Abstract 1131P
Background
Acral melanomas are rare melanoma subtypes with poor prognosis and show limited response to the standard of care for the first line treatment of advanced melanoma (Dacarbazine). In this study, we evaluate the efficacy of the novel combination of pembrolizumab and temozolomide as the first line treatment in Chinese treatment-naïve metastatic acral melanoma patients.
Methods
This was a single arm, open-label, phase II study (ChiCTR2100050073). Eligible patients aged ≥18 years with histopathologically confirmed metastatic acral melanoma (stage III/IV) were enrolled. Patients received pembrolizumab 200 mg Q3W up to 35 cycles (approximately 2 years), and temozolomide 150mg/m2/d on days 1-5 every 4 weeks. For patients who have completed the first treatment cycle without developing dose-limiting toxicity (DLT), Temozolomide would then be administered as 200mg/m2/d on days 1-5, for up to 8 cycles. The primary endpoint was objective response rate (ORR) per RECIST 1.1 by investigator review. Secondary end points were duration of response (DOR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS) and safety.
Results
A total of 38 patients were enrolled. The median age was 58 years (27-71 years), and 23 patients (60.5%) were male. At the data cut-off Apr 10, 2024, 35 patients have received at least one post-treatment radiological evaluation. The ORR was 37.1% (1 CR; 12 PR [95% CI: 21.5% - 55.1%]), 3 unconfirmed PR was included. The median DOR was 7.7 months (95% CI: 5.0-Not reached [NR]). The DCR was 80.0% (1 CR; 12 PR;15 SD [95% CI: 63.1-91.6%]). The median PFS was 7.7 months (95% CI: 4.9-13.2 months). The median OS was NR. No unexpected treatment-related adverse event was reported.
Conclusions
Pembrolizumab combined with Temozolomide is an effective and well-tolerated 1L regimen for Chinese patients with metastatic acral melanoma.
Clinical trial identification
ChiCTR2100050073.
Editorial acknowledgement
Legal entity responsible for the study
Y. Ding.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1111P - Genomic and transcriptomic analysis of Japanese melanoma reveals candidate biomarkers for immune checkpoint inhibitor responders
Presenter: Toshihiro Kimura
Session: Poster session 04
1112P - Immunotherapy after progression to double immunotherapy: Pembrolizumab and Lenvatinib versus conventional chemotherapy for patients with metastatic melanoma after failure of PD-1/CTLA-4 inhibition
Presenter: Dimitrios Ziogas
Session: Poster session 04
1113P - A machine learning model based on computed tomography radiomics to predict prognosis in subjects with stage IV melanoma
Presenter: Maria Teresa Maccallini
Session: Poster session 04
1114P - Deciphering unresectable in-transit metastasis in melanoma: Multi-modal and longitudinal insights
Presenter: Giuseppe Tarantino
Session: Poster session 04
1115P - Multiomics clustering of patients with cutaneous melanoma to reveal survival trends based on tumor immune evasion features
Presenter: Adeliya Leleytner
Session: Poster session 04
1116P - Application of the Scottish inflammatory prognostic score to the south-east Scotland cancer network real-world melanoma cohort
Presenter: Karim El-Shakankery
Session: Poster session 04
1117P - Intratumoral microbiota is associated with prognosis in Chinese patients with skin melanoma
Presenter: Hang Jiang
Session: Poster session 04
1118P - Immunological alterations during neoadjuvant BRAF/MEK inhibition in patients with prior unresectable regionally advanced melanoma: Translational analysis from the REDUCTOR trial
Presenter: Femke Burgers
Session: Poster session 04
1119P - Genomic and transcriptomic predictors of resistance to anti-PD1 monotherapy in patients with advanced melanoma
Presenter: Wenya Wang
Session: Poster session 04
1120P - Tumoral and peripheral immunophenotype of patients with stage II/III melanoma undergoing adjuvant immunotherapy following tumor resection
Presenter: Maria Ascierto
Session: Poster session 04