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
1101P - Efficacy of anti PD-1 therapy in children and adolescent melanoma patients (MELCAYA study)
Presenter: Mario Mandalà
Session: Poster session 04
1102P - Immune checkpoint inhibitor rechallenge after treatment with tumor-infiltrating lymphocytes in unresectable melanoma
Presenter: Allison Betof Warner
Session: Poster session 04
1103P - Real-world efficacy of relatlimab and nivolumab in advanced or resectable melanoma
Presenter: Lilit Karapetyan
Session: Poster session 04
1104P - Early time-point <sup>18</sup>F-FDG-PET/CT at week four (W4) as a prognostic biomarker of survival in metastatic melanoma (mM) patients (pts) on immunotherapy
Presenter: Nezka Hribernik
Session: Poster session 04
1105P - Predicting the outcomes of advanced cutaneous melanoma cases following discontinuation of immune checkpoint inhibition
Presenter: Ka-won Noh
Session: Poster session 04
1106P - NivoLag-when: International real-world study of combination immunotherapy sequences in melanoma
Presenter: Mora Guardamagna
Session: Poster session 04
1107P - Characteristics and quality of life of nine-year survivors from 312 patients with metastatic melanoma treated with pembrolizumab
Presenter: Jessica Hassel
Session: Poster session 04
1108P - Impact of quantitative imaging of all disease on the prognostic value of <sup>18</sup>F-FDG PET/CT in patients treated with immunotherapy for metastatic melanoma
Presenter: Robert Jeraj
Session: Poster session 04
1109P - Association of clinical features with long-term survival in patients with melanoma who responded to distinct checkpoint inhibitors
Presenter: Eva Ellebaek
Session: Poster session 04
1110P - Follow-up brain imaging in patients with melanoma brain metastasis and immune checkpoint inhibitors
Presenter: Imren Ozdamar
Session: Poster session 04