Evidence map›Paper›PMID 38237098›Full record

ArticleJCO precision oncology2024

Cellular Mass Response to Therapy Correlates With Clinical Response for a Range of Malignancies.

Mark M Stevens, Robert J Kimmerling, Selim Olcum, Madeleine Vacha, Rachel LaBella, Anthony Minnah, Katelin Katsis, Juanita Fujii, Zayna Shaheen, Srividya Sundaresan and 13 more

Abstract read
In one paragraph

Article in JCO precision oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

23 authors.

Mark M StevensTravera, Medford, MA.ORCID 0000-0001-9207-4979
Robert J KimmerlingTravera, Medford, MA.
Selim OlcumTravera, Medford, MA.
Madeleine VachaTravera, Medford, MA.
Rachel LaBellaTravera, Medford, MA.
Anthony MinnahTravera, Medford, MA.
Katelin KatsisTravera, Medford, MA.
Juanita FujiiDepartment of Clinical Research, Dignity Health, Sequoia Hospital, Redwood City, CA.
Zayna ShaheenDepartment of Clinical Research, Dignity Health, Sequoia Hospital, Redwood City, CA.
Srividya SundaresanDepartment of Clinical Research, Dignity Health, Sequoia Hospital, Redwood City, CA.
Joseph CriscitielloDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Ruben NiesvizkyWeill Cornell Medicine, New York, NY.
Noopur RajeMassachusetts General Hospital, Boston, MA.ORCID 0000-0003-3066-1275
Andrew BranaganMassachusetts General Hospital, Boston, MA.ORCID 0000-0002-3868-9267
Amrita KrishnanCity of Hope, Los Angeles, CA.ORCID 0000-0002-8484-175X
Sundar JagannathDepartment of Medicine, Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, NY.ORCID 0000-0003-2934-6518
Samir ParekhDepartment of Medicine, Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, NY.ORCID 0000-0001-9694-8469
Adam S SperlingDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-9369-4413
Cara A RosenbaumWeill Cornell Medicine, New York, NY.
Nikhil MunshiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-7344-9795
Marlise R LuskinDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-5781-4529
Anobel TamraziDivision of Vascular and Interventional Radiology, Palo Alto Medical Foundation, Redwood City, CA.
Clifford A ReidTravera, Medford, MA.ORCID 0000-0002-9438-9349

Funding

Defining mechanisms of thalidomide analog resistanceK08CA252174 · NCI · DANA-FARBER CANCER INST · PI SPERLING, ADAM · 2020 to 2024
$1.3M
NCI NIH HHS K08 CA252174
6 · The paper itself

Abstract

purposeCancer patients with advanced-stage disease have poor prognosis, typically having limited options for efficacious treatment, and genomics-based therapy guidance continues to benefit only a fraction of patients. Next-generation ex vivo approaches, such as cell mass-based response testing (MRT), offer an alternative precision medicine approach for a broader population of patients with cancer, but validation of clinical feasibility and potential impact remain necessary. MATERIALS AND

methodsWe evaluated the clinical feasibility and accuracy of using live-cell MRT to predict patient drug sensitivity. Using a unified measurement workflow with a 48-hour result turnaround time, samples were subjected to MRT after treatment with a panel of drugs in vitro. After completion of therapeutic course, clinical response data were correlated with MRT-based predictions of outcome. Specimens were collected from 104 patients with solid (n = 69) and hematologic (n = 35) malignancies, using tissue formats including needle biopsies, malignant fluids, bone marrow aspirates, and blood samples. Of the 81 (78%) specimens qualified for MRT, 41 (51%) patients receiving physician-selected therapies had treatments matched to MRT.

resultsMRT demonstrated high concordance with clinical responses with an odds ratio (OR) of 14.80 (

conclusionMRT showed highly significant correlation with clinical response to therapy. Routine clinical use is technically feasible and broadly applicable to a wide range of samples and malignancy types, supporting the need for future validation studies.

Indexed as

Hematologic NeoplasmsNeoplasmsHumans

Identifiers

PMID38237098
PMCPMC10805426

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.