TY - JOUR
T1 - Long-Term Safety Experience with Telotristat Ethyl Across Five Clinical Studies in Patients with Carcinoid Syndrome
AU - Anthony, Lowell B.
AU - Kulke, Matthew H.
AU - Caplin, Martyn E.
AU - Bergsland, Emily
AU - Öberg, Kjell
AU - Pavel, Marianne
AU - Hörsch, Dieter
AU - Warner, Richard R.P.
AU - O'Dorisio, Thomas M.
AU - Dillon, Joseph S.
AU - Lapuerta, Pablo
AU - Kassler-Taub, Kenneth
AU - Jiang, Wenjun
N1 - Funding Information:
We thank the patients and investigators for participating in the studies. We thank James Banigan, Ph.D. (Chameleon Communications International, with funding provided by Lexicon Pharmaceuticals, Inc.), for medical editorial assistance with this manuscript. We thank the following Lexicon employees: Kristi A. Boehm, M.S., E.L.S., for her assistance with figure preparation, text formatting, and editing of this manuscript; Linda Law, M.D., M.B.A., for study design; Karie Arnold, B.S., and Ernest Wang, B.S., for study monitoring; and Nam Wommack, B.S.N., M.P.H., for data management. Lastly, we would like to thank the team at INC Research (Raleigh, NC) for study conduct, monitoring, analysis, and reporting. We thank Ipsen Pharmaceuticals, Inc., a partner of Lexicon Pharmaceuticals, Inc., for review of this manuscript for medical accuracy. This work was supported by Lexicon Pharmaceuticals, Inc., The Woodlands, TX. Employees of the company were involved in the study designs; the collection, analysis, and interpretation of data; the writing and review
Funding Information:
We thank the patients and investigators for participating in the studies. We thank James Banigan, Ph.D. (Chameleon Communications International, with funding provided by Lexicon Pharmaceuticals, Inc.), for medical editorial assistance with this manuscript. We thank the following Lexicon employees: Kristi A. Boehm, M.S., E.L.S., for her assistance with figure preparation, text formatting, and editing of this manuscript; Linda Law, M.D., M.B.A., for study design; Karie Arnold, B.S., and Ernest Wang, B.S., for study monitoring; and Nam Wommack, B.S.N., M.P.H., for data management. Lastly, we would like to thank the team at INC Research (Raleigh, NC) for study conduct, monitoring, analysis, and reporting. We thank Ipsen Pharmaceuticals, Inc., a partner of Lexicon Pharmaceuticals, Inc., for review of this manuscript for medical accuracy. This work was supported by Lexicon Pharmaceuticals, Inc., The Woodlands, TX. Employees of the company were involved in the study designs; the collection, analysis, and interpretation of data; the writing and review of the manuscript; and the decision to submit for publication. Selected data have been presented in abstract/poster format at the European Society of Medical Oncology Congress, Madrid, Spain, September 8?12, 2017 (442P). Marianne Pavel is currently affiliated with the Department of Medicine 1, Division of Endocrinology, Friedrich-Alexander-Universit?t Erlangen-N?rnberg, Erlangen, Germany.
Publisher Copyright:
© AlphaMed Press 2019
PY - 2019
Y1 - 2019
N2 - Background: Patients with neuroendocrine tumors (NETs) and carcinoid syndrome experience considerable morbidity and mortality; carcinoid syndrome may be associated with shorter survival. Carcinoid syndrome is linked to tumoral secretion of serotonin and other bioactive substances. The subsequent debilitating diarrhea and urgency to defecate pose significant health risks. In previous studies, telotristat ethyl, a tryptophan hydroxylase inhibitor, was effective and well tolerated in treating carcinoid syndrome diarrhea. We present pooled safety data from five clinical trials with telotristat ethyl in patients with carcinoid syndrome. Subjects, Materials, and Methods: Adverse events reported during telotristat ethyl treatment were pooled from two phase II and three phase III clinical trials in 239 patients with carcinoid syndrome. Long-term safety of telotristat ethyl and causes of hospitalization and death were reviewed; overall survival was estimated. Results: Mean (median; range) duration of exposure and follow-up was 1.3 years (1.1 years; 1 week to 5.7 years), with 309 total patient-years of exposure. Leading causes of hospitalization were gastrointestinal disorders or were related to the underlying tumor and related treatment. Survival estimates at 1, 2, and 3 years were 93%, 88%, and 77%. Nearly all deaths were due to progression or complication of the underlying disease; none were attributable to telotristat ethyl. There was one death in year 4. Conclusion: Based on long-term safety data, telotristat ethyl is well tolerated and has a favorable long-term safety profile in patients with carcinoid syndrome. Implications for Practice: Carcinoid syndrome can cause persistent diarrhea, even in patients treated with somatostatin analogs. Across five clinical trials in patients with carcinoid syndrome, telotristat ethyl has been well tolerated and efficacious, providing clinicians with a new approach to help control carcinoid syndrome diarrhea, in addition to somatostatin analog therapy. By reducing the stool frequency in patients with carcinoid syndrome whose diarrhea is refractory to anticholinergics, such as loperamide and atropine/diphenoxylate, and somatostatin analog dose escalation, improvement in quality of life becomes an achievable goal.
AB - Background: Patients with neuroendocrine tumors (NETs) and carcinoid syndrome experience considerable morbidity and mortality; carcinoid syndrome may be associated with shorter survival. Carcinoid syndrome is linked to tumoral secretion of serotonin and other bioactive substances. The subsequent debilitating diarrhea and urgency to defecate pose significant health risks. In previous studies, telotristat ethyl, a tryptophan hydroxylase inhibitor, was effective and well tolerated in treating carcinoid syndrome diarrhea. We present pooled safety data from five clinical trials with telotristat ethyl in patients with carcinoid syndrome. Subjects, Materials, and Methods: Adverse events reported during telotristat ethyl treatment were pooled from two phase II and three phase III clinical trials in 239 patients with carcinoid syndrome. Long-term safety of telotristat ethyl and causes of hospitalization and death were reviewed; overall survival was estimated. Results: Mean (median; range) duration of exposure and follow-up was 1.3 years (1.1 years; 1 week to 5.7 years), with 309 total patient-years of exposure. Leading causes of hospitalization were gastrointestinal disorders or were related to the underlying tumor and related treatment. Survival estimates at 1, 2, and 3 years were 93%, 88%, and 77%. Nearly all deaths were due to progression or complication of the underlying disease; none were attributable to telotristat ethyl. There was one death in year 4. Conclusion: Based on long-term safety data, telotristat ethyl is well tolerated and has a favorable long-term safety profile in patients with carcinoid syndrome. Implications for Practice: Carcinoid syndrome can cause persistent diarrhea, even in patients treated with somatostatin analogs. Across five clinical trials in patients with carcinoid syndrome, telotristat ethyl has been well tolerated and efficacious, providing clinicians with a new approach to help control carcinoid syndrome diarrhea, in addition to somatostatin analog therapy. By reducing the stool frequency in patients with carcinoid syndrome whose diarrhea is refractory to anticholinergics, such as loperamide and atropine/diphenoxylate, and somatostatin analog dose escalation, improvement in quality of life becomes an achievable goal.
KW - Diarrhea
KW - Malignant carcinoid syndrome
KW - Neuroendocrine tumors
KW - Serotonin
KW - Telotristat ethyl
KW - Tryptophan hydroxylase
UR - http://www.scopus.com/inward/record.url?scp=85060148656&partnerID=8YFLogxK
U2 - 10.1634/theoncologist.2018-0236
DO - 10.1634/theoncologist.2018-0236
M3 - Article
C2 - 30651397
AN - SCOPUS:85060148656
SN - 1083-7159
VL - 24
SP - e662-e670
JO - Oncologist
JF - Oncologist
IS - 8
ER -