Evidence map›Paper›PMID 32451495›Full record

Trial reportNature medicine2020

BL-8040, a CXCR4 antagonist, in combination with pembrolizumab and chemotherapy for pancreatic cancer: the COMBAT trial.

Bruno Bockorny, Valerya Semenisty, Teresa Macarulla, Erkut Borazanci, Brian M Wolpin, Salomon M Stemmer, Talia Golan, Ravit Geva, Mitesh J Borad, Katrina S Pedersen and 16 more

Registry-linked trialAbstract readClinical Trial, Phase IIMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Nature medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02826486 (A Phase IIa, Multicenter, Open-label Study to Assess the Safety and Efficacy of the Combination of BL-8040 and Pembrolizumab in Patients With Metastatic Pancreatic Cancer, the COMBAT Study), which is not on this map. Cited by 376 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
376citing papers in PubMed, 8 pooled it
24.5field-weighted citation impact, top 1% of its field
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.

NCT02826486 phase2completednot on this map

A Phase IIa, Multicenter, Open-label Study to Assess the Safety and Efficacy of the Combination of BL-8040 and Pembrolizumab in Patients With Metastatic Pancreatic Cancer, the COMBAT Study (KEYNOTE-202)

TypeinterventionalSponsorBioLineRx, Ltd.Ran2016 to 2022Enrolled80ConditionsMetastatic Pancreatic AdenocarcinomaArmsBL-8040, Pembrolizumab, Chemotherapy
3 · Its place in the literature

Who cites it

376 citing papers in PubMed, 8 syntheses or guidelines pooled it, 514 citations in OpenAlex.

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  15. Interleukin-1α (IL-1α) in pancreatic ductal adenocarcinoma: implications for immunotherapy and molecular biomarkers.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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316 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 17 institutions in 5 countries.

Bruno BockornyDivision of Medical Oncology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Valerya SemenistyOncology, Rambam Health Care Campus, Haifa, Israel.
Teresa MacarullaVall d'Hebron University Hospital, Vall d'Hebron Institute of Oncology, IOB Quirón, Barcelona, Spain.
Erkut BorazanciHonorHealth Research Institute, Scottsdale, AZ, USA.
Brian M WolpinHarvard Medical School, Boston, MA, USA.
Salomon M StemmerInstitute of Oncology, Davidoff Center, Rabin Medical Center, Petah Tikva, Israel.
Talia GolanSackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Ravit GevaOncology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Mitesh J BoradOncology, Mayo Clinic Cancer Center, Scottsdale, AZ, USA.
Katrina S PedersenOncology, Washington University School of Medicine, St. Louis, MO, USA.ORCID http://orcid.org/0000-0003-2793-6901
Joon Oh ParkHematology-Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.ORCID http://orcid.org/0000-0001-6502-2612
Robert A RamirezOncology, Ochsner Medical Center, New Orleans, LA, USA.
David G AbadGrupo Oncologia Fuenlabrada, Madrid, Spain.
Jaime FeliuInstituto de Investigación Hospital Universitario La Paz (IdIPAZ), Cátedra UAM-AMGEN, CIBERONC, Madrid, Spain.
Andres MuñozMedical Oncology Service, Instituto de Investigación Sanitaria Hospital Gregorio Marañón, Universidad Complutense, Madrid, Spain.
Mariano Ponz-SarviseClinica Universidad de Navarra and Program in Solid Tumors (CIMA), Universidad de Navarra, IDISNA, Pamplona, Spain.ORCID http://orcid.org/0000-0002-3240-729X
Amnon PeledGoldyne Savad Institute of Gene Therapy, Hebrew University of Jerusalem, Jerusalem, Israel.
Tzipora M LustigBioLineRx Ltd, Modi'in, Israel.
Osnat Bohana-KashtanBioLineRx Ltd, Modi'in, Israel.
Stephen M ShawBioLineRx Ltd, Modi'in, Israel.
Ella SoraniBioLineRx Ltd, Modi'in, Israel.
Marya ChaneyEarly Oncology Development, Merck & Co., Inc, Kenilworth, NJ, USA.
Shaul KadoshStatExcellence Ltd, Nesher, Israel.
Abi Vainstein HarasBioLineRx Ltd, Modi'in, Israel.
Daniel D Von HoffHonorHealth Research Institute, Scottsdale, AZ, USA.ORCID http://orcid.org/0000-0003-4723-7681
Manuel HidalgoJoan and Sanford I. Weill Department of Medicine, Weill Cornell Medicine, New York, NY, USA. mah4006@med.cornell.edu.ORCID http://orcid.org/0000-0002-3765-3318
Tel Aviv University · ILTranslational Genomics Research Institute · USBeth Israel Deaconess Medical Center · USClinica Universidad de Navarra · ESHarvard University · USHebrew University of Jerusalem · ILHebron University · PSHospital General Universitario Gregorio Marañón · ESHospital Universitario de Fuenlabrada · ESHospital Universitario La Paz · ESMayo Clinic in Arizona · USMerck & Co., Inc., Rahway, NJ, USA (United States) · USNewYork–Presbyterian Hospital · USOchsner Medical Center · USRambam Health Care Campus · ILSamsung Medical Center · KRWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Programmed cell death 1 (PD-1) inhibitors have limited effect in pancreatic ductal adenocarcinoma (PDAC), underscoring the need to co-target alternative pathways. CXC chemokine receptor 4 (CXCR4) blockade promotes T cell tumor infiltration and is synergistic with anti-PD-1 therapy in PDAC mouse models. We conducted a phase IIa, open-label, two-cohort study to assess the safety, efficacy and immunobiological effects of the CXCR4 antagonist BL-8040 (motixafortide) with pembrolizumab and chemotherapy in metastatic PDAC (NCT02826486). The primary outcome was objective response rate (ORR). Secondary outcomes were overall survival (OS), disease control rate (DCR) and safety. In cohort 1, 37 patients with chemotherapy-resistant disease received BL-8040 and pembrolizumab. The DCR was 34.5% in the evaluable population (modified intention to treat, mITT; N = 29), including nine patients (31%) with stable disease and one patient (3.4%) with partial response. Median OS (mOS) was 3.3 months in the ITT population. Notably, in patients receiving study drugs as second-line therapy, the mOS was 7.5 months. BL-8040 increased CD8

Indexed as

AgedAged, 80 and overAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Pancreatic DuctalCD8-Positive T-LymphocytesFemaleFluorouracilHumansIrinotecanLeucovorinLiver NeoplasmsLung NeoplasmsLymphatic MetastasisLymph Nodes4-fluorobenzoyl-TN-14003Antibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalCXCR4 protein, humanFluorouracilIrinotecanLeucovorinpembrolizumabPeptidesReceptors, CXCR4

Identifiers

PMID32451495
OpenAlexW3027648247

What OpenQuestion holds

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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 OpenQuestion graph.