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Last updated: 2017-05-08

Keytruda Approved for Advanced or Recurrent Cervical Cancer in Japan

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Keytruda Approved for Advanced or Recurrent Cervical Cancer in Japan

Keytruda Approved for Advanced or Recurrent Cervical Cancer in Japan

Medical Supporter — Information Notice

This article is a summary of international medical information and is not medical advice; it cannot replace the diagnosis or treatment plan of your attending physician. The medical technologies, drug information and clinical data presented here are compiled from public literature and official statements of major Japanese medical institutions; the applicability and outcome of any therapy vary with each patient and must be assessed individually by a qualified physician.

Any specific treatment plan must be assessed by a licensed physician in Japan

Medical Supporter — Information Notice

This article is a summary of international medical information and is not medical advice; it cannot replace the diagnosis or treatment plan of your attending physician. The medical technologies, drug information and clinical data presented here are compiled from public literature and official statements of major Japanese medical institutions; the applicability and outcome of any therapy vary with each patient and must be assessed individually by a qualified physician.

Any specific treatment plan must be assessed by a licensed physician in Japan

On September 26, 2022, MSD K.K. announced that the anti-PD-1 therapy Keytruda (Pembrolizumab) has received approval in Japan for an expanded indication: the treatment of patients with advanced or recurrent cervical cancer.

Clinical Evidence: KEYNOTE-826 Trial

The approval is supported by the results of the KEYNOTE-826 Phase 3 clinical trial, an international, multicenter, randomized study involving 617 patients with persistent, recurrent, or metastatic cervical cancer who had not received prior systemic chemotherapy.

Participants were randomized to receive:

  1. Keytruda + Chemotherapy (with or without Bevacizumab).
  2. Placebo + Chemotherapy (with or without Bevacizumab).

Key Survival Results

The trial demonstrated that the addition of Keytruda to standard chemotherapy significantly improved outcomes:

  • Overall Survival (OS): Patients in the Keytruda group experienced a statistically significant prolongation of life compared to the placebo group.
  • Progression-Free Survival (PFS): Keytruda also significantly extended the time patients lived without their disease worsening.

Future Outlook

MSD K.K. emphasized its commitment to developing innovative oncology treatments to meet the unmet needs of patients and healthcare professionals in Japan and globally.

Source: MSD K.K. Press Release - Keytruda Approval for Cervical Cancer

#CervicalCancer #Keytruda #Pembrolizumab #KEYNOTE826 #Immunotherapy #CancerResearch #JapanMedicine

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