Therapy for Diffuse Astrocytic and Oligodendroglial Tumors in Adults: ASCO-SNO Guideline.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
01 02 2022
Historique:
pubmed: 14 12 2021
medline: 22 2 2022
entrez: 13 12 2021
Statut: ppublish

Résumé

To provide guidance to clinicians regarding therapy for diffuse astrocytic and oligodendroglial tumors in adults. ASCO and the Society for Neuro-Oncology convened an Expert Panel and conducted a systematic review of the literature. Fifty-nine randomized trials focusing on therapeutic management were identified. Adults with newly diagnosed oligodendroglioma, isocitrate dehydrogenase (IDH)-mutant, 1p19q codeleted CNS WHO grade 2 and 3 should be offered radiation therapy (RT) and procarbazine, lomustine, and vincristine (PCV). Temozolomide (TMZ) is a reasonable alternative for patients who may not tolerate PCV, but no high-level evidence supports upfront TMZ in this setting. People with newly diagnosed astrocytoma, IDH-mutant, 1p19q non-codeleted CNS WHO grade 2 should be offered RT with adjuvant chemotherapy (TMZ or PCV). People with astrocytoma, IDH-mutant, 1p19q non-codeleted CNS WHO grade 3 should be offered RT and adjuvant TMZ. People with astrocytoma, IDH-mutant, CNS WHO grade 4 may follow recommendations for either astrocytoma, IDH-mutant, 1p19q non-codeleted CNS WHO grade 3 or glioblastoma, IDH-wildtype, CNS WHO grade 4. Concurrent TMZ and RT should be offered to patients with newly diagnosed glioblastoma, IDH-wildtype, CNS WHO grade 4 followed by 6 months of adjuvant TMZ. Alternating electric field therapy, approved by the US Food and Drug Administration, should be considered for these patients. Bevacizumab is not recommended. In situations in which the benefits of 6-week RT plus TMZ may not outweigh the harms, hypofractionated RT plus TMZ is reasonable. In patients age ≥ 60 to ≥ 70 years, with poor performance status or for whom toxicity or prognosis are concerns, best supportive care alone, RT alone (for

Identifiants

pubmed: 34898238
doi: 10.1200/JCO.21.02036
doi:

Types de publication

Journal Article Practice Guideline Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

403-426

Auteurs

Nimish A Mohile (NA)

Department of Neurology and Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY.

Hans Messersmith (H)

American Society of Clinical Oncology, Alexandria, VA.

Na Tosha Gatson (NT)

Banner MD Anderson Cancer Center, Phoenix, AZ.
Geisinger Neuroscience Institute. Danville, PA.

Andreas F Hottinger (AF)

Departments of Clinical Neurosciences and Oncology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.

Andrew Lassman (A)

Columbia University Medical Center, New York, NY.

Jordan Morton (J)

University of Oklahoma Health Sciences, Oklahoma City, OK.

Douglas Ney (D)

University of Colorado School of Medicine, Aurora, CO.

Phioanh Leia Nghiemphu (PL)

UCLA David Geffen School of Medicine, Los Angeles, CA.

Adriana Olar (A)

Nomix Laboratories, Denver, CO.

Jeffery Olson (J)

Emory University, Atlanta, GA.

James Perry (J)

Sunnybrook Health Sciences Center, Toronto, Ontario, Canada.

Jana Portnow (J)

City of Hope National Medical Center, Duarte, CA.

David Schiff (D)

University of Virginia Medical Center, Charlottesville, VA.

Anne Shannon (A)

Patient Representative, Honeoye Falls, NY.

Helen A Shih (HA)

Massachusetts General Hospital, Boston, MA.

Roy Strowd (R)

Wake Forest Baptist Health Medical Center, Winston-Salem, NC.

Martin van den Bent (M)

The Brain Tumor Center at Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, the Netherlands.

Mateo Ziu (M)

INOVA Neurosciences and Inova Schar Cancer Institute, Falls Church, VA.

Jaishri Blakeley (J)

Johns Hopkins University School of Medicine, Baltimore, MD.

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Classifications MeSH