Evidence map›Paper›PMID 39707623›Full record

Trial reportClinical pharmacology and therapeutics2025

Investigational Use of Real-World Data as a Hybrid Control in Pancreatic Ductal Adenocarcinoma From the Randomized Phase Ib/II MORPHEUS Trial.

Andrew H Ko, Do-Youn Oh, Janet Lau, Shivani K Mhatre, Bo Ci, Robson Machado, Shi Li, Michael T Bretscher, Irmarie Reyes-Rivera, Jiawen Zhu and 4 more

Abstract readRandomized Controlled TrialClinical Trial, Phase IClinical Trial, Phase II
In one paragraph

Trial report in Clinical pharmacology and therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

14 authors.

Andrew H KoUniversity of California San Francisco, San Francisco, California, USA.
Do-Youn OhSeoul National University Hospital, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
Janet LauGenentech, Inc., South San Francisco, California, USA.ORCID 0009-0006-9149-2320
Shivani K MhatreGenentech, Inc., South San Francisco, California, USA.
Bo CiGenentech, Inc., South San Francisco, California, USA.
Robson MachadoRoche Products Ltd, Welwyn Garden City, UK.
Shi LiGenentech, Inc., South San Francisco, California, USA.
Michael T BretscherF. Hoffmann-La Roche Ltd., Basel, Switzerland.
Irmarie Reyes-RiveraF. Hoffmann-La Roche Ltd., Basel, Switzerland.
Jiawen ZhuGenentech, Inc., South San Francisco, California, USA.
Xiaosong ZhangGenentech, Inc., South San Francisco, California, USA.
Jilpa PatelGenentech, Inc., South San Francisco, California, USA.
Matthew A PsiodaDepartment of Biostatistics, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina, USA.
Mariano Ponz-SarviseCancer Center Clinica Universidad de Navarra and Program in Solid Tumors (CIMA), Universidad de Navarra, IDISNA, Pamplona, Spain.ORCID 0000-0002-3240-729X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enrolling adequate numbers of patients into the control arm of randomized controlled trials (RCTs) often presents barriers. There is interest in leveraging real-world data (RWD) from electronic health records (EHRs) to construct external control (EC) arms to supplement RCT control arms and form hybrid control (HC) arms. This investigation showed the use of an HC arm in second-line metastatic pancreatic ductal adenocarcinoma (PDAC). The RCT experimental arm (atezolizumab + PEGylated recombinant human hyaluronidase (Atezo + PEGPH20)) was compared with an HC arm consisting of patients treated with modified FOLFOX6 or gemcitabine/nab-paclitaxel from the MORPHEUS PDAC internal control arm supplemented with data from a nationwide EHR-derived de-identified database as the EC arm. The EC arm was constructed by applying key inclusion/exclusion criteria from the MORPHEUS PDAC trial to patients from the real-world cohort. Baseline variables were balanced using propensity score matching and covariate adjustment. Three analysis approaches-Cox model with pooled-control data, Cox model with control arm-specific frailty, and Bayesian analysis using a commensurate prior-were assessed. Overall survival was similar between the treatment arms. The direction and magnitude of hazard ratios (HRs) from the multiple HC analyses (HRs ranged from 1.02 to 1.06) were comparable with the reported trial HR (HR 0.91; 95% CI: 0.56, 1.49). This analysis demonstrates the feasibility and applicability of leveraging RWD in clinical trial design to supplement clinical trial control arms.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Pancreatic DuctalPancreatic NeoplasmsAgedAlbuminsAntibodies, Monoclonal, HumanizedDeoxycytidineElectronic Health RecordsFemaleFluorouracilGemcitabineHumansHyaluronoglucosaminidaseLeucovorinMaleMiddle Aged130-nm albumin-bound paclitaxelAlbuminsAntibodies, Monoclonal, HumanizedDeoxycytidineFluorouracilGemcitabineHyaluronoglucosaminidaseLeucovorinOrganoplatinum CompoundsPaclitaxelPolyethylene Glycols

Identifiers

PMID39707623
PMCPMC11924154

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.