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(Colorectal Cancer) Pertuzumab Plus Trastuzumab — Objective Response Rate 32%

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(Colorectal Cancer) Pertuzumab Plus Trastuzumab — Objective Response Rate 32%

(Colorectal Cancer) Pertuzumab Plus Trastuzumab — Objective Response Rate 32%

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HER2-Targeted Therapy: Pertuzumab Plus Trastuzumab in HER2-Amplified Metastatic Colorectal Cancer

  • May 31, 2019
  • Reading time: 1 minute

Objective Response Rate of 32% with Pertuzumab Plus Trastuzumab in HER2-Amplified Metastatic Colorectal Cancer

On March 8, 2019, a Phase 2 clinical trial evaluating the efficacy and safety of the anti-HER2 monoclonal antibody combination of pertuzumab (Perjeta) plus trastuzumab (Herceptin) in patients with HER2-amplified metastatic colorectal cancer who had received multiple prior lines of therapy was published in the medical journal The Lancet Oncology.

Trial Design

This Phase 2 trial administered treatment to patients every 3 weeks, with the treating physician evaluating objective response rate.

Background: Given established evidence of efficacy of anti-HER2 antibodies pertuzumab and trastuzumab in HER2-positive breast cancer, gastric cancer, and other solid tumors, this trial was conducted based on the hypothesis that these agents might also benefit patients with HER2-amplified metastatic colorectal cancer.

Results

Efficacy: Among patients with HER2 amplification, the objective response rate (ORR) was 32%.

Safety: Most common adverse events: diarrhea, fatigue, and nausea. Less common adverse events: hypokalemia and abdominal pain. No treatment-related deaths occurred.

Based on the trial results, heavily pretreated patients with HER2-amplified metastatic colorectal cancer demonstrated acceptable tolerability and meaningful antitumor activity with this combination therapy.

Source: Pertuzumab plus trastuzumab for HER2-amplified metastatic colorectal cancer (MyPathway): an updated report from a multicentre, open-label, phase 2a, multiple basket study. Lancet Oncology, Published: March 08, 2019.

Tags: #ColorectalCancer

  • Clinical trial drug

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