An enormous strength of the Fiona and Stanley Druckenmiller Center for Lung Cancer Research (DCLCR) is the breadth of world-class expertise of its members.

Our leadership alone represents tremendous translational research talent in lung cancer, collaborating on multidisciplinary research in such areas as:

  • genomic characterization of thoracic cancers
  • innovations in minimally invasive surgery
  • advances in medical therapies

Thoracic Surgery

Thoracic surgeon and scientist David Jones is Co-Director of the Fiona and Stanley Druckenmiller Center for Lung Cancer Research. He is Chief of MSK’s Thoracic Service in the Department of Surgery and is the Fiona and Stanley Druckenmiller Chair in Lung Cancer. He is a pioneer in lung cancer metastasis biology and biomarker development. His research focuses on understanding how lung cancer spreads and the biology and regulation of lung cancer metastasis. The Jones laboratory was the first to identify the importance of the metastasis suppressor gene BRMS1 in lung cancer. Dr. Jones is also interested in ADAR-mediated RNA editing and metastases in lung adenocarcinoma, as well as genomic and pathologic biomarkers that may predict recurrence following surgery to remove early-stage lung cancer. The Jones lab uses patient-derived organoids to study the biology of lung cancer metastases and speed new drug development.

Medical Oncology

Medical oncologist Charles Rudin, Chief of MSK’s Thoracic Oncology Service and co-director of the DCLCR, is a translational researcher and leader in the study of lung cancer and other thoracic malignancies as well as developmental therapy for advanced solid tumors. He has conducted novel studies using patient-derived tumor tissue for preclinical drug testing and has led comprehensive analyses of genomic alterations in small cell lung cancer. Dr. Rudin directs a broad research program of therapeutic study including laboratory-based treatment discovery and innovative early- and late-phase clinical trials.

Immunotherapy

Immunotherapy is a new type of cancer treatment. It works by harnessing a patient’s own immune system to fight cancer. This approach has dramatically changed the care of people with lung cancer. Immunotherapies are now a routine part of treatment for nearly all people with lung cancer. Yet there remains a critical need for more progress. In particular, it is important to identify the predictors of response to immunotherapy so these treatments can be given more precisely. Combination therapies that broaden the range of people who can benefit from immunotherapy need to be developed. Within the DCLCR, a multidisciplinary team of scientists and doctors tackle these challenges together, to ultimately improve outcomes for people with lung cancer.

Patient-Derived Xenografts

The DCLCR supports the creation, characterization, and distribution of primary patient-derived xenografts (PDXs). PDXs are created by implanting lung cancer tissue obtained from surgery directly into laboratory models, where they can be grown indefinitely. With a broad cross-section of different types of lung cancer PDXs, scientists can test therapies in the earliest stages of development. MSK’s PDX collection is one of the largest and most deeply annotated in the world containing over 300 lung models. These models have been shared with more than a 100 laboratories at MSK and at collaborating institutions. Studies published in several high-impact publications have used these models, which have also been a part of multiple clinical trials in the Thoracic Service at MSK. For more information about the PDX Program, please contact Kelly Clarke at [email protected].

Patient-Derived Organoids (PDO)

An important part of MSK’s translational lung cancer research program is developing model systems that closely mimic lung cancer in humans. Dr. Jones’s laboratory has established an Institutional Review Board–approved patient-derived organoid (PDO) program for primary lung adenocarcinoma and selected metastatic sites. Using cells from lung adenocarcinoma samples, small tumors are grown in the laboratory. They can then be genetically modified with CRISPR technology and used for in vitro and in vivo experiments. All PDOs are clinically annotated, pathologically confirmed, and genomically profiled using MSK-IMPACT™. Comprehensive PDO models represent a significant advance in scientists’ ability to understand the biologic processes of oncogenesis and metastases. They provide a platform to assess treatment strategies for genomically distinct lung adenocarcinomas. These models have been shared with numerous laboratories at MSK and collaborating institutions. The Jones lab is currently investigating more than 91 lung adenocarcinoma PDOs. For more information about the PDO Program, please contact Yuan Liu, MD, PhD at [email protected]

Thoracic Surgery Oncology Group (TSOG)

In collaboration with the American Association for Thoracic Surgery (AATS), the DCLCR supports the Thoracic Surgery Oncology Group (TSOG), which is led by Dr. Jones. Formed in 2017, the group aims to initiate, rapidly accrue patients for, and complete thoracic surgical oncology clinical trials in North America. Such trials can more rapidly advance the care of people with thoracic cancer. TSOG’s mission encompasses lung, esophageal, thymic, and pleural lining cancers, and tumors that have spread to the lungs. The group focuses on phase I/II studies, window of opportunity trials with correlative analyses, intraoperative imaging studies, relevant registry studies, and multidisciplinary study designs. MSK is the coordinating center for the 37 TSOG institutions. For more information on TSOG, please contact the Project Manager Maria Singh, at [email protected] or Project Coordinator Erin Carrol, at [email protected].

Clinical Trials Currently Open for Enrollment

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73 Clinical Trials found
Researchers want to find the best dose of LY3962673 that can be used safely in people with advanced solid tumors. The people in this study have tumors that have metastasized (spread) or are inoperable (cannot be taken out with surgery). They include people with colorectal cancer, non-small cell lung cancer, and pancreatic cancer.
Researchers want to find the best dose of LY4066434 when given alone and with other drugs to treat solid tumors. The people in this study have cancer that has spread (advanced) or cannot be removed with surgery (inoperable). These include colorectal cancer, non-small cell lung cancer (NSCLC), pancreatic cancer, and other solid tumors.
Researchers want to find the best dose of LY4170156 to treat people with solid tumors. The people in this study have solid tumors that keep growing even after treatment. Their tumors also make a protein called FRA, which plays a role in cancer growth. The tumors treated in this study include:
Researchers want to find the best dose of NT-175 in people with advanced solid tumors. The people in this study have cancers that are inoperable (cannot be surgically removed) or metastatic (have spread). The types of tumors include:
Atezolizumab is a standard treatment for extensive-stage small cell lung cancer (SCLC, cancer which has spread). Researchers want to see if adding valemetostat to atezolizumab therapy is safe for people with SCLC. The people in this study have extensive-stage SCLC and have completed 4 treatment cycles of atezolizumab with chemotherapy.
Researchers are finding the best doses of valemetostat tosylate and datopotamab deruxtecan (Dato-DXd) to use in people with lung cancer. In a second part of the study, researchers are finding the best doses of valemetostat tosylate and trastuzumab deruxtecan (T-DXd) to use in people with digestive cancers.
BNT326 is a type of drug called an antibody-drug conjugate (ADC). ADCs are made of a monoclonal antibody linked to a drug. The antibody binds to a protein on cancer cells called HER3, which plays a role in cancer cell growth. It then releases the anti-cancer drug to kill the cancer cell. By destroying these cells, BNT326 may help slow or stop the growth of your cancer. It is given intravenously (by vein).
Researchers want to find the best dose of ODM-212 to treat advanced solid tumors. The people in this study have solid tumors that have spread and cannot be cured with standard therapies. Examples include:
Researchers are assessing different doses of TNG462 to give with daraxonrasib or zoldonrasib in people with advanced cancer. The people in this study have pancreatic cancer or non-small cell lung cancer (NSCLC) that spread beyond its original location. In addition, their cancers have a mutation (change) in the RAS gene and are missing a protein called MTAP.
Researchers want to find the best dose of EVM14 when used alone or with pembrolizumab in people with solid tumors. The people in this study have a solid tumor that keeps growing after treatment and has spread. This study includes people with: