癌症免疫疗法 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "癌症免疫疗法" in Chinese language version.

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68nih.gov

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64doi.org

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26web.archive.org

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8fda.gov

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3harvard.edu

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2cancer.gov

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2fiercebiotech.com

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2worldcat.org

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1drugs.com

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1asheducationbook.org

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1medicines.org.uk

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1hindawi.com

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1cancer.org

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1archive.today

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1technologyreview.com

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1clinicaltrials.gov

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1globenewswire.com

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1roche.com

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1curetoday.com

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1avactalifesciences.com

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archive.today

Regalado A. Biotech’s Coming Cancer Cure: Supercharge your immune cells to defeat cancer? Juno Therapeutics believes its treatments can do exactly that. MIT Technology Review. June 2015 [2018-10-04]. （原始内容存档于2015-06-20）.

asheducationbook.org

Byrd JC, Stilgenbauer S, Flinn IW. Chronic Lymphocytic Leukemia. （页面存档备份，存于互联网档案馆） Hematology (Am Soc Hematol Educ Program) 2004: 163-183. Date retrieved: 26/01/2006.

avactalifesciences.com

Avacta Life Sciences. Affimer biotherapeutics target cancer's off-switch with PD-L1 inhibitor. [2018-10-04]. （原始内容存档于2016-08-06）.

cancer.gov

Pazdur R. FDA approval for Ipilimumab. [2013-11-07]. （原始内容存档于2015-04-06）.
CAR T-Cell Therapy: Engineering Patients’ Immune Cells to Treat Their Cancers. cancer.gov. 2013-12-06 [2014-05-09]. （原始内容存档于2014-05-12）.

cancer.org

Coriolus Versicolor. American Cancer Society. （原始内容存档于2006-02-15）.

clinicaltrials.gov

Clinical trial number NCT01928394 for "A Study of Nivolumab by Itself or Nivolumab Combined With Ipilimumab in Patients With Advanced or Metastatic Solid Tumors" at ClinicalTrials.gov

curetoday.com

Cure today. Durvalumab continues to progress in treatment of advanced bladder cancer.. [2018-10-04]. （原始内容存档于2017-08-17）.

doi.org

Korneev KV, Atretkhany KN, Drutskaya MS, Grivennikov SI, Kuprash DV, Nedospasov SA. TLR-signaling and proinflammatory cytokines as drivers of tumorigenesis. Cytokine. January 2017, 89: 127–135. PMID 26854213. doi:10.1016/j.cyto.2016.01.021.
Riddell SR. Progress in cancer vaccines by enhanced self-presentation. Proceedings of the National Academy of Sciences of the United States of America. July 2001, 98 (16): 8933–5. Bibcode:2001PNAS...98.8933R. PMC 55350 . PMID 11481463. doi:10.1073/pnas.171326398.
Palucka K, Banchereau J. Dendritic-cell-based therapeutic cancer vaccines. Immunity. July 2013, 39 (1): 38–48. PMC 3788678 . PMID 23890062. doi:10.1016/j.immuni.2013.07.004.
Hirayama M, Nishimura Y. The present status and future prospects of peptide-based cancer vaccines. International Immunology. July 2016, 28 (7): 319–28. PMID 27235694. doi:10.1093/intimm/dxw027.
Gardner TA, Elzey BD, Hahn NM. Sipuleucel-T (Provenge) autologous vaccine approved for treatment of men with asymptomatic or minimally symptomatic castrate-resistant metastatic prostate cancer. Human Vaccines & Immunotherapeutics. April 2012, 8 (4): 534–9. PMID 22832254. doi:10.4161/hv.19795.
Oudard S. Progress in emerging therapies for advanced prostate cancer. Cancer Treatment Reviews. May 2013, 39 (3): 275–89. PMID 23107383. doi:10.1016/j.ctrv.2012.09.005.
Sims RB. Development of sipuleucel-T: autologous cellular immunotherapy for the treatment of metastatic castrate resistant prostate cancer. Vaccine. June 2012, 30 (29): 4394–7. PMID 22122856. doi:10.1016/j.vaccine.2011.11.058.
Shore ND, Mantz CA, Dosoretz DE, Fernandez E, Myslicki FA, McCoy C, Finkelstein SE, Fishman MN. Building on sipuleucel-T for immunologic treatment of castration-resistant prostate cancer. Cancer Control. January 2013, 20 (1): 7–16. PMID 23302902. doi:10.1177/107327481302000103.
Scott AM, Wolchok JD, Old LJ. Antibody therapy of cancer. Nature Reviews. Cancer. March 2012, 12 (4): 278–87. PMID 22437872. doi:10.1038/nrc3236.
Harding FA, Stickler MM, Razo J, DuBridge RB. The immunogenicity of humanized and fully human antibodies: residual immunogenicity resides in the CDR regions. MAbs. May–Jun 2010, 2 (3): 256–65. PMC 2881252 . PMID 20400861. doi:10.4161/mabs.2.3.11641.
Pincetic A, Bournazos S, DiLillo DJ, Maamary J, Wang TT, Dahan R, Fiebiger BM, Ravetch JV. Type I and type II Fc receptors regulate innate and adaptive immunity. Nature Immunology. August 2014, 15 (8): 707–16. PMID 25045879. doi:10.1038/ni.2939.
Topalian SL, Hodi FS, Brahmer JR, Gettinger SN, Smith DC, McDermott DF, Powderly JD, Carvajal RD, Sosman JA, Atkins MB, Leming PD, Spigel DR, Antonia SJ, Horn L, Drake CG, Pardoll DM, Chen L, Sharfman WH, Anders RA, Taube JM, McMiller TL, Xu H, Korman AJ, Jure-Kunkel M, Agrawal S, McDonald D, Kollia GD, Gupta A, Wigginton JM, Sznol M. Safety, activity, and immune correlates of anti-PD-1 antibody in cancer. The New England Journal of Medicine. June 2012, 366 (26): 2443–54. PMC 3544539 . PMID 22658127. doi:10.1056/NEJMoa1200690.
Dahan R, Sega E, Engelhardt J, Selby M, Korman AJ, Ravetch JV. FcγRs Modulate the Anti-tumor Activity of Antibodies Targeting the PD-1/PD-L1 Axis. Cancer Cell. October 2015, 28 (4): 543. PMID 28854351. doi:10.1016/j.ccell.2015.09.011.
Arlauckas SP, Garris CS, Kohler RH, Kitaoka M, Cuccarese MF, Yang KS, Miller MA, Carlson JC, Freeman GJ, Anthony RM, Weissleder R, Pittet MJ. In vivo imaging reveals a tumor-associated macrophage-mediated resistance pathway in anti-PD-1 therapy. Science Translational Medicine. May 2017, 9 (389): eaal3604. PMC 5734617 . PMID 28490665. doi:10.1126/scitranslmed.aal3604.
Dahan R, Barnhart BC, Li F, Yamniuk AP, Korman AJ, Ravetch JV. Therapeutic Activity of Agonistic, Human Anti-CD40 Monoclonal Antibodies Requires Selective FcγR Engagement. Cancer Cell. July 2016, 29 (6): 820–831. PMC 4975533 . PMID 27265505. doi:10.1016/j.ccell.2016.05.001.
Weiner LM, Surana R, Wang S. Monoclonal antibodies: versatile platforms for cancer immunotherapy. Nature Reviews. Immunology. May 2010, 10 (5): 317–27. PMC 3508064 . PMID 20414205. doi:10.1038/nri2744.
Seidel UJ, Schlegel P, Lang P. Natural killer cell mediated antibody-dependent cellular cytotoxicity in tumor immunotherapy with therapeutic antibodies. Frontiers in Immunology. 2013, 4: 76. PMC 3608903 . PMID 23543707. doi:10.3389/fimmu.2013.00076.
Gelderman KA, Tomlinson S, Ross GD, Gorter A. Complement function in mAb-mediated cancer immunotherapy. Trends in Immunology. March 2004, 25 (3): 158–64. PMID 15036044. doi:10.1016/j.it.2004.01.008.
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Demko S, Summers J, Keegan P, Pazdur R. FDA drug approval summary: alemtuzumab as single-agent treatment for B-cell chronic lymphocytic leukemia. The Oncologist. February 2008, 13 (2): 167–74. PMID 18305062. doi:10.1634/theoncologist.2007-0218.
Lemery SJ, Zhang J, Rothmann MD, Yang J, Earp J, Zhao H, McDougal A, Pilaro A, Chiang R, Gootenberg JE, Keegan P, Pazdur R. U.S. Food and Drug Administration approval: ofatumumab for the treatment of patients with chronic lymphocytic leukemia refractory to fludarabine and alemtuzumab. Clinical Cancer Research. September 2010, 16 (17): 4331–8. PMID 20601446. doi:10.1158/1078-0432.CCR-10-0570.
Sharma P, Allison JP. The future of immune checkpoint therapy. Science. April 2015, 348 (6230): 56–61. Bibcode:2015Sci...348...56S. PMID 25838373. doi:10.1126/science.aaa8172.
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Sondak VK, Smalley KS, Kudchadkar R, Grippon S, Kirkpatrick P. Ipilimumab. Nature Reviews. Drug Discovery. June 2011, 10 (6): 411–2. PMID 21629286. doi:10.1038/nrd3463.
Lipson EJ, Drake CG. Ipilimumab: an anti-CTLA-4 antibody for metastatic melanoma. Clinical Cancer Research. November 2011, 17 (22): 6958–62. PMC 3575079 . PMID 21900389. doi:10.1158/1078-0432.CCR-11-1595.
Chambers CA, Kuhns MS, Egen JG, Allison JP. CTLA-4-mediated inhibition in regulation of T cell responses: mechanisms and manipulation in tumor immunotherapy. Annual Review of Immunology. 2001, 19: 565–94. PMID 11244047. doi:10.1146/annurev.immunol.19.1.565.
Castillo J, Perez K. The role of ofatumumab in the treatment of chronic lymphocytic leukemia resistant to previous therapies. Journal of Blood Medicine. 2010, 1: 1–8. PMC 3262337 . PMID 22282677. doi:10.2147/jbm.s7284.
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Keating GM. Rituximab: a review of its use in chronic lymphocytic leukaemia, low-grade or follicular lymphoma and diffuse large B-cell lymphoma. Drugs. July 2010, 70 (11): 1445–76. PMID 20614951. doi:10.2165/11201110-000000000-00000.
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Cerny T, Borisch B, Introna M, Johnson P, Rose AL. Mechanism of action of rituximab. Anti-Cancer Drugs. November 2002,. 13 Suppl 2: S3–10. PMID 12710585. doi:10.1097/00001813-200211002-00002.
Weiner GJ. Rituximab: mechanism of action. Seminars in Hematology. April 2010, 47 (2): 115–23. PMC 2848172 . PMID 20350658. doi:10.1053/j.seminhematol.2010.01.011.
Dranoff G. Cytokines in cancer pathogenesis and cancer therapy. Nature Reviews. Cancer. January 2004, 4 (1): 11–22. PMID 14708024. doi:10.1038/nrc1252.
Dunn GP, Koebel CM, Schreiber RD. Interferons, immunity and cancer immunoediting. Nature Reviews. Immunology. November 2006, 6 (11): 836–48. PMID 17063185. doi:10.1038/nri1961.
Lasfar A, Abushahba W, Balan M, Cohen-Solal KA. Interferon lambda: a new sword in cancer immunotherapy. Clinical & Developmental Immunology. 2011, 2011: 349575. PMC 3235441 . PMID 22190970. doi:10.1155/2011/349575.
Razaghi A, Owens L, Heimann K. Review of the recombinant human interferon gamma as an immunotherapeutic: Impacts of production platforms and glycosylation. Journal of Biotechnology. December 2016, 240: 48–60. PMID 27794496. doi:10.1016/j.jbiotec.2016.10.022.
Coventry BJ, Ashdown ML. The 20th anniversary of interleukin-2 therapy: bimodal role explaining longstanding random induction of complete clinical responses. Cancer Management and Research. 2012, 4: 215–21. PMC 3421468 . PMID 22904643. doi:10.2147/cmar.s33979.
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Mahoney KM, Rennert PD, Freeman GJ. Combination cancer immunotherapy and new immunomodulatory targets. Nature Reviews. Drug Discovery. August 2015, 14 (8): 561–84. PMID 26228759. doi:10.1038/nrd4591.
Tang J, Shalabi A, Hubbard-Lucey VM. Comprehensive analysis of the clinical immuno-oncology landscape. Annals of Oncology. January 2018, 29 (1): 84–91. PMID 29228097. doi:10.1093/annonc/mdx755.
Perry CJ, Muñoz-Rojas AR, Meeth KM, Kellman LN, Amezquita RA, Thakral D, Du VY, Wang JX, Damsky W, Kuhlmann AL, Sher JW, Bosenberg M, Miller-Jensen K, Kaech SM. Myeloid-targeted immunotherapies act in synergy to induce inflammation and antitumor immunity. The Journal of Experimental Medicine. March 2018, 215 (3): 877–893. PMID 29436395. doi:10.1084/jem.20171435.
Rodell CB, Arlauckas SP, Cuccarese MF, Garris CS, Li R, Ahmed MS, Kohler RH, Pittet MJ, Weissleder R. TLR7/8-agonist-loaded nanoparticles promote the polarization of tumour-associated macrophages to enhance cancer immunotherapy. Nature Biomedical Engineering. 2018-05-21. doi:10.1038/s41551-018-0236-8.
Restifo NP, Dudley ME, Rosenberg SA. Adoptive immunotherapy for cancer: harnessing the T cell response. Nature Reviews. Immunology. March 2012, 12 (4): 269–81. PMID 22437939. doi:10.1038/nri3191.
Andersen R, Borch TH, Draghi A, Gokuldass A, Rana MA, Pedersen M, Nielsen M, Kongsted P, Kjeldsen JW, Westergaard MC, Radic HD, Chamberlain CA, Holmich LR, Hendel HW, Larsen MS, Met O, Svane IM, Donia M. T cells isolated from patients with checkpoint inhibitor resistant-melanoma are functional and can mediate tumor regression.. Ann. Oncol. April 2018. PMID 29688262. doi:10.1093/annonc/mdy139.
Wilhelm M, Smetak M, Schaefer-Eckart K, Kimmel B, Birkmann J, Einsele H, Kunzmann V. Successful adoptive transfer and in vivo expansion of haploidentical γδ T cells. Journal of Translational Medicine. February 2014, 12: 45. PMC 3926263 . PMID 24528541. doi:10.1186/1479-5876-12-45.
Jaiswal S, Chao MP, Majeti R, Weissman IL. Macrophages as mediators of tumor immunosurveillance. Trends in Immunology. June 2010, 31 (6): 212–9. PMC 3646798 . PMID 20452821. doi:10.1016/j.it.2010.04.001.
Weiskopf K. Cancer immunotherapy targeting the CD47/SIRPα axis. European Journal of Cancer. May 2017, 76: 100–109. PMID 28286286. doi:10.1016/j.ejca.2017.02.013.
Matlung HL, Szilagyi K, Barclay NA, van den Berg TK. The CD47-SIRPα signaling axis as an innate immune checkpoint in cancer. Immunological Reviews. March 2017, 276 (1): 145–164. PMID 28258703. doi:10.1111/imr.12527.
Veillette A, Chen J. SIRPα-CD47 Immune Checkpoint Blockade in Anticancer Therapy. Trends in Immunology. March 2018, 39 (3): 173–184. PMID 29336991. doi:10.1016/j.it.2017.12.005.
Ahmed M, Cheung NK. Engineering anti-GD2 monoclonal antibodies for cancer immunotherapy. FEBS Letters. January 2014, 588 (2): 288–97. PMID 24295643. doi:10.1016/j.febslet.2013.11.030.
Pardoll DM. The blockade of immune checkpoints in cancer immunotherapy. Nature Reviews. Cancer. March 2012, 12 (4): 252–64. PMC 4856023 . PMID 22437870. doi:10.1038/nrc3239.
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Cameron F, Whiteside G, Perry C. Ipilimumab: first global approval. Drugs. May 2011, 71 (8): 1093–104. PMID 21668044. doi:10.2165/11594010-000000000-00000.
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van Hooren L, Sandin LC, Moskalev I, Ellmark P, Dimberg A, Black P, Tötterman TH, Mangsbo SM. Local checkpoint inhibition of CTLA-4 as a monotherapy or in combination with anti-PD1 prevents the growth of murine bladder cancer. European Journal of Immunology. February 2017, 47 (2): 385–393. PMID 27873300. doi:10.1002/eji.201646583.
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Aleem E. β-Glucans and their applications in cancer therapy: focus on human studies. Anti-Cancer Agents in Medicinal Chemistry. June 2013, 13 (5): 709–19. PMID 23140353. doi:10.2174/1871520611313050007.
Snyder A, Makarov V, Merghoub T, Yuan J, Zaretsky JM, Desrichard A, Walsh LA, Postow MA, Wong P, Ho TS, Hollmann TJ, Bruggeman C, Kannan K, Li Y, Elipenahli C, Liu C, Harbison CT, Wang L, Ribas A, Wolchok JD, Chan TA. Genetic basis for clinical response to CTLA-4 blockade in melanoma. The New England Journal of Medicine. December 2014, 371 (23): 2189–2199. PMC 4315319 . PMID 25409260. doi:10.1056/NEJMoa1406498.
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drugs.com

Opdivo Drug Approval History. [2018-10-04]. （原始内容存档于2017-12-29）.

fda.gov

Commissioner, Office of the. Press Announcements - FDA approval brings first gene therapy to the United States. www.fda.gov. [2017-12-13]. （原始内容存档于2017-09-03）（英语）.
FDA approves CAR-T cell therapy to treat adults with certain types of large B-cell lymphoma. fda.gov. 2017-10-18 [2017-11-08]. （原始内容存档于2017-11-08）.
FDA approves new, targeted treatment for bladder cancer. FDA. 2016-05-18 [2016-05-20]. （原始内容存档于2018-04-24）.
Research, Center for Drug Evaluation and. Approved Drugs - Durvalumab (Imfinzi). www.fda.gov. [2017-05-06]. （原始内容存档于2017-05-08）（英语）.
FDA approves durvalumab after chemoradiation for unresectable stage III NSCLC. （原始内容存档于2018-07-25）.
FDA approval brings first gene therapy to the United States. fda.gov. 2017-08-30 [2017-11-08]. （原始内容存档于2017-09-03）.

accessdata.fda.gov

US Food and Drug Administration - Avelumab Prescribing Label (PDF). （原始内容存档 (PDF)于2017-03-24）.
Pembrolizumab label (PDF). FDA. May 2017 [2018-10-04]. （原始内容存档 (PDF)于2020-10-17）. linked from Index page at FDA website （页面存档备份，存于互联网档案馆） November 2016

fiercebiotech.com

Carroll J. Novartis/Penn's customized T cell wows ASH with stellar leukemia data. Fierce Biotech. December 2013 [2018-10-04]. （原始内容存档于2016-03-04）.
Carroll, John. Servier stages an entry into high-stakes CAR-T showdown with Novartis. FierceBiotech. February 2014 [2018-10-04]. （原始内容存档于2016-03-03）.

globenewswire.com

BeiGene, Ltd. BeiGene Presents Initial Clinical Data on PD-1 Antibody BGB-A317 at the 2016 American Society of Clinical Oncology Annual Meeting. Globe Newswire. [2018-10-04]. （原始内容存档于2017-08-24）.

harvard.edu

ui.adsabs.harvard.edu

Riddell SR. Progress in cancer vaccines by enhanced self-presentation. Proceedings of the National Academy of Sciences of the United States of America. July 2001, 98 (16): 8933–5. Bibcode:2001PNAS...98.8933R. PMC 55350 . PMID 11481463. doi:10.1073/pnas.171326398.
Sharma P, Allison JP. The future of immune checkpoint therapy. Science. April 2015, 348 (6230): 56–61. Bibcode:2015Sci...348...56S. PMID 25838373. doi:10.1126/science.aaa8172.
Schumacher TN, Schreiber RD. Neoantigens in cancer immunotherapy. Science. April 2015, 348 (6230): 69–74. Bibcode:2015Sci...348...69S. PMID 25838375. doi:10.1126/science.aaa4971.

hindawi.com

Thermal Ablative Therapies and Immune Checkpoint Modulation: Can Locoregional Approaches Effect a Systemic Response?. 2015 [2018-10-04]. （原始内容存档于2018-06-02）.

medicines.org.uk

Pembrolizumab label at eMC. UK Electronic Medicines Compendium. 2017-01-27 [2018-10-04]. （原始内容存档于2017-12-13）.

merckgroup.com

Merck Group. Immuno-oncology Avelumab. [2018-10-04]. （原始内容存档于2017-06-11）.

nih.gov

ncbi.nlm.nih.gov

Korneev KV, Atretkhany KN, Drutskaya MS, Grivennikov SI, Kuprash DV, Nedospasov SA. TLR-signaling and proinflammatory cytokines as drivers of tumorigenesis. Cytokine. January 2017, 89: 127–135. PMID 26854213. doi:10.1016/j.cyto.2016.01.021.
Riddell SR. Progress in cancer vaccines by enhanced self-presentation. Proceedings of the National Academy of Sciences of the United States of America. July 2001, 98 (16): 8933–5. Bibcode:2001PNAS...98.8933R. PMC 55350 . PMID 11481463. doi:10.1073/pnas.171326398.
Palucka K, Banchereau J. Dendritic-cell-based therapeutic cancer vaccines. Immunity. July 2013, 39 (1): 38–48. PMC 3788678 . PMID 23890062. doi:10.1016/j.immuni.2013.07.004.
Hirayama M, Nishimura Y. The present status and future prospects of peptide-based cancer vaccines. International Immunology. July 2016, 28 (7): 319–28. PMID 27235694. doi:10.1093/intimm/dxw027.
Gardner TA, Elzey BD, Hahn NM. Sipuleucel-T (Provenge) autologous vaccine approved for treatment of men with asymptomatic or minimally symptomatic castrate-resistant metastatic prostate cancer. Human Vaccines & Immunotherapeutics. April 2012, 8 (4): 534–9. PMID 22832254. doi:10.4161/hv.19795.
Oudard S. Progress in emerging therapies for advanced prostate cancer. Cancer Treatment Reviews. May 2013, 39 (3): 275–89. PMID 23107383. doi:10.1016/j.ctrv.2012.09.005.
Sims RB. Development of sipuleucel-T: autologous cellular immunotherapy for the treatment of metastatic castrate resistant prostate cancer. Vaccine. June 2012, 30 (29): 4394–7. PMID 22122856. doi:10.1016/j.vaccine.2011.11.058.
Shore ND, Mantz CA, Dosoretz DE, Fernandez E, Myslicki FA, McCoy C, Finkelstein SE, Fishman MN. Building on sipuleucel-T for immunologic treatment of castration-resistant prostate cancer. Cancer Control. January 2013, 20 (1): 7–16. PMID 23302902. doi:10.1177/107327481302000103.
Scott AM, Wolchok JD, Old LJ. Antibody therapy of cancer. Nature Reviews. Cancer. March 2012, 12 (4): 278–87. PMID 22437872. doi:10.1038/nrc3236.
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