Skip to main content

Advertisement

Log in

Antibody-Drug Conjugates in Gynecologic Cancers

  • Published:
Current Treatment Options in Oncology Aims and scope Submit manuscript

Opinion Statement

Antibody-drug conjugates (ADCs) are a novel class of targeted cancer therapies with the ability to selectively deliver a cytotoxic drug to a tumor cell using a monoclonal antibody linked to a cytotoxic payload. The technology of ADCs allows for tumor-specificity, improved efficacy, and decreased toxicity compared to standard chemotherapy. Common toxicities associated with ADC use include ocular, pulmonary, hematologic, and neurologic toxicities. Several ADCs have been approved by the United States Food and Drug Administration (FDA) for the management of patients with recurrent or metastatic gynecologic cancers, a population with poor outcomes and limited effective treatment options. The first FDA-approved ADC for recurrent or metastatic cervical cancer was tisotumab vedotin, a tissue factor-targeting agent, after demonstrating response in the innovaTV 204 trial. Mirvetuximab soravtansine targets folate receptor alpha and is approved for use in patients with folate receptor alpha-positive, platinum-resistant, epithelial ovarian cancer based on results from the SORAYA trial. While there are no FDA-approved ADCs for the treatment of uterine cancer, trastuzumab deruxtecan, an anti-human epidermal growth factor receptor 2 (HER2) agent, is actively being investigated. In this review, we will describe the structure and mechanism of action of ADCs, discuss their toxicity profiles, review ADCs both approved and under investigation for the management of gynecologic cancers, and discuss mechanisms of ADC resistance.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

References and Recommended Reading

Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance

  1. SEER Cancer Statistics Factsheets: Common Cancer Sites. National Cancer Institute. Available from: https://seer.cancer.gov/statfacts/html/common.html. Accessed 15 Aug 2023.

  2. Cancer Facts & Figures 2023. American Cancer Society, Inc. 2022.

  3. Schorge JO, et al. The effect of postsurgical therapy on stage III endometrial carcinoma. Gynecol Oncol. 1996;63(1):34–9.

    Article  CAS  PubMed  Google Scholar 

  4. Siegel RL, Miller KD, Wagle NS, Jemal A. Cancer statistics, 2023. CA Cancer J Clin. 2023;73(1):17–48.

    Article  PubMed  Google Scholar 

  5. Armstrong DK, et al. Ovarian Cancer, Version 2.2020, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Canc Netw, 2021;19(2):191-226.

  6. Brooks RA, et al. Current recommendations and recent progress in endometrial cancer. CA Cancer J Clin. 2019;69(4):258–79.

    Article  PubMed  Google Scholar 

  7. Marth C, et al. Cervical cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2018;29(Suppl 4):iv262.

  8. Aghajanian C, et al. OCEANS: a randomized, double-blind, placebo-controlled phase III trial of chemotherapy with or without bevacizumab in patients with platinum-sensitive recurrent epithelial ovarian, primary peritoneal, or fallopian tube cancer. J Clin Oncol. 2012;30(17):2039–45.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Burger RA, et al. Incorporation of bevacizumab in the primary treatment of ovarian cancer. N Engl J Med. 2011;365(26):2473–83.

    Article  CAS  PubMed  Google Scholar 

  10. Pujade-Lauraine E, et al. Bevacizumab combined with chemotherapy for platinum-resistant recurrent ovarian cancer: the AURELIA open-label randomized phase III trial. J Clin Oncol. 2014;32(13):1302–8.

    Article  CAS  PubMed  Google Scholar 

  11. Tewari KS, et al. Improved survival with bevacizumab in advanced cervical cancer. N Engl J Med. 2014;370(8):734–43.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Gonzalez-Martin A, et al. Niraparib in patients with newly diagnosed advanced ovarian cancer. N Engl J Med. 2019;381(25):2391–402.

    Article  CAS  PubMed  Google Scholar 

  13. Monk BJ, et al. A randomized, phase III trial to evaluate rucaparib monotherapy as maintenance treatment in patients with newly diagnosed ovarian cancer (ATHENA-MONO/GOG-3020/ENGOT-ov45). J Clin Oncol. 2022;40(34):3952–64.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Moore K, et al. Maintenance olaparib in patients with newly diagnosed advanced ovarian cancer. N Engl J Med. 2018;379(26):2495–505.

    Article  CAS  PubMed  Google Scholar 

  15. Le DT, et al. PD-1 blockade in tumors with mismatch-repair deficiency. N Engl J Med. 2015;372(26):2509–20.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Marabelle A, et al. Efficacy of pembrolizumab in patients with noncolorectal high microsatellite instability/mismatch repair-deficient cancer: results from the phase II KEYNOTE-158 study. J Clin Oncol. 2020;38(1):1–10.

    Article  CAS  PubMed  Google Scholar 

  17. O’Malley DM, et al. Pembrolizumab in patients with microsatellite instability-high advanced endometrial cancer: results from the KEYNOTE-158 study. J Clin Oncol. 2022;40(7):752–61.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Eskander RN, et al. Pembrolizumab plus chemotherapy in advanced endometrial cancer. N Engl J Med. 2023;388(23):2159–70.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Mirza MR, et al. Dostarlimab for primary advanced or recurrent endometrial cancer. N Engl J Med. 2023;388(23):2145–58.

    Article  CAS  PubMed  Google Scholar 

  20. Colombo N, et al. Pembrolizumab for persistent, recurrent, or metastatic cervical cancer. N Engl J Med. 2021;385(20):1856–67.

    Article  CAS  PubMed  Google Scholar 

  21. Lundqvist EA, Fujiwara K, Seoud M. Principles of chemotherapy. Int J Gynaecol Obstet. 2015;131(Suppl 2):S146-9.

    PubMed  Google Scholar 

  22. Tarantino P, et al. Antibody-drug conjugates: smart chemotherapy delivery across tumor histologies. CA Cancer J Clin. 2022;72(2):165–82.

    Article  PubMed  Google Scholar 

  23. Calo CA, O’Malley DM. Antibody-drug conjugates for the treatment of ovarian cancer. Expert Opin Biol Ther. 2021;21(7):875–87.

    Article  CAS  PubMed  Google Scholar 

  24. Drago JZ, Modi S, Chandarlapaty S. Unlocking the potential of antibody-drug conjugates for cancer therapy. Nat Rev Clin Oncol. 2021;18(6):327–44.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Damelin M, Zhong W, Myers J, Sapra P. Evolving strategies for target selection for antibody-drug conjugates. Pharm Res. 2015;32(11):3494–507.

    Article  CAS  PubMed  Google Scholar 

  26. Donaghy H. Effects of antibody, drug and linker on the preclinical and clinical toxicities of antibody-drug conjugates. MAbs. 2016;8(4):659–71.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Schlothauer T, et al. Novel human IgG1 and IgG4 Fc-engineered antibodies with completely abolished immune effector functions. Protein Eng Des Sel. 2016;29(10):457–66.

    Article  CAS  PubMed  Google Scholar 

  28. Shen BQ, et al. Conjugation site modulates the in vivo stability and therapeutic activity of antibody-drug conjugates. Nat Biotechnol. 2012;30(2):184–9.

    Article  CAS  PubMed  Google Scholar 

  29. Zhang D, Goldberg MV, Chiu ML. Fc Engineering approaches to enhance the Agonism and effector functions of an Anti-OX40 antibody. J Biol Chem. 2016;291(53):27134–46.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Gerlinger M, et al. Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. N Engl J Med. 2012;366(10):883–92.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Chen H, Lin Z, Arnst KE, Miller DD, Li W. Tubulin inhibitor-based antibody-drug conjugates for cancer therapy. Molecules. 2017;22(8):1281.

  32. Pahl A, Lutz C, Hechler T. Amanitins and their development as a payload for antibody-drug conjugates. Drug Discov Today Technol. 2018;30:85–9.

    Article  PubMed  Google Scholar 

  33. Fu Z, et al. Antibody drug conjugate: the “biological missile” for targeted cancer therapy. Signal Transduct Target Ther. 2022;7(1):93.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Hamblett KJ, et al. Effects of drug loading on the antitumor activity of a monoclonal antibody drug conjugate. Clin Cancer Res. 2004;10(20):7063–70.

    Article  CAS  PubMed  Google Scholar 

  35. Jain N, Smith SW, Ghone S, Tomczuk B. Current ADC Linker Chemistry. Pharm Res. 2015;32(11):3526–40.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. Sheyi R, de la Torre BG, Albericio F. Linkers: an assurance for controlled delivery of antibody-drug conjugate. Pharmaceutics. 2022;14(2):396.

  37. Kovtun YV, et al. Antibody-drug conjugates designed to eradicate tumors with homogeneous and heterogeneous expression of the target antigen. Cancer Res. 2006;66(6):3214–21.

    Article  CAS  PubMed  Google Scholar 

  38. Polson AG, et al. Antibody-drug conjugates for the treatment of non-Hodgkin‘s lymphoma: target and linker-drug selection. Cancer Res. 2009;69(6):2358–64.

    Article  CAS  PubMed  Google Scholar 

  39. McCombs JR, Owen SC. Antibody drug conjugates: design and selection of linker, payload and conjugation chemistry. AAPS J. 2015;17(2):339–51.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Masters JC, et al. Clinical toxicity of antibody drug conjugates: a meta-analysis of payloads. Invest New Drugs. 2018;36(1):121–35.

    Article  CAS  PubMed  Google Scholar 

  41. Zhu Y, Liu K, Wang K, Zhu H. Treatment-related adverse events of antibody-drug conjugates in clinical trials: a systematic review and meta-analysis. Cancer. 2023;129(2):283–95.

    Article  CAS  PubMed  Google Scholar 

  42. Eaton JS, Miller PE, Mannis MJ, Murphy CJ. Ocular adverse events associated with antibody-drug conjugates in human clinical trials. J Ocul Pharmacol Ther. 2015;31(10):589–604.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Kim SK, et al. Mitigation and management strategies for ocular events associated with tisotumab vedotin. Gynecol Oncol. 2022;165(2):385–92.

    Article  CAS  PubMed  Google Scholar 

  44. • Gilbert L, et al. Safety and efficacy of mirvetuximab soravtansine, a folate receptor alpha (FRalpha)-targeting antibody-drug conjugate (ADC), in combination with bevacizumab in patients with platinum-resistant ovarian cancer. Gynecol Oncol. 2023;170:241-247. This phase 1b/2 study is of importance as it demonstrates the antitumor effects of mirvetuximab soravtansine in patients with platinum resistant ovarian cancer regardless of level of FRα expression. In addition, it demonstrates that the combination an antibody-drug conjugate with bevacizumab was well-tolerated.

  45. Heitz N, Greer SC, Halford Z. A review of tisotumab vedotin-tftv in recurrent or metastatic cervical cancer. Ann Pharmacother. 2023;57(5):585–96.

    Article  CAS  PubMed  Google Scholar 

  46. Modi S, et al. Trastuzumab deruxtecan in previously treated HER2-low advanced breast cancer. N Engl J Med. 2022;387(1):9–20.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  47. Richardson D, et al. Updated results from the phase 1 expansion study of upifitamab rilsodotin (upri; xmt-1536), a napi2b-directed dolaflexin antibody drug conjugate (ADC) in ovarian cancer (076). Gynecologic Oncology. 2022;166:S48.

    Article  Google Scholar 

  48. Kaufman B, et al. Olaparib monotherapy in patients with advanced cancer and a germline BRCA1/2 mutation. J Clin Oncol. 2015;33(3):244–50.

    Article  CAS  PubMed  Google Scholar 

  49. Ledermann J, et al. Olaparib maintenance therapy in platinum-sensitive relapsed ovarian cancer. N Engl J Med. 2012;366(15):1382–92.

    Article  CAS  PubMed  Google Scholar 

  50. Pujade-Lauraine E, et al. Olaparib tablets as maintenance therapy in patients with platinum-sensitive, relapsed ovarian cancer and a BRCA1/2 mutation (SOLO2/ENGOT-Ov21): a double-blind, randomised, placebo-controlled, phase 3 trial. Lancet Oncol. 2017;18(9):1274–84.

    Article  CAS  PubMed  Google Scholar 

  51. Swisher EM, et al. Rucaparib in relapsed, platinum-sensitive high-grade ovarian carcinoma (ARIEL2 Part 1): an international, multicentre, open-label, phase 2 trial. Lancet Oncol. 2017;18(1):75–87.

    Article  CAS  PubMed  Google Scholar 

  52. Chen YL, et al. Serous ovarian carcinoma patients with high alpha-folate receptor had reducing survival and cytotoxic chemo-response. Mol Oncol. 2012;6(3):360–9.

    Article  CAS  PubMed  Google Scholar 

  53. Kalli KR, et al. Folate receptor alpha as a tumor target in epithelial ovarian cancer. Gynecol Oncol. 2008;108(3):619–26.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  54. •• Matulonis UA, et al. 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. This phase II SORAYA study is of outstanding importance as it demonstrated the antitumor effects of mirvetuximab soravtansine in patients with platinum-resistant epithelial ovarian cancer who have received up to three prior therapies including bevacizumab. The results of this study were practice-changing and led to approval of mirvetuximab for use in folate receptor alpha-positive, platinum resistant, epithelial ovarian cancer.

  55. ImmunoGen Announces FDA Accelerated Approval of ELAHERE™ (mirvetuximab soravtansine-gynx) for the Treatment of Platinum-Resistant Ovarian Cancer. [cited 2023 August 31]; News release]. Available from: https://investor.immunogen.com/news-releases/news-release-details/immunogen-announces-fda-accelerated-approval-elaheretm. Accessed 15 Aug 2023.

  56. •• Moore KN, et al. Phase III MIRASOL (GOG 3045/ENGOT-ov55) study: Initial report of mirvetuximab soravtansine vs. investigator’s choice of chemotherapy in platinum-resistant, advanced high-grade epithelial ovarian, primary peritoneal, or fallopian tube cancers with high folate receptor-alpha expression. J Clin Oncol. 2023;41(17_suppl):LBA5507–LBA5507. While the final results from this study have not yet been published, the initial results report of the phase III MIRASOL study are of outstanding importance. This study confirms mirvetuximab as the first treatment to demonstrate both progression-free and overall survival in platinum-resistant ovarian cancer compared to investigator’s choice chemotherapy. These results will likely result in changes to standard of care treatment for patients with FR alpha-positive platinum resistant ovarian cancer.

  57. O’Malley DM, et al. Phase Ib study of mirvetuximab soravtansine, a folate receptor alpha (FRalpha)-targeting antibody-drug conjugate (ADC), in combination with bevacizumab in patients with platinum-resistant ovarian cancer. Gynecol Oncol. 2020;157(2):379–85.

    Article  CAS  PubMed  Google Scholar 

  58. Naumann RW, et al. Phase 1 dose-escalation study of STRO-002, an antifolate receptor alpha (FRα) antibody drug conjugate (ADC), in patients with advanced, progressive platinum-resistant/refractory epithelial ovarian cancer (EOC). J Clin Oncol. 2021;39(15_suppl): 5550–5550.

  59. Naumann RW, et al. STRO-002-GM2: A phase 1, open-label, safety, pharmacokinetic, and preliminary efficacy study of STRO-002, an anti-folate receptor alpha (FolRα) antibody-drug conjugate (ADC), in combination with bevacizumab in patients with advanced epithelial ovarian cancer (EOC, including fallopian tube or primary peritoneal cancers). J Clin Oncol. 2022;40(16_suppl):TPS5622–TPS5622.

  60. Shimizu T, et al. First-in-human phase 1 study of MORAb-202, an antibody-drug conjugate comprising farletuzumab linked to eribulin mesylate, in patients with folate receptor-α-positive advanced solid tumors. Clin Cancer Res. 2021;27(14):3905–15.

    Article  CAS  PubMed  Google Scholar 

  61. Armstrong DK, et al. Farletuzumab (a monoclonal antibody against folate receptor alpha) in relapsed platinum-sensitive ovarian cancer. Gynecol Oncol. 2013;129(3):452–8.

    Article  CAS  PubMed  Google Scholar 

  62. Vergote I, et al. A randomized, double-blind, placebo-controlled, phase iii study to assess efficacy and safety of weekly farletuzumab in combination with carboplatin and taxane in patients with ovarian cancer in first platinum-sensitive relapse. J Clin Oncol. 2016;34(19):2271–8.

    Article  CAS  PubMed  Google Scholar 

  63. Levan K, et al. Immunohistochemical evaluation of epithelial ovarian carcinomas identifies three different expression patterns of the MX35 antigen, NaPi2b. BMC Cancer. 2017;17(1):303.

    Article  PubMed  PubMed Central  Google Scholar 

  64. • Gerber DE, et al. Phase Ia study of anti-NaPi2b antibody-drug conjugate lifastuzumab vedotin DNIB0600A in patients with non-small cell lung cancer and platinum-resistant ovarian cancer. Clin Cancer Res. 2020;26(2):364–372. This phase I trial of lifastuzumab vedotin in patients with platinum-resistant ovarian cancer is of importance as it identified NaPi2b as a target of interest and demonstrated encouraging antitumor activity with an acceptable safety profile.

  65. • Moore KN, et al. Phase 1b study of anti-NaPi2b antibody-drug conjugate lifastuzumab vedotin (DNIB0600A) in patients with platinum-sensitive recurrent ovarian cancer. Gynecol Oncol. 2020;158(3):631–639. This phase 1b study of lifastuzumab vedotin is also of importance as it demonstrated efficacy in a different patient population, specifically those with recurrent platinum-sensitive ovarian cancer. In addition, this study is important as it evaluates the use of combination therapy with lifastuzumab and carboplatin with or without bevacizumab.

  66. Yurkovetskiy AV, et al. Dolaflexin: a novel antibody-drug conjugate platform featuring high drug loading and a controlled bystander effect. Mol Cancer Ther. 2021;20(5):885–95.

    Article  CAS  PubMed  Google Scholar 

  67. Mersana Therapeutics announces topline data from UPLIFT clinical trial in patients with platinum-resistant ovarian cancer and strategic reprioritization. [cited 2023 August 31]; News release]. Available from: https://finance.yahoo.com/news/mersana-therapeutics-announces-topline-data-110600082.html?guccounter=1. Accessed 15 Aug 2023.

  68. Harter P, et al. UP-NEXT (GOG-3049/ENGOT-Ov71-NSGO-CTU): A study of upitifamab rilsodotin (UpRi), a NaPi2b-directed antibody drug conjugate (ADC), in platinum-sensitive recurrent ovarian cancer. J Clin Oncol. 2023;41(16_suppl):TPS5614–TPS5614.

  69. Mersana Therapeutics announces partial clinical hold on UP-NEXT and UPGRADE-A clinical trials. [cited 2023 August 31]; Press release]. Available from: https://ir.mersana.com/news-releases/news-release-details/mersana-therapeutics-announces-partial-clinical-hold-next-and. Accessed 15 Aug 2023.

  70. Hassan R, Kreitman RJ, Pastan I, Willingham MC. Localization of mesothelin in epithelial ovarian cancer. Appl Immunohistochem Mol Morphol. 2005;13(3):243–7.

    Article  CAS  PubMed  Google Scholar 

  71. Lheureux S, et al. A randomized phase II study of bevacizumab and weekly anetumab ravtansine or weekly paclitaxel in platinum-resistant or refractory ovarian cancer NCI trial#10150. J Clin Oncol. 2022;40(16_suppl):5514–5514.

  72. •• Nishikawa T, et al. Trastuzumab deruxtecan for human epidermal growth factor receptor 2-expressing advanced or recurrent uterine carcinosarcoma (NCCH1615): the STATICE trial. J Clin Oncol. 2023;41(15):2789–2799. This phase II STATICE trial is of outstanding importance as it demonstrates the efficacy of trastuzumab deruxtecan for HER2-expressing advanced or recurrent uterine carcinosarcoma regardless of HER2 status. There are currently no FDA-approved ADCs for use in uterine cancer, and identifying treatments for advanced or recurrent uterine cancer is of utmost importance.

  73. •• Meric-Bernstam F, et al. Efficacy and safety of trastuzumab deruxtecan (T-DXd) in patients (pts) with HER2-expressing solid tumors: DESTINY-PanTumor02 (DP-02) interim results. J Clin Oncol. 2023;41(17_suppl): LBA3000–LBA3000. While the final results are not published, interim results from the DESTINY-PanTumor02 trial are of outstanding importance. Trastuzumab deruxtecan demonstrated efficacy in cervical, endometrial, and ovarian cancer, emphasing the importance of targeting HER2 expressing gynecologic cancers.

  74. Assaraf YG, Leamon CP, Reddy JA. The folate receptor as a rational therapeutic target for personalized cancer treatment. Drug Resist Updat. 2014;17(4–6):89–95.

    Article  PubMed  Google Scholar 

  75. Moore KN, et al. Phase 1 dose-escalation study of mirvetuximab soravtansine (IMGN853), a folate receptor alpha-targeting antibody-drug conjugate, in patients with solid tumors. Cancer. 2017;123(16):3080–7.

    Article  CAS  PubMed  Google Scholar 

  76. Varughese J, et al. Uterine serous papillary carcinomas overexpress human trophoblast-cell-surface marker (Trop-2) and are highly sensitive to immunotherapy with hRS7, a humanized anti-Trop-2 monoclonal antibody. Cancer. 2011;117(14):3163–72.

    Article  CAS  PubMed  Google Scholar 

  77. Goldenberg DM, et al. Trop-2 is a novel target for solid cancer therapy with sacituzumab govitecan (IMMU-132), an antibody-drug conjugate (ADC). Oncotarget. 2015;6(26):22496–512.

    Article  PubMed  PubMed Central  Google Scholar 

  78. Bardia A, et al. Sacituzumab govitecan, a Trop-2-directed antibody-drug conjugate, for patients with epithelial cancer: final safety and efficacy results from the phase I/II IMMU-132-01 basket trial. Ann Oncol. 2021;32(6):746–56.

    Article  CAS  PubMed  Google Scholar 

  79. Francoeur AA, Liao CI, Caesar MA, Chan A, Kapp DS, Cohen JG, Salani R, Chan JK. The increasing incidence of stage IV cervical cancer in the USA: what factors are related?.  Int J Gynecol Cancer. 2022;32(9).

  80. Liao CI, et al. Trends in human papillomavirus-associated cancers, demographic characteristics, and vaccinations in the US, 2001–2017. JAMA Netw Open. 2022;5(3): e222530.

    Article  PubMed  PubMed Central  Google Scholar 

  81. Zhao X, et al. Expression of tissue factor in human cervical carcinoma tissue. Exp Ther Med. 2018;16(5):4075–81.

    PubMed  PubMed Central  Google Scholar 

  82. •• Coleman RL, et al. Efficacy and safety of tisotumab vedotin in previously treated recurrent or metastatic cervical cancer (innovaTV 204/GOG-3023/ENGOT-cx6): a multicentre, open-label, single-arm, phase 2 study. Lancet Oncol. 2021. 22(5):609–619. This phase II study of tisotumab vedotin in previously treated recurrent or metastatic cervical cancer is of outstanding importance as it demonstrated durable antitumor activity with a manageable safety profile. Patients with recurrent or metastatic cervical cancer have very poor prognoses, and effective treatment options in this population are crucial. The results of this study led to FDA-approval of tisotumab vedotin for recurrent or metastatic cervical cancer with progression on or after chemotherapy.

  83. •• Vergote I, et al. Tisotumab Vedotin in combination with carboplatin, pembrolizumab, or bevacizumab in recurrent or metastatic cervical cancer: results from the innovaTV 205/GOG-3024/ENGOT-cx8 study. J Clin Oncol. 2023:JCO2300720. These recently published results from the innovaTV205/GOG-3024/ENGOT-cx8 study are of outstanding importance. This phase Ib/II study of tisotumab vedotin in combination with carboplatin, pembrolizumab, or bevacizumab in patients with recurrent or metastatic cervical cancer. As previously stated, patients with recurrent or metastatic cervical cancer have poor prognoses, and effective treatment options are needed. All combinations demonstrated antitumor activity with manageable safety profiles.

  84. Seagen and Genmab announce TIVDAK® (tisotumab vedotin-tftv) improved overall survival in patients with recurrent or metastatic cervical cancer compared with chemotherapy alone. News release. Seagen Inc. and Genmab A/S. 2023. bit.ly/3r60gnB. Accessed 4 Sep 2023.

  85. Trastuzumab deruxtecan effectively treats HER2-expressing cancers regardless of tumor location. [cited 2023 August 31]; New release]. Available from: https://old-prod.asco.org/about-asco/press-center/news-releases/trastuzumab-deruxtecan-effectively-treats-her2-expressing. Accessed 15 Aug 2023.

  86. Sakai H, et al. HER2 genomic amplification in circulating tumor DNA and estrogen receptor positivity predict primary resistance to trastuzumab emtansine (T-DM1) in patients with HER2-positive metastatic breast cancer. Breast Cancer. 2018;25(5):605–13.

    Article  PubMed  Google Scholar 

  87. Hunter FW, et al. Mechanisms of resistance to trastuzumab emtansine (T-DM1) in HER2-positive breast cancer. Br J Cancer. 2020;122(5):603–12.

    Article  CAS  PubMed  Google Scholar 

  88. Loganzo F, Sung M, Gerber HP. Mechanisms of resistance to antibody-drug conjugates. Mol Cancer Ther. 2016;15(12):2825–34.

    Article  CAS  PubMed  Google Scholar 

  89. Loganzo F, et al. Tumor cells chronically treated with a trastuzumab-maytansinoid antibody-drug conjugate develop varied resistance mechanisms but respond to alternate treatments. Mol Cancer Ther. 2015;14(4):952–63.

    Article  CAS  PubMed  Google Scholar 

  90. Sung M, et al. Caveolae-mediated endocytosis as a novel mechanism of resistance to trastuzumab emtansine (T-DM1). Mol Cancer Ther. 2018;17(1):243–53.

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Contributions

MKA and SS wrote the main manuscript text. MKA prepared figure 1 and tables 1 and 2. All authors reviewed the manuscript.

Corresponding author

Correspondence to Mary Katherine Anastasio MD.

Ethics declarations

Competing interests

The authors declare no competing interests.

Human and Animal Rights and Informed Consent

This article does not contain any studies with human or animal subjects performed by any of the authors.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Anastasio, M.K., Shuey, S. & Davidson, B.A. Antibody-Drug Conjugates in Gynecologic Cancers. Curr. Treat. Options in Oncol. 25, 1–19 (2024). https://doi.org/10.1007/s11864-023-01166-0

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11864-023-01166-0

Keywords

Navigation