Abstract 113P
Background
Patients (pts) with metastatic urothelial carcinoma (mUC) who do not experience disease progression after 4-6 cycles of first-line platinum-based chemotherapy (PBC) may benefit from immunotherapy as maintenance treatment with Avelumab, or receive Pembrolizumab as a second-line.
Methods
AVePEm is a multicenter, observational, retrospective study involving pts with mUC who did not progress after 4 cycles of PBC: GroupA received Avelumab and GroupB Pembrolizumab. The primary endpoints were overall survival (OS) and progression-free survival (PFS), with adverse events (AEs) as secondary endpoints. A p-value of <0.05 was considered significant.
Results
From August 2019 to July 2024, we identified 30 pts. Of those, 53% were in GroupA and 47% in GroupB. Most had transitional cell carcinoma, with 77% from the lower urinary tract and 47% having lymph node-only disease. The median number of PBC cycles was 6, with 40% ineligible for cisplatin. After a median follow-up of 19.9 months (mo) for GroupA and 18.7 mo for GroupB, the mOS was 25 mo and 29.5 mo, respectively (p=0.52) and the mPFS of immunotherapy was 14 mo and 8 mo, respectively (p=0.51). The median time from the end of PBC and the start of Pembrolizumab was 4.1 mo, with a median treatment duration of 7.6 mo for GroupA and 3.5 mo for GroupB. At the time of data analysis, 40% (n=12) of pts were alive and 33% (n=10) on treatment, with 40% still receiving Avelumab, and 50% and 10% on subsequent therapies after Avelumab and Pembrolizumab, respectively. In both groups 50% of pts have a neutrophil-to-lymphocyte ratio (NLR) ≥3 at baseline of PBC. NLR ratio negatively correlates with OS (p=0.099) and PFS (p=0.047). Both treatments were well tolerated, with Grade 3 AEs in 1 pt on Avelumab and 3 on Pembrolizumab, and no Grade 4 AEs reported.
Conclusions
Group A and Group B showed no statistically significant differences in OS and PFS. Of note, more pts were on Avelumab treatment at the data cutoff. AEs were similar in the two groups. Further investigation and follow-up are warranted to gain definitive conclusions on optimal mUC management in the era of immunotherapy and immunoconjugates.
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
D. Pastorelli: Financial Interests, Personal, Advisory Role: MSD Oncology, Amgen, Ipsen, Novartis, Pfizer, Astellas, Leo Pharma, GSK, AbbVie, Bayer. M. Milella: Financial Interests, Personal, Advisory Role: AstraZeneca, MSD Oncology, Janssen Oncology; Financial Interests, Personal, Research Funding: Roche; Financial Interests, Personal, Funding: Ipsen, Servier, Viatris; Financial Interests, Personal, Other: Novartis, Oncosil. All other authors have declared no conflicts of interest.
Resources from the same session
125P - Enhancing the efficacy of neoantigen tumor vaccines in melanoma treatment through different administration times
Presenter: Kai Xiao
Session: Poster Display session
Resources:
Abstract
126P - Combination of oncolytic viruses, radiation therapy, and immune checkpoint inhibitor treatment in a breast cancer model
Presenter: Olga Bezborodova
Session: Poster Display session
Resources:
Abstract
127P - Combining chemotherapy and checkpoint inhibitors with an engineered oncolytic adenovirus encoding a human vIL-2 cytokine to treat pancreatic ductal adenocarcinoma
Presenter: Nea Ojala
Session: Poster Display session
Resources:
Abstract
128P - Non-coding DNA lipid nanoparticles elicit antitumor immune responses and synergize with anti-PDL1 antibodies in mouse models of hepatocellular carcinoma
Presenter: Alba Rodriguez Garcia
Session: Poster Display session
Resources:
Abstract
129P - Computational approaches for enhancing the efficacy of cancer immunotherapy
Presenter: Byungho Lim
Session: Poster Display session
Resources:
Abstract
130P - Neoadjuvant treatment with a bispecific antibody cadonilimab in dMMR/MSI-H locally advanced colorectal cancer: Preliminary results from a phase II trial
Presenter: Caifeng Gong
Session: Poster Display session
Resources:
Abstract
131P - The efficacy and safety of cadonilimab with or without trastuzumab in combination with SOX as first-line (1L) treatment for advanced gastric (G) or gastroesophageal Junction adenocarcinoma (GEJA)
Presenter: Wenhui Yang
Session: Poster Display session
Resources:
Abstract
132P - An open-label, prospective phase II study of cadonilimab in combination with neoadjuvant chemotherapy for patients diagnosed with advanced ovarian cancer (AK104-IIT-003)
Presenter: Jie Tang
Session: Poster Display session
Resources:
Abstract
133P - The efficacy and safety of KN046 combined with axitinib for previously untreated and checkpoint inhibitor treated advanced non-small cell lung cancer: A single-arm, open-label, multicenter phase II clinical trial
Presenter: Li Zhang
Session: Poster Display session
Resources:
Abstract
134P - Intracranial (IC) progression-free survival (PFS) with ivonescimab (Ivo) compared to placebo in the HARMONi-A trial of patients (Pts) with previously treated EGFR mutation-positive (EGFRm+) non-small cell lung cancer (NSCLC)
Presenter: Li Zhang
Session: Poster Display session
Resources:
Abstract