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這幾年,腫瘤治療領(lǐng)域有多項(xiàng)突破性進(jìn)展,誕生了多個(gè)明星“抗癌家族”,比如大家熟知的PD-1/PD-L1家族(多種癌癥)、EGFR家族(肺癌)、ALK家族(肺癌)等,無數(shù)癌癥患者獲得了“新生”。除此之外,還有一個(gè)抗癌新星正在冉冉升起——PARP家族,尤其是最近半年,多個(gè)重磅進(jìn)展相繼公布:近期,多個(gè)國產(chǎn)PARP抑制劑,紛紛獲得國家藥監(jiān)局的臨床試驗(yàn)批文,在國內(nèi)開展了針對卵巢癌、乳腺癌、前列腺癌、胰腺癌等眾多實(shí)體瘤的臨床試驗(yàn)……鑒于此,咚咚給廣大癌種患者總結(jié)一下國內(nèi)外PARP抑制劑的最新進(jìn)展,也期待這些新藥能給更多患者帶來希望。 ① 奧拉帕利(Olaparib):國內(nèi)上市,進(jìn)醫(yī)保 奧拉帕利是阿斯利康公司研發(fā),世界上第一款上市的PARP抑制劑,自2014年底在美國獲批上市后,目前已涵蓋了BRCA突變卵巢癌患者的一二線治療和難治復(fù)發(fā)乳腺癌二三線治療與BRCA突變胰腺癌的一線治療。目前,奧拉帕利已經(jīng)于2018年8月22日在國內(nèi)上市,獲批的適應(yīng)癥包括:無論gBRCA突變狀態(tài),復(fù)發(fā)性卵巢癌二線鉑類化療后維持治療;BRCA突變晚期卵巢癌的一線維持治療。瑞卡帕利是Clovis 研發(fā)的全球第二個(gè)上市的PARP抑制劑,但是卻是全球第一個(gè)被加速批準(zhǔn)用于卵巢癌三線治療的PARP抑制劑。③ 尼拉帕利(Niraparib):國內(nèi)上市 尼拉帕利是Tesaro和GSK聯(lián)合開發(fā)的,全球第三個(gè)上市的PARP抑制劑,雖然比奧拉帕利晚3年在美國上市,但是作為PARP抑制劑中的一匹黑馬進(jìn)展迅速,也創(chuàng)造了兩個(gè)治療領(lǐng)域的第一:目前,尼拉帕利在國外的適應(yīng)癥和臨床數(shù)據(jù)包括:再鼎制藥已經(jīng)將尼拉帕利引進(jìn)中國,正在進(jìn)行小細(xì)胞肺癌和卵巢癌兩個(gè)領(lǐng)域的臨床試驗(yàn),2018年12月向中國藥審中心遞交了上市申請,2019年12月27號,尼拉帕利獲得藥監(jiān)局的批準(zhǔn),正式登陸中國。目前,患者援助項(xiàng)目也已經(jīng)出臺(tái),親民價(jià)格。 他帕唑帕利是輝瑞開發(fā)的全球第四個(gè)上市的PARP抑制劑,首次批準(zhǔn)的適應(yīng)癥為gBRCA突變的乳腺癌,具體臨床數(shù)據(jù)如下:除了已上市“各顯神通”的PARP抑制劑外,還有未上市的新面孔值得期待。雅培公司的維利帕利可能會(huì)是全球第五個(gè)上市的PARP抑制劑,在2019年的ESMO會(huì)議上發(fā)表結(jié)果發(fā)布了卵巢癌和乳腺癌維持治療的結(jié)果。氟唑帕利是恒瑞醫(yī)藥研發(fā)的PARP抑制劑,并已經(jīng)被中國藥審中心納入上市藥物優(yōu)先審評,猜測申報(bào)上市的適應(yīng)癥極有可能為復(fù)發(fā)性卵巢癌患者,該適應(yīng)癥在國內(nèi)已經(jīng)推進(jìn)到III期臨床階段。也就是說,這也許會(huì)是中國第一個(gè)上市的中國自主原研的PARP抑制劑。氟唑帕利在2019年的ESMO會(huì)議上也發(fā)布了優(yōu)異的試驗(yàn)結(jié)果:在BRCA1/2突變的鉑敏感卵巢癌中療效和安全性探索的多中心Ib期研究,ORR高達(dá)55.8%,且截至數(shù)據(jù)發(fā)布日期,尚未達(dá)到中位PFS和OS,這意味著有持續(xù)的生存優(yōu)勢。Pamiparib的研發(fā)進(jìn)展也備受關(guān)注,因?yàn)檫@是創(chuàng)造中國新藥首次在美國成功上市記錄的公司,百濟(jì)神州研發(fā)的PARP抑制劑,目前在包括中國的國家地區(qū)開展了卵巢癌、前列腺癌和胃癌的的關(guān)鍵性試驗(yàn)。在2019年的ESMO會(huì)議上公布了Pamiparib單藥,和與低劑量替莫唑胺聯(lián)合用于實(shí)體瘤患者安全性和劑量探索的I期臨床試驗(yàn)結(jié)果,顯示對多種實(shí)體瘤患者均安全且達(dá)到一定程度的疾病緩解。短短5年時(shí)間內(nèi),PARP抑制劑已經(jīng)成為卵巢癌、乳腺癌的重要治療方法之一,同時(shí)在包括癌王胰腺癌等癌種中顯示出了優(yōu)異的臨床數(shù)據(jù),對患者來說,又多了一份希望。 [1] Domchek, Susan M., et al. “Efficacy and Safety ofOlaparib Monotherapy in Germline BRCA1/2 Mutation Carriers with AdvancedOvarian Cancer and Three or More Lines of Prior Therapy.” Gynecologic Oncology,vol. 140, no. 2, 2016, pp. 199–203.[2] Pujade-Lauraine, Eric, et al. “Olaparib Tabletsas Maintenance Therapy in Patients with Platinum-Sensitive, Relapsed OvarianCancer and a BRCA1/2 Mutation (SOLO2/ENGOT-Ov21): A Double-Blind, Randomised,Placebo-Controlled, Phase 3 Trial.” Lancet Oncology, vol. 18, no.9, 2017, pp. 1274–1284.[3] Moore, Kathleen, et al. “Maintenance Olaparibin Patients With Newly Diagnosed Advanced Ovarian Cancer.” Obstetrical& Gynecological Survey, vol. 74, no. 2, 2019, pp. 86–87.[4] LBA3 – Coleman RL, Fleming GF, Brady MF, etal. VELIA/GOG-3005: Integration of veliparib (V) with front-line chemotherapyand maintenance in women with high-grade serous carcinoma of ovarian, fallopiantube, or primary peritoneal origin (HGSC).[5] Ledermann J, Harter P, Gourley M, et al. Olaparib maintenance therapy inplatinum-sensitive relapsed ovarian cancer. N Engl J Med 2012;366:1382-1392.[6] Moore, Kathleen, et al. “Maintenance Olaparibin Patients With Newly Diagnosed Advanced Ovarian Cancer.” Obstetrical& Gynecological Survey, vol. 74, no. 2, 2019, pp. 86–87.[7] Moore, Kathleen N., et al. “NiraparibMonotherapy for Late-Line Treatment of Ovarian Cancer (QUADRA): A Multicentre,Open-Label, Single-Arm, Phase 2 Trial.” Lancet Oncology, vol. 20,no. 5, 2019, pp. 636–648.[8] Coleman, Robert L., et al. “Rucaparib MaintenanceTreatment for Recurrent Ovarian Carcinoma after Response to Platinum Therapy(ARIEL3): A Randomised, Double-Blind, Placebo-Controlled, Phase 3 Trial.” TheLancet, vol. 390, no. 10106, 2017, pp. 1949–1961.[9] Litton, Jennifer K., et al. “Talazoparib inPatients with Advanced Breast Cancer and a Germline BRCA Mutation.” TheNew England Journal of Medicine, vol. 379, no. 8, 2018, pp. 753–763.[10] LBA9 – Diéras VC, Han HS, Kaufman B, etal. Phase 3 study of veliparib with carboplatin and paclitaxel inHER2-negative advanced/metastatic gBRCA-associated breast cancer.[11] LBA3 – Coleman RL, Fleming GF, Brady MF, etal. VELIA/GOG-3005: Integration of veliparib (V) with front-linechemotherapy and maintenance in women with high-grade serous carcinoma ofovarian, fallopian tube, or primary peritoneal origin (HGSC).[12] Voskoboynik, M., et al. “452PDSafety, AntitumorActivity, and Pharmacokinetics (PK) of Pamiparib (BGB-290), a PARP1/2Inhibitor, in Patients (Pts) with Advanced Solid Tumours: Updated Phase IDose-Escalation/Expansion Results.” Annals of Oncology, vol. 30,2019.[13] Stradella, A., et al. “451PDUpdated Results of the PARP1/2 InhibitorPamiparib in Combination with Low-Dose (Ld) Temozolomide (TMZ) in Patients(Pts) with Locally Advanced or Metastatic Solid Tumours.” Annals ofOncology, vol. 30, 2019.[14] N Li, L Wu, Y Zhang, J Liu, Q Zhou, J Zhu, RYin, L Wang, G Li, X Wu, H Pan, S Yao, Q Wu, K Gu, H Zhang, X Wan, R An, J Zou,Q Wang, 1000PEfficacy and safety of oral poly (ADP-ribose) polymerase inhibitor fluzoparibin patients with BRCA1/2 mutations and platinum sensitive recurrent ovariancancer, Annals of Oncology, Volume 30, Issue Supplement_5, October 2019
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