“DKTK Joint Funding” Program

DKTK has implemented the Joint Funding Program, an intramural competition to trigger and support outstanding research networks on innovational translational and clinical projects in oncology, in order to foster interaction between partner sites and strengthen DKTK’s overall research portfolio. Teams of DKTK researchers from several partner sites are eligible to submit collaborative proposals that are evaluated in a two-step procedure involving the DKTK Research Review Committee and DKTK’s international Scientific Advisory Board. Successful projects will be supported for up to 3 years.

Project “iVacALL”

The clinical 'IvacALL' study is currently investigating the effectiveness of tumour vaccines in children suffering from leukaemia. Relapses after chemo or stem cell therapy are a major problem. Here, customized vaccines open up new treatment options: Children's immune systems are able to recognize the protein changes in tumour cells and to fight them. Therapeutic vaccines using altered protein fragments, or peptides can direct immune cells specifically to the tumour.

As a first step the DNA of both the patient's tumour and their normal healthy tissue extensively analyzed in order to identify the cancer-specific alterations. Following on from that, each patient is vaccinated with a personalized peptide cocktail. The tumour database, which was developed in the course of the study forms the basis of improved treatment options for children in the long-term. The technical progress in genome sequencing in recent years has made these large datasets available for individual therapies.


Prof Dr Peter Lang
University Hospital Tübingen

Prof Dr Stefan Pfister
University Hospital Heidelberg

Prof Dr Hans-Georg Rammensee
University Tübingen

Project “Ga-PSMA-11 in high-risk prostate cancer”

The clinical study 'Ga-PSMA-11 in high-risk prostate cancer' developed by DKFZ scientists has also received an award. This research project is based on a completely new method for the early diagnosis of prostate cancer. The prostate-specific membrane antigen (PSMA) is a transmembrane protein which is enriched in prostate cancer cells. Using a radioactive substance that specifically binds to PSMA, this enrichment can be visualized with positron emission tomography (PET), precisely marking the tumour tissue and any metastases.

Currently there are no reliable early non-invasive diagnostic method for prostate cancer. The Joint Funding now enables DKTK scientists to test PSMA diagnostics in a clinical study at the DKTK sites. The DKTK investigators will look at a large number of tissue samples from prostate cancer patients and compare the findings using PSMA diagnostics. This method also presents a potential clinical approach for cancer therapy: If labeled with a strongly radioactive marker, the PSMA-binding substance could also specifically destroy cancer cells.


Prof Dr Frederik Giesel
University Hospital Heidelberg

Project “NonCoMs in Cancer Genomes”

So far, the focus of genetic tumour analysis has been on mutations that result in altered proteins. They are often considered to be the trigger for malignant tumours. Identifying and understanding non-coding mutations in cancer genomes is a project that goes an important step further and traces mutations in tumour cells that do not lead to altered proteins, but are located in regions that change the activity of important cancer genes. Plans include investigations particularly on skin tumours (melanoma) and brain tumours (glioblastoma). Being able to identify these mutations in a collaborative effort represents a major chance to track down the causes of cancer.


Prof Dr Alfred Nordheim
University Tübingen

Prof Dr Dirk Schadendorf
University Hospital Essen

Project “Molecular Stratification Program”

The DKTK project 'Molecular Stratification Program' at the National Center for Tumour Diseases (NCT) in Heidelberg focuses on customized therapies. The term 'stratification' refers to the initiative to assign patients with the same initial diagnosis to subgroups according to molecular results in order to be able to offer them a tailored therapy. The project promotes the development of a central database containing gene defects and changes in gene activity of tumour cells. The tumour profiles will help hospitals to tailor therapy for individual patients.


Project “Overcoming therapy resistance in pancreatic cancers”

Pancreatic cancer is one of the most aggressive cancers with a dismal prognosis and for which effective treatment options are desperately needed. In this Joint Funding Project DKTK experts in molecular oncology, animal model development, drug development and clinical oncology join forces for rationally developing effective combination therapies against pancreatic cancer. To this end, the team explores molecular mechanisms that are responsible for the resistance that pancreatic tumors possess or develop to established therapies. These mechanisms are studied in sophisticated cell culture and animal models of different molecular subtypes of pancreatic cancer that the DKTK investigators recently described. Notably, these subtypes were found to respond differently to anticancer drugs. Based on the understanding of molecular mechanisms of treatment resistance, the research team explores new drugs and develops combination therapies tailored to each pancreatic cancer subtype with the goal to effectively kill resistant cancer cells or avoid the development of secondary resistance that established monotherapies induce. The overall aim is to establish drug combinations that break tumor resistance as novel treatment options for pancreatic cancer patients.


Prof Dr Ulrich Keilholz
Charité Comprehensive Cancer Center

Prof Dr Jens Siveke
University Hospital Essen

Project “Elucidating the basis of primary resistance to first-line combined anti-EGFR /chemotherapy and establishment of a tumor repository for analysis of secondary resistance in metastatic colorectal cancer"

Antibodies are increasingly being used as targeted therapies for treating cancer patients. They can recognize specific molecules on the surface of cancer cells and block their function specifically, or activate the patient’s immune system to attack the tumor. Antibodies are also administered in combination with chemotherapy, for instance in cases of advanced colon cancer. Even with this combination treatment, however, physicians are seeing primary and secondary therapy resistance: some patients do not respond to the treatment and in some patients success is only temporary. The sequencing of tumor samples is increasingly helping scientists identify genetic modifications in cancer cells. However, it is not yet known which of these changes are responsible for therapy resistance in colon cancer patients. 

This multicenter project aims to uncover the molecular causes of primary and secondary therapy resistance in colon cancer. When planning treatment, oncologists would then be able to take into account which cancer drugs a patient is resistant to or is highly likely to develop resistance to. The scientists are pursuing two approaches: in order to understand primary tumor resistance, they are analyzing tumor samples from patients who have already been treated with a combination of antibody therapy and chemotherapy and for whom the outcome is known. They are isolating DNA from the samples and sequencing around 500 genes associated with colon cancer to identify genetic changes. At the same time, they are establishing whether cells from the immune system have migrated to the tumor, since DKTK scientists have observed indications that this kind of immune cell infiltration  correlates with a better treatment outcome. The researchers are concentrating primarily on changes that are significantly different between patients who responded particularly well or particularly poorly to treatment. In the subsequent, second approach, the scientists at the two participating sites will take tumor biopsies from 60 patients before treatment and in the event of a recurrence. These samples will be analyzed for molecular changes, as in the first approach. The results will enable the researchers to verify their conclusions from the first approach and, for the first time, to investigate the causes of secondary therapy resistance (by comparing the biopsies taken before and after treatment from patients who suffer a relapse).  In future, genetic and immune analyses will be used as a routine diagnostic method so that every colon cancer patient can be offered the best treatment option for them.


Project “Novel risk adapted prevention strategies among people with higher risk profiles for colorectal cancer (RaPS)”

People between the ages of 40 and 60 have a two to four times higher risk of developing colon cancer if they have first-degree relatives affected by the disease. Experts recommend that people in this risk group take part in early colon cancer screening programs. In Germany, however, colonoscopies for colon cancer prevention  are only offered as standard from the age of 55 onwards.

The aim of the joint project is firstly to establish how frequently people aged 40–55 who have family members with the condition present signs of colon cancer or its precursor stages that can be identified via a colonoscopy and removed. For this part of the project, the participating physicians are offering colonoscopies to 1200 test subjects between the ages of 40 and 54 who have close relatives affected by colon cancer. The data can then be used to develop improved preventative measures for this risk group. In addition, the scientists hope to establish new, less invasive detection methods for early cancer diagnosis. They are examining blood and stool samples for molecular risk factors and biomarkers that would be suitable for early cancer diagnosis.

The aim is for this study to produce new findings that can improve colon cancer prevention in the risk group of people with family members already affected by the disease. This could enable a considerable proportion of the 15,000 or so cases of colon cancer that occur each year in Germany among people below the age of 65 to be prevented or identified early and treated effectively.


Prof Dr Hermann Brenner

German Cancer Research Center (DKFZ)


The DKTK project “PARADIGM” investigates the interaction between radio- and immunotherapy in the treatment of patients with metastatic melanoma. In the multicenter clinical study “IRINA” patients with metastatic melanoma will be randomized to perceive either immunotherapy only or in combination with radiation treatment. Increasing reports of cancer patients have shown that radiotherapy can also affect tumors outside the irradiated area – the so-called abscopal effect. This effect might result from radiation-induced activation of the patients’ immune system to attack cancer cells.

The interdisciplinary DKTK team will analyze the patients’ tumors and blood in order to shed light on how radiotherapy induces anti-tumor immunity. The researchers aim to boost the anti-tumor activity in patients by combining radiotherapy with a specific immunotherapy approach - blocking the tumors’ defense mechanisms against an immune attack. Furthermore, the team searches for biomarkers, molecular profiles to identify patients that are most likely to benefit from this new combination therapy. The aim is to unravel the molecular mechanism behind the abscopal effect and exploit it for treatment of melanoma patients by combination therapy in the “IRINA” study.  The DKTK study will be performed at all eight DKTK sites bringing together experts in radiotherapy, immunotherapy and molecular diagnostics.


Dr Dr Amir Abdollahi​
German Cancer Research Center