Abstract 1678P
Background
Chemotherapy alone has limited efficacy in treating advanced pancreatic cancer (APC). The addition of nimotuzumab (nimo) to gemcitabine had been shown to be more effective in our previous studies: the progression-free survival (PFS) was up to 5.1 months, 1.5 months longer than gemcitabine alone for 1st line treatment of APC, but its efficacy and safety in combination with other chemotherapy regimens are unknown.
Methods
In this study, patients with APC were treated with standard of care (routine chemotherapy) combined with or without nimo in a real-world data setting. Demographic and clinical data were collected from electronic medical records of First Affiliated Hospital of Xi’an Jiaotong University from April 2018 to May 2023. The primary efficacy endpoint was progression-free survival (PFS).
Results
We identified 282 APC patients, of which 36.8% received nimo combined with routine chemotherapy. After 1:1 propensity score matching (PSM), we created 65 pairs patients (median age was 62 years, range, 55-69) who received routine chemotherapy with or without nimo as first-line treatment. Among them, 55 pairs were treated with albumin paclitaxel-gemcitabine (AG), 3 pairs with gemcitabine-tegafur (GS) and 7 pairs with others. The median dosage of nimo was 400mg weekly. Up to May 2023, the median follow-up time was beyond 24 months. Survival analysis showed that nimo was associated with longer PFS (10.9 months vs 9.1 months; p<0.05, HR=0.5(95%CI, 0.29-0.88) after matching), but the OS was not evaluated due to the missing date of death. No grade 3 or above toxicities were observed.
Conclusions
Gemcitabine-based combination chemotherapy (eg, AG regimen, GS regimen) were commonly used as first-line treatment for APC in China. The addition of nimotuzumab to combination chemotherapy was a strong regimen and found to prolong the survival time for APC, with a manageable safety profile.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1664P - Italian Association for Medical Oncology (AIOM) guideline application in real-world: Multi-institutional based survey of adjuvant and first-line pancreatic ductal adenocarcinoma treatment in Italy (GARIBALDI) - survival analyses in the metastatic cohort
Presenter: Michele Reni
Session: Poster session 22
1665P - Prognostic impact of diabetes and antidiabetic medication in pancreatic cancer patients
Presenter: Alexander Friedrich
Session: Poster session 22
1667P - Clinical and molecular features of young onset pancreatic adenocarcinoma
Presenter: Maxime Remond
Session: Poster session 22
1668P - Prevalence and management of pancreatic ductal adenocarcinoma (PDAC) over a decade in France: A population-based study
Presenter: Léo Mas
Session: Poster session 22
1670P - Tumoral and non-tumoral thrombosis associated with pancreatic ductal adenocarcinoma (PDAC): Survival impact, assessment of predictive scales and rethrombosis
Presenter: Alejandra Cardozo
Session: Poster session 22
1671P - Treatment patterns and efficacy in patients (pt) with pancreatic cancer (PC) from the Spanish RETUD registry
Presenter: Teresa Macarulla
Session: Poster session 22
1673P - Trajectories of immune-related serum proteins and quality of life in patients with pancreatic and other periampullary cancer: The champ study
Presenter: Sofie Olsson Hau
Session: Poster session 22
1674P - VILP registry of patients with metastatic pancreatic cancer treated with pegylated liposomal irinotecan plus 5-fluoroucil and leucovorin in the Czech Republic
Presenter: Stanislav Batko
Session: Poster session 22
1675P - Diagnostic performance of blood-based DNA methylation assay using epigenetic-specific peptide nucleic acid in pancreatic adenocarcinoma
Presenter: Hongsik Kim
Session: Poster session 22