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 225Ac-ABD147 to treat advanced lung cancer. The people in this study have small cell lung cancer (SCLC) or large cell neuroendocrine carcinoma of the lung (LCNEC). Their cancer keeps growing even after treatment that included platinum-based chemotherapy.
Researchers want to find the best dose of AZD9592 to use in people with lung and head and neck cancers. They will assess AZD9592 when it is given alone and with the anti-cancer drug osimertinib. The people in this study have advanced non-small cell lung cancer (NSCLC) or head and neck cancer with mutations (changes or variants) in the EGFR gene.
Researchers want to find the best dose of BBO-10203 to use in people with advanced solid tumors. The people in this study have one of these types of cancer that has spread (metastasized):
Researchers want to find the best dose of BDTX-4933 to use in people with advanced lung cancer. The people in this study have non-small cell lung cancer that has a mutation (change or variant) in the BRAF or KRAS genes (KRAS non-G12C mutation). This mutation can cause cancer cells to grow.
BG-60366 is designed to break down the mutated EGFR protein, which promotes the growth of NSCLC. BG-60366 is taken orally (by mouth).
DAY301 is a type of drug called an antibody-drug conjugate (ADC). ADCs are substances made up of a monoclonal antibody (special protein) linked to a drug. The antibody binds to specific proteins on certain types of cells, including cancer cells. The linked drug enters these cells and kills them. With ADCs, there is a lower risk of harming normal cells, since they usually do not have the target protein.
Researchers want to find the highest dose of ERAS-0015 that can be given safely in people with advanced solid tumors. The people in this study have cancer that has metastasized (spread) and has a mutation in the RAS gene.
Researchers are assessing different doses of FT825 alone or with cetuximab to treat people with advanced solid tumors. Their tumors have high levels of the HER2 protein. Altered HER2 proteins can fuel cancer growth. 
Researchers want to find the best dose of INCB161734 to use in people with advanced cancer. The people in this study have solid tumors that have spread. In addition, their cancers have a genetic mutation (change) called KRAS G12D.