A Phase IIb Randomized Controlled Trial of the TLPLDC Vaccine As Adjuvant Therapy After Surgical Resection of Stage III/IV Melanoma: A Primary Analysis
Overview
Authors
Affiliations
Background: Melanoma therapy has changed dramatically over the last decade with improvements in immunotherapy, yet many patients do not respond to current therapies. This novel vaccine strategy may prime a patient's immune system against their tumor and work synergistically with immunotherapy against advanced-stage melanoma.
Methods: This was a prospective, randomized, double-blind, placebo-controlled, phase IIb trial of the tumor lysate, particle-loaded, dendritic cell (TLPLDC) vaccine administered to prevent recurrence in patients with resected stage III/IV melanoma. Patients were enrolled and randomized 2:1 to the TLPLDC vaccine or placebo (empty yeast cell wall particles and autologous dendritic cells). Both intention-to-treat (ITT) and per treatment (PT) analyses were predefined, with PT analysis including patients who remained disease-free through the primary vaccine/placebo series (6 months).
Results: A total of 144 patients were randomized (103 vaccine, 41 control). Therapy was well-tolerated with similar toxicity between treatment arms; one patient in each group experienced related serious adverse events. While disease-free survival (DFS) was not different between groups in ITT analysis, in PT analysis the vaccine group showed improved 24-month DFS (62.9% vs. 34.8%, p = 0.041).
Conclusions: This phase IIb trial of TLPLDC vaccine administered to patients with resected stage III/IV melanoma shows TLPLDC is well-tolerated and improves DFS in patients who complete the primary vaccine series. This suggests patients who do not recur early benefit from TLPLDC in preventing future recurrence from melanoma. A phase III trial of TLPLDC + checkpoint inhibitor versus checkpoint inhibitor alone in patients with advanced, surgically resected melanoma is under development.
Trial Registration: NCT02301611.
Updates in Immunotherapy for Pancreatic Cancer.
Chick R, Pawlik T J Clin Med. 2024; 13(21).
PMID: 39518557 PMC: 11546190. DOI: 10.3390/jcm13216419.
Levin N, Kim S, Marquardt C, Vale N, Yu Z, Sindiri S J Immunother Cancer. 2024; 12(5).
PMID: 38816232 PMC: 11141192. DOI: 10.1136/jitc-2023-008645.
Understanding yeast shells: structure, properties and applications.
Macedo L, Pinho S, Silva A, Moura I, Espinoza B, Invencao M ADMET DMPK. 2024; 12(2):299-317.
PMID: 38720922 PMC: 11075163. DOI: 10.5599/admet.2118.
Utility of cell-based vaccines as cancer therapy: Systematic review and meta-analysis.
Tiwari A, Alcover K, Carpenter E, Thomas K, Krum J, Nissen A Hum Vaccin Immunother. 2024; 20(1):2323256.
PMID: 38544385 PMC: 10984131. DOI: 10.1080/21645515.2024.2323256.
Dendritic Cells in Cancer Immunology and Immunotherapy.
Hato L, Vizcay A, Eguren I, Perez-Gracia J, Rodriguez J, Gallego Perez-Larraya J Cancers (Basel). 2024; 16(5).
PMID: 38473341 PMC: 10930494. DOI: 10.3390/cancers16050981.