University Hospital Zürich, Zurich, Switzerland
Reinhard Dummer , Keith Flaherty , Caroline Robert , Ana Maria Arance , Jan Willem de Groot , Claus Garbe , Helen Gogas , Ralf Gutzmer , Ivana Krajsová , Gabriella Liszkay , Carmen Loquai , Mario Mandalà , Dirk Schadendorf , Naoya Yamazaki , Michael D. Pickard , Fabian Zohren , Michelle L. Edwards , Paolo Antonio Ascierto
Background: Combined BRAF/MEK inhibitor therapy has demonstrated benefits on progression-free survival (PFS) and OS and is standard of care for the treatment of advanced BRAF V600-mutant melanoma. Here we report a 5-year update from the COLUMBUS trial. Methods: In Part 1 of COLUMBUS, 577 pts with advanced/metastatic BRAF V600-mutant melanoma, untreated or progressed after first-line immunotherapy, were randomized 1:1:1 to encorafenib 450 mg QD + binimetinib 45 mg BID (COMBO450), encorafenib 300 mg QD (ENCO300), or vemurafenib 960 mg BID (VEM). An updated analysis including PFS, OS, objective response rate (ORR; by blinded independent central review), and safety was conducted after minimum follow-up of 65.2 months (mo). Data are as is; study is ongoing. Results: At data cut-off (Sep 15, 2020), there were 131 (68%), 117 (60%), and 145 (76%) deaths in the COMBO450, ENCO300, and VEM treatment arms, respectively. The median OS (95% CI) and 5-year OS rate (95% CI) with COMBO450 were 33.6 (24.4–39.2) mo and 34.7% (28.0–41.5), respectively (median follow-up: 70.4 mo). The 5-year OS rate (95% CI) in COMBO450 pts who had normal lactate dehydrogenase (LDH) levels at baseline was 45.1% (36.5–53.2). Median OS and 5-year OS rates for ENCO300 and VEM, as well as for pts with normal and high LDH levels and > 3 organs involved at baseline, are shown in the table. For COMBO450, ENCO300, and VEM, the 5-year PFS rate was 22.9%, 19.3%, and 10.2%; ORR (95% CI) was 64.1% (56.8–70.8), 51.5% (44.3–58.8), and 40.8% (33.8–48.2); and the median duration of response (DOR) was 18.6, 15.5, and 12.3 mo, respectively. Safety results were consistent with the known tolerability profile of COMBO450. Additional efficacy and updated safety analyses will be presented. Following study drug discontinuation, the most common subsequent treatment in all arms was checkpoint inhibitors. Conclusions: Updated OS and DOR results with COMBO450 demonstrate continued long-term benefits in pts with BRAF V600-mutant melanoma. Clinical trial information: NCT01909453
COMBO450 | ENCO300 | VEM | |||||||
---|---|---|---|---|---|---|---|---|---|
Events/pts (%) | Median OS (95% CI), mo* | 5-year OS rate (95% CI) | Events/pts (%) | Median OS (95% CI), mo* | 5-year OS rate (95% CI) | Events/pts (%) | Median OS (95% CI), mo* | 5-year OS rate (95% CI) | |
All pts | 131/192 (68.2) | 33.6 (24.4–39.2) | 34.7% (28.0–41.5) | 117/194 (60.3) | 23.5 (19.6–33.6) | 34.9% (27.9–42.0) | 145/191 (75.9) | 16.9 (14.0–24.5) | 21.4% (15.7–27.8) |
LDH normal | 81/137 (59.1) | 51.7 (36.8–67.3) | 45.1% (36.5–53.2) | 79/147 (53.7) | 35.3 (23.7–60.5) | 41.8% (33.3–50.1) | 95/139 (68.3) | 24.5 (18.6–29.1) | 28.4% (20.9–36.4) |
LDH high | 50/55 (90.9) | 11.4 (9.0–17.4) | 9.1% (3.3–18.4) | 38/47 (80.9) | 9.2 (7.0–16.2) | 13.8% (5.6–25.6) | 50/52 (96.2) | 9.6 (8.5–11.5) | 4.0% (0.7–12.1) |
> 3 organs involved | 35/42 (83.3) | 11.6 (9.1–20.8) | – | 32/44 (72.7) | 15.7 (7.9–19.7) | – | 39/45 (86.7) | 10.9 (8.6–15.7) | – |
*Unstratified Cox regression model.
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Abstract Disclosures
2019 ASCO Annual Meeting
First Author: Gabriella Liszkay
2020 ASCO Virtual Scientific Program
First Author: Helen Gogas
2018 ASCO Annual Meeting
First Author: Reinhard Dummer
2022 ASCO Annual Meeting
First Author: Erika Richtig