Abstract
Analysis of patient diaries in the NETTER-1 Study of 177Lu-DOTATATE versus high-dose octreotide in progressive midgut neuroendocrine tumors.
Author
person
Jonathan R. Strosberg
Moffitt Cancer Center, Tampa, FL
info_outline
Jonathan R. Strosberg, Edward M. Wolin, Beth A. Chasen, Matthew H. Kulke, David L Bushnell, Martyn Caplin, Richard P. Baum, Timothy J. Hobday, Andrew Eugene Hendifar, Paola Santoro, Per Broberg, Arnaud Demange, Kjell E. Oberg, Philippe B. Ruszniewski, Laura Ravasi, Eric Krenning
Full text
Authors
person
Jonathan R. Strosberg
Moffitt Cancer Center, Tampa, FL
info_outline
Jonathan R. Strosberg, Edward M. Wolin, Beth A. Chasen, Matthew H. Kulke, David L Bushnell, Martyn Caplin, Richard P. Baum, Timothy J. Hobday, Andrew Eugene Hendifar, Paola Santoro, Per Broberg, Arnaud Demange, Kjell E. Oberg, Philippe B. Ruszniewski, Laura Ravasi, Eric Krenning
Organizations
Moffitt Cancer Center, Tampa, FL, University of Kentucky, Lexington, KY, Department of Nuclear Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, Boston Medical Center, Boston, MA, Veterans Administration Medical Center, Iowa City, IA, Royal Free Hospital, London, United Kingdom, Zentralklinik, Bad Berska, Bad Berska, Germany, Mayo Clinic, Rochester, MN, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, Advanced Accelerator Applications, Geneva, Switzerland, Uppsala University Hospital, Uppsala, Sweden, Beaujon Hospital, Clichy, France, Erasmus MC, Rotterdam, Netherlands
Abstract Disclosures
Research Funding
Pharmaceutical/Biotech Company
Background:
The primary statistical analysis for the NETTER-1 trial showed a clinically and statistically significant PFS benefit with
177
Lu-DOTATATE vs. high-dose octreotide.
177
Lu-DOTATATE treatment was also correlated with a significant delay in time to deterioration in HRQoL. In addition to HRQoL questionnaires, patients were asked to record presence or absence of a range of symptoms in a daily diary.
Methods:
A Mixed Model Repeated Measures (MMRM) was used to analyze the change, compared to baseline, of the occurrence of abdominal Pain, diarrhea and cutaneous flushing as these symptoms were regarded as the most relevant to judge the overall disease status. For each visit (week = 0, 4, 8, etc.) the number of days with symptoms during the previous period was calculated. At baseline, the number of days with symptoms was counted over the previous 6 weeks, whereas the time frame between visits lasted 4 weeks.
Results:
The estimated number of days with symptoms declined significantly more in the
177
Lu-dotatate arm compared to the octreotide arm. The difference in change and the confidence intervals for the symptoms abdominal pain, diarrhea and flushing of skin are, respectively: -3.11 [-4.88; -1.34], -3.11 [-5.04; -1.18] and -1.98 [-3.88; -0.08]
.
Conclusions:
Analysis of symptom diaries confirms that
177
Lu-Dotatate can palliate clinically relevant symptoms when compared to high-dose octreotide.