Claudin-6 (CLDN6) and Folate Receptor Alpha (FRα) Targeted Antibody-Drug Conjugates: Bypassing Platinum Resistance and Tumor Heterogeneity in High-Grade Serous Ovarian Carcinoma

Authors

  • Anwar Shareef Alkunani OB/GYNE and Infertility center, SC, Chicago, Illinois, U.S
  • Laith Ghadhanfer Shareef Department of Clinical Pharmacy, College of Pharmacy, University of Mashreq, Baghdad, Iraq https://orcid.org/0000-0001-7773-8474
  • Ahmed Zakaria Al Arajy Department of Pharmacy, Al-Farabi University College, Baghdad, Iraq https://orcid.org/0000-0003-3593-990X

DOI:

https://doi.org/10.54133/ajms.v11i2.3258

Keywords:

High-Grade Serous Ovarian Carcinoma, Folate Receptor Alpha, Mirvetuximab, Soravtansine, Platinum Resistance

Abstract

High-grade serous ovarian carcinoma (HGSOC) is the most lethal gynecologic malignancy, and predicting its outcomes is complicated by two interlinked adversaries: the near-inevitable development of platinum resistance that depletes the most successful drug class against the disease and a profound molecular and antigenic heterogeneity that defies targeted therapy. Antibody-drug conjugates (ADCs) directed against tumor-associated antigens offer a strategically attractive answer to both because they kill through a cytotoxic mechanism of microtubule disruption by a delivered payload that is wholly independent of the DNA-repair and drug-handling pathways that confer platinum resistance and because the bystander effect of their membrane-permeable payloads can reach antigen-negative cells within a heterogeneous tumor. This review examines two complementary antigens that researchers are pursuing in HGSOC. Folate receptor alpha (FRα), overexpressed in the great majority of these tumors, is the target of mirvetuximab soravtansine, the first agent of any class to demonstrate an overall-survival benefit in platinum-resistant ovarian cancer and the first ADC approved for this disease. Claudin-6 (CLDN6), an oncofetal tight-junction protein essentially absent from normal adult tissue and expressed in roughly half of HGSOC, is the target of the first-in-class ADC TORL-1-23, which has shown encouraging response rates in platinum-resistant disease in early-phase testing. We detail the biology and resistance mechanisms of HGSOC; the rationale by which antigen-directed payload delivery bypasses platinum resistance; the design, clinical validation, and pipeline of FRα- and CLDN6-targeted ADCs; the way bystander killing, complementary antigen coverage, and biomarker-guided selection address heterogeneity; the safety; and resistance.

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References

Grither WR, et al. Rethinking ovarian cancer III: the past decade and future directions. Nat Rev Cancer. 2026:1-20. doi: 10.1038/s41568-026-00916-0. DOI: https://doi.org/10.1038/s41568-026-00916-0

Konstantinopoulos PA, Matulonis UA. Clinical and translational advances in ovarian cancer therapy. Nat Cancer. 2023;4(9):1239-1257. doi: 10.1038/s43018-023-00617-9. DOI: https://doi.org/10.1038/s43018-023-00617-9

Pujade-Lauraine E, Banerjee S, Pignata S. Management of platinum-resistant, relapsed epithelial ovarian cancer. J Clin Oncol. 2019;37(27):2437-2448. doi: 10.1200/JCO.19.00194. DOI: https://doi.org/10.1200/JCO.19.00194

Richardson DL, Eskander RN, O’Malley DM. Advances in ovarian cancer care and unmet treatment needs for patients with platinum resistance: a narrative review. JAMA Oncol. 2023;9(6). doi: 10.1001/jamaoncol.2023.0197. DOI: https://doi.org/10.1001/jamaoncol.2023.0197

Matulonis UA, Lorusso D, Oaknin A. Efficacy and safety of mirvetuximab soravtansine in patients with platinum-resistant ovarian cancer with high folate receptor alpha expression: results from the SORAYA study. J Clin Oncol. 2023;41(13):2436-2445. doi: 10.1200/JCO.22.01900. DOI: https://doi.org/10.1200/JCO.22.01900

Kefas J, Flynn M. Unlocking the potential of immunotherapy in platinum-resistant ovarian cancer: Rationale, challenges, and novel strategies. Cancer Drug Resist. 2024;7:39. doi: 10.20517/cdr.2024.67. DOI: https://doi.org/10.20517/cdr.2024.67

Chen B, Zheng X, Wu J, Chen G, Yu J, Xu Y, et al. Antibody–drug conjugates in cancer therapy: current landscape, challenges, and future directions. Mol Cancer. 2025;24(1):279. doi: 10.1186/s12943-025-02489-2. DOI: https://doi.org/10.1186/s12943-025-02489-2

Cheng X, Li P, Jiang R, Meng E, Wu H. ADC: A deadly killer of platinum resistant ovarian cancer. J Ovarian Res. 2024;17(1):196. doi: 10.1186/s13048-024-01523-z. DOI: https://doi.org/10.1186/s13048-024-01523-z

Popov D. Diagnostic and Therapeutic Antibodies in Oncology: Mechanisms, Clinical Applications, and Future Directions. Precision Oncology through Cancer Antigens: Diagnostic and Therapeutic Antibody Approaches.

An M, Yan J, Liu B, Liu Q. Harnessing the power of CAR-NK cells for solid tumors: challenges, innovations, and future frontiers in immunotherapy. Cancer Commun. 2026;46:0023. doi: 10.34133/cancomm.0023. DOI: https://doi.org/10.34133/cancomm.0023

Network CGAR. Integrated genomic analyses of ovarian carcinoma. Nature. 2011;474(7353):609-615. doi: 10.1038/nature10166. DOI: https://doi.org/10.1038/nature10166

Ortega MA, Fraile-Martínez O, García-Montero C. Ovarian cancer—insights into platinum resistance and overcoming it. Medicina (Kaunas). 2023;59(3):544. doi: 10.3390/medicina59030544. DOI: https://doi.org/10.3390/medicina59030544

Patch AM, Christie EL, Etemadmoghadam D. Whole-genome characterization of chemoresistant ovarian cancer. Nature. 2015;521(7553):489-494. doi: 10.1038/nature14410. DOI: https://doi.org/10.1038/nature14410

Galluzzi L, Senovilla L, Vitale I. Molecular mechanisms of cisplatin resistance. Oncogene. 2012;31(15):1869-83. doi: 10.1038/onc.2011.384. DOI: https://doi.org/10.1038/onc.2011.384

Norouzi-Barough L, Sarookhani MR, Sharifi M. Molecular mechanisms of drug resistance in ovarian cancer. J Cell Physiol. 2018;233(6):4546-4562. doi: 10.1002/jcp.26289. DOI: https://doi.org/10.1002/jcp.26289

McGranahan N, Swanton C. Clonal heterogeneity and tumor evolution: past, present, and the future. Cell. 2017;168(4):613-628. doi: 10.1016/j.cell.2017.01.018. DOI: https://doi.org/10.1016/j.cell.2017.01.018

Schwarz RF, Ng CKY, Cooke SL. Spatial and temporal heterogeneity in high-grade serous ovarian cancer: a phylogenetic analysis. PLoS Med. 2015;12(2):e1001789. doi: 10.1371/journal.pmed.1001789. DOI: https://doi.org/10.1371/journal.pmed.1001789

Nasiri F, Safarzadeh Kozani P, Salem F, Mahboubi Kancha M, Dashti Shokoohi S, Safarzadeh Kozani P. Mechanisms of antigen-dependent resistance to chimeric antigen receptor (CAR)-T cell therapies. Cancer Cell Int. 2025;25(1):64. doi: 10.1186/s12935-025-03697-y. DOI: https://doi.org/10.1186/s12935-025-03697-y

Drago JZ, Modi S, Chandarlapaty S. Unlocking the potential of antibody-drug conjugates for cancer therapy. Nat Rev Clin Oncol. 2021;18(6):327-344. doi: 10.1038/s41571-021-00470-8. DOI: https://doi.org/10.1038/s41571-021-00470-8

Tsuchikama K, Anami Y, Ha SYY, Yamazaki CM. Exploring the next generation of antibody-drug conjugates. Nat Rev Clin Oncol. 2024;21(3):203-223. doi: 10.1038/s41571-023-00850-2. DOI: https://doi.org/10.1038/s41571-023-00850-2

Hao Y, Song Z. Mechanisms of resistance to antibody-drug conjugates in cancer therapy: molecular basis and therapeutic strategies. Cancer Drug Resist. 2025;8:59. doi: 10.20517/cdr.2025.148. DOI: https://doi.org/10.20517/cdr.2025.148

Staudacher AH, Brown MP. Antibody drug conjugates and bystander killing: is antigen-dependent internalisation required? Br J Cancer. 2017;117(12):1736-1742. doi: 10.1038/bjc.2017.367. DOI: https://doi.org/10.1038/bjc.2017.367

McDermott MS, O'Brien NA, Hoffstrom B, Gong K, Lu M, Zhang J, et al. Preclinical efficacy of the antibody-drug conjugate CLDN6-23-ADC for the treatment of CLDN6-positive solid tumors. Clin Cancer Res. 2023;29(11):2131-243. doi: 10.1158/1078-0432.CCR-22-2981. DOI: https://doi.org/10.1158/1078-0432.CCR-22-2981

Marine J-C, Bartok O, Sagie S, Vitiello PP, Bardelli A, Weller C, et al. Mapping intratumor heterogeneity across layers for advancing immunotherapy. Cell. 2026;189(8):2416-2440. doi: 10.1016/j.cell.2026.03.025. DOI: https://doi.org/10.1016/j.cell.2026.03.025

Zwicke GL, Ali Mansoori G, Jeffery CJ. Utilizing the folate receptor for active targeting of cancer nanotherapeutics. Nano Rev. 2012;3(1):18496. doi: 10.3402/nano.v3i0.18496. DOI: https://doi.org/10.3402/nano.v3i0.18496

Scaranti M, Cojocaru E, Banerjee S, Banerji U. Exploiting the folate receptor α in oncology. Nat Rev Clin Oncol. 2020;17(6):349-359. doi: 10.1038/s41571-020-0339-5. DOI: https://doi.org/10.1038/s41571-020-0339-5

Kalli KR, Oberg AL, Keeney GL. Folate receptor alpha as a tumor target in epithelial ovarian cancer. Gynecol Oncol. 2008;108(3):619-626. doi: 10.1016/j.ygyno.2007.11.020. DOI: https://doi.org/10.1016/j.ygyno.2007.11.020

Dilawari A, Shah M, Ison G. FDA approval summary: mirvetuximab soravtansine-gynx. Clin Cancer Res. 2023;29(19):3835-3840. doi: 10.1158/1078-0432.CCR-23-0991. DOI: https://doi.org/10.1158/1078-0432.CCR-23-0991

Kokori E, Olatunji G, Komolafe R, Abraham IC, Ukoaka B, Samuel O, et al. Mirvetuximab soravtansine: A breakthrough in targeted therapy for platinum-resistant ovarian cancer. Medicine. 2024;103(20):e38132. doi: 10.1097/MD.0000000000038132. DOI: https://doi.org/10.1097/MD.0000000000038132

Coleman RL, Lorusso D, Oaknin A. Mirvetuximab soravtansine in folate receptor alpha (FRα)-high platinum-resistant ovarian cancer: final overall survival from the SORAYA trial. Gynecol Oncol. 2024;186:1-9. doi: 10.1136/ijgc-2024-005401. DOI: https://doi.org/10.1136/ijgc-2024-005401

Moore KN, Angelergues A, Konecny GE. Mirvetuximab soravtansine in FRα-positive, platinum-resistant ovarian cancer (MIRASOL): a phase 3 trial. N Engl J Med. 2023;389(23):2162-2174. doi: 10.1056/NEJMoa2309169. DOI: https://doi.org/10.1056/NEJMoa2309169

Ascione L, Guidi L, Prakash A, Trapani D, LoRusso P, Lou E, et al. Unlocking the potential: biomarkers of response to antibody-drug conjugates. Am Soc Clin Oncol Edu Book. 2024;44(3):e431766. doi: 10.1200/EDBK_431766. DOI: https://doi.org/10.1200/EDBK_431766

Li X, Abrahams C, Embry M. Discovery of STRO-002, a novel homogeneous ADC targeting folate receptor alpha, for the treatment of ovarian and endometrial cancers. Mol Cancer Ther. 2023;22(2):155-167. doi: 10.1158/1535-7163.MCT-22-0322. DOI: https://doi.org/10.1158/1535-7163.MCT-22-0322

Oaknin A, Fariñas-Madrid L, García-Duran C, Martin LP, O'Malley DM, Schilder RJ, et al. Luveltamab tazevibulin (STRO-002), an anti-folate receptor alpha (FolRα) antibody drug conjugate (ADC), safety and efficacy in a broad distribution of FolRα expression in patients with recurrent epithelial ovarian cancer (OC): Update of STRO-002-GM1 phase 1 dose expansion cohort. J Clin Oncol. 2024;188:8-16. doi: 10.1200/JCO.2023.41.16_suppl.5508. DOI: https://doi.org/10.1200/JCO.2023.41.16_suppl.5508

Shimizu T, Fujiwara Y, Yonemori K. First-in-human phase 1 study of farletuzumab ecteribulin (MORAb-202), an antibody-drug conjugate targeting folate receptor alpha. Clin Cancer Res. 2021;27(14):3905-3915. doi: 10.1158/1078-0432.CCR-20-4740. DOI: https://doi.org/10.1158/1078-0432.CCR-20-4740

Ab O, Bartle LM, Yoder NC. IMGN151, a next-generation folate receptor alpha-targeting antibody-drug conjugate with a biparatopic design. Mol Cancer Ther. 2024;23(5):667-680.

Reinhard K, Rengstl B, Oehm P. An RNA vaccine drives expansion and efficacy of claudin-CAR-T cells against solid tumors. Science. 2020;367(6476):446-453. doi: 10.1126/science.aay5967. DOI: https://doi.org/10.1126/science.aay5967

Hendrickson AW, Konecny GE, Winterhoff B, Adjei AA, Pulaski H, Yoon S, et al. 1074P Claudin- 6 (CLDN6) is a therapeutic target in ovarian cancer (OC): Emerging results from the CATALINA 1 (CAT1) study. Ann Oncol. 2025;36(suppl). doi: 10.1016/j.annonc.2025.08.1713. DOI: https://doi.org/10.1016/j.annonc.2025.08.1714

Kim H, Lee SY, Choi YJ. Claudin-6 expression in primary and recurrent epithelial ovarian cancer: a potential therapeutic target for high-grade serous ovarian cancer. Ann Oncol. 2024;35(suppl 2):S571. doi: 10.1016/j.annonc.2024.08.832. DOI: https://doi.org/10.1016/j.annonc.2024.08.832

Konecny GE, Hamilton EP, Richardson DL. First-in-human phase I study of a novel claudin-6 (CLDN6)-targeted antibody-drug conjugate, TORL-1-23, in advanced solid tumors (CATALINA-1). Ann Oncol. 2023;34(suppl 2):S550. doi: 10.1016/j.annonc.2023.09.193. DOI: https://doi.org/10.1016/j.annonc.2023.09.1935

Du H, Yang X, Fan J, Du X. Claudin 6: Therapeutic prospects for tumours, and mechanisms of expression and regulation. Mol Med Rep. 2021;24(3):677. doi: 10.3892/mmr.2021.12316. DOI: https://doi.org/10.3892/mmr.2021.12316

Hamagawa K, Yoshida H, Yagishita S, Shintani D, Yano M, Yasuda M, et al. 71O Profiling antibody-drug conjugate (ADC) target expression in high-grade serous ovarian cancer (HGSOC): opportunities for targeted treatment strategies. ESMO Open. 2025;10. doi: 10.1016/j.esmoop.2025.105200. DOI: https://doi.org/10.1016/j.esmoop.2025.105200

Mackensen A, Haanen JBAG, Koenecke C. CLDN6-specific CAR-T cells plus amplifying RNA vaccine (BNT211) in relapsed or refractory solid tumours: a phase 1 trial. Nat Med. 2023;29(11):2844-53. doi: 10.1038/s41591-023-02612-0. DOI: https://doi.org/10.1038/s41591-023-02612-0

Menon R, Bako E, Liu S, Stec J, Thakur S, Deutschman E, et al. Mirvetuximab soravtansine: mechanism of action, clinical and translational science. Clin Transl Sci. 2026;19(1):e70447. doi: 10.1111/cts.70447. DOI: https://doi.org/10.1111/cts.70447

Nwabufo CK. Mirvetuximab soravtansine in ovarian cancer therapy: expert opinion on pharmacological considerations. Cancer Chemother Pharmacol. 2024;93(2):89-105. doi: 10.1007/s00280-023-04575-y. DOI: https://doi.org/10.1007/s00280-023-04575-y

Yuan R, McGeehan A, Zhou S, Cheng C, Armanini M, Smith J, et al. The anti-FRα antibody–drug conjugate luveltamab tazevibulin demonstrates efficacy in non–small cell lung cancer preclinical models and induces immunogenic cell death. Mol Cancer Ther. 2025;24(9):1428-1441. doi: 10.1158/1535-7163.MCT-24-0649. DOI: https://doi.org/10.1158/1535-7163.MCT-24-0649

Lewis GD. Antibody–drug conjugates: The past, present and future. Ann Rev Cancer Biol. 2025;10. doi: 10.1146/annurev-cancerbio-070524-032954. DOI: https://doi.org/10.1146/annurev-cancerbio-070524-032954

Kim ET, Kim JH, Park EY, Song IH, Park HS, Park SY, et al. The efficacy and safety of folate receptor α‐targeted antibody‐drug conjugate therapy in patients with high‐grade epithelial ovarian, primary peritoneal, or fallopian tube cancers: A systematic review and meta‐analysis. Cancer Med. 2024;13(21):e70392. doi: 10.1002/cam4.70392. DOI: https://doi.org/10.1002/cam4.70392

Niquille DL, Fitzgerald KM, Gera N. Biparatopic antibodies: therapeutic applications and prospects. MAbs. 2024;16(1):2310890. doi: 10.1080/19420862.2024.2310890. DOI: https://doi.org/10.1080/19420862.2024.2310890

Lorenzon I. Chemoresistance in epithelial ovarian cancer: in vitro selection and characterization of platinum resistant cells. Thesis. 2020. Available at: https://air.uniud.it/retrieve/e27ce0c8-8369-055e-e053-6605fe0a7873/Tesi_Lorenzon_Ilaria.pdf

Ogundipe OD, Olajubutu O, Adesina SK. Targeted drug conjugate systems for ovarian cancer chemotherapy. Biomed Pharmacother. 2023;165:115151. doi: 10.1016/j.biopha.2023.115151. DOI: https://doi.org/10.1016/j.biopha.2023.115151

García-Alonso S, Ocaña A, Pandiella A. Resistance to antibody-drug conjugates: an issue of intracellular trafficking. Cancer Res. 2018;78(9):2159-2165. doi: 10.1158/0008-5472.CAN-17-3671. DOI: https://doi.org/10.1158/0008-5472.CAN-17-3671

Loganzo F, Sung M, Gerber HP. Mechanisms of resistance to antibody-drug conjugates. Mol Cancer Ther. 2016;15(12):2825-2834. doi: 10.1158/1535-7163.MCT-16-0408. DOI: https://doi.org/10.1158/1535-7163.MCT-16-0408

Liu Y, Liu Y, Wu T, Bai X, Wang S, Zhang L, et al. Drug resistance to antibody-drug conjugates: mechanisms, challenges, and perspectives. Cancer Biol Med. 2026. doi: 10.20892/j.issn.2095-3941.2025.0707. DOI: https://doi.org/10.20892/j.issn.2095-3941.2025.0707

Vonniessen B, Tabariès S, Siegel PM. Antibody-mediated targeting of Claudins in cancer. Front Oncol. 2024;14:1320766. doi: 10.3389/fonc.2024.1320766. DOI: https://doi.org/10.3389/fonc.2024.1320766

Holm J, Hansen SI. Characterization of soluble folate receptors (folate binding proteins) in humans. Biological roles and clinical potentials in infection and malignancy. Biochim Biophys Acta Proteins Proteom. 2020;1868(10):140466. doi: 10.1016/j.bbapap.2020.140466. DOI: https://doi.org/10.1016/j.bbapap.2020.140466

Azzalini E, Stanta G, Canzonieri V, Bonin S. Overview of tumor heterogeneity in high-grade werous ovarian cancers. Int J Mol Sci. 2023;24(20):15077. doi: 10.3390/ijms242015077. DOI: https://doi.org/10.3390/ijms242015077

Wang WD, Guo YY, Yang ZL, Su GL, Sun ZJ. Sniping cancer stem cells with nanomaterials. ACS Nano. 2023;17(23):23262-23298. doi: 10.1021/acsnano.3c07828. DOI: https://doi.org/10.1021/acsnano.3c07828

Paul S, Konig MF, Pardoll DM, Bettegowda C, Papadopoulos N, Wright KM, et al. Cancer therapy with antibodies. Nat Rev. Cancer. 2024;24(6):399-426. doi: 10.1038/s41568-024-00690-x DOI: https://doi.org/10.1038/s41568-024-00690-x

Screnci B, Stafford LJ, Barnes T, Shema K, Gilman S, Wright R, et al. Antibody specificity against highly conserved membrane protein Claudin 6 driven by single atomic contact point. iScience. 2022;25(12):105665. doi: 10.1016/j.isci.2022.105665. DOI: https://doi.org/10.1016/j.isci.2022.105665

Cheung A, Liu Y, Chenoweth AM, Montaseri H, Esapa B, Chudasama V, et al. Antibody-drug conjugate design and mechanisms of action for cancer treatment: state of the art and beyond. Physiol Rev. 2026;106(3):1681-1756. doi: 10.1152/physrev.00039.2025. DOI: https://doi.org/10.1152/physrev.00039.2025

Li F, Emmerton KK, Jonas M, Zhang X, Miyamoto JB, Setter JR, et al. Intracellular released payload influences potency and bystander-killing effects of antibody-drug conjugates in preclinical models. Cancer Res. 2016;76(9):2710-2719. doi: 10.1158/0008-5472.CAN-15-1795. DOI: https://doi.org/10.1158/0008-5472.CAN-15-1795

Silverstein J, Karlan B, Herrington N, Konecny G. Antibody–drug conjugates as targeted therapy for treating gynecologic cancers: update 2025. Curr Opin Obstetr Gynecol. 2024;37(1):5. doi: 10.1097/GCO.0000000000000925. DOI: https://doi.org/10.1097/GCO.0000000000001002

Putra AD, Darmawan NS, Rahman AT, Syariatin L. Minimal residual disease detection: Bridging molecular and clinical strategies for recurrence prevention in gynecologic cancers. Int J Mol Sci. 2025;26(23):11708. doi: 10.3390/ijms262311708. DOI: https://doi.org/10.3390/ijms262311708

Shin HG, Yang HR, Yoon A, Lee S. Bispecific Antibody-Based Immune-Cell Engagers and Their Emerging Therapeutic Targets in Cancer Immunotherapy. Int J Mol Sci. 2022;23(10). doi: 10.3390/ijms23105686. DOI: https://doi.org/10.3390/ijms23105686

Feng F, Han X, Fang Z, Xi K, Wang Z, Shen J, et al. Synthetic M13 phage engagers expand CAR-T cell antigen recognition to overcome tumor heterogeneity. Trend Biotechnol. 2026. doi: 10.1016/j.tibtech.2026.02.008. DOI: https://doi.org/10.1016/j.tibtech.2026.02.008

Wang J, Zhang Q, Cao Y, Wang C, Hamzeh S. Precision theranostics in oncology: integrating antibody-drug conjugates, radioimmunotherapy, and immuno‑PET for adaptive cancer care. Discover Oncol. 2026. doi: 10.1007/s12672-026-03124-x DOI: https://doi.org/10.1007/s12672-026-05151-5

Yamazaki CM, Yamaguchi A, Anami Y. Antibody-drug conjugates with dual payloads for combating breast tumor heterogeneity and drug resistance. Nat Commun. 2021;12:3528. doi: 10.1038/s41467-021-23793-7. DOI: https://doi.org/10.1038/s41467-021-23793-7

Lorusso D, Ceni V, Daniele G. Newer ADCs and their role in ovarian cancer: the heterogeneity challenge. Ann Oncol. 2023;34(suppl). doi: 10.1016/j.annonc.2023.10.017. DOI: https://doi.org/10.1016/j.annonc.2023.10.017

Scandurra G, Marano F, Gebbia V, Valerio MR, Sambataro D, Lombardo V, et al. Management of ocular toxicity in patients with gynecologic cancer receiving novel antibody–drug conjugates: a narrative review. Clin Transl Oncol. 2026;28(3):746-756. doi: 10.1007/s12094-025-04050-5 DOI: https://doi.org/10.1007/s12094-025-04050-5

Yang M, Huang Y, Qian W, Zhu J, Fei L, Jiao Z, et al. Multifunctional nanotherapeutics for tumor microenvironment modulation in solid tumor therapy. Discover Nano. 2026;21(1):286. doi: 10.1186/s11671-026-04736-x DOI: https://doi.org/10.1186/s11671-026-04736-x

Waseem S, Zhan J, Xiao X, Bai P. Precision oncology in gynecologic cancers: molecular taxonomy, biomarker-guided therapeutics, and the challenge of therapeutic resistance. Front Oncol. 2026;16:1785469. doi: 10.3389/fonc.2026.1785469. DOI: https://doi.org/10.3389/fonc.2026.1785469

Zhou K, Liu X, Zhu H. Overcoming resistance to antibody-drug conjugates: from mechanistic insights to cutting-edge strategies. J Hematol Oncol. 2025;18(1):96. doi: 10.1186/s13045-025-01752-9. DOI: https://doi.org/10.1186/s13045-025-01752-9

Tew WP, Lacchetti C, Kohn EC. Poly(ADP-ribose) polymerase inhibitors in the management of ovarian cancer: ASCO guideline. J Clin Oncol. 2020;38(30):3468-3493. doi: 10.1200/JCO.20.01924. DOI: https://doi.org/10.1200/JCO.20.01924

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2026-10-19

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Alkunani, A. S., Shareef, L. G., & Al Arajy, A. Z. (2026). Claudin-6 (CLDN6) and Folate Receptor Alpha (FRα) Targeted Antibody-Drug Conjugates: Bypassing Platinum Resistance and Tumor Heterogeneity in High-Grade Serous Ovarian Carcinoma. Al-Rafidain Journal of Medical Sciences ( ISSN 2789-3219 ), 11(2), 140–151. https://doi.org/10.54133/ajms.v11i2.3258

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