Phase 3 Study of Rucaparib as Switch Maintenance After Platinum in Relapsed High Grade Serous and Endometrioid Ovarian Cancer (ARIEL3)

Trial ID # NCT01968213; ARIEL3
Phase III
Drug Class DNA Damage Repair Pathway Inhibitors: PARP
Drug Name Rucaparib
Alternate Drug Names AG-014699, PF 01367338, CO-338, Rubraca
Drugs in Trial Rucaparib
Eligible Participant

Platinum sensitive recurrence and CR or PR in most recent platinum-based therapy, ≥ 2 platinum-based regimens

Patients Enrolled

564

Therapy Setting

Maintenance

Study Design

Double Blind, Randomized

Endpoints

PFS, OS, PFS2, TFST, evaluated per RECIST

Biomarkers

Exploratory: BRCA1/2; LOH (by FoundationFocus CDx BRCA LOH), HRR gene alterations

Efficacy

Ruc maint vs Placebo (investigator review):

All (n=564):
PFS: 10.8 vs 5.4 months, HR: 0.36 (0.30-0.45, p<0.0001)
PFS2: 20.6 vs 16.3 months, HR: 0.703 (0.579-0.854, p<0.01)
OS: 36.0 vs 43.2 months, HR: 0.995 (0.809-1.223, p=0.96)
BRCA MUT (n=196):
PFS: 16.6 vs 5.4 months, HR: 0.23 (0.16-0.34, p<0.0001)
PFS2: 26.1 vs 18.4 months, HR: 0.672 (0.480-0.941, p=0.02)
OS: 45.9 vs 47.8 months, HR: 0.832 (0.581-1.192, p=0.32)
BRCA MUT/BRCA WT LOH High (n=354):
PFS: 13.6 vs 5.4 months, HR: 0.32 (0.24-0.42, p<0.0001)
PFS2: 24.7 vs 18.4 months, HR: 0.718 (0.558-0.923, p=0.01)
OS: 40.5 vs 47.8 months, HR: 1.005 (0.766-1.320, p=0.97)

Ruc maint vs Placebo (BICR):

All (n=564):
PFS: 13.7 vs 5.4 months, HR: 0.35 (0.28-0.45, p<0.0001)
BRCA MUT (n=196):
PFS: 26.8 vs 5.4 months, HR: 0.20 (0.13-0.32, p<0.0001)
BRCA MUT/BRCA WT LOH High (n=354):
PFS: 22.9 vs 5.5 months, HR: 0.34 (0.24-0.47, p<0.0001)

Exploratory analysis BRCA WT patients:
BRCA WT/LOH Low (n=161): PFS: 8.2 vs 5.3 months, HR: 0.47 (0.31-0.71, p=0.0002)
BRCA WT/LOH High (n=158): PFS: 11.1 vs 5.6 months, HR: 0.55 (0.35-0.89, p=0.0135)

Ruc maint vs Placebo (investigator review):

All (n=564):
PFS: 10.8 vs 5.4 months, HR: 0.36 (0.30-0.45, p<0.0001)
BRCA MUT (n=196):
PFS: 16.6 vs 5.4 months, HR: 0.23 (0.16-0.34, p<0.0001)
BRCA MUT/BRCA WT LOH High (n=354):
PFS: 13.6 vs 5.4 months, HR: 0.32 (0.24-0.42, p<0.0001)

Exploratory analysis BRCA status, patients w/ HRR alterations:
BRCA WT/LOH Low (n=161): PFS: 6.7 vs 5.4 months, HR: 0.58 (0.40-0.85, p=0.0049)
BRCA WT/LOH High (n=158): PFS: 9.7 vs 5.4 months, HR: 0.44 (0.29-0.66, p<0.001)
w/ HRR gene alterations (n=43):
PFS: 11.1 vs 5.5 months, HR: 0.21 (0.09-0.50); TFST: 16.9 vs 6.3 months, HR: 0.16 (0.06-0.40)
PFS2: 21.1 vs 17.3 months, HR: 0.30 (0.12-0.72); TSST: 24.4 vs 17.9 months, HR: 0.43 (0.18-1.04)
BRCA1 MUT (n=117):
TFST: 16.8 vs 8.1 months, HR: 0.41 (0.27-0.64); PFS2: 25.1 vs 21.8 month, HR: 0.84 (0.53-1.32); TSST: 25.9 vs 18.5 months, HR: 0.65 (0.41-1.04)
BRCA2 MUT (n=79):
TFST: 30.4 vs 7.1 months, HR: 0.17 (0.09-0.33); PFS2: 34.1 vs 18.4 month, HR: 0.51 (0.29-0.91); TSST: 34.2 vs 19.4 months, HR: 0.55 (0.31-0.96)

Exploratory analysis prior PFS interval, w/ or w/o prior Bev:
PFS interval >6 to ≤12 months:
8.2 vs 4.1 months, HR 0.33 (0.24-0.46, p<0.0001)
PFS interval >12 months: 
13.6 vs 5.6 months, HR 0.39 (0.30 to 0.52, p<0.0001)
w/ prior Bev:
10.3 vs 5.4 months, HR 0.42 (0.26 to 0.68, p=0.0004)
w/o prior Bev:
10.9 vs 5.4 months, HR 0.35 (0.28 to 0.45, p<0.0001)

Clinically Significant Adverse Events

Ruc vs Placebo:
Serious AE: any (21 vs 11%), AML/MDS (3.8 vs 3.2%) - two treatment related deaths in Ruc arm
Grade 3-4 AE: any (54 vs 14%), anemia (19 vs 1% ), elevated liver enzymes (11 vs 0%)

Conclusion

Improved PFS but no benefit for all patients with rucaparib maintenance treatment

Reference

Coleman RL et al. Rucaparib maintenance treatment for recurrent ovarian carcinoma after response to platinum therapy (ARIEL3): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet (2017) 390(10106): 1949-1961)
https://www.ncbi.nlm.nih.gov/pubmed/28916367

Ledermann JA et al. Rucaparib for patients with platinum-sensitive, recurrent ovarian carcinoma (ARIEL3): post-progression outcomes and updated safety results from a randomised, placebo-controlled, phase 3 trial. Lancet Oncol (2020) 21(5):710-722
https://pubmed.ncbi.nlm.nih.gov/32359490/

Kwan T et al. Clinical and molecular characteristics of ARIEL3 patients who derived exceptional benefit from rucaparib maintenance treatment for high-grade ovarian cancer (HGOC). J Clin Oncol (2021) 39 (suppl 15; abstr 5537)
https://meetinglibrary.asco.org/record/197247/abstract

Kwan T et al. Poster
https://www.clearityfoundation.org/wp-content/uploads/2021/06/ARIEL-3-Exceptional-benefit-poster-ASCO-2021-scaled.jpeg

Clamp A et al. Rucaparib maintenance treatment for recurrent ovarian carcinoma: the effects of progression-free interval and prior therapies on efficacy and safety in the randomized phase III trial ARIEL3. Int J Gynecol Cancer (2021) 31(7):949-958
https://pubmed.ncbi.nlm.nih.gov/34103386/

Oaknin A et al. Maintenance treatment with rucaparib for recurrent ovarian carcinoma in ARIEL3, a randomized phase 3 trial: The effects of best response to last platinum-based regimen and disease at baseline on efficacy and safety. Cancer Med (2021) 10(20):7162-7173
https://pubmed.ncbi.nlm.nih.gov/34549539/

Coleman RM et al. OVERALL SURVIVAL RESULTS FROM ARIEL3: A PHASE 3 RANDOMIZED, DOUBLE-BLIND STUDY OF RUCAPARIB VS PLACEBO FOLLOWING RESPONSE TO PLATINUM-BASED CHEMOTHERAPY FOR RECURRENT OVARIAN CARCINOMA. IGCS 2022, O003/#557
https://www.clearityfoundation.org/wp-content/uploads/2022/11/ARIEL3-IGCS-2022-abstract.pdf

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