Evidence map›Paper›PMID 41741368›Full record

Trial reportThe oncologist2026

Atezolizumab and motixafortide, cobimetinib or simlukafusp alfa in pretreated advanced pancreatic cancer: phase I/IIb MORPHEUS-PDAC umbrella study.

Gulam A Manji, Vincent Chung, Do-Youn Oh, Jill Lacy, Charles D Lopez, Mariano Ponz-Sarvisé, Teresa Macarulla, Roby Thomas, Ben George, Angela Alistar and 6 more

Registry-linked trialAbstract readClinical Trial, Phase IRandomized Controlled TrialClinical Trial, Phase II
In one paragraph

Trial report in The oncologist, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03193190 (A Phase Ib/II, Open-Label, Multicenter, Randomized Umbrella Study Evaluating the Efficacy and Safety of Multiple Immunotherapy-Based Treatment Combinations in Patients With Metastatic Pancreatic Ductal Adenocarcinoma), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03193190 phase1 / phase2completednot on this map

A Phase Ib/II, Open-Label, Multicenter, Randomized Umbrella Study Evaluating the Efficacy and Safety of Multiple Immunotherapy-Based Treatment Combinations in Patients With Metastatic Pancreatic Ductal Adenocarcinoma (Morpheus-Pancreatic Cancer)

TypeinterventionalSponsorHoffmann-La RocheRan2017 to 2025Enrolled341ConditionsPancreatic AdenocarcinomaArmsNab-Paclitaxel, Gemcitabine, Oxaliplatin, Leucovorin, Fluorouracil
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Gulam A ManjiDivision of Hematology and Oncology, Columbia University Irving Medical Center, New York, NY, 10032, United States.ORCID 0009-0000-7459-6036
Vincent ChungCity of Hope National Medical Center, Duarte, CA, 91010, United States.ORCID 0000-0001-9475-808X
Do-Youn OhCancer Research Institute, Seoul National University College of Medicine; Department of Internal Medicine, Seoul National University Hospital; Integrated Major in Innovative Medical Science, Seoul National University Graduate School, Seoul, 03080, Republic of Korea.
Jill LacyDepartment of Medicine, Section of Medical Oncology, Yale School of Medicine, Yale University, New Haven, CT, 06510, United States.
Charles D LopezDivision of Hematology Oncology, Oregon Health & Science University, Knight Cancer Institute, Portland, OR, 97239, United States.
Mariano Ponz-SarviséCancer Center Clinica Universidad de Navarra and Program in Solid Tumors (CIMA), Universidad de Navarra, Pamplona, 31008, Spain.
Teresa MacarullaGastrointestinal Cancer Unit, Vall d'Hebron University Hospital and Vall d'Hebron Institute of Oncology (VHIO), Barcelona, 08035, Spain.
Roby ThomasDepartment of Medical Oncology, University of Pittsburgh Medical Center, Pittsburgh, PA, 15219, United States.
Ben GeorgeGastrointestinal Oncology, Medical College of Wisconsin, Milwaukee, WI, 53226, United States.
Angela AlistarAtlantic Hematology Oncology, Morristown, NJ, 07960, United States.
Jens T SivekeDepartment of Medical Oncology and Division of Solid Tumor Translational Oncology, German Cancer Consortium, West German Cancer Center, University Hospital Essen, Essen, 45147, Germany.
Yun XuRoche (China) Holding Ltd., Shanghai, 201203, China.
Janet LauGenentech, Inc.  South San Francisco 94080, United States.
Edward ChaGenentech, Inc.  South San Francisco 94080, United States.
Kyu-Pyo KimDepartment of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, 05505, Republic of Korea.
Eileen M O'ReillyDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, United States.ORCID 0000-0002-8076-9199

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI FRANCESCA M GANY · 1985 to 2026
$347.4M
F. Hoffmann-La Roche LtdNCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundThe MORPHEUS platform comprised multiple open-label, randomized, phase Ib/II trials to identify early signals with different treatment combinations across multiple cancers. MORPHEUS-PDAC (NCT03193190) evaluated atezolizumab combinations in pancreatic ductal adenocarcinoma (PDAC). We describe outcomes with atezolizumab plus either motixafortide, cobimetinib, or two simlukafusp alfa regimens.

methodsEligible patients with advanced, pretreated PDAC were randomized to receive second-line (2 L) atezolizumab plus either motixafortide (BL8040; n = 15), cobimetinib (n = 14), simlukafusp alfa every 2 weeks (q2w; n = 15), or simlukafusp alfa every 3 weeks (q3w; n = 16); or control (mFOLFOX6 [n = 25] or gemcitabine plus nab-paclitaxel [n = 25]). Patients experiencing disease progression or toxicity who met eligibility criteria were enrolled to receive third-line (3 L) atezolizumab plus cobimetinib (n = 14), or atezolizumab plus simlukafusp alfa q2w (n = 1) or q3w (n = 6). Primary endpoints were objective response rates (ORRs) per RECIST 1.1 and safety.

resultsORRs were 7.1% with atezolizumab-simlukafusp alfa q2w, 8.7% with mFOLFOX6 (both 2 L; 0% in other arms), 14.3% with atezolizumab-cobimetinib, and 16.7% with atezolizumab-simlukafusp alfa q3w (both 3 L). Grade 3-5 adverse event rates were 53.3% (2 L atezolizumab-motixafortide), 64.3% (2 L atezolizumab-cobimetinib), 57.1% (2 L atezolizumab-simlukafusp alfa q2w), 53.3% (2 L atezolizumab-simlukafusp alfa q3w), 63.0% (2 L mFOLFOX6 or gemcitabine-nab-paclitaxel), 50.0% (3 L atezolizumab-cobimetinib), and 100% (3 L atezolizumab-simlukafusp alfa q3w).

conclusionsThe overall safety of atezolizumab combinations was manageable and consistent with each agent's known safety profile. This novel trial design enabled rapid evaluations of 3 atezolizumab combinations; all had limited efficacy as 2 L or 3 L treatment for metastatic PDAC. New treatments are needed to improve outcomes in previously treated PDAC.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsAzetidinesCarcinoma, Pancreatic DuctalPancreatic NeoplasmsPiperidinesAgedFemaleFluorouracilHumansLeucovorinMaleMiddle AgedAntibodies, Monoclonal, HumanizedatezolizumabAzetidinescobimetinibFluorouracilLeucovorinPiperidinesatezolizumab combinationCXCR4 inhibitorFAP-IL2vimmunotherapyMAP/ERK kinase inhibitorpancreatic ductal adenocarcinoma

Identifiers

PMID41741368
PMCPMC12971112

What Socratic holds

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LicenceCC BY
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.