https://doi.org/10.55788/a4b22dd9
Dr Alison Birtle (Rosemere Cancer Centre, UK) shared results from an updated analysis of the POUT trial (NCT01993979), a randomised, multi-centre, phase 3 trial assigning 260 post-nephroureterectomy patients with advanced UTUC either to surveillance only or to four 21-day cycles of adjuvant chemotherapy. For participants in the chemotherapy arm, treatment was initiated within 90 days post-surgery and consisted of either a combination of gemcitabine-cisplatin or, in patients with impaired renal function, gemcitabine-carboplatin. Follow-up visits to monitor for signs of recurrence occurred at the same frequency in both treatment arms; namely, at 4, 7, 10, and 13 weeks corresponding to the end of each chemotherapy treatment cycle. Patients underwent imaging and cystoscopy every 6 months for 2 years and then annually up to the 5-year point.
The primary endpoint was DFS within a 3-year time frame. The occurrence of 88 deaths triggered a (pre-planned) updated analysis with data cut-off 11 January 2021; after a median follow-up period of 49.2 months, 109 (41.9%) participants had reached the primary endpoint of DFS; 64/129 (49.6%) in the surveillance group and 45/131 (34.4%) in the chemotherapy group (adjusted HR 0.54; 95% CI 0.36–0.79; P=0.002). There had also occurred 93 deaths: 52 of the 129 patients in the surveillance arm (40.3%) and 41 of the 131 patients in the chemotherapy arm (31.3%) had died.
Secondary outcome measures included overall survival, metastasis-free survival, acute and late toxicity, and quality of life. All secondary outcome measures were tracked for 5 years except quality of life, which was only monitored for up to 2 years. Updated overall survival rates are 57% (95% CI 46–66) for patients under surveillance and 65% (95% CI 71–86) for patients receiving gemcitabine-cisplatin/carboplatin (adjusted HR=0.77; 95% CI 0.50–1.17; P=0.21). Metastasis-free survival was achieved by 66 of the 129 (51.2%) participants assigned to surveillance and by 45 of the 131 (34.4%) participants assigned to chemotherapy (adjusted HR=0.55; 95% CI 0.37–0.82; P=0.003). In the chemotherapy group, 44% of participants experienced grade ≥3 treatment-emergent adverse events (AEs) compared with only 4% of participants in the surveillance group [2]. These AEs were consistent with previous AEs reported for this chemotherapy protocol. The most common AEs experienced were hypertension (25/240, 10.4%), lethargy (25/240, 10.4%), urinary tract infection (14/240, 5.8%), and hearing loss (13/240, 5.4%). Chemotherapy was not associated with any long-term toxicity. Regarding quality-of-life outcomes, no differences were seen between the groups.
Despite a non-significant improvement in overall survival, the improved DFS and metastasis-free survival outcomes achieved by patients treated with platinum-based chemotherapy within 90 days post-nephroureterectomy have prompted the researchers to recommend this protocol be considered a new standard of care for these patients.
- Birtle AJ. Updated outcomes of POUT: A phase III randomized trial of peri-operative chemotherapy versus surveillance in upper tract urothelial cancer (UTUC). Abstract 455, ASCO Genitourinary Cancers Symposium, 11–13 February 2021.
- Birtle A et al. Lancet. 2020 Apr 18;395(10232):1268–77.
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