Institute, Boston, MA;

4. Mayo Clinic, Rochester, MN;

5. Stanford Cancer Clinical Trials Office, Palo Alto, CA;

6. Memorial Sloan Kettering Cancer Center, New York, NY;

7. Stanford University School of Medicine, Stanford, CA;

8. New York Presbyterian-Weill Cornell Medical Center, New York, NY;

Abstract

321 Background: G3 NENs are aggressive, and optimal systemic treatment is unclear. Temozolomide (TEM)-based regimens have been used to treat grade 1-2 NETs, but their efficacy in G3 NENs (Ki-67 > 20%) remains undetermined. Aims: To assess the clinical efficacy of TEM-containing regimens in advanced grade III gastroenteropancreatic NENs (GEPNENs). Methods: A multicentre retrospective review (2008-2017) of patients with metastatic/unresectable G3 GEPNENs who received a TEM-containing regimen. The primary endpoint was time to treatment failure (TTF). Radiologic response was extracted from local reports without formal RECIST criteria. Results: 118 patients in six centers were included (median age 55, 65% male, 15% functional, 75% pancreatic NEN). 57% were well-differentiated, 35% poorly-differentiated, and 18% unknown based on local pathology reports. The regimen used was CAPTEM in 93% and TEM in 7%. Best radiological responses were: complete response (1%), partial response (39%), stable disease (22%), progressive disease (31%), unknown (7%) not by RECIST. Median TTF was 150 days and median overall survival (OS) 18.0 months. Fifteen patients (14%) required dose reductions/discontinuation due to adverse events. TTF was shorter for patients on TEM alone (p = 0.02, Table 1). Well-differentiated NENs had better response rate (52% vs 26%, p = 0.02) and overall survival (30.1 vs 12.0 mo, p = 0.008) compared to poorly-differentiated NEN. Conclusions: This is the largest TEM treatment series in G3 NEN, involving collaboration of several major North American NET centers. 40% of patients showed some degree of response, and treatment was generally well-tolerated. TEM-based regimens should be considered a viable treatment option in this setting. Prospective confirmatory trials (such as EA2142) may face difficulties in accrual due to disease rarity. [Table: see text]

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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