Jelmyto Induces Durable Responses in Low-Grade UTUC

Article

Data for a key study secondary outcome measure showed that 56.1% of patients who achieved a complete response to Jelmyto maintained that response at 12 months.

More than half of patients with low-grade upper tract urothelial carcinoma (UTUC) receiving treatment with mitomycin-containing reverse thermal gel (Jelmyto) achieved a complete response (CR) maintained that response at 1 year, according to the final results of the pivotal phase 3 OLYMPUS trial presented during the 21st Annual Meeting of the Society of Urologic Oncology (SUO).1

Data for a key study secondary outcome measure reported at SUO showed that 56.1% of patients who achieved a CR to Jelmyto maintained that response at 12 months. This translated to an 81.8% probability of maintaining a CR at the 12-month visit.

Of note, maintenance therapy was allowed by the study protocol; however, it was modified by study investigators and there was no evidence that maintenance treatment enhanced the durability of patient responses.

The durability data from the final analysis sustained the positive primary efficacy results from OLYMPUS.2 The primary data showed that 59.2% (n = 42) of the 71-patient intent-to-treat (ITT) population achieved a CR. Eight patients had a partial response. Additionally, 20 (58.8%) of 34 patients considered unresectable at baseline by the treating urologist achieved a CR.

These primary data supported the April 2020 FDA approval of Jelmyto as the first therapy to treat patients with low-grade UTUC.

“[Jelmyto] is an innovative [treatment] and the first approved kidney-sparing approach for patients with low-grade UTUC, including for those whose tumors are difficult to treat endoscopically,” said presenting author Surena F. Matin, MD, The University of Texas MD Anderson Cancer Center in Houston.

The open-label, single-arm, phase 3 OLYMPUS trial included patients from 24 academic centers in the United States and Israel. To be eligible for enrollment, adult patients had to have treatment-naïve or recurrent disease, 1 or more measurable papillary low-grade tumors 15 mm or smaller, and a wash urine cytology sampled from the pyelocaliceal system showing the absence of high-grade disease.

Patients received 6 once-weekly intravesical instillations with a retrograde catheter to the renal pelvis and calyces. Primary disease evaluation occurred 4 to 6 weeks following the completion of treatment. The study defined CR using 3 components: negative 3-month ureteroscopic evaluation, negative cytology, and negative for-cause biopsy.

Seventy-one patients received at least 1 dose of treatment. The most commonly occurring adverse events (AEs) were ureteric stenosis (44%), urinary tract infection (32%), hematuria (32%), flank pain (31%), and nausea (25%).

“Ureteric obstruction may be associated with an increasing number of doses/procedures,” said Matin. Ureteric stenosis was the most common obstruction event and was reported after a median of 6 instillations.

Matin said anecdotal reports from study investigators suggested that, “At initial development of ureteral narrowing, stricture formation might be mitigated by treatment holiday and steroid therapy.”

There were 5 patient deaths; however, none were determined by investigators to be related to the study treatment or study procedure. All deaths occurred at least 30 days following the final dose of study treatment.

References

1. Lerner S, Matin S, Kleinmann N, et al. Durability of response to chemoablative treatment of low-grade upper tract urothelial carcinoma with a mitomycin-containing reverse thermal hydrogel: Final results of the OLYMPUS trial. Presented at: 21st Annual Meeting of the Society of Urologic Oncology; December 2-5, 2020; Virtual. Abstract 16

2. Kleinmann N, Matin SF, Pierorazio PM, et al. Primary chemoablation of low-grade upper tract urothelial carcinoma using UGN-101, a mitomycin-containing reverse thermal gel (OLYMPUS): an open-label, single-arm, phase 3 trial.Lancet Oncol. 2020;21(6):776-785.doi:10.1016/S1470-2045(20)30147-9

Recent Videos
Preliminary phase 2 trial data show durvalumab plus lenalidomide was superior to durvalumab alone in refractory/advanced cutaneous T-cell lymphoma.
Performance status, age, and comorbidities may impact benefit seen with immunotherapy vs chemotherapy in patients with breast cancer.
Developing odronextamab combinations following CAR T-cell therapy failure may help elicit responses in patients with diffuse large B-cell lymphoma.
Cytokine release syndrome was primarily low or intermediate in severity, with no grade 5 instances reported among those with diffuse large B-cell lymphoma.
Safety results from a phase 2 trial show that most toxicities with durvalumab treatment were manageable and low or intermediate in severity.
Updated results from the 1b/2 ELEVATE study elucidate synergizing effects observed with elacestrant plus targeted therapies in ER+/HER2– breast cancer.
Patients with ESR1+, ER+/HER2– breast cancer resistant to chemotherapy may benefit from combination therapy with elacestrant.
Related Content