Abstract
Immunotherapy is one of the most promising treatments for multiple tumor types. The significant clinical benefits and durable responses of immunotherapy have led to the emergence of various immune-related clinical response patterns that extend beyond those achieved with cytotoxic agents. Various studies investigated the efficacy of immunotherapy, including the effect on tumor size, long-term survival benefits, and the ability to overcome the particularly challenging survival curves tailing phenomenon. The current immune-related methods guidelines, such as immune-related Response Criteria (irRC), immune-related Response Evaluation Criteria in Solid Tumors (irRECIST), immune Response Evaluation Criteria in Solid Tumors (iRECIST), and immune-modified Response Evaluation Criteria in Solid Tumors (imRECIST), could be well-adapted to identify the heterogeneity of responses that appear in patients receiving immunotherapy, such as pseudoprogression (PsPD) and hyperprogressive disease (HPD), and to some extent to overcome the limitation of evaluating the efficacy of immunotherapy on tumor size by imaging. Additionally, a second type of evaluation method was proposed based on survival, which includes milestone analysis and restricted mean survival time. Currently, milestone analysis is a complementary tool to summarize and interpret trial results along with more conventional measures of survival and other less established metrics. A golden standard evaluation method to distinguish the efficacy of immunotherapy may improve the process of imaging and aid survival-based efficacy evaluation in patients with solid tumors.
Highlights
The most direct method of evaluating treatment efficacy involves the imaging of changes in the tumor size
The results showed that compared with the measures made according to RECISTv1.1, the progression free survival (PFS) increased by 1.5 months, overall survival (OS) increased slightly by 2%, the disease control rate increased by 13%, and the assessment of progressive disease (PD) decreased by 16% when evaluated by imRECIST, which laid the foundation for the proposition of imRECIST
These evaluation methods are constantly evolving to improve their accuracy of efficacy evaluation in tumor treatment and identify patients who can benefit from immunotherapy
Summary
The most direct method of evaluating treatment efficacy involves the imaging of changes in the tumor size. For the appearance of new lesions, the irRC consider that progressive disease (PD) would not be assigned as long as the total tumor burden does not increase by >25%, and patients with a stable clinical status would be recommended treatment continuation and reassessed after at least 4 weeks.
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