LUME-Meso trial enrols first patient: Boehringer Ingelheim’s new pivotal study investigating nintedanib for the treatment of malignant pleural mesothelioma

09 May 2016
  • The trial will evaluate efficacy and safety of nintedanib* as a first-line oral treatment in combination with pemetrexed/cisplatin followed by continuing nintedanib monotherapy
  • Nintedanib targets receptors that play a role in tumour growth and development of metastasis in malignant pleural mesothelioma where no other targeted therapies are currently approved
  • Follows EU approval of nintedanib (Vargatef®) in combination with docetaxel for treatment of adenocarcinoma of the lung after first-line chemotherapy

Ingelheim, Germany, 09 May 2016 - Boehringer Ingelheim today announced the enrolment of the first patient in the global Phase III trial evaluating the efficacy and safety of nintedanib in combination with pemetrexed/cisplatin, followed by continuing nintedanib monotherapy, as a first-line treatment for patients with unresectable malignant pleural mesothelioma (MPM). Patients will qualify for enrolment in the trial if they are not eligible to undergo surgical resection, have received no prior first-line therapies for MPM and hold an Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.

Lead investigator, Professor Giorgio V. Scagliotti, University of Torino, Chair of the Department of Oncology, Italy, commented, “Malignant pleural mesothelioma is a rare cancer and despite years of research, patients continue to have a poor prognosis – less than 10% survive for five years following diagnosis. Due to the mode of action of nintedanib, it has the potential to be an effective treatment option for patients with pleural mesothelioma.”

LUME-Meso [NCT01907100 (link is external)] will randomise 397 patients in a double-blind, multi-centre, global comparison of nintedanib in combination with pemetrexed/cisplatin or matching placebo in combination with pemetrexed/cisplatin as a first-line treatment.1 For patients whose disease has not progressed after a maximum of six cycles of chemotherapy, nintedanib or matching placebo will continue to be administered orally as a monotherapy on a daily basis, until disease progression or unmanageable side effects. The primary endpoint of the trial is progression-free survival and overall survival is the key secondary endpoint. Other secondary endpoints include objective tumour response and disease control.

Through its mode of action nintedanib targets the receptors of the vascular endothelial growth factor (VEGF), fibroblast growth factor (FGF), platelet-derived growth factor (PDGF) and proto-oncogene tyrosine-protein kinase (Src) pathways which play a role in tumour growth and the development of metastasis in MPM. No targeted therapies are currently approved for the treatment of this rare and difficult-to-treat cancer.2

Dr Jörg Barth, Corporate Senior Vice President, Therapy Area Head Oncology, Boehringer Ingelheim said, “Over the last few years Boehringer Ingelheim has accumulated considerable expertise in the field of thoracic oncology. With the approval of Giotrif® and Vargatef® as well as a broad clinical pipeline we are building up a strong presence in this setting. The effort to develop a potential efficacious treatment for malignant pleural mesothelioma demonstrates our long-term commitment for patients with significant unmet medical need.”

Nintedanib is also being evaluated in the LUME-Colon 1 trial [NCT02149108 (link is external)], a global Phase III trial in patients with advanced colorectal cancer. Recruitment is now complete and data are expected to be available later in 2016.3

Notes to editors

Intended audiences

This press release is issued from our Corporate Headquarters in Ingelheim, Germany and is intended to provide information about our global business. Please be aware that information relating to the approval status and labels of approved products may vary from country to country, and a country-specific press release on this topic may have been issued in the countries where we do business.

About mesothelioma

https://www.boehringer-ingelheim.com/sites/default/files/Documents/Mesothelioma_Backgrounder.pdf

Mesothelioma is a rare and difficult-to-treat cancer that represents less than 1% of all cancers.2 Following diagnosis, surgery is not an option for the majority of patients due to the diffuse spreading growth of neoplasm and there is a high unmet medical need for novel, effective first-line treatments.4

About nintedanib

https://www.boehringer-ingelheim.com/sites/default/files/Documents/Vargatef_Backgrounder.pdf

About Boehringer Ingelheim in Oncology

https://www.boehringer-ingelheim.com/sites/default/files/Infographics/bi_in_oncology_backgrounder.pdf

About Boehringer Ingelheim

Boehringer Ingelheim is one of the world’s 20 leading pharmaceutical companies. Headquartered in Ingelheim, Germany, Boehringer Ingelheim operates globally through 145 affiliates and a total of some 47,500 employees. The focus of the family-owned company, founded in 1885, is on researching, developing, manufacturing and marketing new medications of high therapeutic value for human and veterinary medicine.

Social responsibility is an important element of the corporate culture at Boehringer Ingelheim. This includes worldwide involvement in social projects through, for example, the initiative “Making More Health” while also caring for employees. Respect, equal opportunity and reconciling career and family form the foundation of mutual cooperation. The company also focuses on environmental protection and sustainability in everything it does.

In 2015, Boehringer Ingelheim achieved net sales of about 14.8 billion euros. R&D expenditure corresponds to 20.3 per cent of net sales.

For more information please visit www.boehringer-ingelheim.com

References: 

* Nintedanib is approved in the EU under the brand name VARGATEF® for use in combination with docetaxel in adult patients with locally advanced, metastatic or locally recurrent NSCLC of adenocarcinoma tumour histology after first-line chemotherapy. Nintedanib is under regulatory review by health authorities in other countries outside the EU. Nintedanib is not approved in other oncology indications.

  1. Clinicaltrials.gov. Nintedanib (BIBF 1120) in Mesothelioma. Available at: https://clinicaltrials.gov/ct2/show/NCT01907100?term=nintedanib+mesothelioma&rank=2 (last accessed April 2016).
  2. Moore A. et al. Malignant mesothelioma. Orphanet J Rare Dis. 2008;3(34).
  3. Clinicaltrials.gov. A double-blind randomised, placebo-controlled, Phase III study of nintedanib plus best supporting care (BSC) versus placebo plus BSC, in patients with colorectal cancer refractory to standard therapies: https://clinicaltrials.gov/ct2/show/NCT02149108?term=nintedanib+AND+Colon&rank=2 (last accessed April 2016).
  4. Zaragoulidis P. et al. Malignant pleural mesothelioma: current and future perspectives. J Thorac Dis. 2013;5(4):S39.
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