In elderly patients with glioblastoma, the addition of temozolomide to short-course radiotherapy resulted in longer survival than short-course radiotherapy alone. (Funded by the Canadian Cancer Society Research Institute and others; ClinicalTrials.gov number, NCT00482677 .).
PsPD has a clinical impact on chemotherapy-treated GBM, as it may express the glioma killing effects of treatment and is significantly correlated with MGMT status. Improvement in the early recognition of psPD patterns and knowledge of mechanisms underlying this phenomenon are crucial to eliminating biases in evaluating the results of clinical trials and guaranteeing effective treatment.
Immunotherapy represents a promising area of therapy among neuro-oncology
patients. However, early phase studies reveal unique challenges associated with assessment
of radiological changes reflecting delayed responses or therapy-induced inflammation.
Clinical benefit, including long-term survival and tumor regression, can still occur
following initial apparent progression or appearance of new lesions. Refinement of
response assessment criteria for neuro-oncology patients undergoing immunotherapy is
therefore warranted. A multinational and multidisciplinary panel of neuro-oncology
immunotherapy experts describes immunotherapy response assessment for neuro-oncology
(iRANO) criteria that are based on guidance for determination of tumor progression
outlined by the immune-related response criteria (irRC) and the response assessment in
neuro-oncology (RANO) working group. Among patients who demonstrate imaging findings
meeting RANO criteria for progressive disease (PD) within six months of initiating
immunotherapy including the development of new lesions, confirmation of radiographic
progression on follow-up imaging is recommended provided that the patient is not
significantly worse clinically. The proposed criteria also include guidelines for use of
corticosteroids. The role of advanced imaging techniques and measurement of clinical
benefit endpoints including neurologic and immunologic functions are reviewed. The iRANO
guidelines put forth herein will evolve successively to improve their utility as further
experience from immunotherapy trials in neuro-oncology accumulate.
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