Loco-regional immunotherapy with recombinant interleukin-2 and adherent lymphokine-activated killer cells (A-LAK) in recurrent glioblastoma patients
Cancer Immunology Immunotherapy, ISSN: 0340-7004, Vol: 39, Issue: 3, Page: 193-197
1994
- 61Citations
- 21Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations61
- Citation Indexes60
- 60
- CrossRef51
- Patent Family Citations1
- 1
- Captures21
- Readers21
- 21
Article Description
Nine patients with recurrent glioblastoma were given autologous adherent lymphokine-activated killer (A-LAK) cells and interleukin-2 (IL-2) administered directly into the tumor cavity through an Ommaya tube placed during surgery/biopsy. The immunotherapy was well tolerated and the response rate was 33% (one complete response, two partial responses, four with stable disease and two with progressive disease). However, survival 18 months from initial diagnosis did not differ from that reported in the literature for patients treated conventionally. Serial determinations of IL-2 in the tumor cavity during the course of treatment revealed that IL-2 concentrations were sufficient to maintain lymphocyte activation. Since steroid medication was discontinued during treatment and A-LAK cells have greater antitumor activity than standard LAK cells, other factors are discussed that might explain the limited results. © 1994 Springer-Verlag.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0028108663&origin=inward; http://dx.doi.org/10.1007/bf01533386; http://www.ncbi.nlm.nih.gov/pubmed/7923250; http://link.springer.com/10.1007/BF01533386; http://www.springerlink.com/index/10.1007/BF01533386; http://www.springerlink.com/index/pdf/10.1007/BF01533386; https://dx.doi.org/10.1007/bf01533386; https://link.springer.com/article/10.1007/BF01533386
Springer Science and Business Media LLC
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