NEW YORK, NY and MAINZ, GERMANY – November 9, 2011 – The Association for Cancer Immunotherapy (CIMT) Immunoguiding Program (CIP) and the Cancer Immunotherapy Consortium (CIC) of the Cancer Research Institute (CRI) today announced the publication of a joint paper discussing recent results of independent international, cross-laboratory immune assay harmonization studies. More than 120 academic, pharmaceutical, biotechnology, contract research, and government laboratories from the United States and Europe have participated in CIMT-CIP and CRI-CIC sponsored proficiency panels to test and compare immune response assays, including measurement variability and reproducibility. The collaboration between both organizations dedicated to cancer immunotherapy has enabled this successful program, which represents the largest in the field and delivers an important practical advance to the research community.
Unlike most anticancer treatments, immune-based therapies primarily target the immune system and not the tumor. Therefore, an essential component of immunotherapy trials is the study of the patient’s immune response to such treatment, measuring clinical efficacy and ultimately deciding on the progress of early clinical studies. However, differing protocols between laboratories for measuring immune responses often result in high data variability and poor reproducibility. This precludes an objective comparison of data across studies and the identification of biomarkers.
“To save costs and prevent redundant trials one should be able to use the datasets from many different phase I/II clinical trials as building blocks for strategies. This, however, requires a reduction in data variability and the implementation of cross-laboratory harmonization guidelines,” says Sjoerd van der Burg, Ph.D., chairman of the CIMT Immunoguiding Program and professor of Experimental Cancer Immunology and Therapy at Leiden Medical Center, Netherlands. “A higher probability to identify biomarkers through harmonization of immunological assays will in the end guide timely and rational decisions about candidate agents that move through the clinical trial process.”
According to van der Burg, any size laboratory, regardless of experience level, can benefit from participating in proficiency panels as an effective mechanism for quality control in assay development and application.
“The proposed methodological improvements to clinical cancer immunology that have resulted from our international collaborations, such as our assay harmonization guidelines, when implemented, have been shown to reduce data variability and enhance the clinical development process,” says Sylvia Janetzki, Ph.D., leader of the proficiency panel program of the CRI Cancer Immunotherapy Consortium. “With many new promising immune-based therapeutic agents now in development, it’s important that members of the broader cancer immunotherapy community consider these simple harmonization guidelines as a possible means to increasing efficiencies across laboratories and shortening the time it takes to develop biomarkers and bring effective new treatments to cancer patients.”
Since 2005, the Cancer Immunotherapy Consortium (CIC) of the Cancer Research Institute in the United States and the Association for Cancer Immunotherapy Immunoguiding Program (CIP) in Europe have conducted large proficiency panel experiments to address assay harmonization. Enrollment instructions for new laboratories and clinical trial sites interested in participating in the harmonization process initiated by CIP and CIC are available on their websites, www.cimt.eu and www.cancerresearch.org/cic, respectively.
Sjoerd H. van der Burg, Michael Kalos, Cecile Gouttefangeas, Sylvia Janetzki, Christian Ottensmeier, Marij J.P. Welters, Pedro Romero, Cedrik M. Britten, Axel Hoos. Harmonization of immune biomarker assays for clinical studies. Science Translational Medicine 3, 108ps44 (2011).
Note: To view the open access version of this paper, you must visit the CIC publications library and then select this publication from the list.
Christine S. Castle, Communications Director
Association for Cancer Immunotherapy (CIMT)
+49 (0) 6131 178166 or email@example.com
Brian M. Brewer, Director of Marketing & Communications
Cancer Research Institute
(212) 688-7515, ext. 242 or firstname.lastname@example.org
About the Association for Cancer Immunotherapy (CIMT)
The Association for Cancer Immunotherapy (CIMT) is an international networking and education platform aiming to facilitate the development of new immunotherapies against cancer for the benefit of patients. CIMT was founded in 2002, and has its home office in Mainz, Germany. The association hosts the largest European expert meetings on cancer immunotherapy, publishes therapeutic guidelines and has established two topic-specific working groups: the CIMT Regulatory Research Party, focusing on the regulatory aspects of drug development, which is pioneering the regulatory framework of actively personalized vaccines for single patient use only; and the CIMT Immunoguiding Program (CIP), which focuses on the quality control and harmonization of immunomonitoring assays. To reach its goals, CIMT closely cooperates with various partners, among them the Cancer Research Institute’s Cancer Immunotherapy Consortium (CRI-CIC). Visit www.cimt.eu for more information.
About the Cancer Immunotherapy Consortium of the Cancer Research Institute
The Cancer Immunotherapy Consortium (CIC), a program of the nonprofit Cancer Research Institute, is an international association of more than 100 pharmaceutical and biotechnology companies and academic institutions that share a common interest in immunotherapy research and development.
CIC’s mission is to improve patient care by making cancer immunotherapies part of the standard-of-care in oncology. CIC provides a platform that allows its stakeholders to advance the field by working together to achieve solutions to scientific and developmental challenges creating a single and powerful voice within the biomedical research community. From these collaborative, community-wide efforts, CIC has developed and published a number of landmark recommendations for practical solutions to key challenges in the field, including the development of new immune related response criteria and clinical trial endpoints for evaluation of cancer immunotherapy impact on patient health.
Founded in 2002 as the Cancer Vaccine Consortium (CVC), CIC amended its name in early 2010 to represent more accurately the broader diversity of the many promising clinical developments in immune-based treatment of cancer beside vaccines, including monoclonal antibodies and other modulators of immunity.