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
156P - Liver Metastases Correlate with Shortened Survival and Increased Dissociate Response in Patients Treated with T-Cell Engagers.
Presenter: Noé Herbel
Session: Poster Display session
Resources:
Abstract
157P - Preliminary results of a multicentric randomized phase I/IIa trial of an immunotherapy targeting dendritic cells (DC), CD40HVac, in patients with HPV16-positive oropharyngeal carcinoma (OPC)
Presenter: Caroline Even
Session: Poster Display session
Resources:
Abstract
158P - XCR1+ dendritic cell (DC) role in antitumoral response to anti PD-L1 antibody: Data from the phase Ib/II trial of DC vaccination in small cell lung cancer patients
Presenter: Maria Gonzalez Cao
Session: Poster Display session
Resources:
Abstract
159P - Unveiling the impact of DC vaccination on systemic immunity in advanced malignant melanoma: Preliminary results from the ABSIDE study
Presenter: Giada Sabatino
Session: Poster Display session
Resources:
Abstract
160P - Oral DNA vaccination targeting personalised neoantigens in immune checkpoint-inhibitor treated solid tumor patients: Interim results
Presenter: Domas Vaitiekus
Session: Poster Display session
Resources:
Abstract
161P - Safety of TrimelVax vaccine for patients with advanced melanoma: Clinical results
Presenter: ROBERTO ESTAY
Session: Poster Display session
Resources:
Abstract
162P - EO4010 (EO) + nivolumab (N) ± bevacizumab (B) in patients (pts) with microsatellite stable (MSS) metastatic colorectal carcinoma (mCRC)
Presenter: Romain Cohen
Session: Poster Display session
Resources:
Abstract
163P - Effect of split intravenous dosing of oncolytic adenovirus TILT-123 on normal tissue versus tumor macrophages and virus bioavailability in patients with advanced solid tumors
Presenter: Elise Jirovec
Session: Poster Display session
Resources:
Abstract
164P - Roginolisib (IOA-244), the first highly selective oral allosteric modulator of phosphoinositide 3-kinase inhibitor delta (PI3K_), has immuno-modulatory effects associated with clinical benefits in patients with metastatic uveal melanoma
Presenter: Anna Di Giacomo
Session: Poster Display session
Resources:
Abstract
165P - TIGIT inhibition in non-small cell lung cancer: Meta-analysis of clinical efficacy and biomarker correlation
Presenter: Hashim Talib Hashim
Session: Poster Display session
Resources:
Abstract