Evidence map›Paper›PMID 38748739›Full record

ArticlePloS one2024

Safety and efficacy of peptide receptor radionuclide therapy in neuroendocrine tumors: A single center experience.

Vineeth Sukrithan, Heather Armbruster, Sherise Rogers, Sherry Mori Vogt, Cassandra Grenade, Claire Verschraegen, Ye Zhou, Ashima Goyal, Mona Natwa, Akram Hussein and 10 more

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Targeted Radionuclide Therapy: Current Landscape and Combination Approaches to Improve Oncology Outcomes.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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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

20 authors.

Vineeth SukrithanDivision of Medical Oncology, Department of Internal Medicine, The Ohio State University and Arthur G. James Cancer Center, Columbus, Ohio, United States of America.
Heather ArmbrusterDepartment of Pharmacy, The Ohio State University, Columbus, Ohio, United States of America.
Sherise RogersDivision of Hematology Oncology, Department of Medicine, University of Florida, Gainesville, FL, United States of America.
Sherry Mori VogtDivision of Pharmacy, Medical University of South Carolina, Charleston, South Carolina, United States of America.
Cassandra GrenadeDivision of Hematology Oncology, Department of Medicine, Ohio Health, Delaware, OH, United States of America.
Claire VerschraegenDivision of Medical Oncology, Department of Internal Medicine, The Ohio State University and Arthur G. James Cancer Center, Columbus, Ohio, United States of America.
Ye ZhouDivision of Medical Oncology, Department of Internal Medicine, The Ohio State University and Arthur G. James Cancer Center, Columbus, Ohio, United States of America.
Ashima GoyalDivision of Medical Oncology, Department of Internal Medicine, The Ohio State University and Arthur G. James Cancer Center, Columbus, Ohio, United States of America.
Mona NatwaDepartment of Radiology, The Ohio State University, Columbus, Ohio, United States of America.
Akram HusseinDepartment of Nuclear Medicine Pharmacy, The Ohio State University, Columbus, Ohio, United States of America.
Hallie BarrDepartment of Pharmacy, The Ohio State University, Columbus, Ohio, United States of America.
Dramane KonateDepartment of Environmental Health and Safety, The Ohio State University, Columbus, Ohio, United States of America.
Rochelle BatdorfDepartment of Environmental Health and Safety, The Ohio State University, Columbus, Ohio, United States of America.
Andrew BrownCardinal Health, Dublin, Ohio, United States of America.
Bonnie WilliamsDepartment of Radiology, The Ohio State University, Columbus, Ohio, United States of America.ORCID 0009-0006-5648-1861
Songzhu ZhaoDepartment of Biostatistics, The Ohio State University, Columbus, Ohio, United States of America.
Lai WeiDepartment of Biostatistics, The Ohio State University, Columbus, Ohio, United States of America.
Menglin XuDivision of Medical Oncology, Department of Internal Medicine, The Ohio State University and Arthur G. James Cancer Center, Columbus, Ohio, United States of America.
Manisha H ShahDivision of Medical Oncology, Department of Internal Medicine, The Ohio State University and Arthur G. James Cancer Center, Columbus, Ohio, United States of America.
Bhavana KondaDivision of Medical Oncology, Department of Internal Medicine, The Ohio State University and Arthur G. James Cancer Center, Columbus, Ohio, United States of America.ORCID 0000-0002-9099-5990

Funding

The Ohio State University Center for clinical and Translational ScienceUL1TR001070 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2013 to 2017
$22.6M
NCATS NIH HHS UL1 TR001070
6 · The paper itself

Abstract

Peptide receptor radionucleotide therapy (PRRT) with 177Lu-dotatate is widely used for the treatment of patients with neuroendocrine tumors (NETs). We analyzed data from 104 patients with NETs treated with 177Lu -dotatate at a US academic center between December 2017 and October 2020 to better understand patterns of long-term efficacy, safety, and toxicity in the real-world setting. 177Lu-dotatate (200 mCi) was administered every eight weeks for four doses. The most common sites of primary disease were small intestine NETs (n = 49, 47%), pancreatic NETs (n = 32, 31%), and lung NETs (n = 7, 7%). Twenty-seven percent had Ki-67 <3%, 49% had Ki-67 between 3-20%, and 13.5% had Ki-67 >20%. The cohort had been pretreated with a median of two prior lines of treatment. Forty percent had received prior liver-directed treatment. Seventy-four percent of patients completed all four doses of treatment. The objective response rate was 18%. The median time-to-treatment failure/death was significantly longer for small-bowel NETs when compared to pancreatic NETs (37.3 months vs. 13.2 months, p = 0.001). In a multivariate model, Ki-67, primary site, and liver tumor burden ≥50% were found to independently predict time-to-treatment failure/death. Around 40% of patients experienced adverse events of ≥grade 3 severity. Treatment-related adverse events leading to discontinuation of therapy happened in 10% of patients. Preexisting mesenteric/peritoneal disease was present in 33 patients; seven of these patients developed bowel-related toxicities including two grade 5 events. We also report two cases of delayed-onset minimal change nephrotic syndrome, which occurred 14 and 27 months after the last dose of PRRT. Lastly, we describe six patients who developed rapid tumor progression in the liver leading to terminal liver failure within 7.3 months from the start of PRRT, and identify potential risk factors associated with this occurrence, which will need further study.

Indexed as

Neuroendocrine TumorsOctreotideReceptors, PeptideAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedOrganometallic CompoundsPancreatic NeoplasmsRadiopharmaceuticalsRetrospective StudiesTreatment OutcomeOctreotideOrganometallic CompoundsRadiopharmaceuticalsReceptors, Peptide

Identifiers

PMID38748739
PMCPMC11095666

What OpenQuestion holds

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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.