Home > Endocrinology > Promising first results of mitazalimab in metastatic pancreatic ductal adenocarcinoma

Promising first results of mitazalimab in metastatic pancreatic ductal adenocarcinoma

Presented by
Dr Teresa Macarulla, Vall d’Hebron University Hospital, Spain
Conference
ESMO GI 2024
Trial
Phase 1/2, OPTIMIZE-1
The anti-CD40 antibody mitazalimab, in combination with mFOLFIRINOX, demonstrated a manageable safety profile and promising clinical efficacy in patients with metastatic pancreatic ductal adenocarcinoma (mPDAC) in the phase 1/2 OPTIMIZE-1 trial.

With a 5-year overall survival (OS) rate below 5%, current systemic therapies for mPDAC are associated with poor outcomes. Previously, CD40 agonists were shown to alter macrophage phenotype polarisation to favour the M1 phenotype and suppress pancreatic cancer [1].

The phase 1/2 OPTIMIZE-1 trial (NCT04888312) explored the safety and efficacy of mitazalimab, a second-generation CD40 agonist, combined with modified FOLFIRINOX in mPDAC patients. The primary endpoint was overall response rate (ORR); secondary endpoints included duration of response (DoR), progression-free survival (PFS), overall survival (OS), and safety. Dr Teresa Macarulla (Vall d’Hebron University Hospital, Spain) presented the first results [2].

In phase 1b of OPTIMIZE-1, 900 µg/kg mitazalimab was determined to be the recommended phase 2 dose. A total of 70 patients were enrolled in phase 2 (efficacy set: n=57; safety set: n=70). After a median follow-up of 18 months, confirmed ORR was 42.1%. Median DoR was 12.6 months, median PFS was 7.7 months, and median OS was 14.9 months. A high CD4 effector T-cell expansion after the first cycle of mitazalimab correlated with a better median OS.

Treatment-emergent adverse events (TEAEs) of grade ≥3 were observed in 55 (79%) participants, with neutropenia (25.7%), hypokalemia (15.7%), and thrombocytopenia (11.4%) being the most common. Safety was overall consistent with the known mFOLFIRINOX safety profile.

Based on these results, Dr Macarulla concluded that “mitazalimab in combination with mFOLFIRINOX demonstrated a well-manageable safety profile and a promising clinical efficacy. These encouraging results warrant continued development in a randomised phase 3 trial.”

  1. Lim CY, et al. Gut Liver. 2022;16:645-659.
  2. Macarulla T, et al. CD40 agonist mitazalimab combined with mFOLFIRINOX (mFFX) in patients with metastatic pancreatic ductal adenocarcinoma (mPDAC): Primary analysis of the OPTIMIZE-1 phase 1b/2 study. Abstract 280MO. ESMO Gastrointestinal Cancers Congress 2024, 26–29 June, Munich, Germany.

Medical writing support was provided by Dr Marten Dooper.
Copyright ©2024 Medicom Medical Publishers



Posted on