Case series of outcomes in advanced cancer patients with single pathway alterations receiving N-of-One therapies.


Journal

NPJ precision oncology
ISSN: 2397-768X
Titre abrégé: NPJ Precis Oncol
Pays: England
ID NLM: 101708166

Informations de publication

Date de publication:
28 Mar 2022
Historique:
received: 07 09 2021
accepted: 11 02 2022
entrez: 29 3 2022
pubmed: 30 3 2022
medline: 30 3 2022
Statut: epublish

Résumé

Though advanced cancers generally display complex molecular portfolios, there is a subset of patients whose malignancies possess only one genomic alteration or alterations in one oncogenic pathway. We assess how N-of-One therapeutic strategies impact outcomes in these patients. From 12/2012 to 9/2018, 429 therapy-evaluable patients with diverse treatment-refractory cancers were presented at Molecular Tumor Boards at Moores Cancer Center at UC San Diego. The clinical benefit rate, defined by RECIST1.1, was assessed for patients with solid tumors who underwent next-generation sequencing (NGS) profiling revealing one genomic or pathway alteration, subsequently managed with N-of-One therapies. Nine of 429 patients (2.1%) met evaluation criteria. Using matched therapy indicated by NGS, the clinical benefit rate (stable disease ≥ 6 months/partial/complete response) was 66.7%. Median progression-free survival was 11.3 months (95% CI: 3.4-not evaluable). Thus, a small subset of diverse cancers has single pathway alterations on NGS testing. These patients may benefit from customized therapeutic matching.

Identifiants

pubmed: 35347205
doi: 10.1038/s41698-022-00259-7
pii: 10.1038/s41698-022-00259-7
pmc: PMC8960821
doi:

Types de publication

Journal Article

Langues

eng

Pagination

18

Subventions

Organisme : U.S. Department of Health & Human Services | NIH | NCI | Division of Cancer Epidemiology and Genetics, National Cancer Institute (National Cancer Institute Division of Cancer Epidemiology and Genetics)
ID : Grants P30 CA023100
Organisme : NCI NIH HHS
ID : K08 CA168999
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA023100
Pays : United States
Organisme : U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI)
ID : K08CA168999 and R21CA192072
Organisme : NCI NIH HHS
ID : R21 CA192072
Pays : United States

Informations de copyright

© 2022. The Author(s).

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Auteurs

Diviya Gupta (D)

School of Medicine, University of California San Diego, La Jolla, CA, USA.

Razelle Kurzrock (R)

School of Medicine, University of California San Diego, La Jolla, CA, USA. teoam2011@gmail.com.
Center for Personalized Cancer Therapy, UC San Diego Moores Cancer Center, La Jolla, CA, USA. teoam2011@gmail.com.
Division of Hematology/Oncology, UC San Diego, San Diego, CA, USA. teoam2011@gmail.com.

Suzanna Lee (S)

Center for Personalized Cancer Therapy, UC San Diego Moores Cancer Center, La Jolla, CA, USA.

Ryosuke Okamura (R)

Center for Personalized Cancer Therapy, UC San Diego Moores Cancer Center, La Jolla, CA, USA.
Division of Hematology/Oncology, UC San Diego, San Diego, CA, USA.

Hyo Jeong Lim (HJ)

Department of Internal Medicine, Veterans Health Service Medical Center, Seoul, Republic of Korea.

Ki Hwan Kim (KH)

Division of Hematology and Medical Oncology, Seoul National University Boramae Medical Center, Seoul, Republic of Korea.

Jason K Sicklick (JK)

School of Medicine, University of California San Diego, La Jolla, CA, USA.
Center for Personalized Cancer Therapy, UC San Diego Moores Cancer Center, La Jolla, CA, USA.
Department of Surgery, Division of Surgical Oncology, UC San Diego, San Diego, CA, USA.

Shumei Kato (S)

School of Medicine, University of California San Diego, La Jolla, CA, USA. smkato@health.ucsd.edu.
Center for Personalized Cancer Therapy, UC San Diego Moores Cancer Center, La Jolla, CA, USA. smkato@health.ucsd.edu.
Division of Hematology/Oncology, UC San Diego, San Diego, CA, USA. smkato@health.ucsd.edu.

Classifications MeSH