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TIL Therapy Breakthroughs for Oncologists and Oncology Professionals

Dr. Allison Betof Warner presenting TIL therapy melanoma breakthroughs at Stanford, showing 96% survival and 67% response rates.

Dr. Allison Betof Warner unveils TIL therapy innovations at Stanford, boasting 96% 10-year survival and 67% response rates in melanoma treatment, October 2025.

TIL Therapy Breakthroughs for Oncologists and Oncology Professionals

Tumor-Infiltrating Lymphocyte (TIL) therapy is transforming melanoma care and continues to provide new insights into TIL therapy melanoma management. Dr. Allison Betof Warner, Director of the Melanoma Program at Stanford University, leads this effort. Her work delivers stunning results for oncologists.

Unmatched Survival and Response Rates

Firstly, TIL therapy with lifileucel achieves a 96% 10-year survival rate for responders (Seitter et al. Clin Cancer Res 2021). This suggests a potential cure for metastatic cases. Additionally, for PD-1 refractory melanoma, the objective response rate (ORR) is 31.4%. Moreover, the disease control rate (DCR) reaches 77.7% (Chesney et al. JITC 2022). Furthermore, engineered OBX-115 boosts this to a 67% response rate at the recommended phase 2 dose (Chesney…Betof Warner. ASCO 2025). Lastly, the median duration of response (DoR) is 36.5 months, with many patients staying in remission beyond five years without further treatment in the context of TIL therapy melanoma advancements.

Comparative Efficacy and Safety

In contrast, TIL therapy outperforms ipilimumab. It offers a median progression-free survival (PFS) of 7.2 months versus 3.1 months (hazard ratio 0.50, 95% CI 0.35-0.72, P<0.001) (Rohaan et al. NEJM 2022). Similarly, the ORR is 49% with TIL, compared to 21% with ipilimumab. Additionally, complete responses hit 20% versus 7%. Meanwhile, safety data shows 94.9% of patients experience at least one treatment-emergent adverse event (TEAE). These decrease within two weeks post-infusion (Sarnaik et al. SITC 2022). Furthermore, OBX-115 adds safety, with no Grade 5 events and only 5 patients with Grade 3 nonhematologic TRAEs at 34 weeks, showcasing the progress in TIL therapy melanoma safety.

Expanding Horizons with TILVANCE-301

Consequently, the TILVANCE-301 Phase 3 trial (NCT05727904) is key. It randomizes ~670 patients 1:1 to lifileucel plus pembrolizumab or pembrolizumab alone. Primary endpoints are ORR and PFS per RECIST v1.1. Moreover, secondary goals include overall survival (OS) and complete response (CR) rate. Therefore, early results may shift TIL therapy melanoma treatment to frontline use.

Safety Innovations and Beyond Melanoma

Alternatively, OBX-115 uses regulatable mbIL-15, avoiding high-dose IL-2. Acetazolamide regulates it, reducing risks. Additionally, no dose-limiting toxicities (DLTs) or severe cytokine release syndrome (CRS) occur. Furthermore, trials now target non-small cell lung cancer, cervical cancer, and breast cancer. Thus, this one-time treatment differs from endless chemo and marks a significant step in TIL therapy melanoma application.

Why Oncologists Should Act

However, hematologic issues like leukopenia (100%) and chills (75.0%) are common but manageable within weeks. Dr. Warner focuses on shorter manufacturing and safer lymphodepletion. Moreover, the stats—96% survival, 67% response, 36.5-month DoR—signal a shift. Finally, engineered cells enhance efficacy. Regarding TIL therapy melanoma, these developments offer exciting opportunities for oncologists.

Join Dr. Warner (@DrBetofMDPhD) to explore these advances.

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