Abstract 450P
Background
Anamorelin (ANAM), a ghrelin receptor agonist, was effective in increasing skeletal muscle mass, weight gain, and appetite in the Ono-7643-05 study for gastrointestinal cancer, including pancreatic cancer (PC) with cancer cachexia (CC), and ANAM was approved in Japan as the world's first treatment for CC. In the Ono-7643-05 study, weight gain and appetite improvement were observed at 3 weeks, and the ANAM package insert states that ANAM should be discontinued if no effectiveness is observed within 3 weeks. The data on factors associated with discontinuation within the first 3 weeks may facilitate the decision to initiate or continue ANAM.
Methods
Patients with unresectable or recurrent PC who started ANAM between 21 April 2021 and 31 March 2022 at the National Cancer Center Hospital and National Cancer Center Hospital East were retrospectively analyzed. Patient characteristics and reasons for discontinuation of ANAM at 3 weeks were collected. Using the clinical data at the time of ANAM initiation, logistic regression analysis was performed to evaluate the background factors associated with the discontinuation of ANAM within 3 weeks.
Results
The study included 110 patients (median age: 70 years; male: 55; Eastern Cooperative Oncology Group performance status 0/1/2/3/unknown: 15/70/15/6/4; prior chemotherapy regimen 0/1/2/3 or more/best supportive care: 5/59/24/15/7 patients). ANAM was discontinued within 3 weeks in 47 patients. The main reasons for discontinuation were disease progression in 23 patients (49%), adverse events (AEs) in 12 patients (26%), and the ineffectiveness of ANAM in 8 patients (17%). The main AEs were gastrointestinal disorders such as nausea and vomiting. Multivariate analysis of factors correlated with the discontinuation of ANAM within 3 weeks revealed a significant association with a Glasgow prognostic score (GPS) of 2.
Conclusions
Among PC patients with CC, the discontinuation rate at 3 weeks after starting ANAM was 43%. The main reason for discontinuation was disease progression. A GPS of 2, which may reflect a high degree of inflammation and low nutritional status, was associated with discontinuation within 3 weeks. Appropriate patient selection may improve the continuation rate of ANAM.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
National Cancer Center Hospital.
Funding
National Cancer Center Hospital and National Cancer Center Hospital East.
Disclosure
A. Ohba: Financial Interests, Personal, Invited Speaker: Yakult, Ono, Servier, Taiho, Eisai; Financial Interests, Personal, Advisory Board: Zymeworks; Financial Interests, Institutional, Local PI: Ono, Chugai, Novartis. S. Mitsunaga: Financial Interests, Personal, Invited Speaker: Ono Pharmaceutical CO., LTD. T. Satake: Financial Interests, Institutional, Local PI: Ono, NIHON Servier. H. Imaoka: Financial Interests, Personal, Invited Speaker: Yakult Honsha, AstraZeneca, Nihon Servier, Kaneka Medix, SB KAWASUMI LABORATORIES; Financial Interests, Personal, Advisory Board: Nihon Servier, Kaneka Medix; Financial Interests, Personal, Writing Engagement: Medico's Hirata; Financial Interests, Institutional, Local PI: Ono Pharmaceutical, Novartis, Nihon Servier. C. Morizane: Financial Interests, Personal, Advisory Board: Yakult, MSD, Servier, Boehringer Ingelheim, AstraZeneca, Taiho Pharmaceutical, Merck biopharma; Financial Interests, Personal, Invited Speaker: Novartis, Teijin Pharma; Financial Interests, Institutional, Coordinating PI: Yakult Honsha, Ono Pharmaceutical, Taiho Pharmaceutical, Eisai, MSD K.K., J-Pharma, AstraZeneca, Merck biopharma; Financial Interests, Institutional, Funding: Daiichi Sankyo RD Novare, Hitachi. M. Ikeda: Financial Interests, Personal, Advisory Board: AstraZeneca, Chugai, Eli Lilly Japan, Eisai, NIHON Servier, Novartis, MSD; Financial Interests, Personal, Invited Speaker: AstraZeneca, Bristol Myers Squibb, Chugai, Eli Lilly Japan, Eisai, NIHON Servier, Novartis, Taiho, Yakult, Teijin Pharma, AbbVie, Abbott Japan, Fujifilm Toyama Chemical, Incyte Biosciences Japan, Takeda, Ono, MSD, Taisho Pharmaceutical, Nippon Kayaku, Guardant Health Japan; Financial Interests, Institutional, Coordinating PI: Bayer, Bristol Myers Squibb, Eisai, AstraZeneca, Eli Lilly Japan, Chugai Pharmaceutical, MSD, Ono, Novartis, J-Pharma, Pfizer, Chiome Bioscience, NIHON Servier, Delta-Fly Pharma, Syneos Health, Merus.N.V., Merck biopharma, Boehringer Ingelheim, Invitae; Financial Interests, Personal, Steering Committee Member: Chugai, NIHON Servier, Takeda, Novartis, Eisai, Rakuten Medical. T. Okusaka: Financial Interests, Personal, Advisory Board: Eisai, Nihon Servier, AstraZeneca, Ono Pharmaceutical, FUJIFILM Toyama Chemical, Daiihon-Sumitomo, Novartis; Financial Interests, Personal, Invited Speaker: AstraZeneca, Eisai, Chugai Pharma, Nihon Servier, Incyte, Johnson & Johnson, Daiichi Sankyo, Taiho; Financial Interests, Institutional, Local PI: AstraZeneca, Chugai Pharma, Eisai, Novartis, Bristol Myers Squibb, MSD, Incyte, Syneos Health. All other authors have declared no conflicts of interest.
Resources from the same session
485P - LDCT lung cancer screening of never-smokers meta-analysis subgroup analysis: Adenocarcinoma is the highly predictive histology identified in never-smokers
Presenter: Sai-Hong Ou
Session: Poster Display
Resources:
Abstract
486P - Fiscal feasibility and implications of integrating lung cancer screening into Hong Kong’s healthcare system
Presenter: Herbert Ho Fung Loong
Session: Poster Display
Resources:
Abstract
487P - Evaluating the performance of the USPSTF lung cancer screening guidelines in an Asian population of lung cancer patients
Presenter: Jian Wei Tan
Session: Poster Display
Resources:
Abstract
488P - Pulmonary ground glass opacity lesions: Immune ecosystem and its clinical relevances of early-stage lung adenocarcinoma
Presenter: Shensi Shen
Session: Poster Display
Resources:
Abstract
489TiP - BGB-LC-202 (NCT05577702): Phase II Umbrella study of tislelizumab (TIS) monotherapy and TIS-based immunotherapy combinations +/- chemotherapy (CT) as neoadjuvant treatment in Chinese patients (pts) with resectable stage II to IIIA non-small cell lung cancer (NSCLC)
Presenter: Wentao Yu
Session: Poster Display
Resources:
Abstract
491P - Furmonertinib as adjuvant therapy for elderly patients in resected EGFR-mutated non-small cell lung cancer: A double-center, real-world experience
Presenter: Ziheng Wu
Session: Poster Display
Resources:
Abstract
492P - Penpulimab-based combination neoadjuvant/adjuvant therapy for patients with resectable locally advanced non-small cell lung cancer: Preliminary results from a phase II study (ALTER-L043)
Presenter: Changli Wang
Session: Poster Display
Resources:
Abstract
493P - The prognostic value of 4L lymph node dissection in left-sided operable non-small cell lung cancer: A systematic review and meta-analysis
Presenter: Lei Peng
Session: Poster Display
Resources:
Abstract
495P - Intrinsic STING of CD8+T cells regulates self-metabolic reprogramming and exerts anti-tumor effects
Presenter: Qiuli Xu
Session: Poster Display
Resources:
Abstract
496P - Fruquintinib plus sintilimab in patients (pts) with advanced non-small cell lung cancer (NSCLC) with PD-L1-positive expression: A multicenter, single-arm phase II study
Presenter: Shun Lu
Session: Poster Display
Resources:
Abstract