乳腺癌是全球女性面临的主要健康威胁之一,其发病率居高不下。幸运的是,随着医学研究的不断深入,新的治疗策略层出不穷,其中免疫检查点抑制剂(Immune Checkpoint Inhibitor, ICI)的出现,为乳腺癌治疗带来了革命性的变化。ICI通过重新激活人体自身的免疫系统来对抗癌细胞,在多种癌症中显示出显著疗效。本文将聚焦ICI在不同类型乳腺癌(包括激素受体阳性型、HER2过表达型和三阴性乳腺癌)中的最新临床研究进展,探讨其应用前景与挑战,希望能为关注乳腺癌治疗,特别是对靶向药、免疫治疗药物感兴趣的患者和家属提供有价值的参考信息。
HR阳性乳腺癌:ICI治疗的新探索
激素受体(HR)阳性乳腺癌是最常见的亚型,约占所有病例的70%-75%。虽然内分泌治疗是其主要手段,但部分患者仍会面临耐药或复发。近年来,ICI联合疗法为这类患者带来了新的希望。
早期HR阳性乳腺癌的治疗进展
在新辅助治疗(术前治疗)领域,多项研究显示ICI联合化疗能提高疗效。例如:
- KEYNOTE-756研究:这项大型III期临床试验评估了帕博利珠单抗(Pembrolizumab)联合化疗用于高风险早期ER阳性/HER2阴性乳腺癌的效果。结果显示,与单纯化疗相比,加入帕博利珠单抗显著提高了病理学完全缓解(pCR,指手术切除的组织中检测不到浸润性癌细胞)率。值得注意的是,PD-L1表达水平越高的患者,从帕博利珠单抗治疗中获益似乎越大。
- CheckMate 7FL研究:该研究评估了另一种ICI药物纳武利尤单抗(Nivolumab)联合化疗的效果,同样观察到pCR率的提高,尤其是在PD-L1阳性的患者中。
这两项研究提示,对于部分高风险的早期HR阳性乳腺癌患者,新辅助ICI联合化疗可能是一种有效的策略。然而,研究也发现在亚洲人群(包括中国亚组)中,pCR率的提高并不显著,这可能与人种差异、样本量或肿瘤生物学特性有关,需要进一步研究。此外,对于ER低表达(1%-10%)的HER2阴性乳腺癌,PROMENADE研究发现其对ICI治疗的反应更接近三阴性乳腺癌(TNBC),提示这类患者或许应按照TNBC的管理策略进行治疗。
Neo-CheckRay研究还探索了新辅助化疗联合放疗(SBRT)和度伐利尤单抗(Durvalumab)的疗效,初步结果显示这种联合方式安全可行,并可能对PD-L1阴性的“冷肿瘤”患者带来获益。
晚期HR阳性乳腺癌的联合策略
对于晚期或转移性HR阳性乳腺癌,ICI与其他药物的联合也在积极探索中:
- SACI-IO研究:初步评估了抗体药物偶联物(ADC)戈沙妥珠单抗(Sacituzumab Govitecan, SG)联合帕博利珠单抗的疗效。虽然总体人群的生存期改善不明显,但在PD-L1阳性亚组中观察到积极趋势。
- DOLAF研究:探索了PARP抑制剂奥拉帕利(Olaparib)、度伐利尤单抗和内分泌治疗药物氟维司群的联合方案。结果显示,在携带特定基因突变(如BRCA)或对PARP抑制剂可能敏感的患者中,该联合方案展现出良好的疗效和可接受的安全性。
这些研究表明,ICI联合ADC或PARP抑制剂可能为特定的晚期HR阳性乳腺癌患者群体带来新的治疗选择。对于需要这些前沿靶向药、免疫治疗药物或ADC药物的患者,了解可靠的海外购药渠道,例如MedFind提供的代购服务,可能有助于获得治疗所需药品,同时也需要关注相关药物的价格和可能的仿制药信息。
HER2过表达型乳腺癌:ICI联合抗HER2治疗的探索
HER2过表达型乳腺癌约占20%-25%,抗HER2靶向治疗是其标准疗法。研究发现抗HER2治疗后,肿瘤微环境中的PD-L1表达可能升高,提示联合ICI或许能增强疗效。
早期HER2阳性乳腺癌
多项研究尝试将ICI融入早期HER2阳性乳腺癌的治疗:
- Keyriched-1研究:探索了帕博利珠单抗联合曲妥珠单抗和帕妥珠单抗(双靶)的无化疗新辅助方案,在HR阴性/HER2阳性患者中显示出较高的pCR率。
- 一项II期研究评估了度伐利尤单抗联合双靶治疗,也获得了不错的pCR率。
- Neo-PATH研究:评估了阿替利珠单抗(Atezolizumab)联合化疗和双靶的新辅助方案,整体pCR率良好,尤其在PD-L1阳性患者中pCR率高达100%。
然而,并非所有研究都取得了阳性结果。Impassion-050研究显示,在新辅助化疗联合双靶的基础上加用阿替利珠单抗,并未进一步提高pCR率,反而增加了不良事件。这提示在HER2阳性乳腺癌中,ICI的应用仍需谨慎,需要更精准地筛选获益人群。
晚期HER2阳性乳腺癌
在晚期HER2阳性乳腺癌中,ICI的应用探索也遇到了一些挑战:
- PANACEA研究:显示帕博利珠单抗联合曲妥珠单抗在PD-L1阳性的经治晚期患者中有一定疗效,但在PD-L1阴性患者中无效。
- KATE2研究:评估了ADC药物恩美曲妥珠单抗(T-DM1)联合阿替利珠单抗,结果并未改善总体患者的无进展生存期(PFS),但PD-L1阳性亚组显示出潜在获益。后续的KATE3研究正在进一步验证这一发现在PD-L1阳性人群中的效果。
目前,对于HER2阳性乳腺癌,ICI尚未成为标准疗法,其确切地位和最佳联合策略仍在研究中。
三阴性乳腺癌(TNBC):ICI治疗的重大突破
三阴性乳腺癌(TNBC)约占10%-20%,因缺乏明确的治疗靶点,一度治疗选择有限,预后较差。ICI的出现显著改变了TNBC的治疗格局。
早期TNBC
在新辅助和辅助治疗阶段,ICI联合化疗已显示出明确获益:
- KEYNOTE-522研究:是TNBC免疫治疗领域的里程碑。研究证实,在新辅助化疗中加入帕博利珠单抗,并在术后继续使用帕博利珠单抗辅助治疗,不仅能显著提高pCR率,更能带来长期的生存获益(EFS和OS改善)。最新的长期随访数据(超过6年)进一步巩固了这一结论,该方案已成为高风险早期TNBC的标准治疗之一。
- CamRelief研究:在中国患者中评估了卡瑞利珠单抗(Camrelizumab)联合新辅助化疗的效果,同样显著提高了pCR率,为中国高危早期TNBC患者提供了新的有效选择。
- 其他研究如A-BRAVE、BELLINI、NSABP B-59等也在探索不同ICI药物(如阿维鲁单抗、纳武利尤单抗联合伊匹木单抗/Relatlimab、阿替利珠单抗)在早期TNBC辅助或新辅助治疗中的应用,结果各有不同,提示需要更精细的患者选择和方案设计。
- ADC药物联合ICI也显示出潜力。I-SPY2.2研究中,德达博妥单抗(Dato-DXd)联合度伐利尤单抗在新辅助治疗中取得了很高的pCR率。
晚期TNBC
对于晚期或转移性TNBC,ICI联合化疗已成为部分患者的一线标准治疗:
- Impassion-130研究:证实阿替利珠单抗联合白蛋白紫杉醇可改善PD-L1阳性晚期TNBC患者的PFS和OS。
- KEYNOTE-355研究:显示帕博利珠单抗联合化疗可改善PD-L1阳性(CPS≥10)晚期TNBC患者的PFS和OS。
- TORCHLIGHT研究:在中国人群中证实特瑞普利单抗(Toripalimab)联合白蛋白紫杉醇可改善PD-L1阳性晚期TNBC患者的PFS。
然而,并非所有联合方案都成功(如Impassion-131/132研究),提示化疗药物的选择、PD-L1检测标准等因素都可能影响疗效。除了联合化疗,其他联合策略也在探索中:
- 联合PARP抑制剂:对于携带BRCA突变的TNBC患者,奥拉帕利联合度伐利尤单抗(MEDIOLA研究)或尼拉帕利联合帕博利珠单抗(TOPACIO/KEYNOTE-162研究)显示出潜力。
- 联合抗血管生成药物:如卡瑞利珠单抗联合阿帕替尼,或替雷利珠单抗联合Sitravatinib及化疗(SPARK研究),初步结果显示出令人鼓舞的疗效。
- 联合ADC药物:戈沙妥珠单抗(SG)已是晚期TNBC的重要选择,其与帕博利珠单抗的联合正在研究中(ASCENT-04)。Dato-DXd联合度伐利尤单抗(BEGONIA研究)在一线治疗中也展现出非常高的缓解率和持久疗效,且似乎不受PD-L1表达影响。
获取这些先进的抗癌药物,无论是免疫检查点抑制剂、PARP抑制剂还是ADC药物,对于患者来说至关重要。考虑到部分药物在国内的可及性和价格,通过MedFind这样的海外靶向药代购平台,了解和获取治疗方案中所需的药物(包括潜在的仿制药选项),不失为一种途径。同时,面对复杂的治疗信息和决策,利用AI问诊服务进行初步咨询,或查阅药物信息和诊疗指南,也能帮助患者更好地理解病情和治疗选择。
总结与展望:乳腺癌免疫治疗的未来
免疫检查点抑制剂(ICI)无疑为乳腺癌治疗带来了新的曙光,尤其是在三阴性乳腺癌和部分HR阳性、HER2阳性乳腺癌亚型中。目前,ICI联合化疗、靶向治疗、内分泌治疗、ADC药物、PARP抑制剂或抗血管生成药物是主流研究方向,旨在通过协同作用提高疗效。
PD-L1表达、肿瘤浸润淋巴细胞(TILs)、基因表达谱(如TcellinfGEP)等生物标志物在预测疗效、筛选获益人群方面扮演着越来越重要的角色,推动着乳腺癌治疗走向精准化。
然而,挑战依然存在:
- 耐药机制:部分患者对ICI原发性耐药或产生继发性耐药,其机制复杂,需要深入研究以开发克服耐药的策略。
- 疗效异质性:即使在同一亚型中,患者对ICI的反应也存在很大差异,需要更精准的生物标志物来预测疗效。
- 免疫相关不良事件(irAEs):ICI可能引起独特的副作用,需要及时识别和妥善管理。
- 最佳联合策略和时机:如何选择最佳的联合药物、确定最佳的治疗时机(新辅助、辅助或晚期)仍需更多研究探索。
未来,乳腺癌免疫治疗的研究将聚焦于优化患者分层、探索新的联合方案、深入理解肿瘤免疫微环境、攻克耐药机制,并开发更优的伴随诊断技术。随着这些研究的不断深入,相信ICI将在乳腺癌治疗中发挥更大作用,为更多患者带来长期生存的希望。获取准确的药物信息、理解最新的临床研究成果,并找到可靠的途径获取治疗所需的靶向药或免疫治疗药物,将是患者战胜疾病过程中的重要环节。
[参考文献]
[1] SIEGEL R L, GIAQUINTO A N, JEMAL A. Cancer statistics, 2024[J]. CA A Cancer J Clin, 2024, 74(1): 12-49.
[2] HARBECK N, GNANT M. Breast cancer[J]. Lancet, 2017, 389(10074): 1134-1150.
[3] 张 琪, 修秉虬, 吴 炅. 2023年中国乳腺癌重要临床研究成果及最新进展[J]. 中国癌症杂志, 2024, 34(2): 135-142.
ZHANG Q, XIU B Q, WU J. Progress of important clinical research of breast cancer in China in 2023[J]. Chin Oncol, 2024, 34(2): 135-142.
[4] HARBECK N, PENAULT-LLORCA F, CORTES J, et al. Breast cancer[J]. Nat Rev Dis Primers, 2019, 5(1): 66.
[5] DALL’OLIO F G, MARABELLE A, CARAMELLA C, et al. Tumour burden and efficacy of immune-checkpoint inhibitors[J]. Nat Rev Clin Oncol, 2022, 19(2): 75-90.
[6] C A R D O S O F , O ’S H A U G H N E S S Y J , L I U Z Z , e t a l . Pembrolizumab and chemotherapy in high-risk, early-stage, ER+/HER2- breast cancer: a randomized phase 3 trial[J]. Nat Med, 2025[Online ahead of print].
[7] LOI S, SALGADO R, CURIGLIANO G, et al. Neoadjuvant nivolumab and chemotherapy in early estrogen receptor positive breast cancer: a randomized phase 3 trial[J]. Nat Med, 2025 [Online ahead of print].
[8] CHERIFI F, CABEL L, BOUSRIH C, et al. PROMENADE: PembROlizuMab for early triple negative ER-low breast caNcer, reAl worlD FrEnch cohort[J]. Ann Oncol, 2024, 35: S312-S313.
[9] CARDOSO F, MCARTHUR H L, SCHMID P, et al. LBA21 KEYNOTE-756: Phase Ⅲ study of neoadjuvant pembrolizumab (pembro) or placebo (pbo) + chemotherapy (chemo), followed by adjuvant pembro or pbo + endocrine therapy (ET) for earlystage high-risk ER+/HER2-breast cancer[J]. Ann Oncol, 2023, 34: S1260-S1261.
[10] SCHMID P, CORTES J, PUSZTAI L, et al. Pembrolizumab for early triple-negative breast cancer[J]. N Engl J Med, 2020, 382(9): 810-821.
[11] DE CALUWE A, DESMOULINS I, CAO K, et al. Primary endpoint results of the Neo-CheckRay phase Ⅱ trial evaluating stereotactic body radiation therapy (SBRT) +/- durvalumab (durva) +/- oleclumab (ole) combined with neo-adjuvant chemotherapy (NACT) for early-stage, high risk ER+/HER2- breast cancer (BC)[J]. Ann Oncol, 2024, 35: S1205.
[12] GARRIDO-CASTRO A C, KIM S E, DESROSIERS J, et al. SACI-IO HR+: a randomized phase Ⅱ trial of sacituzumab govitecan with or without pembrolizumab in patients with metastatic hormone receptor-positive/HER2-negative breast cancer[J]. J Clin Oncol, 2024, 42(17_suppl): LBA1004.
[13] GUIU LAHAYE S, BALMANA GELPI J, GAUTHIER L, et al. DOLAF: an international multicenter phase Ⅱ trial of durvalumab (MEDI4736) plus olaparib plus fulvestrant in patients with metastatic or locally advanced ER-positive, HER2-negative breast cancer selected using criteria that predict sensitivity to olaparib[J]. J Clin Oncol, 2022, 40(16_suppl): TPS1116.
[14] SU S C, ZHAO J H, XING Y, et al. Immune checkpoint inhibition overcomes ADCP-induced immunosuppression by macrophages[J]. Cell, 2018, 175(2): 442-457.e23.
[15] KUEMMEL S, GLUZ O, REINISCH M, et al. Abstract PD10- 11: Keyriched-1-a prospective, multicenter, open label, neoadjuvant phase Ⅱ single arm study with pembrolizumab in combination with dual anti-HER2 blockade with trastuzumab and pertuzumab in early breast cancer patients with molecular HER2-enriched intrinsic subtype[J]. Cancer Res, 2022, 82(4_Suppl): PD10-11-PD10-11.
[16] GUAN J, SUN K, JAIN D, et al. Chemotherapy-free neoadjuvant regimen with durvalumab, trastuzumab and pertuzumab (DTP) in HER2-enriched early breast cancer: a prospective, openlabel phase Ⅱ trial[J]. Cancer Res, 2022.
[17] AHN H K, SIM S H, SUH K J, et al. Response rate and safety of a neoadjuvant pertuzumab, atezolizumab, docetaxel, and trastuzumab regimen for patients with ERBB2-positive stage Ⅱ/Ⅲ breast cancer: the neo-PATH phase 2 nonrandomized clinical trial[J]. JAMA Oncol, 2022, 8(9): 1271-1277.
[18] HUOBER J, BARRIOS C H, NIIKURA N, et al. Atezolizumab with neoadjuvant anti-human epidermal growth factor receptor 2 therapy and chemotherapy in human epidermal growth factor receptor 2-positive early breast cancer: primary results of the randomized phase Ⅲ IMpassion050 trial[J]. J Clin Oncol, 2022, 40(25): 2946-2956.
[19] L O I S , G I O B B I E – H U R D E R A , G O M B O S A , e t a l . Pembrolizumab plus trastuzumab in trastuzumab resistant, advanced, HER2-positive breast cancer (PANACEA): a singlearm, multicentre, phase 1b-2 trial[J]. Lancet Oncol, 2019, 20(3): 371-382.
[20] EMENS L A, ESTEVA F J, BERESFORD M, et al. Trastuzumab emtansine plus atezolizumab versus trastuzumab emtansine plus placebo in previously treated, HER2-positive advanced breast cancer (KATE2): a phase 2, multicentre, randomised, doubleblind trial[J]. Lancet Oncol, 2020, 21(10): 1283-1295.
[21] LOI S, SCHNEEWEISS A, SONG E, et al. 329TiP KATE3: a phase Ⅲ study of trastuzumab emtansine (T-DM1) in combination with atezolizumab or placebo in patients with previously treated HER2-positive and PD-L1-positive locally advanced or metastatic breast cancer[J]. Ann Oncol, 2021, 32: S509.
[22] CONTE P F, DIECI M V, BISAGNI G, et al. A-BRAVE trial: a phase Ⅲ randomized trial with avelumab in early triplenegative breast cancer with residual disease after neoadjuvant chemotherapy or at high risk after primary surgery and adjuvant chemotherapy[J]. J Clin Oncol, 2024, 42(17_suppl): LBA500.
[23] NEDERLOF I, ROLFES A L, GIELEN R C A M, et al. LBA11 Neoadjuvant nivolumab/relatlimab or nivolumab/ipilimumab in triple-negative breast cancer with high tumor-infiltrating lymphocytes (TILs)[J]. Ann Oncol, 2024, 35: S1206.
[24] GEYER C. GS3-05: NSABP B-59/GBG-96-GeparDouze: a randomized double-blind phase Ⅲ clinical trial of neoadjuvant chemotherapy with atezolizumab or placebo followed by adjuvant atezolizumab or placebo in patients with stage Ⅱ and Ⅲ triple-negative breast cancer[C]. San Antonio Breast Cancer Conference, 2024, December 10-13, GS3-05.
[25] SCHMID P, CORTES J, DENT R, et al. Event-free survival with pembrolizumab in early triple-negative breast cancer[J]. N Engl J Med, 2022, 386(6): 556-567.
[26] PUSZTAI L, DENKERT C, O’SHAUGHNESSY J, et al. Eventfree survival by residual cancer burden with pembrolizumab in early-stage TNBC: exploratory analysis from KEYNOTE-522[J]. Ann Oncol, 2024, 35(5): 429-436.
[27] SCHMID P, CORTES J, DENT R, et al. Overall survival with pembrolizumab in early-stage triple-negative breast cancer[J]. N Engl J Med, 2024, 391(21): 1981-1991.
[28] O’SHAUGHNESSY J. Exploratory biomarker analysis of the phase 3 KEYNOTE-522 study of neoadjuvant pembrolizumab or placebo plus chemotherapy followed by adjuvant pembrolizumab or placebo for early-stage TNBC[C]. San Antonio Breast Cancer Symposium, 2024, December 10-13, LB1-07.
[29] CHEN L, LI H, ZHANG H, et al. Camrelizumab vs placebo in combination with chemotherapy as neoadjuvant treatment in patients with early or locally advanced triple-negative breast cancer: the CamRelief randomized clinical trial[J]. JAMA, 2024 Dec 13 [Online ahead of print].
[30] SHIMIZU T, SANDS J, YOH K, et al. First-in-human, phase Ⅰ dose-escalation and dose-expansion study of trophoblast cell-surface antigen 2-directed antibody-drug conjugate datopotamab deruxtecan in non-small cell lung cancer: TROPION-PanTumor01[J]. J Clin Oncol, 2023, 41(29): 4678-4687.
[31] KHOURY K, MEISEL J L, YAU C, et al. Datopotamabderuxtecan in early-stage breast cancer: the sequential multiple assignment randomized I-SPY2.2 phase 2 trial[J]. Nat Med, 2024, 30(12): 3728-3736.
[32] BARDIA A, PUSZTAI L, ALBAIN K, et al. TROPIONBreast03: a randomized phase Ⅲ global trial of datopotamab deruxtecan °¿ durvalumab in patients with triple-negative breast cancer and residual invasive disease at surgical rep after neoadjuvant therapy[J]. Ther Adv Med Oncol, 2024, 16: 17588359241248336.
[33] SCHMID P, ADAMS S, RUGO H S, et al. Atezolizumab and nab-paclitaxel in advanced triple-negative breast cancer[J]. N Engl J Med, 2018, 379(22): 2108-2121.
[34] EMENS L A, ADAMS S, BARRIOS C H, et al. First-line atezolizumab plus nab-paclitaxel for unresectable, locally advanced, or metastatic triple-negative breast cancer: IMpassion130 final overall survival analysis[J]. Ann Oncol, 2021, 32(8): 983-993.
[35] CORTES J, CESCON D W, RUGO H S, 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.
[36] JIANG Z F, OUYANG Q C, SUN T, et al. Toripalimab plus nab-paclitaxel in metastatic or recurrent triple-negative breast cancer: a randomized phase 3 trial[J]. Nat Med, 2024, 30(1): 249-256.
[37] MO H N, YU Y P, SUN X Y, et al. Metronomic chemotherapy plus anti-PD-1 in metastatic breast cancer: a Bayesian adaptive randomized phase 2 trial[J]. Nat Med, 2024, 30(9): 2528-2539.
[38] MILES D, GLIGOROV J, ANDRÉ F, et al. Primary results from IMpassion131, a double-blind, placebo-controlled, randomised phase Ⅲ trial of first-line paclitaxel with or without atezolizumab for unresectable locally advanced/metastatic triple-negative breast cancer[J]. Ann Oncol, 2021, 32(8): 994-1004.
[39] DENT R, ANDRÉ F, GONÇALVES A, et al. IMpassion132 double-blind randomised phase Ⅲ trial of chemotherapy with or without atezolizumab for early relapsing unresectable locally advanced or metastatic triple-negative breast cancer[J]. Ann Oncol, 2024, 35(7): 630-642.
[40] DOMCHEK S M, POSTEL-VINAY S, IM S A, et al. Olaparib and durvalumab in patients with germline BRCA mutated metastatic breast cancer (MEDIOLA): an open-label, multicentre, phase 1/2, basket study[J]. Lancet Oncol, 2020, 21(9): 1155-1164.
[41] VINAYAK S, TOLANEY S M, SCHWARTZBERG L, et al. Open-label clinical trial of niraparib combined with pembrolizumab for treatment of advanced or metastatic triplenegative breast cancer[J]. JAMA Oncol, 2019, 5(8): 1132-1140.
[42] CHEN W Z, SHEN L S, JIANG J X, et al. Antiangiogenic therapy reverses the immunosuppressive breast cancer microenvironment[J]. Biomark Res, 2021, 9(1): 59.
[43] LIU J Q, LIU Q, LI Y, et al. Efficacy and safety of camrelizumab combined with apatinib in advanced triple-negative breast cancer: an open-label phase Ⅱ trial[J]. J Immunother Cancer, 2020, 8(1): e000696.
[44] LIU X, SUI X, XU Y, et al. Tislelizumab plus sitravatinib and nab-paclitaxel in patients with untreated locally recurrent or metastatic triple-negative breast cancer (TNBC): updated efficacy and safety results[C]. San Antonio Breast Cancer Symposium, 2024, December 10-13: PS3-01.
[45] 国家肿瘤质控中心乳腺癌专家委员会, 中国抗癌协会乳腺癌专业委员会, 中国抗癌协会肿瘤药物临床研究专业委员会. 中国晚期乳腺癌规范诊疗指南(2020版)[J]. 中华肿瘤杂志, 2020, 42(10): 781-797.
Breast Cancer Expert Committee of National Cancer Quality Control Center, Breast Cancer Expert Committee of China Anti-Cancer Association, Cancer Drug Clinical Research Committee of China Anti-Cancer Association. Guidelines for clinical diagnosis and treatment of advanced breast cancer in China (2020 edition)[J]. Chin J Oncol, 2020, 42(10): 781-797.
[46] TOLANEY S M, DE AZAMBUJA E, EMENS L A, et al. 276TiP ASCENT-04/KEYNOTE-D19: Phase Ⅲ study of sacituzumab govitecan (SG) plus pembrolizumab (pembro) vs treatment of physician’s choice (TPC) plus pembro in first-line (1L) programmed death-ligand 1-positive (PD-L1+) metastatic triple-negative breast cancer (mTNBC)[J]. Ann Oncol, 2022, 33: S664-S665.
[47] S C H M I D P , WY S O C K I P J , M A C X , e t a l . 3 7 9 M O Datopotamab deruxtecan (Dato-DXd) + durvalumab (D) as firstline (1L) treatment for unresectable locally advanced/metastatic triple-negative breast cancer (a/mTNBC): updated results from BEGONIA, a phase Ⅰb/Ⅱ study[J]. Ann Oncol, 2023, 34: S337.
[48] SCHMID P, OLIVEIRA M, O’SHAUGHNESSY J, et al. 261TiP TROPION-Breast05: phase (Ph) Ⅲ study of datopotamab deruxtecan (Dato-DXd) °¿ durvalumab (D) vs chemotherapy (CT) + pembrolizumab (pembro) in patients (pts) with PD-L1+locally recurrent inoperable or metastatic triple-negative breast cancer (TNBC)[J]. ESMO Open, 2024, 9: 103282.