Himisha Beltran, MD (Damon Runyon-Gordon Family Clinical Investigator ’13-’16) of Weill Cornell Medicine, New York, and colleagues, used next-generation sequencing technologies to analyze neuroendocrine prostate cancer, an aggressive resistant form of cancer which sometimes develops in certain patients. The researchers examined resistance in samples collected from 81 patients and discovered the distinctive genetic, epigenetic and molecular features that underlie neuroendocrine prostate cancer.

Madhav Dhodapkar, MD (Damon Runyon-Lilly Clinical Investigator ‘02-‘07) of Yale Cancer Center, New Haven, and colleagues have determined that chronic stimulation of the immune system by lipids made in the context of inflammation underlies the origins of at least a third of all myelomas, a type of cancer affecting plasma cells. The study suggests that newer approaches to lower the levels of these lipids in patients with precursors for myeloma.

Piero D. Dalerba, MD (Damon Runyon-Rachleff Innovator ‘16-‘17), of Columbia University Medical Center, New York, and colleagues, have identified a biomarker, the CDX2 gene, that could be used to predict which stage II colon cancer patients may benefit from chemotherapy after surgery to prevent a recurrence of their disease. They found that cancers that do not express the gene have a worse prognosis than those that do. The study was published in the online edition of the New England Journal of Medicine.

David G. Kirsch, MD, PhD (Damon Runyon-Rachleff Innovator '08-'10, Innovation Award Committee Member) at the Duke University School of Medicine, Durham, and colleagues, have tested a new injectable agent that causes cancer cells in a tumor to fluoresce, potentially increasing a surgeon's ability to locate and remove all of a cancerous tumor on the first attempt.

Mark A. Lemmon, PhD (Damon Runyon Scholar ’97-‘98, Damon Runyon Fellow ’93-’96) of Yale University, New Haven, and colleagues at The Children's Hospital of Philadelphia reported that a next-generation ALK inhibitor drug, called PF-06463922, shows promise in treating pediatric neuroblastoma. In animal models, it caused rapid and sustained tumor regression and was more effective than the FDA-approved ALK inhibitor crizotinib.