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
519P - Final results and subgroup analysis of ORIENTAL: A phase IIIB study of durvalumab plus platinum-etoposide in first-line treatment of Chinese patients with extensive-stage small-cell lung cancer (ES-SCLC)
Presenter: Ying Cheng
Session: Poster Display
Resources:
Abstract
520P - Role of atezolizumab in controlling CNS progression in ES-SCLC
Presenter: Yoon Namgung
Session: Poster Display
Resources:
Abstract
521P - Camrelizumab combined with chemotherapy and apatinib as first-line therapy for extensive-stage small cell lung cancer: A phase II, single-arm, exploratory research
Presenter: Yanbin Zhao
Session: Poster Display
Resources:
Abstract
522P - Durvalumab plus etoposide and carboplatin for extensive-stage small cell lung cancer with mild idiopathic interstitial pneumonia
Presenter: Ichiro Nakachi
Session: Poster Display
Resources:
Abstract
523P - Camrelizumab plus apatinib as maintenance treatment in patients with extensive-stage small cell lung cancer who were responding or stable after standard first-line chemotherapy (CAMERA): Results from a single-arm, phase II trial
Presenter: Qi Wang
Session: Poster Display
Resources:
Abstract
524P - Treatment pattern and overall survival by lines of therapy among patients with advanced small cell lung cancer in Taiwan
Presenter: Kelly Huang
Session: Poster Display
Resources:
Abstract
525P - Development of diagnostic prediction score for malignant pleural effusion in lung cancer: MPE-Lung score
Presenter: Chaichana Chantharakhit
Session: Poster Display
Resources:
Abstract
526P - Burden and trends of tracheal, bronchus, and lung (TBL) cancer in Southeast Asia, East Asia, and Oceania from 1990-2019, and its projection of deaths to 2040: A benchmarking analysis
Presenter: Monika Chhayani
Session: Poster Display
Resources:
Abstract
527P - Efficacy of intraventricular chemotherapy with pemetrexed for leptomeningeal metastasis from lung adenocarcinoma: A retrospective study
Presenter: Fang Cun
Session: Poster Display
Resources:
Abstract
528P - Socioeconomic determinants of access to standard-of-care treatments in advanced and metastatic NSCLC in Hong Kong: A territory-wide study
Presenter: Ka Man Cheung
Session: Poster Display
Resources:
Abstract