Home > For Consumers > Pembrolizumab (Keytruda) for advanced...

PubMed Health. A service of the National Library of Medicine, National Institutes of Health.

Informed Health Online [Internet]. Cologne, Germany: Institute for Quality and Efficiency in Health Care (IQWiG); 2006-.

Informed Health Online [Internet].

Pembrolizumab (Keytruda) for advanced lung cancer: Overview

Last Update: June 1, 2017; Next update: 2020.

Introduction

The drug pembrolizumab (trade name: Keytruda) has been approved in Germany since July 2016 for the treatment of advanced non-small-cell lung cancer. It can be used in adult patients who have mutated cancer cells that can lead to faster tumor growth.

Lung cancer is caused by the growth of malignant cells in the airways (bronchi) and their branches (bronchioles). It is also referred to as a bronchogenic carcinoma. There are two main types:

NSCLC is surgically removed, if possible. But sometimes the tumor has already become too large or the cancer has spread to other parts of the body (metastasis) through the blood or lymphatic system. It is then called advanced lung cancer.

Pembrolizumab has been approved for use in people who have a tumor with elevated levels of the protein PD-L1. This protein weakens the body's immune response, particularly the activity of T cells, against the tumor cells.

Those who are affected might also have a mutated receptor in the tumor tissue called an epidermal growth factor receptor (EGFR). And the tumor cells may produce a specific enzyme called anaplastic lymphoma kinase (ALK). Both of these changes cause further uncontrolled tumor growth as well. Pembrolizumab is also an option for this group of people if earlier treatments for EGFR or the enzyme ALK have been unsuccessful.

Pembrolizumab blocks the effect of the PD-L1 protein produced by the tumor tissue and initiates an immune response to the cancer cells in order to inhibit tumor growth.

Application

Pembrolizumab comes in the form of a powder that is dissolved in a liquid and then given through an infusion (an IV drip), entering the bloodstream directly through a vein. The infusion is given every three weeks and lasts about 30 minutes each time. The dose will depend on the patient's body weight. This treatment is discontinued if severe side effects occur or if the cancer continues to grow.

Other treatments

The following treatments are available for people with advanced lung cancer and the PD-L1 mutation:

  • As first-line treatment for a tumor without mutated EGFR or ALK, depending on general health and the side effects, the options are either platinum-based chemotherapy (using drugs such as cisplatin or carboplatin combined with vinorelbine, gemcitabine, docetaxel, paclitaxel or pemetrexed) or treatment with gemcitabine or vinorelbine.
  • As second-line treatment, if previous chemotherapy was unsuccessful, the standard approach is treatment with docetaxel, pemetrexed or nivolumab. These standard treatments are also an option for adults with an additional EGFR or ALK mutation who have previously had unsuccessful therapy. If none of these standard treatments are possible, best supportive care (BSC) is used. BSC should be tailored to the patient's individual needs, relieve pain and other symptoms, and improve quality of life.

Assessment

In 2017, the Institute for Quality and Efficiency in Health Care (IQWiG, Germany) looked into the advantages and disadvantages of pembrolizumab for people with advanced lung cancer and a PD-L1 mutation compared to the standard therapies so far.

The manufacturer provided two relevant studies for the following groups:

More information

This information summarizes the main results of reviews produced by the Institute for Quality and Efficiency in Health Care (IQWiG, Germany). The reviews were commissioned by the German Federal Joint Committee (G-BA) as part of the “early benefit assessment of medications.” On the basis of the reviews and the hearings received, the G-BA passed a resolution on the added benefit of pembrolizumab (Keytruda).

Sources

  • Institute for Quality and Efficiency in Health Care (IQWiG, Germany). Pembrolizumab (non-small cell lung cancer) - Benefit assessment according to §35a Social Code Book V. Dossier assessment; commission A16-55. November 10, 2016. (IQWiG reports; Volume 459). [PubMed: 29144639]
  • Institute for Quality and Efficiency in Health Care (IQWiG, Germany). Pembrolizumab (non-small cell lung cancer) - Benefit assessment according to §35a Social Code Book V. Dossier assessment; commission A17-06. May 10, 2017. (IQWiG reports; Volume 509).
  • IQWiG health information is written with the aim of helping people understand the advantages and disadvantages of the main treatment options and health care services.

    Because IQWiG is a German institute, some of the information provided here is specific to the German health care system. The suitability of any of the described options in an individual case can be determined by talking to a doctor. We do not offer individual consultations.

    Our information is based on the results of good-quality studies. It is written by a team of health care professionals, scientists and editors, and reviewed by external experts. You can find a detailed description of how our health information is produced and updated in our methods.

© IQWiG (Institute for Quality and Efficiency in Health Care)

Download

IQWiG (Institute for Quality and Efficiency in Health Care)

PubMed Health Blog...

read all...

Informed Health Links

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...