Evidence map›Paper›PMID 35884377›Full record

ArticleCancers2022

Factors Contributing to Tumor Shrinkage after Peptide Receptor Radionuclide Therapy in Patients with Unresectable Neuroendocrine Tumors.

Sho Hasegawa, Noritoshi Kobayashi, Damian Wild, Fesupplix Kaul, Naoki Okubo, Akihiro Suzuki, Yusuke Kurita, Shoko Takano, Atsushi Nakajima, Yasushi Ichikawa

Abstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

3 citing papers in PubMed.

  1. Trial
  2. Article
  3. 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

10 authors.

Sho HasegawaGastroenterology and Hepatology Division, Yokohama City University Hospital, Yokohama 2360004, Japan.
Noritoshi KobayashiOncology Division, Yokohama City University Hospital, Yokohama 2360004, Japan.
Damian WildNuclear Medicine Division, University Hospital Basel, 4031 Basel, Switzerland.ORCID 0000-0002-8135-5350
Fesupplix KaulNuclear Medicine Division, University Hospital Basel, 4031 Basel, Switzerland.ORCID 0000-0002-0621-4072
Naoki OkuboOncology Division, Yokohama City University Hospital, Yokohama 2360004, Japan.
Akihiro SuzukiOncology Division, Yokohama City University Hospital, Yokohama 2360004, Japan.
Yusuke KuritaGastroenterology and Hepatology Division, Yokohama City University Hospital, Yokohama 2360004, Japan.
Shoko TakanoRadiation Oncology Division, Yokohama City University Hospital, Yokohama 2360004, Japan.
Atsushi NakajimaGastroenterology and Hepatology Division, Yokohama City University Hospital, Yokohama 2360004, Japan.ORCID 0000-0002-6263-1436
Yasushi IchikawaOncology Division, Yokohama City University Hospital, Yokohama 2360004, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peptide receptor activation therapy (PRRT) is a promising treatment option for metastatic neuroendocrine tumors (NETs). However, predicting tumor shrinkage before treatment is challenging. We analyzed the shrinkage rate of each metastatic tumor lesion to identify predictive factors related to shrinkage. Patients with metastatic NET who underwent PRRT were included in this retrospective study. For each patient, between one to five metastatic lesions were selected in descending order of size, and the change in the maximum tumor diameter after treatment was defined as the shrinkage rate per lesion (L-SR). We analyzed the relationship between pretreatment clinicopathological factors and L-SR. The median L-SR of all 75 lesions in 20 patients was 20% (95% CI: 4.8−26.1%). While previous treatment with cytotoxic agents (34.4%, p < 0.05) and primary tumor of the pancreas (27.8%, p < 0.05) were significantly favorable factors, a primary tumor of the rectum was significantly more resistant to shrinkage (−20.5%, p < 0.001). Therefore, lesion-based analysis of PRRT for NETs showed that pancreatic NET and previous treatment with cytotoxic agents were favorable factors for tumor shrinkage; however, rectal NET was a factor associated with resistance to shrinkage.

Indexed as

lesion-based analysisneuroendocrine tumorspeptide receptor radionuclide therapy

Identifiers

PMID35884377
PMCPMC9313286

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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.