Evidence map›Paper›PMID 32910338›Full record

ArticleInvestigational new drugs2021

Immunologic and tumor responses of pegilodecakin with 5-FU/LV and oxaliplatin (FOLFOX) in pancreatic ductal adenocarcinoma (PDAC).

J Randolph Hecht, Kyriakos P Papadopoulos, Gerald S Falchook, Manish R Patel, Jeffrey R Infante, Raid Aljumaily, Deborah J Wong, Karen A Autio, Zev A Wainberg, Todd M Bauer and 11 more

Registry-linked trialOpen access · greenAbstract readClinical Trial, Phase I
In one paragraph

Article in Investigational new drugs, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02009449 (A Phase 1, Open-Label Dose Escalation First-in-Human Study to Evaluate the Tolerability, Safety, Maximum Tolerated Dose, Preliminary Clinical Activity and Pharmacokinetics of AM0010 in Patients With Advanced Solid Tumors), which is not on this map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 30% 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.

NCT02009449 phase1completednot on this map

A Phase 1, Open-Label Dose Escalation First-in-Human Study to Evaluate the Tolerability, Safety, Maximum Tolerated Dose, Preliminary Clinical Activity and Pharmacokinetics of AM0010 in Patients With Advanced Solid Tumors

TypeinterventionalSponsorEli Lilly and CompanyRan2013 to 2023Enrolled353ConditionsMelanoma, Prostate Cancer, Ovarian Cancer, Renal Cell CarcinomaArmsPegilodecakin, Paclitaxel or Docetaxel and Carboplatin or Cisplatin, FOLFOX (Oxaliplatin/Leucovorin/5-Fluorouracil), gemcitabine/nab-paclitaxel, Capecitabine
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
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  6. Targeting inflammation as cancer therapy.Journal of hematology & oncology · 2024
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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

21 authors at 6 institutions in 1 country.

J Randolph HechtDavid Geffen School of Medicine, UCLA, 10833 Le Conte Avenue, Santa Monica, CA, USA. jrhecht@mednet.ucla.edu.ORCID 0000-0003-2277-4157
Kyriakos P PapadopoulosSTART Center for Cancer Care, 4383 Medical Drive, San Antonio, TX, USA.
Gerald S FalchookSarah Cannon Research Institute at HealthONE, 1800 N Williams Street Suite 300, Denver, CO, USA.
Manish R PatelSarah Cannon Research Institute/Florida Cancer Specialists, 600 N Cattlemen Road Suite 200, Sarasota, FL, USA.
Jeffrey R InfanteSarah Cannon Research Institute/Tennessee Oncology, PLLC, 300 20th Avenue N, Nashville, TN, USA.
Raid AljumailySarah Cannon Research Institute/Tennessee Oncology, PLLC, 300 20th Avenue N, Nashville, TN, USA.
Deborah J WongDavid Geffen School of Medicine, UCLA, 10833 Le Conte Avenue, Santa Monica, CA, USA.
Karen A AutioMemorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY, USA.
Zev A WainbergDavid Geffen School of Medicine, UCLA, 10833 Le Conte Avenue, Santa Monica, CA, USA.
Todd M BauerSarah Cannon Research Institute/Tennessee Oncology, PLLC, 300 20th Avenue N, Nashville, TN, USA.
Milind JavleMD Anderson Cancer Center, 1515 Holcombe, Houston, TX, USA.
Shubham PantStephenson Cancer Center of the University of Oklahoma, 800 NE 10th, Oklahoma City, OK, USA.
Johanna BendellSarah Cannon Research Institute/Tennessee Oncology, PLLC, 300 20th Avenue N, Nashville, TN, USA.
Annie HungEli Lilly and Company, Indianapolis, IN, USA.
Navneet RattiARMO BioSciences, a wholly owned subsidiary of Eli Lilly and Company, 575 Chesapeake Dr., Redwood City, CA, USA.
Peter VanVlasselaerARMO BioSciences, a wholly owned subsidiary of Eli Lilly and Company, 575 Chesapeake Dr., Redwood City, CA, USA.
Rakesh VermaARMO BioSciences, a wholly owned subsidiary of Eli Lilly and Company, 575 Chesapeake Dr., Redwood City, CA, USA.
Joseph LevequeDavid Geffen School of Medicine, UCLA, 10833 Le Conte Avenue, Santa Monica, CA, USA.
Sujata RaoEli Lilly and Company, Indianapolis, IN, USA.
Martin OftARMO BioSciences, a wholly owned subsidiary of Eli Lilly and Company, 575 Chesapeake Dr., Redwood City, CA, USA.
Aung NaingMD Anderson Cancer Center, 1515 Holcombe, Houston, TX, USA.
Eli Lilly (United States) · USSarah Cannon · USThe University of Texas MD Anderson Cancer Center · USMemorial Sloan Kettering Cancer Center · USSouth Texas Accelerated Research Therapeutics · USUCLA Health · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Background Treatment options for pancreatic ductal adenocarcinoma (PDAC) are limited and checkpoint blockade inhibitors have been disappointing in this disease. Pegilodecakin has demonstrated single agent anti-tumor activity in immune-sensitive tumors. Phase 1 and preclinical data indicate synergy of pegilodecakin with 5-FU and platins. We assessed the safety and activity of pegilodecakin+FOLFOX in patients with PDAC. Methods IVY (NCT02009449) was an open-label phase 1b trial in the United States. Here we report on all enrolled patients from cohort C. Heavily pretreated patients were treated with pegilodecakin (self-administered subcutaneously daily at 2.5, 5, or 10 μg/kg) + 5-flurouracil/leucovorin/oxaliplatin (FOLFOX), dosed per manufacturers prescribing information, until tumor progression. Eligible patients had measurable disease per immune-related response criteria (irRC), were ≥ 18 years of age, and had ECOG performance status of 0 or 1. Patients were evaluated for primary(safety) and secondary (tumor response per irRC) endpoints. Results From 5 August 2014-12 July 2016, 39 patients enrolled in cohort C. All patients were evaluable for safety. In this advanced population, regimen had manageable toxicities with no immune-related adverse events (irAEs) greater than grade 1. The most common grade 3/4/5 TEAEs were thrombocytopenia (21[53.8%] of 39) and anemia (17[43.6%] of 39). In evaluable PDAC patients, the best overall response of pegilodecakin+FOLFOX was 3(14%) with CRs in 2(9%) patients. Conclusions Pegilodecakin+FOLFOX had an acceptable tolerability profile in PDAC, with no substantial irAEs seen, and promising efficacy with the combination yielding a 2-year OS of 24% (95% CI 10-42). These data led to the phase 3 study with pegilodecakin+FOLFOX as second-line therapy of PDAC (SEQUOIA).

Indexed as

AdultAgedAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Pancreatic DuctalDose-Response Relationship, DrugFluorouracilHumansInterleukin-10Kaplan-Meier EstimateLeucovorinMiddle AgedNeoplasm StagingOrganoplatinum CompoundsPancreatic NeoplasmsPolyethylene GlycolsProgression-Free SurvivalFluorouracilInterleukin-10LeucovorinOrganoplatinum CompoundspegilodecakinPolyethylene GlycolsFOLFOXIL-10Metastatic pancreatic adenocarcinomaPegilodecakinPegylated IL-10Phase 1

Identifiers

PMID32910338
PMCPMC8944136
OpenAlexW3086777363

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.