Abstract 1585P
Background
The IVY study (UMIN000033376) investigated the impact of first-line platinum-induced PN on the incidence of PN during second-line PTX-based chemotherapy and its efficacy in patients with unresectable AGC.
Methods
The study utilized the Common Terminology Criteria for Adverse Events (CTCAE), the Patient Neurotoxicity Questionnaire (PNQ), and the Functional Assessment of Cancer Therapy/Gynecologic Oncology Group-Neurotoxicity (FACT/GOG-Ntx) to assess PN. The primary endpoint was to determine the incidence of grade 3 or greater PN during second-line treatment in patients with and without PN at the start of treatment. The secondary objective was to examine the relationship between PN and the efficacy.
Results
Of 162 patients enrolled in this study, 156 received second-line PTX-based chemotherapy and were divided into two groups based on their PN status at the start of the treatment. The characteristics of 156 patients are as follows: the median age was 69 years, 72% were male, 90% were ECOG PS: 0 or 1, 81% used oxaliplatin in their first-line chemotherapy regimen. Of the 156 patients, 90 patients (58%) were in the group with PN (CTCAE grade: 1 to 3), and 66 were in the group without PN (grade: 0). The group with PN had a higher incidence of grade 3 or greater PN than the group without PN (16.7% vs. 4.6%, p=0.02). The progression-free survival and the overall response rate were not significantly different between the two groups (4.0 months in the group with PN vs. 3.5 months without PN, p=0.20; and 23% vs. 19%, p=0.69). However, the median overall survival was significantly better in the group with PN (10.3 months vs. 8.1 months, p=0.04). The quality-of-life scores, as assessed by PNQ and FACT/GOG-Ntx, were lower in the group with PN than the scores of the group without PN during two months of treatment.
Conclusions
Starting second-line PTX-based chemotherapy with existing PN increased the severity of PN during treatment. However, this adverse effect did not impact the effectiveness of second-line PTX-based chemotherapy for patients with unresectable AGC.
Clinical trial identification
UMIN000033376.
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
T. Ando: Financial Interests, Institutional, Research Grant: Chugai Pharmaceutical Co., Ltd.; Financial Interests, Institutional, Invited Speaker: Otsuka Pharmaceutical Co., Ltd., Taiho, Daiichi Sankyo Company, Limited., Nippon Kayaku Co.,Ltd. All other authors have declared no conflicts of interest.
Resources from the same session
1590P - Real-world gastric cancer (GC) in Latin America (LATAM) and Europe (EU)
Presenter: Berenice Freile
Session: Poster session 22
1591P - Gastric cancer in young patients under 40 years: 5-year analyses of Georgian cancer registry
Presenter: Tamar Esakia
Session: Poster session 22
1617P - PRODIGE 29-UCGI 26 (NEOPAN): Quality of life results of a phase III randomised trial comparing chemotherapy with folfirinox (FFX) or gemcitabine (gem) in locally advanced pancreatic carcinoma (LAPC)
Presenter: Michel Ducreux
Session: Poster session 22
1618P - Durable efficacy of zenocutuzumab, a HER2 x HER3 bispecific antibody, in advanced NRG1 fusion positive (NRG1+) pancreatic ductal adenocarcinoma (PDAC)
Presenter: Alison Schram
Session: Poster session 22
1620P - A phase II study of perioperative nalirifox in patients with resectable pancreatic ductal adenocarcinoma (rPDAC): Survival update and biomarkers analysis of the NITRO trial
Presenter: Davide Melisi
Session: Poster session 22
1621P - Efficacy and safety of erdafitinib in adults with pancreatic cancer and prespecified fibroblast growth factor receptor alterations (FGFRalt) in the phase II open-label: Single-arm RAGNAR trial
Presenter: Shubham Pant
Session: Poster session 22
1622P - D-1553 in patients with KRAS G12C mutated advanced pancreatic cancer (pca)
Presenter: Shunsuke Kondo
Session: Poster session 22
1623P - Pelareorep (pela) + atezolizumab (atezo) and chemotherapy in first-line (1L) advanced or metastatic pancreatic ductal adenocarcinoma (PDAC) patients: Results from the GOBLET study
Presenter: Dirk Arnold
Session: Poster session 22
1624P - Predictive factors for treatment success of second-line Nal-IRI/5-FU/FA in patients with metastatic pancreatic ductal adenocarcinoma (PDAC) (AIO-PAK-0216)
Presenter: Manfred Lutz
Session: Poster session 22