Evidence map›Paper›PMID 37569668›Full record

ArticleInternational journal of molecular sciences2023

Perspectives of Cell Sensitivity/Resistance Assay in Soft Tissue Sarcomas Chemotherapy.

Timur I Fetisov, Sofya A Khazanova, Polina A Shtompel, Ekaterina S Trapeznikova, Victoria Y Zinovieva, Valeria I Marshall, Anastasia A Lovenger, Dmitriy V Rogozhin, Tararykova A Anastasia, Beniamin Yu Bokhyan and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. 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
0.8field-weighted citation impact, top 24% 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.

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, 3 citations in OpenAlex.

  1. Article
  2. Review
  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

13 authors at 2 institutions in 1 country.

Timur I FetisovN.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.
Sofya A KhazanovaN.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.
Polina A ShtompelN.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.ORCID 0009-0000-8673-597X
Ekaterina S TrapeznikovaFaculty of Medicine, Sechenov University, 119991 Moscow, Russia.
Victoria Y ZinovievaN.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.
Valeria I MarshallN.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.
Anastasia A LovengerN.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.
Dmitriy V RogozhinN.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.
Tararykova A AnastasiaN.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.
Beniamin Yu BokhyanN.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.
Gennady A BelitskyN.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.
Marianna G YakubovskayaN.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.ORCID 0000-0002-9710-8178
Kirill I KirsanovN.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.ORCID 0000-0002-8599-6833
Peoples' Friendship University of Russia · RUSechenov University · RU

Funding

Russian Science Foundation 22-75-00100
6 · The paper itself

Abstract

Treatment of highly malignant soft tissue sarcomas (STSs) requires multicomponent therapy including surgery, radiotherapy, and chemotherapy. Despite the advancements in targeted cancer therapies, cytostatic drug combinations remain the gold standard for STS chemotherapy. The lack of algorithms for personalized selection of STS chemotherapy leads to unhelpful treatment of chemoresistant tumors, causing severe side effects in patients. The goal of our study is to assess the applicability of in vitro chemosensitivity/resistance assays (CSRAs) in predicting STS chemoresistance. Primary cell cultures were obtained from 148 surgery samples using enzymatic and mechanical disaggregation. CSRA was performed using resazurin-based metabolic activity measurement in cells cultured with doxorubicin, ifosfamide, their combination and docetaxel, gemcitabine, and also their combination for 7 days. Both the clinical data of patients and the CSRA results demonstrated a higher resistance of some cancer histotypes to specific drugs and their combinations. The correlation between the CSRA results for doxorubicin and ifosfamide and clinical responses to the combination chemotherapy with these drugs was demonstrated via Spearman rank order correlation. Statistically significant differences in recurrence-free survival were also shown for the groups of patients formed, according to the CSRA results. Thus, CSRAs may help both practicing physicians to avoid harmful and useless treatment, and researchers to study new resistance markers and to develop new STS drugs.

Indexed as

SarcomaSoft Tissue NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsDoxorubicinHumansIfosfamideDoxorubicinIfosfamidechemoresistancedocetaxeldoxorubicingemcitabineifosfamidesoft tissue sarcomasynovial sarcomaundifferentiated pleomorphic sarcoma

Identifiers

PMID37569668
PMCPMC10418362
OpenAlexW4385455475

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.