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Combined Lanreotide Autogel and Temozolomide Treatment of Progressive Pancreatic and Intestinal Neuroendocrine Tumors: The Phase II SONNET Study
被引:4
|作者:
Pavel, Marianne
[1
,2
,3
,4
,5
,16
]
Lahner, Harald
[6
]
Hoersch, Dieter
[7
]
Rinke, Anja
[8
,9
]
Denecke, Timm
[10
,11
]
Koch, Arend
[2
,3
,4
,12
]
Regnault, Benjamin
[13
]
Helbig, Dorit
[14
]
Hoffmanns, Philipp
[14
]
Raderer, Markus
[15
]
机构:
[1] Charite Univ Med Berlin, Dept Hepatol & Gastroenterol, Berlin, Germany
[2] Free Univ Berlin, Berlin, Germany
[3] Humboldt Univ, Berlin, Germany
[4] Berlin Inst Hlth BIH, Berlin, Germany
[5] Friedrich Alexander Univ Erlangen Nuernberg, Univ Hosp Erlangen, Dept Med 1, Erlangen, Germany
[6] Univ Hosp Essen, Dept Endocrinol & Metab, Essen, Germany
[7] Zentralklin Bad Berka, Dept Gastroenterol Endocrinol, Bad Berka, Germany
[8] Univ Hosp Giessen & Marburg, Dept Gastroenterol, Marburg, Germany
[9] Philipps Univ Marburg, Marburg, Germany
[10] Charite Univ Med Berlin, Dept Radiol, Campus Virchow Klinikum, Berlin, Germany
[11] Univ Med Ctr Leipzig, Dept Diagnost & Intervent Radiol, Leipzig, Germany
[12] Charite Univ Med Berlin, Dept Neuropathol, Berlin, Germany
[13] Ipsen Pharma, Boulogne Billancourt, France
[14] Ipsen Pharm GmbH, Munich, Germany
[15] Med Univ Vienna, Div Oncol, Internal Med 1, Vienna, Austria
[16] Friedrich Alexander Univ Erlangen Nurnberg, Med Klin 1, Endokrinol & Diabetol, Ulmenweg 18, D-91054 Erlangen, Germany
来源:
关键词:
neuroendocrine tumors;
gastrointestinal neoplasms;
O(6)-methylguanine-DNA methyltransferase;
temozolomide;
lanreotide;
receptors;
somatostatin;
ENETS CONSENSUS GUIDELINES;
MGMT PROMOTER METHYLATION;
NEOPLASMS;
THERAPY;
IMMUNOHISTOCHEMISTRY;
CAPECITABINE;
MULTICENTER;
EVEROLIMUS;
SPANISH;
D O I:
10.1093/oncolo/oyad325
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Background In advanced neuroendocrine tumors (NET), antiproliferative treatment options beyond somatostatin analogs remain limited. Temozolomide (TMZ) has shown efficacy in NET alone or combined with other drugs.Materials and Methods SONNET (NCT02231762) was an open, multicenter, prospective, phase II study to evaluate lanreotide autogel 120 mg (LAN) plus TMZ in patients with progressive advanced/metastatic grade 1/2 gastroenteropancreatic (GEP) NET or of unknown primary. Patients could be enrolled at first-line or higher therapy line. The primary endpoint was disease control rate ([DCR], rate of stable disease [SD], partial [PR], and complete response [CR]) at 6 months of LAN and TMZ. Patients with nonfunctioning (NF) NET without progression at 6 months were randomized to 6-month LAN maintenance or watch and wait, patients with functioning (F)-NET with clinical benefit (PR, SD) continued on LAN.Results Fifty-seven patients were recruited. The majority of patients received the study drug at second or higher treatment line and had an NET G2. DCR at 6 months LAN and TMZ was 73.5%. After 6 months of further LAN maintenance, 54.5% of patients with F-NET and 71.4% with NF-NET had SD or PR vs 41.7% with NF-NET on observation only. LAN and TMZ were effective in all subgroups analyzed. At 12 months of follow-up, median progression-free survival was 11.1 months. Median serum chromogranin A decreased except in NF-NET on observation. O6-methylguanine DNA methyltransferase promoter methylation appeared to better reflect TMZ response than loss of gene expression. During combination therapy, the most frequent treatment-emergent adverse events grade 3/4 reported were nausea (14%), thrombocytopenia (12.3%), and neutropenia (8.8%). Four deaths were reported resulting from severe adverse events not considered related to study medication.Conclusions LAN plus TMZ is a treatment option for patients with progressive GEP-NET with more aggressive biological profile showing a manageable safety profile. Drugs that control tumor growth and/or inhibit hormone release are a mainstay of management of neuroendocrine tumors. This study investigated the combined treatment with lanreotide, a drug derived from the naturally occurring inhibitory hormone somatostatin, and the chemotherapeutic agent temozolomide.
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页码:e643 / e654
页数:12
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