Developments in Combining Targeted Radionuclide Therapies and Immunotherapies for Cancer Treatment

被引:16
|
作者
Kerr, Caroline P. [1 ,2 ]
Grudzinski, Joseph J. [1 ]
Nguyen, Thanh Phuong [2 ]
Hernandez, Reinier [3 ]
Weichert, Jamey P. [1 ]
Morris, Zachary S. [2 ]
机构
[1] Univ Wisconsin Madison, Sch Med & Publ Hlth, Dept Radiol, Madison, WI 53705 USA
[2] Univ Wisconsin Madison, Sch Med & Publ Hlth, Dept Human Oncol, Madison, WI 53705 USA
[3] Univ Wisconsin Madison, Sch Med & Publ Hlth, Dept Med Phys, Madison, WI 53705 USA
关键词
targeted radionuclide therapy (TRT); anti-tumor immunity; external beam radiation therapy (EBRT); tumor microenvironment (TME); IMMUNE-CHECKPOINT BLOCKADE; RESISTANT PROSTATE-CANCER; RANDOMIZED PHASE-II; RADIOPHARMACEUTICAL THERAPY; SIPULEUCEL-T; TUMOR-CELLS; MOUSE MODEL; X-RAY; DOSIMETRY; RADIATION;
D O I
10.3390/pharmaceutics15010128
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Targeted radionuclide therapy (TRT) and immunotherapy are rapidly growing classes of cancer treatments. Basic, translational, and clinical research are now investigating therapeutic combinations of these agents. In comparison to external beam radiation therapy (EBRT), TRT has the unique advantage of treating all disease sites following intravenous injection and selective tumor uptake and retention-a particularly beneficial property in metastatic disease settings. The therapeutic value of combining radiation therapy with immune checkpoint blockade to treat metastases has been demonstrated in preclinical studies, whereas results of clinical studies have been mixed. Several clinical trials combining TRT and immune checkpoint blockade have been initiated based on preclinical studies combining these with EBRT and/or TRT. Despite the interest in translation of TRT and immunotherapy combinations, many questions remain surrounding the mechanisms of interaction and the optimal approach to clinical implementation of these combinations. This review highlights the mechanisms of interaction between anti-tumor immunity and radiation therapy and the status of basic and translational research and clinical trials investigating combinations of TRT and immunotherapies.
引用
收藏
页数:15
相关论文
共 50 条
  • [1] Combining immunotherapy and targeted therapies in cancer treatment
    Vanneman, Matthew
    Dranoff, Glenn
    NATURE REVIEWS CANCER, 2012, 12 (04) : 237 - 251
  • [2] Combining immunotherapy and targeted therapies in cancer treatment
    Matthew Vanneman
    Glenn Dranoff
    Nature Reviews Cancer, 2012, 12 : 237 - 251
  • [3] Neurological Complications of Targeted Therapies and Immunotherapies for Cancer
    McFaline-Figueroa, J. Ricardo
    Lee, Eudocia Q.
    CURRENT TREATMENT OPTIONS IN NEUROLOGY, 2021, 23 (03)
  • [4] Neurological Complications of Targeted Therapies and Immunotherapies for Cancer
    J. Ricardo McFaline-Figueroa
    Eudocia Q. Lee
    Current Treatment Options in Neurology, 2021, 23
  • [5] Neurological sequelae of cancer immunotherapies and targeted therapies
    Wick, Wolfgang
    Hertenstein, Anne
    Platten, Michael
    LANCET ONCOLOGY, 2016, 17 (12): : E529 - E541
  • [6] Targeted radionuclide therapies for pancreatic cancer
    Shah, M.
    Da Silva, R.
    Gravekamp, C.
    Libutti, S. K.
    Abraham, T.
    Dadachova, E.
    CANCER GENE THERAPY, 2015, 22 (08) : 375 - 379
  • [7] Targeted radionuclide therapies for pancreatic cancer
    M Shah
    R Da Silva
    C Gravekamp
    S K Libutti
    T Abraham
    E Dadachova
    Cancer Gene Therapy, 2015, 22 : 375 - 379
  • [8] Combining Targeted Radionuclide Therapy and Immune Checkpoint Inhibition for Cancer Treatment
    Kleinendorst, Simone C.
    Oosterwijk, Egbert
    Bussink, Johan
    Westdorp, Harm
    Konijnenberg, Mark W.
    Heskamp, Sandra
    CLINICAL CANCER RESEARCH, 2022, 28 (17) : 3652 - 3657
  • [9] Combining immunotherapies for the treatment of prostate cancer
    Redman, Jason M.
    Gulley, James L.
    Madan, Ravi A.
    UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, 2017, 35 (12) : 694 - 700
  • [10] Combining targeted therapies in ovarian cancer
    Scambia, Giovanni
    Salutari, Vanda
    Ferrandina, Gabriella
    LANCET ONCOLOGY, 2014, 15 (11): : 1179 - 1181