Nirogacestat Approval Offers Choice to Desmoid Tumor Population

Commentary
Video

The difference in adverse effect profiles between sorafenib and nirogacestat may make one treatment more appealing than the other for certain patients with desmoid tumors, says Brian Van Tine, MD, PhD.

In an interview with CancerNetwork®, Brain Van Tine, MD, PhD, spoke about how the FDA approval of nirogacestat (Ogsiveo) in progressing desmoid tumors may offer patients a choice when it comes to managing their disease.1

Van Tine, a professor of medicine in the Division of Oncology, Section of Medical Oncology at Washington University School of Medicine’s Siteman Cancer Center, discussed how nirogacestat may have a different adverse effect (AE) profile compared with sorafenib (Nexavar), which may produce rashes and some nausea. Although nirogacestat may cause ovarian failure in some younger female patients, he stated that this wouldn’t be a concern in male patients or those who have undergone menopause. He continued to say that nirogacestat’s approval will allow for patients to decide which agent would be more suitable for them as part of a patient-centered discussion.

Supporting data for the approval of nirogacestat came from the phase 3 DeFi trial (NCT03785964), in which the agent elicited a statistically significant progression-free survival (PFS) benefit compared with placebo in those with desmoid tumors (HR, 0.29; 95% CI, 0.15-0.55; P <.001).2

Transcript:

I think the most important thing that comes out of having a second active drug and the first FDA-approved drug for the treatment of desmoid tumors is that patients actually have choices. The [adverse] effect profile of these two drugs is different.

Sorafenib is a drug that you have to use carefully because [patients] can get rashes on [their] hands and feet; you have some tolerance for nausea and some tolerance for fatigue. Nirogacestat has a different adverse effect profile and some things you have to watch for. Overall, it is something that may be more appealing to the average patient. There is some concern that this can induce ovarian failure in younger women, but for older women and male patients, this is not a concern. There may be a selective advantage for one drug over the other depending on a patient-centered discussion of which drug they'd like to try. The biggest thing that comes out of an FDA approval here is actually choice.

References

  1. FDA approves nirogacestat for desmoid tumors. News release. FDA. November 27, 2023. Accessed November 27, 2023. https://tinyurl.com/3zezwe53
  2. Gounder M, Ratan R, Alcindor T, et al. Nirogacestat, a γ-secretase inhibitor for desmoid tumors. N Engl J Med. 2023;388:898-912. doi:10.1056/NEJMoa2210140
Recent Videos
Data from the SPOTLIGHT and GLOW trials reveal that zolbetuximab increased survival in patients with CLDN18.2-positive gastric or GEJ adenocarcinoma.
The incorporation of zolbetuximab in addition to chemotherapy has shown benefit in patients with Claudin 18.2–positive gastric cancers in clinical trials.
Michael J. Hall, MD, MS, FASCO, discusses the need to reduce barriers to care for those with Li-Fraumeni syndrome, including those who live in rural areas.
Patrick Oh, MD, highlights next steps for further research in treating patients with systemic therapy in addition to radiotherapy for early-stage NSCLC.
The ability of metformin to disrupt mitochondrial metabolism may help mitigate the risk of cancer in patients with Li-Fraumeni syndrome.
Increased use of systemic therapies, particularly among patients with high-risk node-negative NSCLC, were observed following radiotherapy.
Heather Zinkin, MD, states that reflexology improved pain from chemotherapy-induced neuropathy in patients undergoing radiotherapy for breast cancer.
A prospective trial may help affirm ctDNA as a non-invasive option of predicting responses to radiotherapy among those with gynecologic cancers.
Interest in novel therapies to improve outcomes initiated an investigation of the use of immunotherapy in early-stage non-small cell lung cancer.
ctDNA reductions or clearance also appeared to correlate with a decrease in disease burden during the pre-boost phase of radiotherapy.
Related Content