DCE-MRI perfusion predicts pseudoprogression in metastatic melanoma treated with immunotherapy.


Journal

Journal of neuro-oncology
ISSN: 1573-7373
Titre abrégé: J Neurooncol
Pays: United States
ID NLM: 8309335

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 13 08 2019
accepted: 20 12 2019
pubmed: 25 12 2019
medline: 27 10 2020
entrez: 25 12 2019
Statut: ppublish

Résumé

It can be challenging to differentiate pseudoprogression from progression. We assessed the ability of dynamic contrast enhanced T1 MRI (DCE-MRI) perfusion to identify pseudoprogression in melanoma brain metastases. Patients with melanoma brain metastases who underwent immunotherapy and DCE-MRI were identified. Enhancing lesions ≥  5mm in diameter on DCE-MRI and that were new or increased in size between a week from beginning the treatment, and a month after completing the treatment were included in the analysis. The 90th percentiles of rVp and rKtrans and the presence or absence of hemorrhage were recorded. Histopathology served as the reference standard for pseudoprogression. If not available, pseudoprogression was defined as neurological and radiographic stability or improvement without any new treatment for ≥ 2 months. Forty-four patients were identified; 64% received ipilimumab monotherapy for a median duration of 9 weeks (range, 1-138). Sixty-four lesions in 44 patients were included in the study. Of these, nine lesions in eight patients were determined to be pseudoprogression and seven lesions were previously irradiated. Forty-four progression lesions and eight pseudoprogression lesions were hemorrhagic. Median lesion volume for pseudoprogression and progression were not significantly different, at 2.3 cm Pseudoprogression exhibited significantly lower rVp

Identifiants

pubmed: 31873875
doi: 10.1007/s11060-019-03379-6
pii: 10.1007/s11060-019-03379-6
pmc: PMC7545497
mid: NIHMS1611598
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

339-346

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : R25 CA020449
Pays : United States
Organisme : Core Grant P30
ID : CA008748
Organisme : National Cancer Institute of the National Institutes of Health
ID : R25CA020449

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Auteurs

Yoshie Umemura (Y)

Department of Neurology, University of Michigan, 1914 Taubman Center, 1500 E. Medical Center Dr., SPC 5316, Ann Arbor, MI, 48109 5316, USA. yoshie@med.umich.edu.

Diane Wang (D)

Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Kyung K Peck (KK)

Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Jessica Flynn (J)

Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Zhigang Zhang (Z)

Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Robin Fatovic (R)

Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Erik S Anderson (ES)

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Kathryn Beal (K)

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Brain Tumor Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Alexander N Shoushtari (AN)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Thomas Kaley (T)

Department of Neurology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Brain Tumor Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Robert J Young (RJ)

Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Brain Tumor Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

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Classifications MeSH