A phase III study (APROMISS) of AL3818 (Catequentinib, Anlotinib) hydrochloride monotherapy in subjects with metastatic or advanced synovial sarcoma.

Author:

Van Tine Brian Andrew1,Chawla Sant P.2,Trent Jonathan C.3,Wilky Breelyn A.4,Chugh Rashmi5,Chmielowski Bartosz6,Kummar Shivaani7,Basu Mallick Atrayee8,Somaiah Neeta9,Cranmer Lee D.10,Agulnik Mark11,Keedy Vicki Leigh12,Stacchiotti Silvia13,Vincenzi Bruno14,Badalamenti Giuseppe15,Siontis Brittany L16,Attia Steven17

Affiliation:

1. Siteman Cancer Center, Washington University in St. Louis, St. Louis, MO;

2. Sarcoma Oncology Research Center, Santa Monica, CA;

3. University of Miami-Sylvester Comprehensive Cancer Center, Jackson Memorial Hospital, Miami, FL;

4. University of Colorado, Aurora, CO;

5. University of Michigan, Ann Arbor, MI;

6. Division of Hematology-Oncology, David Geffen School of Medicine at UCLA, Los Angeles, CA;

7. Phase I Clinical Research Program Stanford University School of Medicine, Stanford, CA;

8. NSABP Foundation and Thomas Jefferson University Hospital, Philadelphia, PA;

9. Department of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX;

10. University of Washington/Fred Hutchinson Cancer Research Center, Seattle, WA;

11. Northwestern University, Chicago, IL;

12. Vanderbilt University Medical Center, Nashville, TN;

13. Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy;

14. Policlinico Universitario Campus, Bio-Medico, Rome, Italy;

15. Department of Surgical, Oncological, and Oral Sciences, Section of Medical Oncology, University of Palermo, Palermo, Italy;

16. Mayo Clinic, Rochester, MN;

17. Mayo Clinic, Jacksonville, FL;

Abstract

11505 Background: AL3818 (Catequentinib, Anlotinib) is a novel, orally administered, small molecule tyrosine kinase inhibitor. The primary objective of this Phase 3 study is to evaluate the efficacy of AL3818 monotherapy in patients (pts) with synovial sarcoma (SS) comparing with dacarbazine in randomization setting. Methods: Patients with a diagnosis of synovial sarcoma requiring second line or further line treatment were eligible for enrollment. The regimen was a 21-day cycle with oral AL3818 administered on 14 days on and 7 days off. This phase 3 trial is randomized in 2:1 ratio of AL3818 comparing to dacarbazine with option of crossover after PD of dacarbazine treatment. Progression free survival (PFS) with Log Rank test is the primary endpoint and this trial for SS is currently completed enrolled in US and Italy. Results: Total 79 pts initiated treatment and are evaluable, 52 received AL3818 as treatment arm (T), and 27 received dacarbazine (D) as control arm (C). Arms T/C median ages were 40.5/42.0 years (range: 18-70+) and 20/16 (38.5%/59.3%) were male. Overall, PFS was 2.89 months (95% CI: 2.73 – 6.87) for AL3818 and 1.64 (95% CI: 1.45 – 2.70) for D. The PFS of study met the primary endpoint with a p-value of 0.0015 and a HR of 0.449 (95% CI: 0.270– 0.744). At the month 4, 6, and 12, the percentages of progression free patients for AL3818 were 48.1%, 42.3% and 26.9%; and for D were 14.85%, 11.1% and 3.7%. For grade 3 treatment-related adverse events, 12(23.1%) of pts experienced for AL3818 and 7(25.9%) of pts experienced for D. The most common AL3818 related grade 3 AEs were diarrhea (5.8%) and hypertension (3.8%). Conclusions: This phase III trial demonstrates improved disease control and superior progression free survival for AL3818 vs dacarbazine in advanced SS. In addition, the study further confirms the acceptable benefit-risk profile of AL3818 from the prior randomized Phase 2b soft tissue sarcoma study (NCT02449343). AL3818 is a meaningful treatment option for pts with advanced SS. Clinical trial information: NCT 03016819 Clinical trial information: NCT03016819.

Funder

Advenchen Laboratories

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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