ESMO 2016: New data from Eisai’s oncology portfolio for halaven (eribulin), lenvima (lenvatinib) and kisplyx (lenvatinib)
Posted: 4 October 2016 | | No comments yet
European Pharmaceutical Review will of course keep you up to date with all the latest pharma news from the conference. Here’s a preview snippet…
Eisai highlights nine new data abstracts in hard to treat cancers for eribulin and lenvatinib at the European Society for Medical Oncology (ESMO) Congress, Copenhagen, 7-11 October 2016.
Lenvatinib data in thyroid cancer, renal cell carcinoma and other solid tumours
An investigational phase II study for lenvatinib focuses on the treatment of KIF5B-RET–positive adenocarcinoma of the lung. Adenocarcinoma is a type of non-small cell lung carcinoma, one of the most common forms of lung cancer. RET fusions activate RET kinase and occur in 1-2% of patients.
Exploratory early phase data will review lenvatinib with anti PD-1 therapy including a phase Ib/II study in people with selected solid tumours.
Subanalyses from the pivotal SELECT study investigate responses in specific metastasis sites following treatment with lenvatinib for patients with radioiodine-refractory (RAI-R) differentiated thyroid cancer (DTC). SELECT is a multicentre randomised, double-blind, placebo-controlled phase III study to compare the progression-free survival (PFS) of patients with radioiodine-refractory differentiated thyroid cancer.
A pre-clinical study examines the VEGFR and FGFR signalling pathway participation in tumour growth and angiogenesis in human renal cell carcinoma xenografts treated with the combination of lenvatinib plus everolimus. A further pre-clinical study analyses immune response in syngeneic murine tumour models to understand the antitumour effect and mechanism of action of the combination of lenvatinib and PD-1 blockade treatment in a number of cancer models.
Epidemiological data in metastatic breast cancer
This study investigates the progressive decline in efficacy of active agents in locally advanced
or metastatic breast cancer with each successive therapy cycle. The study includes data from 443 patients in Spain with locally advanced or metastatic breast cancer.
Eribulin data in metastatic breast cancer
A study investigates the safety of eribulin in third-line chemotherapy in 59 patients with HER2-negative metastatic or locally advanced breast cancer.
Exploratory data from the investigational, phase II, multicenter, single arm trial (MERIBEL) will examine the efficacy and safety of eribulin as a first-line therapy for HER2- metastatic breast cancer.
Eribulin data in soft tissue sarcomas
Results will be presented from a pre-specified subgroup analysis in leiomyosarcomas of the phase III 309 study comparing eribulin to dacarbazine. Eribulin is not licensed in leiomyosarcomas in the European Union.
“Eisai is committed to the development of innovative treatments for people with cancer and always gives first thought to patients and their families. Eribulin has demonstrated a unique overall survival benefit in advanced or metastatic breast cancer and unresectable liposarcoma. Lenvatinib delivers rapid, pronounced and durable responses; and significantly prolongs the time before a cancer progresses in both advanced thyroid and advanced kidney cancer,” comments Gary Hendler, Chairman & CEO EMEA and Chief Commercial Officer, Global Oncology Business Group.
Video snippet
M. Ducreux says that the main focus of genomic research in upper GI cancers is in gastric carcinoma. He emphasizes that understanding of carcinogenesis is key in achieving progress in the treatment and discusses molecular subtypes of gastric cancer. He predicts that in a near future oncologists will be able to select patients and to propose immunotherapy probably in a sub-population of patients with MSI type gastric carcinoma.Video produced by the European Society for Medical Oncology (ESMO).
Table of Eisai’s products and where to find them
Product | Abstract Name | Presentation Details |
Lenvatinib Poster: 1204PD | Phase 2 study of lenvatinib in patients with RET Velcheti V et al
| Poster Discussion: NSCLC, metastatic Date: 09 Oct 16 Time: 14:45-16:15 Room: Oslo |
Lenvatinib Poster: 776PD | A phase 1b trial of lenvatinib plus pembrolizumab in patients with selected solid tumours Taylor M et al | Poster Discussion: Genitourinary tumours, non-prostate Date: 09 Oct 16 Time: 16:30-17:30 Room: Athens |
Lenvatinib Poster: 2PD | Lenvatinib mesylate enhanced antitumour activity of PD-1 blockade agent by potentiating Th1 immune response Kato Y et al | Poster Discussion: Basic science and translational research Date: 09 Oct 16 Time: 16:30-17:30 Room: Berlin |
Lenvatinib Poster: 962P | Responses in specific metastases following treatment with lenvatinib: results from the phase 3 SELECT study Robinson B et al | Poster Presentation: Poster display Date: 09 Oct 16 Time: 13:00-14:00 Room: Hall E |
Lenvatinib Poster: 6P | The antitumour activity of lenvatinib in combination with everolimus in human RCC xenograft models is dependent on VEGFR and FGFR signalling Kimura T et al | Poster Presentation: Poster display Date: 10 Oct 16 Time: 13:00-14:00 Room: Hall E |
Epidemiological Data Poster: 248P | CASCADE study: pronounced decline in treatment efficacy through the metastatic life of breast cancer patients De Paz L et al
| Poster Presentation: Poster display Date: 10 Oct 16 Time: 13:00-14:00 Room: Hall E |
Eribulin Poster: 238P | MERIBEL study: Single-agent eribulin as first-line therapy for taxane-resistant HER2[-] metastatic breast cancer (MBC) patients Ortega V et al | Poster Presentation: Poster display Date: 10 Oct 16 Time: 13:00-14:00 Room: Hall E |
Eribulin Poster: 246P | Single arm, multicentre, non-randomized open-label trial to evaluate the safety of eribulin in third line chemotherapy in patients with HER2-negative metastatic or locally advanced breast cancer previously treated with anthracyclines and taxanes: Onsite study (ONCOSUR 2012-02) Sanchez L et al | Poster Presentation: Poster display Date: 10 Oct 16 Time: 13:00-14:00 Room: Hall E |
Eribulin Poster: 1401PD | Subgroup analysis in leiomyosarcoma (LMS) patients from a phase 3, open-label, randomised study of eribulin versus dacarbazine in patients with advanced liposarcoma (LPS) and LMS Blay J et al | Poster Discussion: Sarcoma Date: 10 Oct 16 Time: 11:00-12:00 Room: Brussels |
European Pharmaceutical Review hopes the event will be informative, interesting and impassioned – and of course we’ll keep you up to date with all the latest pharma news from the conference. Our advice? Attend as much as you can and download the ESMO events app to keep yourself in the loop.