[1]Bianchini G, Balko JM, Mayer IA, et al. Triple-negative breast cancer: challenges and opportunities of a heterogeneousdisease[J]. Nat Rev Clin Oncol, 2016,13(11):674-690.
[2]Rigiracciolo DC, Nohata N, Lappano R, et al. IGF-1/IGF-1R/FAK/YAP Transduction Signaling Prompts Growth Effects in Triple-Negative Breast Cancer (TNBC) Cells[J]. Cells, 2020,9(4):1010.
[3]Lin NU, Vanderplas A, Hughes ME, et al. Clinicopathologic features, patterns of recurrence and survival among women with triple-negative breast cancer in the National Comprehensive Cancer Network[J]. Cancer, 2012, 118(22): 5463-5472.
[4]Fosu-Mensah N, Peris MS, Weeks HP, et al. Advances in small-molecule drug discovery for triple-negative breast cancer[J]. Future Med Chem, 2015,7(15):2019-2039.
[5]Hwang S, Park S, Kwon Y. Recent therapeutic trends and promising targets in triple negative breastcancer[J]. Pharmacol Ther, 2019, 199:30-57.
[6]Lotfinejad P, Kazemi T, Mokhtarzadeh A, et al. PD-1/PD-L1 axis importance and tumor microenvironment immune cells[J]. Life Sci, 2020, 259:118297.
[7]Hollern DP, Xu N, Thennavan A, et al. B Cells and T Follicular Helper Cells Mediate Response to Checkpoint Inhibitors in High Mutation Burden Mouse Models of Breast Cancer[J]. Cell,2019,179(5):1191-1206.
[8]Seidel JA, Otsuka A, Kabashima K. Anti-PD-1 and anti-CTLA-4 therapies incancer: mechanisms of action, efficacy,and limitations[J]. Front Oncol,2018,8:86.
[9]Asano Y, Kashiwagi S, Goto W, et al. Prediction of treatment responses to neoadjuvant chemotherapy in triple-negative breast cancer by analysis of immune checkpoint protein expression[J]. J Transl Med,2018,16(1):87.
[10]Kwa MJ, Adams S. Checkpoint inhibitors in triple-negative breast cancer(TNBC):where to go from here[J]. Cancer-Am Cancer Soc,2018,124(10):2086-2103.
[11]Qin G, Wang X, Ye S, et al. NPM1 upregulates the transcription of PD-L1 and suppresses T cell activity in triple-negative breast cancer[J]. Nat Commun, 2020,11(1):1669.
[12]Wang Y, Wang H, Yao H, et al.Regulation of PD-L1: emerging routes for targeting tumor immuneevasion[J]. Front Pharmacol, 2018,9:536.
[13]Mazza C, Escudier B, Albiges L. Nivolumab in renal cell carcinoma: latest evidence and clinicalpotential[J]. Ther Adv Med Oncol,2017,9(3):171-181.
[14]Voorwerk L, Slagter M, Horlings HM, et al. Immune induction strategies in metastatic triple-negative breast cancer to enhance the sensitivity to PD-1 blockade: the TONIC trial[J]. Nat Med,2019,25(6):920-928.
[15]Kleef R, Moss R, Szasz AM, et al. Complete Clinical Remission of Stage IV Triple-Negative Breast Cancer Lung Metastasis Administering Low-Dose Immune Checkpoint Blockade in Combination With Hyperthermia and Interleukin-2[J]. Integr Cancer Ther, 2018,17(4):1297-1303.
[16]Cortes J, Cescon DW, Rugo HS, et al.Pembrolizumab plus chemotherapy versus placebo plus chemotherapy for previously untreated locally recurrent inoperable or metastatic triple-negative breast cancer (KEYNOTE-355): a randomised, placebo-controlled, double-blind, phase 3 clinical trial[J]. Lancet, 2020,396(10265):1817-1828.
[17]Kwapisz D. Pembrolizumab and atezolizumab in triple-negative breastcancer[J]. Cancer Immunol Immunother, 2021,70(3):607-617.
[18]Amens LA, Cruz C, Eder JP, et al. Long-term clinical outcomes and biomarker analyses of atezolizumab therapy for patients with metastatic triple-negative breastcancer[J]. JAMA Oncol,2019,5(1):74.
[19]Mohan N, Hosain S, Zhao J, et al. Atezolizumab potentiates Tcell-mediated cytotoxicity and coordinates with FAK to suppress cell invasion and motility in PD-L1+triple negative breast cancer cells[J]. Oncoimmunology,2019,8(9):e1624128.
[20]Loibl S, Untch M, Burchardi N, et al. A randomised phase Ⅱ study investigating durvalumab in addition to an anthracycline taxane-based neoadjuvant therapy in earlytriple-negative breast cancer: clinical results and biomarker analysis of GeparNuevo study[J]. Ann Oncol,2019, 30(8):1279-1288.
[21]Tarantino P, Gandini S, Trapani D, et al.Immunotherapy addition to neoadjuvant chemotherapy for early triple negative breast cancer: A systematic review and meta-analysis of randomized clinicaltrials[J]. Crit Rev Oncol Hematol, 2021,159:103223.
[22]Dirix LY, Takacs I, Jerusalem G, et al. Avelumab, an anti-PD-L1 antibody, in patients with locally advanced or metastatic breast cancer: a phase 1b JAVELIN Solid Tumor study[J]. Breast Cancer Res Treat,2018,167(3): 671-686.
[23]Kadono T. Immune-related adverse events by immune checkpointinhibitors[J]. Nihon Rinsho Meneki Gakkai Kaishi,2017,40(2):83-89.
[24]Ramos-Casals M, Brahmer JR, Callahan MK, et al. Immune-related adverse events of checkpoint inhibitors[J]. Nat Rev Dis Primers,2020,6(1):38.
[25]Geisler AN, Phillips GS, Barrios DM,et al. Immune checkpoint inhibitor-related dermatologic adverse events[J]. J Am Acad Dermatol,2020,83(5):1255-1268.
[26]Bukamur H, Katz H, Alsharedi M, et al. Immune Checkpoint Inhibitor-Related Pulmonary Toxicity: Focus on Nivolumab[J]. South Med J,2020,113(11):600-605.