Literature DB >> 27875387

Clinical Response Rates From Interleukin-2 Therapy for Metastatic Melanoma Over 30 Years' Experience: A Meta-Analysis of 3312 Patients.

Richard Bright1, Brendon J Coventry, Nathan Eardley-Harris, Nancy Briggs.   

Abstract

Interleukin-2 (IL-2), initially used in 1986, can induce clinical regression-complete responses (CR) and partial responses (PR) of metastatic malignant melanoma. IL-2 has been used alone or in combination, and in different dosage schedules, as an immunotherapeutic agent for melanoma treatment. This meta-analysis aimed to document and evaluate the spectrum of reported clinical response rates from the combined experience of almost 30 years of IL-2 clinical usage. Clinical trials using IL-2 for metastatic melanoma therapy that reported: dosage, combinations, study details, definitions and clinical CR, PR, and overall response (OR) rates were included. A meta-analysis was conducted using the preferred reporting items for systematic reviews and meta-analyses (PRISMA) guidelines. In total, 34 studies met inclusion criteria, with 41 separate treatment arms. For all IL-2 treatment modalities collectively, the CR rate was 4.0% [95% confidence interval (CI), 2.8-5.3], PR 12.5% (95% CI, 10.1-15.0), and OR 19.7% (95% CI, 15.9-23.5). CR pre-1994 was 2.7% versus 6.1% post-1994. High and intermediate-IL-2 dosage showed no CR difference, while low-dose IL-2 showed a nonstatistical trend toward an increased CR rate. The highest CR rate resulted from IL-2 combined with vaccine at 5.0%. The meta-analysis showed that IL-2 immunotherapy for advanced metastatic melanoma delivered a CR rate of 4% (range, 0-23%) across nearly 30 years of clinical studies, with gradual improvement over time. The significance is that, contrary to popular belief, the data demonstrated that CR rates were similar for intermediate versus high-IL-2 dosing.

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Year:  2017        PMID: 27875387     DOI: 10.1097/CJI.0000000000000149

Source DB:  PubMed          Journal:  J Immunother        ISSN: 1524-9557            Impact factor:   4.456


  12 in total

1.  Is immunity in cancer the key to improving clinical outcome?: Report on the International Symposium on Immunotherapy, The Royal Society, London, UK, 12-13 May 2017.

Authors:  Peter L Stern
Journal:  Ther Adv Vaccines       Date:  2017-07-20

Review 2.  The role for chemotherapy in the modern management of melanoma.

Authors:  Avinash Gupta; Fabio Gomes; Paul Lorigan
Journal:  Melanoma Manag       Date:  2017-05-19

3.  Beta blocker use correlates with better overall survival in metastatic melanoma patients and improves the efficacy of immunotherapies in mice.

Authors:  Kathleen M Kokolus; Ying Zhang; Jeffrey M Sivik; Carla Schmeck; Junjia Zhu; Elizabeth A Repasky; Joseph J Drabick; Todd D Schell
Journal:  Oncoimmunology       Date:  2017-12-21       Impact factor: 8.110

4.  Single injection of IL-12 coacervate as an effective therapy against B16-F10 melanoma in mice.

Authors:  Mintai P Hwang; Ronald J Fecek; Tianyue Qin; Walter J Storkus; Yadong Wang
Journal:  J Control Release       Date:  2019-12-19       Impact factor: 9.776

5.  Melanoma therapeutics: a literature review.

Authors:  Pavan Kumar Dhanyamraju; Trupti N Patel
Journal:  J Biomed Res       Date:  2022-02-28

Review 6.  Melanoma treatment in review.

Authors:  Beatriz Domingues; José Manuel Lopes; Paula Soares; Helena Pópulo
Journal:  Immunotargets Ther       Date:  2018-06-07

Review 7.  Therapeutic vaccination immunomodulation: forming the basis of all cancer immunotherapy.

Authors:  Brendon J Coventry
Journal:  Ther Adv Vaccines Immunother       Date:  2019-08-01

Review 8.  Combination of Immunotherapy With Targeted Therapy: Theory and Practice in Metastatic Melanoma.

Authors:  Chune Yu; Xiaowei Liu; Jiqiao Yang; Min Zhang; Hongyu Jin; Xuelei Ma; Hubing Shi
Journal:  Front Immunol       Date:  2019-05-07       Impact factor: 7.561

Review 9.  Cardiotoxicity of Anticancer Therapeutics.

Authors:  Jerry Dong; Hong Chen
Journal:  Front Cardiovasc Med       Date:  2018-02-07

Review 10.  Modulation of Inflammation-Induced Tolerance in Cancer.

Authors:  Vladimir Rogovskii
Journal:  Front Immunol       Date:  2020-06-26       Impact factor: 7.561

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