First-in-human phase I study of the oral inhibitor of indoleamine 2,3-dioxygenase-1 epacadostat (INCB024360) in patients with advanced solid malignancies
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Abstract Purpose: Indoleamine 2,3-dioxygenase-1 (IDO1) catalyzes the degradation of tryptophan to N-formyl-kynurenine. Overexpressed in many solid malignancies, IDO1 can promote tumor escape from host immunosurveillance. This first-in-human phase I study investigated the maximum tolerated dose, safety, pharmacokinetics, pharmacodynamics, and antitumor activity of epacadostat (INCB024360), a potent and selective inhibitor of IDO1. Experimental Design: Fifty-two patients with advanced solid malignancies were treated with epacadostat [50 mg once daily or 50, 100, 300, 400, 500, 600, or 700 mg twice daily (BID)] in a dose-escalation 3 + 3 design and evaluated in 28-day cycles. Treatment was continued until disease progression or unacceptable toxicity. Results: One dose-limiting toxicity (DLT) occurred at the dose of 300 mg BID (grade 3, radiation pneumonitis); another DLT occurred at 400 mg BID (grade 3, fatigue). The most common adverse events in >20% of patients overall were fatigue, nausea, decreased appetite, vomiting, constipation, abdominal pain, diarrhea, dyspnea, back pain, and cough. Treatment produced significant dose-dependent reductions in plasma kynurenine levels and in the plasma kynurenine/tryptophan ratio at all doses and in all patients. Near maximal changes were observed at doses of ≥100 mg BID with >80% to 90% inhibition of IDO1 achieved throughout the dosing period. Although no objective responses were detected, stable disease lasting ≥16 weeks was observed in 7 of 52 patients. Conclusions: Epacadostat was generally well tolerated, effectively normalized kynurenine levels, and produced maximal inhibition of IDO1 activity at doses of ≥100 mg BID. Studies investigating epacadostat in combination with other immunomodulatory drugs are ongoing. Clin Cancer Res; 23(13); 3269–76. ©2017 AACR.
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Epacadostat 100 mg was taken forward from phase I despite higher dose levels being tolerable and no maximum tolerated dose being established.
“Regarding dosing of epacadostat, 100 mg was taken forward out of the phase I study despite higher dose levels being tolerable and no maximum tolerated dose being established (59).”
From Reimagining IDO Pathway Inhibition in Cancer Immunotherapy via Downstream Focus on the Tryptophan–Kynurenine–Aryl Hydrocarbon Axis (2019) · cites this paper as [59]
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Cites
PD-1 and PD-L1 Immune Checkpoint Blockade to Treat Breast Cancer
Hartkopf, A. D., Taran, F., Wallwiener, M., Walter, C. B., Krämer, B., Grischke, E., & Brucker, S. Y. (2016) · Breast Care · doi:10.1159/000453569 · Cited by 30,989 · see citing works
Improved Survival with Ipilimumab in Patients with Metastatic Melanoma
Hodi, F. S., O'Day, S. J., McDermott, D. F., Weber, R. W., Sosman, J. A., Haanen, J. B., Gonzalez, R., Robert, C., Schadendorf, D., Hassel, J. C., et al. (2010) · New England Journal of Medicine · doi:10.1056/nejmoa1003466 · Cited by 15,155 · see citing works
Self-citationPD-1 Blockade in Tumors with Mismatch-Repair Deficiency
Le, D. T., Uram, J. N., Wang, H., Bartlett, B. R., Kemberling, H., Eyring, A. D., Skora, A. D., Luber, B. S., Azad, N. S., Laheru, D., et al. (2015) · New England Journal of Medicine · doi:10.1056/nejmoa1500596 · Cited by 9,377 · see citing works
Nivolumab in Previously Untreated Melanoma without <i>BRAF</i> Mutation
Robert, C., Long, G. V., Brady, B., Dutriaux, C., Maio, M., Mortier, L., Hassel, J. C., Rutkowski, P., McNeil, C., Kalinka-Warzocha, E., et al. (2015) · New England Journal of Medicine · doi:10.1056/nejmoa1412082 · Cited by 5,519 · see citing works
The future of immune checkpoint therapy
Sharma, P., & Allison, J. P. (2015) · Science · doi:10.1126/science.aaa8172 · Cited by 4,878 · see citing works
Ipilimumab plus Dacarbazine for Previously Untreated Metastatic Melanoma
Robert, C., Thomas, L., Bondarenko, I., O'Day, S., Weber, J., Garbe, C., Lebbe, C., Baurain, J.-F., Testori, A., Grob, J.-J., et al. (2011) · New England Journal of Medicine · doi:10.1056/nejmoa1104621 · Cited by 4,496 · see citing works
Innate and adaptive immune cells in the tumor microenvironment
Gajewski, T. F., Schreiber, H., & Fu, Y.-X. (2013) · Nature Immunology · doi:10.1038/ni.2703 · Cited by 4,148 · see citing works
Self-citationPrevention of Allogeneic Fetal Rejection by Tryptophan Catabolism
Munn, D. H., Zhou, M., Attwood, J. T., Bondarev, I. E., Conway, S. J., Marshall, B., Brown, C. C., & Mellor, A. L. (1998) · Science · doi:10.1126/science.281.5380.1191 · Cited by 2,589 · see citing works
Ido expression by dendritic cells: tolerance and tryptophan catabolism
Mellor, A. L., & Munn, D. H. (2004) · Nature Reviews Immunology · doi:10.1038/nri1457 · Cited by 2,341 · see citing works
Uyttenhove, C., Pilotte, L., Théate, I., Stroobant, V., Colau, D., Parmentier, N., Boon, T., & Van den Eynde, B. J. (2003) · Nature Medicine · doi:10.1038/nm934 · Cited by 2,305 · see citing works
Schadendorf, D., Hodi, F. S., Robert, C., Weber, J. S., Margolin, K., Hamid, O., Patt, D., Chen, T.-T., Berman, D. M., & Wolchok, J. D. (2015) · Journal of Clinical Oncology · doi:10.1200/jco.2014.56.2736 · Cited by 2,141 · see citing works
Inhibition of T Cell Proliferation by Macrophage Tryptophan Catabolism
Munn, D., Shafizadeh, E., Attwood, J., Bondarev, I., Pashine, A., & Mellor, A. (1999) · Journal of Experimental Medicine · doi:10.1084/jem.189.9.1363 · Cited by 1,721 · see citing works
Spranger, S., Spaapen, R. M., Zha, Y., Williams, J., Meng, Y., Ha, T. T., & Gajewski, T. F. (2013) · Science Translational Medicine · doi:10.1126/scitranslmed.3006504 · Cited by 1,677 · see citing works
Self-citationAn Interaction between Kynurenine and the Aryl Hydrocarbon Receptor Can Generate Regulatory T Cells
Mezrich, J. D., Fechner, J. H., Zhang, X., Johnson, B. P., Burlingham, W. J., & Bradfield, C. A. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903670 · Cited by 1,617 · see citing works
Llosa, N. J., Cruise, M., Tam, A., Wicks, E. C., Hechenbleikner, E. M., Taube, J. M., Blosser, R. L., Fan, H., Wang, H., Luber, B. S., et al. (2015) · Cancer Discovery · doi:10.1158/2159-8290.cd-14-0863 · Cited by 1,487 · see citing works
Frumento, G., Rotondo, R., Tonetti, M., Damonte, G., Benatti, U., & Ferrara, G. B. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20020121 · Cited by 1,133 · see citing works
Immune Escape Mechanisms as a Guide for Cancer Immunotherapy
Beatty, G. L., & Gladney, W. L. (2015) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-14-1860 · Cited by 1,078 · see citing works
Self-citationIndoleamine 2,3-dioxygenase and tumor-induced tolerance
Munn, D. H., & Mellor, A. L. (2007) · Journal of Clinical Investigation · doi:10.1172/jci31178 · Cited by 1,074 · see citing works
Muller, A. J., DuHadaway, J. B., Donover, P. S., Sutanto-Ward, E., & Prendergast, G. C. (2005) · Nature Medicine · doi:10.1038/nm1196 · Cited by 1,064 · see citing works
Tryptophan Catabolism in Cancer: Beyond IDO and Tryptophan Depletion
Platten, M., Wick, W., & den Eynde, B. J. V. (2012) · Cancer Research · doi:10.1158/0008-5472.can-12-0569 · Cited by 708 · see citing works
Holmgaard, R., Zamarin, D., Munn, D. H., Wolchok, J. D., & Allison, J. P. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20130066 · Cited by 633 · see citing works
Brandacher, G., Perathoner, A., Ladurner, R., Schneeberger, S., Obrist, P., Winkler, C., Werner, E. R., Werner-Felmayer, G., Weiss, H. G., G√∂bel, G., et al. (2006) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-05-1966 · Cited by 614 · see citing works
Spranger, S., Koblish, H. K., Horton, B., Scherle, P. A., Newton, R., & Gajewski, T. F. (2014) · Journal for ImmunoTherapy of Cancer · doi:10.1186/2051-1426-2-3 · Cited by 552 · see citing works
Self-citationSelective inhibition of IDO1 effectively regulates mediators of antitumor immunity
Liu, X., Shin, N., Koblish, H. K., Yang, G., Wang, Q., Wang, K., Leffet, L., Hansbury, M., Thomas, B. A., Rupar, M. J., et al. (2010) · Blood · doi:10.1182/blood-2009-09-246124 · Cited by 549 · see citing works
Self-citationIDO Activates Regulatory T Cells and Blocks Their Conversion into Th17-Like T Cells
Baban, B., Chandler, P., Sharma, M. D., Pihkala, J. P. S., Koni, P. A., Munn, D. H., & Mellor, A. L. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900986 · Cited by 494 · see citing works
Sharma, M. D., Hou, D., Liu, Y., Koni, P. A., Metz, R. A., Chandler, P., Mellor, A. L., He, Y., & Munn, D. H. (2009) · Blood · doi:10.1182/blood-2008-12-195354 · Cited by 406 · see citing works
Chiesa, M. D., Carlomagno, S., Frumento, G., Balsamo, M., Cantoni, C., Conte, R., Moretta, L., Moretta, A., & Vitale, M. (2006) · Blood · doi:10.1182/blood-2006-03-006700 · Cited by 402 · see citing works
Indoleamine 2,3-Dioxygenase Expression in Human Cancers: Clinical and Immunologic Perspectives
Godin-Ethier, J., Hanafi, L., Piccirillo, C. A., & Lapointe, R. (2011) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-11-1331 · Cited by 398 · see citing works
Okamoto, A., Nikaido, T., Ochiai, K., Takakura, S., Saito, M., Aoki, Y., Ishii, N., Yanaihara, N., Yamada, K., Takikawa, O., et al. (2005) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-04-2671 · Cited by 391 · see citing works
Indoleamine 2,3-dioxygenase is a novel prognostic indicator for endometrial cancer
Ino, K., Yoshida, N., Kajiyama, H., Shibata, K., Yamamoto, E., Kidokoro, K., Takahashi, N. K., Terauchi, M., Nawa, A., Nomura, S., et al. (2006) · British Journal of Cancer · doi:10.1038/sj.bjc.6603477 · Cited by 247 · see citing works
Koblish, H. K., Hansbury, M., Bowman, K., Yang, G., Neilan, C. L., Haley, P. J., Burn, T. C., Waeltz, P., Sparks, R. B., Yue, E. W., et al. (2010) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-09-0628 · Cited by 243 · see citing works
Self-citationInaba, T., Ino, K., Kajiyama, H., Yamamoto, E., Shibata, K., Nawa, A., Nagasaka, T., Akimoto, H., Takikawa, O., & Kikkawa, F. (2009) · Gynecologic Oncology · doi:10.1016/j.ygyno.2009.07.015 · Cited by 217 · see citing works
Tolerance to apoptotic cells is regulated by indoleamine 2,3-dioxygenase
Ravishankar, B., Liu, H., Shinde, R. S., Chandler, P., Baban, B., Tanaka, M., Munn, D. H., Mellor, A. L., Karlsson, M. C. I., & McGaha, T. L. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1117736109 · Cited by 199 · see citing works
Grohmann, U., Fallarino, F., Bianchi, R., Belladonna, M. L., Vacca, C., Orabona, C., Uyttenhove, C., Fioretti, M. C., & Puccetti, P. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.2.708 · Cited by 175 · see citing works
Indoleamine 2,3-dioxygenase is a critical regulator of acute graft-versus-host disease lethality
Jasperson, L. K., Bucher, C. M., Panoskaltsis‐Mortari, A., Taylor, P. A., Mellor, A. L., Munn, D. H., & Blazar, B. R. (2007) · Blood · doi:10.1182/blood-2007-06-096081 · Cited by 145 · see citing works
Takao, M., Okamoto, A., Nikaido, T., Urashima, M., Takakura, S., Saito, M., Saito, M., Okamoto, S., Takikawa, O., Sasaki, H., et al. (2007) · Oncology Reports · doi:10.3892/or.17.6.1333 · Cited by 97 · see citing works
Immune Checkpoint Blockade: A New Paradigm in Treating Advanced Cancer
Kreamer, K. M. (2014) · Journal of the Advanced Practitioner in Oncology · doi:10.6004/jadpro.2014.5.6.3 · Cited by 61 · see citing works
Gangadhar, T. C., Hamid, O., Smith, D. C., Bauer, T. M., Wasser, J. S., Olszanski, A. J., Luke, J. J., Balmanoukian, A. S., Kaufman, D. R., Zhao, Y., et al. (2016) · Annals of Oncology · doi:10.1093/annonc/mdw379.06 · Cited by 58 · see citing works
Self-citationGibney, G. T., Hamid, O., Lutzky, J., Olszanski, A. J., Gangadhar, T. C., Gajewski, T. F., Chmielowski, B., Hanks, B. A., Boasberg, P. D., Zhao, Y., et al. (2015) · European Journal of Cancer · doi:10.1016/s0959-8049(16)30312-4 · Cited by 34 · see citing works
Self-citation
Flagged first, then by citations
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Cited by
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Tryptophan metabolism as a common therapeutic target in cancer, neurodegeneration and beyond
Platten, M., Nollen, E. A. A., Röhrig, U. F., Fallarino, F., & Opitz, C. A. (2019) · Nature Reviews Drug Discovery · doi:10.1038/s41573-019-0016-5 · Cited by 1,586 · see citing works
Regulatory T cells in cancer immunosuppression — implications for anticancer therapy
Togashi, Y., Shitara, K., & Nishikawa, H. (2019) · Nature Reviews Clinical Oncology · doi:10.1038/s41571-019-0175-7 · Cited by 1,553 · see citing works
Natural killer cells and other innate lymphoid cells in cancer
Chiossone, L., Dumas, P., Vienne, M., & Vivier, É. (2018) · Nature reviews. Immunology · doi:10.1038/s41577-018-0061-z · Cited by 1,003 · see citing works
Long, G. V., Dummer, R., Hamid, O., Gajewski, T. F., Caglevic, C., Dalle, S., Arance, A., Carlino, M. S., Grob, J.-J., Kim, T. M., et al. (2019) · The Lancet Oncology · doi:10.1016/s1470-2045(19)30274-8 · Cited by 960 · see citing works
Self-citationNext generation of immune checkpoint therapy in cancer: new developments and challenges
Marin-Acevedo, J. A., Dholaria, B., Soyano, A. E., Knutson, K. L., Chumsri, S., & Lou, Y. (2018) · Journal of Hematology & Oncology · doi:10.1186/s13045-018-0582-8 · Cited by 802 · see citing works
Lu, K., He, C., Guo, N., Chan, C., Ni, K., Lan, G., Tang, H., Pelizzari, C. A., Fu, Y., Spiotto, M. T., et al. (2018) · Nature Biomedical Engineering · doi:10.1038/s41551-018-0203-4 · Cited by 602 · see citing works
Discovery of IDO1 Inhibitors: From Bench to Bedside
Prendergast, G. C., Malachowski, W. P., DuHadaway, J. B., & Muller, A. J. (2017) · Cancer Research · doi:10.1158/0008-5472.can-17-2285 · Cited by 563 · see citing works
Spranger, S., Koblish, H. K., Horton, B., Scherle, P. A., Newton, R., & Gajewski, T. F. (2014) · Journal for ImmunoTherapy of Cancer · doi:10.1186/2051-1426-2-3 · Cited by 552 · see citing works
Self-citationTherapeutic targets and biomarkers of tumor immunotherapy: response versus non-response
Wang, D., Wu, X., & Sun, Y. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01136-2 · Cited by 518 · see citing works
Targeting the IDO1/TDO2–KYN–AhR Pathway for Cancer Immunotherapy – Challenges and Opportunities
Cheong, J. E., & Sun, L. (2017) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2017.11.007 · Cited by 489 · see citing works
Steggerda, S. M., Bennett, M. K., Chen, J., Emberley, E. D., Huang, T. C., Janes, J. R., Li, W., MacKinnon, A. L., Makkouk, A., Marguier, G. M., et al. (2017) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-017-0308-4 · Cited by 488 · see citing works
Classification of current anticancer immunotherapies
Galluzzi, L., Vacchelli, E., Pedro, J. M. B., Buqué, A., Senovilla, L., Baracco, E. E., Bloy, N., Castoldi, F., Abastado, J., Agostinis, P., et al. (2014) · Oncotarget · doi:10.18632/oncotarget.2998 · Cited by 471 · see citing works
Resistance Mechanisms to Anti-PD Cancer Immunotherapy
Vesely, M. D., Zhang, T., & Chen, L. (2022) · Annual Review of Immunology · doi:10.1146/annurev-immunol-070621-030155 · Cited by 468 · see citing works
Targeting the IDO1 pathway in cancer: from bench to bedside
Liu, M., Wang, X., Wang, L., Ma, X., Gong, Z., Zhang, S., & Li, Y. (2018) · Journal of Hematology & Oncology · doi:10.1186/s13045-018-0644-y · Cited by 449 · see citing works
IDO1 in cancer: a Gemini of immune checkpoints
Zhai, L., Ladomersky, E., Lenzen, A. C., Nguyen, B., Patel, R., Lauing, K. L., Wu, M., & Wainwright, D. A. (2018) · Cellular and Molecular Immunology · doi:10.1038/cmi.2017.143 · Cited by 441 · see citing works
Broadening the Impact of Immunotherapy to Pancreatic Cancer: Challenges and Opportunities
Balachandran, V. P., Beatty, G. L., & Dougan, S. K. (2019) · Gastroenterology · doi:10.1053/j.gastro.2018.12.038 · Cited by 444 · see citing works
Self-citationMetabolism of Amino Acids in Cancer
Wei, Z. C., Liu, X., Cheng, C., Yu, W., & Yi, P. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.603837 · Cited by 439 · see citing works
Labadie, B. W., Bao, R., & Luke, J. J. (2019) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-18-2882 · Cited by 413 · see citing works
Mitchell, T. C., Hamid, O., Smith, D. C., Bauer, T. M., Wasser, J. S., Olszanski, A. J., Luke, J. J., Balmanoukian, A. S., Schmidt, E. V., Zhao, Y., et al. (2018) · Journal of Clinical Oncology · doi:10.1200/jco.2018.78.9602 · Cited by 388 · see citing works
Self-citationEmerging targets in cancer immunotherapy
Burugu, S., Dancsok, A. R., & Nielsen, T. O. (2017) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2017.10.001 · Cited by 316 · see citing works
Migrating into the tumor: a roadmap for T cells
van der Woude, L. L., Gorris, M. A. J., Halilovic, A., Figdor, C. G., & de Vries, I. J. M. (2017) · Trends in cancer · doi:10.1016/j.trecan.2017.09.006 · Cited by 307 · see citing works
Indoleamine 2,3-dioxygenase (IDO) inhibitors and cancer immunotherapy
Fujiwara, Y., Kato, S., Nesline, M., Conroy, J. M., DePietro, P., Pabla, S., & Kurzrock, R. (2022) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2022.102461 · Cited by 307 · see citing works
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Opitz, C. A., Somarribas Patterson, L. F., Mohapatra, S. R., Dewi, D. L., Sadik, A., Platten, M., & Trump, S. (2020) · British Journal of Cancer · doi:10.1038/s41416-019-0664-6 · Cited by 300 · see citing works
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Lemos, H. D. P., Huang, L., Prendergast, G. C., & Mellor, A. L. (2019) · Nature reviews. Cancer · doi:10.1038/s41568-019-0106-z · Cited by 275 · see citing works
Indoleamine 2,3-Dioxygenase and Its Therapeutic Inhibition in Cancer
Prendergast, G. C., Malachowski, W. P., Mondal, A., Scherle, P., & Muller, A. J. (2017) · International review of cytology · doi:10.1016/bs.ircmb.2017.07.004 · Cited by 274 · see citing works
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Muller, A. J., Manfredi, M. G., Zakharia, Y., & Prendergast, G. C. (2018) · Seminars in Immunopathology · doi:10.1007/s00281-018-0702-0 · Cited by 265 · see citing works
Next-generation immuno-oncology agents: current momentum shifts in cancer immunotherapy
Pan, C.-X., Liu, H., Robins, E., Song, W., Liu, D., Li, Z., & Zheng, L. (2020) · Journal of Hematology & Oncology · doi:10.1186/s13045-020-00862-w · Cited by 245 · see citing works
Lu, J., Liu, X., Liao, Y., Wang, X., Ahmed, A., Jiang, W., Ji, Y. C., Meng, H., & Nel, A. E. (2018) · ACS Nano · doi:10.1021/acsnano.8b05189 · Cited by 222 · see citing works
RetractedRegulatory T cells: a potential target in cancer immunotherapy
Shitara, K., & Nishikawa, H. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13625 · Cited by 215 · see citing works
Yang, L., Li, A., Lei, Q., & Zhang, Y. (2019) · Journal of Hematology & Oncology · doi:10.1186/s13045-019-0804-8 · Cited by 215 · see citing works
Bishnupuri, K. S., Alvarado, D. M., Khouri, A. N., Shabsovich, M., Chen, B., Dieckgraefe, B. K., & Ciorba, M. A. (2019) · Cancer Research · doi:10.1158/0008-5472.can-18-0668 · Cited by 212 · see citing works
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Prendergast, G. C., Mondal, A., Dey, S., Laury‐Kleintop, L. D., & Muller, A. J. (2017) · Trends in cancer · doi:10.1016/j.trecan.2017.11.005 · Cited by 198 · see citing works
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Nayak-Kapoor, A., Hao, Z., Sadek, R., Dobbins, R., Marshall, L., Vahanian, N. N., Ramsey, W. J., Kennedy, E. P., Mautino, M. R., Link, C. J., et al. (2018) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-018-0351-9 · Cited by 163 · see citing works
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Wang, Y., Wang, Y., Ren, Y., Zhang, Q., Yi, P., & Cheng, C. (2022) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2022.02.010 · Cited by 146 · see citing works
A phase I study of indoximod in patients with advanced malignancies
Soliman, H. H., Minton, S. E., Han, H. S., Ismail-Khan, R. R., Neuger, A. M., Khambati, F. A., Noyes, D. R., Lush, R. M., Chiappori, A., Roberts, J. D., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.8216 · Cited by 145 · see citing works
Crosignani, S., Bingham, P., Bottemanne, P., Cannelle, H., Cauwenberghs, S., Cordonnier, M., Dalvie, D., Deroose, F. D., Feng, J. L., Gomes, B., et al. (2017) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.7b00974 · Cited by 144 · see citing works
Indoleamine 2,3-dioxygenase (Ido) inhibitors and their nanomedicines for cancer immunotherapy
Guo, Y., Liu, Y., Wu, W., Ling, D., Zhang, Q., Peng, Z. M., & Hu, X. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.121018 · Cited by 132 · see citing works
Limitations and Off-Target Effects of Tryptophan-Related IDO Inhibitors in Cancer Treatment
Günther, J., Däbritz, J., & Wirthgen, E. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01801 · Cited by 133 · see citing works
Kynurenine emerges from the shadows – Current knowledge on its fate and function
Marszałek‐Grabska, M., Walczak, K., Gaweł, K., Wicha-Komsta, K., Wnorowska, S., Wnorowski, A., & Turski, W. A. (2021) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.107845 · Cited by 126 · see citing works
Targeting Tryptophan Catabolism in Cancer Immunotherapy Era: Challenges and Perspectives
Peyraud, F., Guégan, J., Bodet, D., Cousin, S., Bessede, A., & Italiano, A. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.807271 · Cited by 130 · see citing works
Mechanisms of resistance to immune checkpoint inhibitors
Nagasaki, J., Ishino, T., & Togashi, Y. (2022) · Cancer Science · doi:10.1111/cas.15497 · Cited by 127 · see citing works
Tuning the Tumor Myeloid Microenvironment to Fight Cancer
Jahchan, N. S., Mujal, A. M., Pollack, J. L., Binnewies, M., Sriram, V., Reyno, L. M., & Krummel, M. F. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01611 · Cited by 120 · see citing works
Microenvironmental influences on T cell immunity in cancer and inflammation
Heintzman, D. R., Fisher, E. L., & Rathmell, J. C. (2022) · Cellular and Molecular Immunology · doi:10.1038/s41423-021-00833-2 · Cited by 119 · see citing works
Li, Z., Song, W., Rubinstein, M. P., & Liu, D. (2018) · Journal of Hematology & Oncology · doi:10.1186/s13045-018-0684-3 · Cited by 118 · see citing works
Chen, B., Alvarado, D. M., Iticovici, M. S., Kau, N. S., Park, H., Parikh, P. J., Thotala, D. K., & Ciorba, M. A. (2020) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-19-0282 · Cited by 118 · see citing works
The footprint of kynurenine pathway in every cancer: a new target for chemotherapy
Ala, M. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.173921 · Cited by 108 · see citing works
Kristeleit, R. S., Давиденко, І., Shirinkin, V., El-Khouly, F., Bondarenko, I., Goodheart, M. J., Горбунова, В. А., Penning, C. A., Shi, J. G., Liu, X., et al. (2017) · Gynecologic Oncology · doi:10.1016/j.ygyno.2017.07.005 · Cited by 100 · see citing works
Self-citationTargeting indoleamine-2,3-dioxygenase in cancer: Scientific rationale and clinical evidence
Ricciuti, B., Leonardi, G. C., Puccetti, P., Fallarino, F., Bianconi, V., Sahebkar, A., Baglivo, S., Chiari, R., & Pirro, M. (2018) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2018.12.004 · Cited by 96 · see citing works
The evolving landscape of ‘next-generation’ immune checkpoint inhibitors: A review
Mazzarella, L., Duso, B. A., Trapani, D., Belli, C., D’Amico, P., Ferraro, E., Viale, G., & Curigliano, G. (2019) · European Journal of Cancer · doi:10.1016/j.ejca.2019.04.035 · Cited by 98 · see citing works
Dill, E. A., Dillon, P. M., Bullock, T. N. J., & Mills, A. M. (2018) · Modern Pathology · doi:10.1038/s41379-018-0061-3 · Cited by 92 · see citing works
Beyond CTLA-4 and PD-1 Inhibition: Novel Immune Checkpoint Molecules for Melanoma Treatment
Ziogas, D. C., Theocharopoulos, C., Lialios, P., Foteinou, D., Koumprentziotis, I., Xynos, G., & Gogas, H. J. (2023) · Cancers · doi:10.3390/cancers15102718 · Cited by 92 · see citing works
The aryl hydrocarbon receptor: structure, signaling, physiology and pathology
Coumoul, X., Barouki, R., Esser, C., Haarmann‐Stemmann, T., Lawrence, B. P., Lehmann, J., Moura‐Alves, P., Murray, I. A., Opitz, C. A., Perdew, G. H., et al. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02500-8 · Cited by 103 · see citing works
Kiyozumi, Y., Baba, Y., Okadome, K., Yagi, T., Ishimoto, T., Iwatsuki, M., Miyamoto, Y., Yoshida, N., Watanabe, M., Komohara, Y., et al. (2018) · Annals of Surgery · doi:10.1097/sla.0000000000002754 · Cited by 88 · see citing works
Recent advances in clinical trials targeting the kynurenine pathway
Pires, A. S., Sundaram, G., Heng, B., Krishnamurthy, S., Brew, B. J., & Guillemin, G. J. (2021) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.108055 · Cited by 84 · see citing works
Gomes, B., Driessens, G., Bartlett, D. W., Cai, D., Cauwenberghs, S., Crosignani, S., Dalvie, D., Denies, S., Dillon, C. P., Fantin, V. R., et al. (2018) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-17-1104 · Cited by 84 · see citing works
Gibney, G. T., Hamid, O., Lutzky, J., Olszanski, A. J., Mitchell, T. C., Gajewski, T. F., Chmielowski, B., Hanks, B. A., Zhao, Y., Newton, R. C., et al. (2019) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-019-0562-8 · Cited by 84 · see citing works
Self-citationGiglio, A. D., Federico, A. D., Nuvola, G., Deiana, C., & Gelsomino, F. (2021) · Current Oncology Reports · doi:10.1007/s11912-021-01124-9 · Cited by 83 · see citing works
Hong, D. S., Parikh, A. R., Shapiro, G. I., Varga, A., Naing, A., Meric‐Bernstam, F., Ataman, Ö., Reyderman, L., Binder, T. A., Ren, M., et al. (2020) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2019-000222 · Cited by 82 · see citing works
Present and future of cancer immunotherapy: A tumor microenvironmental perspective (Review)
Yu, Y., & Cui, J. (2018) · Oncology Letters · doi:10.3892/ol.2018.9219 · Cited by 78 · see citing works
Odunsi, K. O., Qian, F., Lugade, A. A., Yu, H., Geller, M. A., Fling, S. P., Kaiser, J. C., Lacroix, A. M., D’Amico, L., Ramchurren, N., et al. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abg8402 · Cited by 77 · see citing works
Next generation immune-checkpoints for cancer therapy
Donini, C., D’Ambrosio, L., Grignani, G., Aglietta, M., & Sangiolo, D. (2018) · Journal of Thoracic Disease · doi:10.21037/jtd.2018.02.79 · Cited by 72 · see citing works
A Phase II Study of Epacadostat and Pembrolizumab in Patients with Advanced Sarcoma
Kelly, C. M., Qin, L., Whiting, K. A., Richards, A. L., Avutu, V., Chan, J. E., Chi, P., Dickson, M. A., Gounder, M. M., Keohan, M. L., et al. (2023) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-22-3911 · Cited by 73 · see citing works
Indoleamine 2,3-Dioxygenase (IDO) Inhibition as a Strategy to Augment Cancer Immunotherapy
Yentz, S. E., & Smith, D. C. (2018) · BioDrugs · doi:10.1007/s40259-018-0291-4 · Cited by 70 · see citing works
Beyond PD-1/PD-L1 Inhibition: What the Future Holds for Breast Cancer Immunotherapy
Chrétien, S., Zerdes, I., Bergh, J. C. S., Matikas, A., & Foukakis, T. (2019) · Cancers · doi:10.3390/cancers11050628 · Cited by 70 · see citing works
IDO1 inhibition potentiates vaccine-induced immunity against pancreatic adenocarcinoma
Blair, A. B., Kleponis, J., Thomas, D. L., Muth, S. T., Murphy, A. G., Kim, V., & Zheng, L. (2019) · Journal of Clinical Investigation · doi:10.1172/jci124077 · Cited by 70 · see citing works
Kreidieh, M., Mukherji, D., Temraz, S. N., & Shamseddine, A. I. (2020) · BioMed Research International · doi:10.1155/2020/9037217 · Cited by 68 · see citing works
Metabolic reprogramming in colorectal cancer: regulatory networks and therapy
Zhang, J., Zou, S., & Fang, L. (2023) · Cell & Bioscience · doi:10.1186/s13578-023-00977-w · Cited by 69 · see citing works
The Role of Indoleamine 2, 3-Dioxygenase 1 in Regulating Tumor Microenvironment
Huang, X., Zhang, F., Wang, X., & Liu, K. (2022) · Cancers · doi:10.3390/cancers14112756 · Cited by 66 · see citing works
Phan, T. X., Nguyen, V. H., Salazar, M. D., Manuel, E. R., Kaltcheva, T. I., Tsai, W., Blazar, B. R., Diamond, D. J., & Melstrom, L. G. (2019) · Cancer Gene Therapy · doi:10.1038/s41417-019-0089-7 · Cited by 65 · see citing works
Kao, H., & Lou, P. (2019) · Head & Neck · doi:10.1002/hed.25930 · Cited by 65 · see citing works
Kynurenine/Tryptophan Ratio as a Potential Blood-Based Biomarker in Non-Small Cell Lung Cancer
Mandarano, M., Orecchini, E., Bellezza, G., Vannucci, J., Ludovini, V., Baglivo, S., Tofanetti, F. R., Chiari, R., Loreti, E., Puma, F., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094403 · Cited by 64 · see citing works
Major Developments in the Design of Inhibitors along the Kynurenine Pathway
Jacobs, K. R., Castellano‐González, G., Guillemin, G. J., & Lovejoy, D. B. (2017) · Current Medicinal Chemistry · doi:10.2174/0929867324666170502123114 · Cited by 63 · see citing works
Li, J., Huang, J., Jiang, Z., Li, R., Sun, A., Leung, E. L., & Yan, P. (2019) · Integrative Cancer Therapies · doi:10.1177/1534735419890020 · Cited by 62 · see citing works
Dendritic Cell Vaccines in Ovarian Cancer
Zhang, X., He, T., Li, Y., Chen, L., Liu, H., Wu, Y., & Guo, H. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.613773 · Cited by 62 · see citing works
Reardon, D. A., Desjardins, A., Rixe, O., Cloughesy, T. F., Alekar, S., Williams, J. H., Li, R., Taylor, C. T., & Lassman, A. B. (2020) · Investigational New Drugs · doi:10.1007/s10637-020-00950-1 · Cited by 61 · see citing works
Fujiwara, Y., Mittra, A., Naqash, A. R., & Takebe, N. (2020) · Cancer Drug Resistance · doi:10.20517/cdr.2020.11 · Cited by 63 · see citing works
Advancing Cancer Therapy with Present and Emerging Immuno-Oncology Approaches
Kamta, J., Chaar, M., Ande, A., Altomare, D. A., & Ait‐Oudhia, S. (2017) · Frontiers in Oncology · doi:10.3389/fonc.2017.00064 · Cited by 61 · see citing works
Balog, A., Lin, T.-A., Maley, D., Gullo-Brown, J. L., Kandoussi, E. H., Zeng, J., & Hunt, J. T. (2020) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-20-0251 · Cited by 61 · see citing works
Adamantinomatous craniopharyngioma: moving toward targeted therapies
Hengartner, A. C., Prince, E. W., Vijmasi, T., & Hankinson, T. C. (2020) · Neurosurgical FOCUS · doi:10.3171/2019.10.focus19705 · Cited by 60 · see citing works
Can Metabolic Pathways Be Therapeutic Targets in Rheumatoid Arthritis?
Sánchez‐López, E., Cheng, A., & Gumá, M. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8050753 · Cited by 57 · see citing works
Affolter, T., Llewellyn, H. P., Bartlett, D. W., Zong, Q., Xia, S., Torti, V. R., & Ji, C. (2019) · PLoS ONE · doi:10.1371/journal.pone.0217276 · Cited by 58 · see citing works
Liang, F., Wang, G., Wang, Y., Yang, Y., Wen, Z., Chen, D. S., Fang, W., Zhang, B., Yang, L., Zhang, C., et al. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01127-3 · Cited by 55 · see citing works
Indoleamine Dioxygenase Inhibitors: Clinical Rationale and Current Development
Zhu, M. M. T., Dancsok, A. R., & Nielsen, T. O. (2019) · Current Oncology Reports · doi:10.1007/s11912-019-0750-1 · Cited by 55 · see citing works
Furazans in Medicinal Chemistry
Mancini, R. S., Barden, C., Weaver, D. F., & Reed, M. A. (2021) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.0c01901 · Cited by 54 · see citing works
Yu, Y., Liang, H., Fang, X., Zhang, S., Xing, Z., Shi, L., Kuang, C., Seliger, B., & Yang, Q. (2021) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-021-01847-4 · Cited by 54 · see citing works
Miyasato, Y., Takashima, Y., Takeya, H., Yano, H., Hayano, A., Nakagawa, T., Makino, K., Takeya, M., Yamanaka, R., & Komohara, Y. (2018) · Journal of the Japan Society of the Reticuloendothelial System · doi:10.3960/jslrt.18001 · Cited by 51 · see citing works
Anari, F. M., Ramamurthy, C., & Zibelman, M. R. (2018) · Future Oncology · doi:10.2217/fon-2017-0585 · Cited by 50 · see citing works
Chinn, Z., Stoler, M. H., & Mills, A. M. (2018) · Histopathology · doi:10.1111/his.13723 · Cited by 50 · see citing works
The Role of Immune Checkpoint Inhibitors in Colorectal Adenocarcinoma
Almquist, D., Ahn, D. H., & Bekaii‐Saab, T. (2020) · BioDrugs · doi:10.1007/s40259-020-00420-3 · Cited by 50 · see citing works
Mapping the Binding Trajectory of a Suicide Inhibitor in Human Indoleamine 2,3-Dioxygenase 1
Pham, K., & Yeh, S. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b07994 · Cited by 51 · see citing works
- Authors
- Beatty, G. L., O'Dwyer, P. J., Clark, J., Shi, J. G., Bowman, K. J., Scherle, P. A., Newton, R. C., Schaub, R., Maleski, J., Leopold, L., & Gajewski, T. F.
- Affiliations
- Abramson Cancer Center (US)
- Incyte (United States) (US)
- University of Chicago (US)
- Corresponding author
- Beatty, Gregory L.
- ORCID
- Venue
- Clinical Cancer Research
- Published
- 2017-07-01
- Volume
- 23
- Issue
- 13
- Pages
- 3269-3276
- ISSN
- 1078-0432 (ISSN-L)
- 1557-3265
- PMC
- PMC5496788
- OpenAlex
- W2570766240
- Cited by
- 314
- References
- 40
- Citations by year
- 2026: 14 · 2025: 18 · 2024: 42 · 2023: 21 · 2022: 26 · 2021: 36 · 2020: 33 · 2019: 44 · 2018: 53 · 2017: 24 · 2016: 1 · 2014: 2
- FWCI
- 18.80
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Clinical Cancer Research (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- University of Chicago
- Abramson Cancer Center
- National Cancer Institute (K08CA138907)
- Topics
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Keywords
- epacadostat, IDO1, IDO1 inhibitors, advanced solid tumors, kynurenine, kynurenine/tryptophan ratio, tryptophan degradation, tumor immunosuppression, radiation pneumonitis, dose-limiting toxicity, pharmacokinetics, pharmacodynamics, anticancer activity, maximum tolerated dose
- MeSH terms
- Administration, Oral, Adult, Aged, Dose-Response Relationship, Drug, Drug Administration Schedule, Female, Humans, Male, Middle Aged, Neoplasm Staging, Neoplasms, Oximes, Sulfonamides, Indoleamine-Pyrrole 2,3,-Dioxygenase, Drug-Related Side Effects and Adverse Reactions
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