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Semir Vranic Orcid logo
Semir Vranic

College of Medicine, QU Health, Qatar University, Doha, Qatar,

Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book. It has survived not only five centuries, but also the leap into electronic typesetting, remaining essentially unchanged. It was popularised in the 1960s with the release of Letraset sheets containing Lorem Ipsum passages, and more recently with desktop publishing software like Aldus PageMaker including versions of Lorem Ipsum_711


Antibody-drug conjugates (ADCs) are novel, highly potent drugs composed of a small molecule of an anticancer drug (payload) attached to humanized antibody recognizing an epitope on the surface of cancer cells. ADCs are rapidly expanding in the oncology field. By 2022, >180 ADC-based clinical trials have been conducted [1]. Most of these clinical trials are in phases I or II [1]. Several ADCs have been approved and used for the treatment of various malignancies (e.g., brentuximab vedotin (BV) for the treatment of CD30+ lymphomas, trastuzumab emtansine (T-DM1) for advanced/metastatic/or early-stage high-risk HER2-positive breast cancer with residual disease after neoadjuvant treatment) [2]. Among the new ADCs is sacituzumab govitecan (SG)/Trodelvy®, a conjugate of anti-Trop-2 antibody and SN-38 payload (an active metabolite of irinotecan). SG has been recently approved by the Food and Drug Administration (FDA) for the treatment of metastatic triple-negative breast (2020) and urothelial carcinomas (2021) [3]. SG activity is based on targeting the trophoblast cell-surface antigen-2 (Trop-2). Trop-2 (or EpCAM/Trop-1) acts as an epithelial-specific cell adhesion molecule, exhibiting a growth-stimulatory effects [4, 5]. It also transduces intracellular calcium signaling, which can occur without extracellular Ca2+ [6].

Trop-2 expression was initially described in trophoblasts and fetal tissues, but subsequently, Trop-2 activity has been demonstrated in various solid (e.g., breast, urothelial, ovarian, colorectal, pancreatic, gastric, prostate, cervical, lung, salivary gland, and oral squamous cell carcinomas) and hematologic malignancies (e.g., leukemias and non-Hodgkin lymphomas) [3, 6–9]. In the breast, Trop-2 expression has been observed in different histologic and molecular subtypes, including luminal and triple-negative breast cancers [8, 10–12].

In contrast to its prognostic value [13], the predictive value of Trop-2 expression has not been established yet. Consequently, predictive testing was not done in any of the trials that led to the approval of SG. However, some ongoing clinical trials, like the one exploring the therapeutic effects of SG in patients with endometrial carcinoma (ClinicalTrials.gov Identifier: NCT04251416) set as an inclusion criterion the availability of endometrial carcinoma tissue and “at least 2+ staining for Trop-2” by immunohistochemistry [14]. Similarly, an ongoing clinical trial (ClinicalTrials.gov Identifier: NCT04152499) will explore the therapeutic utility of SKB264, a monoclonal anti-Trop-2 antibody, in advanced/refractory cancers with a prior predictive Trop-2 testing by immunohistochemistry [15].

The most recent (third) FDA approval of SG occurred on February 3, 2023. It is related to luminal breast cancers (estrogen receptor-positive [ER+], HER2-negative [HER2−]), the largest (70%) subgroup of breast carcinomas. The approval was based on a phase 3 randomized clinical trial (TROPiCS-02 study) that involved locally advanced/metastatic luminal breast cancers (ER+/HER2−), previously treated with endocrine and at least two additional systemic treatment modalities [16]. In the TROPiCS-02 study, SG exhibited a significant and clinically meaningful overall survival (OS) benefit of 3.2 months compared with single-agent chemotherapy (median OS: 14.4 months vs 11.2 months; hazard ratio [HR] ═ 0.79; 95% CI: 0.65–0.96; p ═ 0.02). SG also demonstrated a substantial (34%) reduction risk of disease progression or death (median progression-free survival: 5.5 vs 4.0 months; HR: 0.66; 95% CI: 0.53–0.83; p ═ 0.0003). Notably, 21% of patients treated with SG were progression-free at one year compared with 7% of those treated with conventional chemotherapy [16].


In advanced/metastatic settings, the treatment of luminal breast cancers remains challenging. Endocrine resistance, poor response to conventional chemotherapy and resistance to several targeted treatment modalities, such as PIK3CA and CDK4/6 inhibitors, are commonly seen in daily practice. Therefore, the approval with SG expands the therapeutic options for the largest subpopulation of breast cancer patients.

Ongoing clinical trials targeting Trop-2 protein appear to be more promising since they include predictive testing for Trop-2 expression and a more individualized therapeutic approach.


This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 

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