Robert A. Figlin, MD, on Understanding the Cancer Journey in GU Malignancies

Video

Robert A. Figlin, MD, details how his institution, Cedars-Sinai Cancer, is aiming to fully understand the cancer journey for those with genitourinary malignancies.

At the 2021 American Society of Clinical Oncology (ASCO) Annual Meeting, CancerNetwork® sat down with Robert A. Figlin, MD, professor of Biomedical Sciences and Medicine, Steven Spielberg Family Chair in Hematology-Oncology, and deputy director of Cedars-Sinai Cancer, to discuss efforts to fully understand the cancer journey in genitourinary malignancies. This includes the process of identifying high-risk patients, as well as implementing genetic testing on a wider scale.

Transcript:

What we are spending a lot of time on at Cedars-Sinai is really [understanding] the totality of the cancer journey. What do I mean by that? I mean, that screening is still a part [of identifying] high-risk patients. The entry of genomics into the high-risk screening population with organizations like Grail—where they looked at a signature for identifying people who do not have overt cancer but may be able to pick up cancers through a blood test—[is] very important to watch. I also think it is absolutely critical that we make sure that we penetrate using next-generation sequencing [on] all of our patients where appropriate because, ultimately, matching a targeted agent with an abnormal genetic profile is always better than treating patients randomly. Whether it is BRCA...or homologous repair, integrating that into our clinical practice and understanding that is going to be critical for the next 5 years of cancer care.

Recent Videos
Brett L. Ecker, MD, focused on the use of de-escalation therapy, which is gaining momentum in neuroendocrine tumors.
Certain bridging therapies and abundant steroid use may complicate the T-cell collection process during CAR T therapy.
Educating community practices on CAR T referral and sequencing treatment strategies may help increase CAR T utilization.
Harmonizing protocols across the health care system may bolster the feasibility of giving bispecifics to those with lymphoma in a community setting.
Although accuracy remains a focus in whole-body MRI testing in patients with Li-Fraumeni syndrome, comfortable testing experiences may ease anxiety.
Subsequent testing among patients in a prospective study may affirm the ability of cfDNA sequencing to detect cancers in those with Li-Fraumeni syndrome.
cfDNA sequencing may allow for more accessible, frequent, and sensitive testing compared with standard surveillance in Li-Fraumeni syndrome.
STX-478 showed efficacy in patients with advanced solid tumors regardless of whether they had kinase domain or helical PI3K mutations.
STX-478 may avoid adverse effects associated with prior PI3K inhibitors that lack selectivity for the mutated protein vs the wild-type protein.
Related Content