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✓ Translated by DotMD AI Clinical Council Source: Gynecologic oncology • Phase III Randomized Trial
Verify Primary Source: NIH PubMed PMID #38052110 ↗

Phase III Randomized Trial: Lunchbox trial (N = 42)

Original Paper Title: “Lunchbox trial: A randomized phase III trial of cisplatin and irradiation followed by carboplatin and paclitaxel versus sandwich therapy of carboplatin and paclitaxel followed by irradiation then carboplatin and paclitaxel for advanced endometrial carcinoma”

Elena Rostova (AI Quant) Rigor Score
82 / 100
Sample Size (Participants)
N = 42
Evidence Classification
Phase III Randomized Trial
Sarah Jenkins, RN (AI Plain-English Editor) • Key Takeaways
  • There was no observed significant difference between chemoRT then chemo compared to sandwich therapy in terms of RFS, OS, or adverse events, although the trial was underpowered and closed early due to low accrual.
  • Study Design & Sample: Phase III Randomized Trial published in Gynecologic oncology (N = 42 human participants).
  • Biostatistical Rigor Score: 82/100 audited by Elena Rostova (AI Biostatistician & openFDA Quant).

What the Study Found (In Plain English)

Published in Gynecologic oncology (2024), this phase iii randomized trial evaluating 42 human participants investigated: The objective was to compare sequencing strategies for treatment of advanced endometrial carcinoma. Key clinical takeaway: There was no observed significant difference between chemoRT then chemo compared to sandwich therapy in terms of RFS, OS, or adverse events, although the trial was underpowered and closed early due to low accrual.

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

Primary Endpoint & Quantitative Summary (Gynecologic oncology, 2024-01-15; N = 42; Rigor 82/100): There was no observed significant difference between chemoRT then chemo compared to sandwich therapy in terms of RFS, OS, or adverse events, although the trial was underpowered and closed early due to low accrual.

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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