
Lung, Kidney, and Neuroendocrine Tumor Cancer Studies Led by Dana-Farber Presented at ESMO Congress 2023
Novel treatments, combination therapies, and personalized medicine headline several studies led by Dana-Farber Cancer Institute and presented for the first time at the European Society of Medical Oncology Congress 2023 in Madrid, Spain.
MADRID – Novel treatments, combination therapies, and personalized medicine headline several studies led by
A pivotal lung cancer study (LBA65) led by
Data from the phase 3 CABINET study (LBA53) in advanced neuroendocrine tumors (NET) will be presented for the first time by
Other key research from Dana-Farber shows new treatments and advances in personalized medicine in prostate, head and neck, bladder, and many other cancer types. Select studies include:
Combination of two antibody-drug conjugates found safe in patients with advanced bladder cancer, may have implications in other cancer types
In patients with metastatic urothelial carcinoma (mUC) who progressed on prior treatments, the combination of antibody-drug conjugates (ADC) sacituzumab govitecan plus enfortumab vedotin was found safe with encouraging efficacy. Data from the phase 1 double antibody-drug conjugate trail, dubbed the DAD trial, shows the combination of these unique ADCs, which have different payloads with different targets, did not present any new toxicity signals. Furthermore, the data shows robust clinical activity in this small trial with an objective response rate of 70%. To the researchers' knowledge, this is the first study to combine 2 ADCs in any malignancy and they plan to study this combination further in a phase 2 expansion. The data presented at ESMO on double antibody-drug conjugates may have implications beyond bladder cancer in other malignancies.
Largest epigenomic cell-free DNA dataset reported to date
Cancer cells shed DNA into the bloodstream, and analyzing this DNA can help doctors diagnose or monitor cancer using a blood sample in an approach known as a ‘liquid biopsy.’ Liquid biopsy has focused mainly on detecting changes in the DNA sequence (mutations) in cancer. In this study led by Dana-Farber, scientists developed a test that can measure changes in gene regulation – signals that turn genes on and off – from blood. This is the largest epigenomic cell-free DNA dataset reported to date. This approach may allow researchers to understand how cancer becomes resistant to treatment and to do a better job choosing the right treatment for a given patient.
Prostate cancer study offers guidance on which patients most likely to benefit from treatment intensification
Radiation therapy and long-term androgen deprivation therapy (RT+ltADT) is standard of care treatment for patients with high-risk, locally advanced prostate cancer (HR/LA-PC). In this pooled analysis of more than 3,500 patients with HR/LA-PC treated on randomized trials of RT+ltADT, researchers found outcomes vary significantly depending on the number of adverse risk factors and the presence of clinically node positive disease. The risk factors looked at were Gleason Score, T stage, PSA level, or node positive disease. Researchers found these risk factors highly prognostic. Poorer outcomes in overall survival and metastasis-free survival were seen in patients with 2 or 3 risk factors. The poorest outcomes were seen in patients with node-positive disease. Researchers say these findings have implications for selecting patients for intensification of therapy beyond RT+ltADT and will guide interpretation of ongoing adjuvant trials in HR/LA-PC.
First targeted therapy found safe and shows anti-tumor activity in patients with rare head and neck cancer
HRAS mutations are seen in 4-8% of patients with recurrent and/or metastatic head and neck squamous cell carcinoma (HNSCC) and prognosis remains poor. Tipifarnib, a farnesyltransferase inhibitor that disrupts HRAS function, was found safe, tolerable and to have encouraging efficacy, according to the AIM-HN phase 2 study. This study enrolled 59 patients who were treated with oral tipifarnib. Tipifarnib has previously shown promising activity in patients with HNSCC harboring high variant allele frequency (VAF). 50 of the 59 patients in this study had high VAF of ≥ 20% (Median 34%)
The primary endpoint was objective response rate (ORR). ORR was 30% by investigator assessment and 20% by independent review. Median progression free survival was 2.6 months and median overall survival 6.9 months. 44% of patients received immunotherapy prior to enrolling on the trial. Grade 3+ treatment-related adverse events (TRAEs) were observed in 56% of patients, however, only 7% discontinued treatment due to TRAEs. Ongoing combination studies are targeting adaptive resistance pathways (PI3K/mTOR/Akt) to further improve outcomes.
Dana-Farber’s
A full list of Dana-Farber Oral Presentations at the 2023 ESMO Congress is available



































