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
1121P - Artificial Intelligence to predict BRAF mutational status from whole slide images in melanoma
Presenter: Céline Bossard
Session: Poster session 04
1122P - The role of imaging during follow-up after radical surgery of stage IIb-c and III cutaneous malignant melanoma: Survival results from an interim analysis of a randomized prospective multicenter study (TRIM)
Presenter: Cecilia Ladjevardi
Session: Poster session 04
1123P - Melanoma incidence and mortality decline in younger adults in Sweden: Start of a shift in the upgoing trend?
Presenter: Hildur Helgadottir
Session: Poster session 04
1124P - Adjuvant treatment of patients with stage III melanoma: 4-year follow-up time of multicenter real-world study
Presenter: Elisabeth Livingstone
Session: Poster session 04
1125P - Accuracy of PET-CT to assess extent of nodal disease in clinical stage III melanoma
Presenter: Ronen Stoff
Session: Poster session 04
1126P - A phase II study of nivolumab/relatlimab in metastatic uveal melanoma
Presenter: Jose Lutzky
Session: Poster session 04
1127P - Subgroup analysis of FOCUS phase III trial efficacy results
Presenter: Matthew Wheater
Session: Poster session 04
1128P - Preliminary results of first-in-human study of 225-Actinium MTI-201 (225Ac-MTI-201) in metastatic uveal melanoma
Presenter: Nikhil Khushalani
Session: Poster session 04
1129P - Clinical outcomes from a tebentafusp UK expanded access program in patients with metastatic uveal melanoma (mUM)
Presenter: Paul Nathan
Session: Poster session 04
1130P - Phase II trial on nivolumab plus radiotherapy in patients with metastatic mucosal melanoma: PORTER-M3 trial
Presenter: Motoo Nomura
Session: Poster session 04