✓ Translated by DotMD AI Clinical Council Source: Future oncology (London, England) • Phase III Randomized Trial
Verify Primary Source: NIH PubMed PMID #33263418 ↗

Phase III Randomized Trial: MAHOGANY: margetuximab combination in HER2+ unresectable/metastatic gastric/gastroesophageal junction adenocarcinoma

Original Paper Title: “MAHOGANY: margetuximab combination in HER2+ unresectable/metastatic gastric/gastroesophageal junction adenocarcinoma”

Elena Rostova (AI Quant) Rigor Score
82 / 100
Sample Size (Participants)
Systematic Review
Evidence Classification
Phase III Randomized Trial
Sarah Jenkins, RN (AI Plain-English Editor) • Key Takeaways
  • Primary end points include objective response rate, overall survival and safety/tolerability. Clinical trial registration: NCT04082364
  • Study Design & Sample: Phase III Randomized Trial published in Future oncology (London, England) (Multi-cohort synthesis).
  • Biostatistical Rigor Score: 82/100 audited by Elena Rostova (AI Biostatistician & openFDA Quant).

What the Study Found (In Plain English)

Published in Future oncology (London, England) (2021), this phase iii randomized trial evaluating human clinical outcomes investigated: Standard-of-care, first-line therapy for patients with advanced HER2+ gastric/gastroesophageal junction adenocarcinoma is chemotherapy plus trastuzumab, a monoclonal antibody (mAb) targeting HER2. Key clinical takeaway: Primary end points include objective response rate, overall survival and safety/tolerability. Clinical trial registration: NCT04082364

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

Primary Endpoint & Quantitative Summary (Future oncology (London, England), 2021-04-15; Phase III Randomized Trial; Rigor 82/100): Primary end points include objective response rate, overall survival and safety/tolerability. Clinical trial registration: NCT04082364

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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