✓ Translated by DotMD AI Clinical Council Source: The British journal of surgery • Phase III Randomized Trial
Verify Primary Source: NIH PubMed PMID #40474841 ↗

Phase III Randomized Trial: Surgical considerations for tumour-infiltrating lymphocyte therapy in melanoma: results from a randomized phase III trial (N = 80)

Original Paper Title: “Surgical considerations for tumour-infiltrating lymphocyte therapy in melanoma: results from a randomized phase III trial”

Elena Rostova (AI Quant) Rigor Score
82 / 100
Sample Size (Participants)
N = 80
Evidence Classification
Phase III Randomized Trial
Sarah Jenkins, RN (AI Plain-English Editor) • Key Takeaways
  • Tumour resections for TIL-IMP manufacture lead to limited surgical complications. Manufacture with a therapeutic response was successful using lesions of varying sizes from different anatomical locations, with highest rates for lymph nodes.
  • Study Design & Sample: Phase III Randomized Trial published in The British journal of surgery (N = 80 human participants).
  • Biostatistical Rigor Score: 82/100 audited by Elena Rostova (AI Biostatistician & openFDA Quant).

What the Study Found (In Plain English)

Published in The British journal of surgery (2025), this phase iii randomized trial evaluating 80 human participants investigated: The aim of this study was to describe the impact of surgical resections on tumour-infiltrating lymphocyte (TIL) therapy, based on results from a randomized phase III trial comparing TIL therapy with standard ipilimumab in patients with metastatic melanoma (NCT02278887). Key clinical takeaway: Tumour resections for TIL-IMP manufacture lead to limited surgical complications. Manufacture with a therapeutic response was successful using lesions of varying sizes from different anatomical locations, with highest rates for lymph nodes.

Dr. Lin (AI Evidence Lead): Statistical Endpoints & Numbers

Primary Endpoint & Quantitative Summary (The British journal of surgery, 2025-05-31; N = 80; Rigor 82/100): Tumour resections for TIL-IMP manufacture lead to limited surgical complications. Manufacture with a therapeutic response was successful using lesions of varying sizes from different anatomical locations, with highest rates for lymph nodes.

Study Limitations & Caveats Before You Act

Clinical trials evaluate specific inclusion/exclusion cohorts under protocol-controlled conditions (Phase III Randomized Trial). Individual response, hepatic/renal clearance, CYP450 drug interactions, and baseline comorbidities vary; verify applicability with a board-certified physician before modifying any prescription or supplement regimen.

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