Abstract
Enfortumab vedotin (EV), a nectin-4-directed antibody conjugated to monomethyl auristatin E (MMAE), has been approved for patients with advanced urothelial carcinoma (aUC) previously treated with platinum-based chemotherapy and immune inhibitors. Taxane agents and MMAE share antitumor mechanisms through microtubule disruption, thus raising a notable concern regarding cross-resistance between these drugs. This case report describes two patients with taxane-based chemotherapy-refractory aUC who responded well to EV. A 71-year-old man (case 1) with pT3N0M0 renal pelvic UC showed a partial response to EV in metastatic lesions of the bilateral lungs and right pelvic lymph nodes after three cycles of paclitaxel plus gemcitabine chemotherapy. A 53-year-old man (case 2) with cT3bN2M0 bladder UC underwent platinum-based neoadjuvant chemotherapy and the following radial cystectomy (ypTis ypN0). He developed bilateral lung metastases and showed a complete response to EV in the metastatic lesions after 20 cycles of paclitaxel plus nedaplatin chemotherapy. Our experience of two cases demonstrated that tumor response to EV can be expected in patients with taxane-refractory aUC.
1. Introduction
Urothelial cancer (UC) of the bladder is the 12th most common cancer worldwide, accounting for 573,278 new cases and 212,536 deaths annually [1]. In spite recent advancements in systemic therapy, the prognosis of patients with advanced (aUC), unresectable, or metastatic UC remains poor. Platinum-based chemotherapy, immune checkpoint inhibitors, taxane-based chemotherapy, and FGFR-targeted therapy are currently available for patients with aUC [2]. Taxane agents, such as paclitaxel and docetaxel, exert anticancer activity by promoting polymerization of tubulin dimers, stabilizing microtubules, and inhibiting cell division [3, 4]. Evaluation of 370 patients from eight phase 2 trials demonstrated that taxane plus other chemotherapeutic agents was associated with prolonged overall survival as late-line systemic therapy following prior platinum-based therapy [5].
Recently, enfortumab vedotin (EV), a nectin-4-directed antibody conjugated to monomethyl auristatin E (MMAE), has been approved for patients with aUC previously treated with platinum-based chemotherapy and programmed cell death-1 (PD-1)/programmed death-ligand 1 (PD-L1) inhibitors [6]. MMAE is a synthetic derivative of dolastatin-10 and is similar to taxanes, which disrupt microtubule dynamics through inhibition of tubulin polymerization [7, 8]. The two-dimensional structure of three microtubule-disrupting anticancer agents is shown in Figure 1 demonstrating that the structure of MMAE is not similar to two taxane agents. The treatment sequence in cancer management is vital to achieve long survival.
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One of the biggest clinical concerns is whether taxane-refractory tumors can respond to EV and if EV-resistant tumors can respond to taxane agents. However, data regarding the cross-resistance between taxane anticancer agents and MMAE in urothelial cancer is limited. This case report describes two patients with taxane-based chemotherapy-refractory aUC who responded well to EV.
2. Case Presentation
2.1. Case 1
The patient was a 71-year-old man with localized UC of the right renal pelvis (pT3pN0 in a nephroureterectomy specimen). He received three cycles of adjuvant gemcitabine plus cisplatin (GC) chemotherapy. One year after radical surgery, right iliac lymph node metastasis developed, and he was treated with three cycles of paclitaxel plus gemcitabine (PG) chemotherapy consisting of paclitaxel 175 mg/m2 on day 1 and 1,000 mg/m2 on days 1 and 8, every three weeks. The metastatic lesion did not respond to taxane-based chemotherapy (Figure 2(a)). We observed that the development of multiple lung metastases and lymph node metastases further progressed and invaded the bladder, followed by palliative radiotherapy to the bladder-invading lesion to control urinary bleeding. After he received a total of 23 doses of pembrolizumab and 13 cycles of M-VAC (50%-reduced dose of methotrexate, vinblastine, and doxorubicin and 50%-reduced dose of cisplatin) chemotherapy, multiple lung metastases, and lymph node metastasis progressed (Figure 2(a)). He was started on a 1.25 mg/kg dose of EV (on days 1, 8, and 15 of a 28-day cycle). Because he presented with grade 3 erythema multiforme during the first cycle, the dose of EV was reduced by 20% (1.00 mg/kg) thereafter. The metastatic lesions responded to EV (partial response) after three cycles of EV (Figure 2(a)). The treatment is ongoing.
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2.2. Case 2
A 53-year-old man presented with cT3bN2M0 muscle-invasive bladder UC. After receiving a cycle of GC chemotherapy and a cycle of gemcitabine plus carboplatin chemotherapy as a neoadjuvant setting, laparoscopic radical cystectomy accompanied with lymph node dissection and ileal conduit was performed, and the pathological diagnosis was ypTis and ypN0. Because multiple lung metastases developed within 12 months after the last dose of perioperative chemotherapy, pembrolizumab was initiated, and he received a total of eight cycles [9]. Then, paclitaxel plus nedaplatin (PN) chemotherapy consisting of paclitaxel 200 mg/m2 on day 1 and nedaplatin 100 mg/m2 on day 1, every three to four weeks was administered to mitigate pembrolizumab-refractory disease. After 20 cycles of PN, multiple lung metastases progressed; however, he developed hearing impairment due to platinum agents (Figure 2(b)). He was started on a 1.25 mg/kg dose of EV. The metastatic lesions became undetectable (complete response) after four cycles of EV (Figure 2(b)). The treatment is still ongoing without any severe adverse events.
3. Discussion
We described the clinical courses of two patients in whom taxane-based chemotherapy-refractory metastatic lesions responded to EV. EV is a nectin-4-directed anticancer drug conjugate (ADC) approved as a salvage treatment for aUC. ADCs are an emerging class of drugs designed to increase selectivity for cancer cells and potentially reduce toxicity by conjugating cytotoxic agents to highly specific monoclonal antibodies [4]. Hoffman-Censits et al. performed immunohistochemical staining analysis to compare nectin-4 expression and reported that 58% of the muscle-invasive UC were positive for nectin-4 expression with a histoscore (-score, 0 to 300) cutoff of 15 [10]. Conjugating MMAE to the nectin-4-biding antibody provided significant clinical benefit in EV-201 and EV-301 trials [6, 11, 12]. However, EV treatment can cause severe adverse events, including skin reactions, hematologic toxicity, hyperglycemia, and peripheral neuropathy [13]. When patients are indicated for EV administration, physicians need to pay attention to balance of oncological benefit and risk of potential adverse events.
The two patients described in this report responded well to EV even after the patients acquired taxane resistance. Taxane agents and MMAE share antitumor mechanisms through microtubule disruption, which raises a significant concern regarding cross-resistance between these drugs. The molecular mechanisms underlying taxane resistance in UC are not fully understood. Activation of the fibroblast growth factor receptor signaling pathway and epithelial–mesenchymal transition plays an important role in cancer progression and paclitaxel resistance [14, 15]. Chu et al. reported that EV sensitivity is strongly associated with the luminal subtype and nectin-4 expression [16]. Some studies have suggested that exposure to cisplatin-based chemotherapy could decrease nectin-4 expression in UC cells, indicating that pretreatment could induce EV resistance [17–19]. However, only little is known about the molecular mechanisms underlying MMAE resistance, especially in UC. Chen et al. utilized a functional genomics approach to identify putative biomarkers of resistance to paclitaxel and MMAE in breast cancer and found that amplification of the chromosome 17q21 region encoding the ABCC3 drug transporter gene is highly associated with resistance to both drugs [20]. Further analyses using MMAE-resistant UC and MMAE-sensitive UC are required to determine the exact mechanism underpinning EV resistance and to develop combined interventions for patients with aUC and EV resistance. Another issue to be discussed is the difference of drug delivery efficiency between EV and standard chemotherapy drugs. EV is designed to efficiently deliver its payload and MMAE by actively targeting nectin-4, which is highly expressed in UC. It could be a marked concern whether enough uptake of paclitaxel into the tumor was delivered to tumor tissue to exert an antitumor effect, because the tumor biopsy was not performed and intratumoral concentration of paclitaxel was not measured during treatment in our cases.
4. Conclusion
This case report suggests that a tumor response to EV can be expected in taxane-refractory aUC. However, in this case report, patients treated with taxane agents for EV-refractory aUC were excluded. More clinical evidence should be accumulated to establish better treatment strategies consisting of multiple systemic treatments, such as platinum-based chemotherapy, immune checkpoint inhibitors, taxane-based chemotherapy, and EV.
Data Availability
The data used to support the findings of this study are included within the article.
Conflicts of Interest
M. Miyake received honoraria from Pfizer Inc., Merck Biopharma Co., Ltd., MSD K.K., and Astellas Pharma Inc. and served in a consulting or advisory role for Pfizer Inc. and Astellas Pharma Inc. K. Fujimoto received honoraria from Pfizer Inc., Merck Biopharma Co., Ltd., MSD K.K., Ono Pharmaceutical Co., Ltd., and Astellas Pharma Inc.; received research funding from Pfizer Inc., MSD K.K., Ono Pharmaceutical Co., Ltd., and Astellas Pharma Inc.; and served in a consulting or advisory role for Pfizer Inc. and Ono Pharmaceutical Co., Ltd. Other authors disclose no potential conflicts of interest.
Acknowledgments
The authors thank the patients for their important contribution to this study.