MORPHEUS: A phase Ib/II study platform evaluating the safety and clinical efficacy of cancer immunotherapy (CIT)–based combinations in gastrointestinal (GI) cancers.

Author:

Desai Jayesh1,Kortmansky Jeremy S.2,Segal Neil Howard3,Fakih Marwan4,Oh Do-Youn5,Kim Kyu-Pyo6,Rahma Osama E.7,Ko Andrew H.8,Chung Hyun Cheol9,Alsina Maria10,Yeh Kun-Huei11,Li Shi12,Al-Sakaff Nedal Jaffer Abdulla13,Patel Jilpa12,Barak Hila12,Wang Jun13,Zhang Xiaosong12,Bleul Conrad13,Cha Edward12,Lee Jeeyun14

Affiliation:

1. Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne, Australia;

2. Yale School of Medicine, New Haven, CT;

3. Memorial Sloan Kettering Cancer Center, New York, NY;

4. City of Hope, Duarte, CA;

5. Seoul National University Hospital, Seoul, Korea, Republic of (South);

6. Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea, Republic of (South);

7. Dana Farber Cancer Institute, Boston, MA;

8. UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco, CA;

9. Yonsei Cancer Center, Seoul, Korea, Republic of (South);

10. Vall d'Hebron Institute of Oncology, Barcelona, Spain;

11. National Taiwan University Hospital, Taipei, Taiwan;

12. Genentech, Inc., South San Francisco, CA;

13. F. Hoffmann-La Roche Ltd., Basel, Switzerland;

14. Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea, Republic of (South);

Abstract

TPS467 Background: CIT has significant survival benefits across multiple tumor types, but durable response is experienced by only subsets of patients (pts). To extend clinical benefit to more pts, efficacious CIT combinations (combos) targeting multiple cancer immune escape mechanisms need to be identified. The MORPHEUS platform includes multiple ph Ib/II trials designed to identify early signals of safety and efficacy of CIT combos. Using a randomized trial design, multiple treatment (tx) arms are compared with a single control arm in each pt cohort. We present three GI-specific MORPHEUS trials, each assessing CIT combos that could concurrently enhance multiple aspects of the cancer immune response. Methods: The MORPHEUS trials described here are global, open-label, randomized, Ph Ib/II trials enrolling pts with pancreatic ductal adenocarcinoma (PDAC), gastric or gastroesophageal junction cancers or colorectal cancer (CRC). New arms with novel CIT combos (table) are opened as new txs become available, and arms with minimal efficacy or unacceptable toxicity are closed. Studies include multiple cohorts for pts receiving different lines of tx (1L and 2L PDAC and gastric; 3L CRC). Pts with loss of clinical benefit or unacceptable toxicity may be eligible to enroll in a different CIT combo arm. Primary endpoints include safety and investigator-assessed ORR (RECIST v1.1); secondary endpoints: PFS, OS, DCR and DOR. Clinical trial information: NCT03193190, NCT03281369, NCT03555149. [Table: see text]

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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