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memo - Magazine of European Medical Oncology

, Volume 11, Issue 4, pp 284–290 | Cite as

ASCO 2018: highlights of urothelial cancer and prostate cancer

  • Renate Pichler
  • Wolfgang Horninger
  • Isabel Heidegger
Open Access
short review
  • 636 Downloads

Summary

Prostate cancer and urothelial carcinoma are the two most common urological cancers. The aim of this short review is to highlight abstracts from this year’s ASCO Annual Meeting. The phase III SPCG-13 trial showed no difference in biochemical disease-free survival by the addition of docetaxel after primary radiation therapy of localized high-risk prostate cancer. In bone dominant metastatic castration resistant prostate cancer, the phase II radium-223 dose escalation study concluded that the currently used dose with 6 cycles of 55 kBq/kg remains the standard of care. The PARP inhibitor olaparib plus abiraterone provided a significant benefit in radiological progression-free survival compared with abiraterone alone, independent of homologous recombination repair (HRR) mutation status. In localized muscle-invasive urothelial carcinoma, two phase II trials (ABACUS and PURE-01) exploring the pathological complete remission rate of atezolizumab and pembrolizumab prior to cystectomy in cisplatin-unfit or cisplatin-fit patients are presented. Novel targeted therapies such as fibroblast growth factor receptor (FGFR) inhibitors or monoclonal antibodies against nectin-4 confirmed astonishing objective response rates in heavily pretreated metastatic urothelial carcinoma (mUC) patients, resulting in a median overall survival (OS) up to 13.8 months. Finally, updated 1‑year and 2‑year OS survival rates of pembrolizumab and atezolizumab in the first line setting of mUC are presented.

Keywords

Prostate cancer Bladder cancer Urothelial carcinoma PARP inhibitors Immunotherapy Neoadjuvant chemotherapy 

Prostate cancer and urothelial cancer are the two leading urological tumor entities [1, 2]. Consequently, multiple clinical studies are ongoing either to cure patients with localized disease or to delay tumor progression in advanced stages of the disease.

Even at the latest ASCO 2018 meeting a large number of clinical studies were reported, with clinical practice changing studies in the near future especially in bladder cancer.

Localized prostate cancer

Adjuvant docetaxel after primary radiation therapy

The authors of the SPCG-13 trial presented data from a phase III randomized study analyzing the impact of adjuvant docetaxel therapy after primary radiation (≥74 Gy) in patients with localized prostate cancer. All patients were required to harbor an intermediate (PSA 10–20 ng/ml or biopsy Gleason score 7 or cT2b–cT2c) or high risk (PSA > 20 ng/ml or biopsy Gleason score 8–10 or ≥cT3a) stage of the disease. In addition to the routinely used androgen deprivation therapy, all patients were randomized either to 6 cycles docetaxel (75 mg/m2) or to placebo after radiation. The primary endpoint of the study was biochemical recurrence defined as a rising PSA ≥ 2 ng/ml above the nadir PSA value.

Although promising former studies on this issue, statistical analyses including 378 patients revealed no significant difference in biochemical disease-free survival in both arms at 5‑year follow-up (progression: +docetaxel vs. surveillance: 31% vs. 30.3%, p = 0.631), [3]. To summarize, the present study showed that adjuvant docetaxel treatment does not improve biochemical disease-free survival after radiotherapy in intermediate- or high-risk prostate cancer. However, final results of the RTOG0521 study [4] as well as the subanalysis of the STAMPEDE trial [5] also investigating this topic have to be awaited before drawing any final conclusion of the impact of adjuvant docetaxel therapy in patients with intermediate- or high-risk prostate cancer.

Metastatic castration resistant prostate cancer (mCRPC)

Androgen deprivation therapy is an important backbone treatment in advanced/metastatic prostate cancer; however, most patients will develop a castration-resistant status after 2–3 years. According to the current EAU guidelines castration resistant prostate cancer (CRPC) is defined as serum testosterone < 50 ng/dL or 1.7 nmol/L plus (1) biochemical progression (3 consecutive PSA rises one week apart resulting in two 50% increases over the nadir, and a PSA > 2 ng/mL) or (2) radiological progression (new lesions either 2 or more new bone lesions on bone scan or a soft tissue lesion) [6]. In recent years, several new treatment options have been approved for this stage of the disease (Fig. 1); however, recent data from a hospital-based registry revealed that these new agents since 2010 showed a modest benefit on overall survival rates in metastatic CRPC patients, with a median improvement of 6 months [7].
Fig. 1

Overview of approved agents in metastatic castration resistant prostate cancer (blue arrows) including their year of approval. Future new treatment options are highlighted in black, treatment options discussed in this manuscript are marked in red with *. PARP poly ADP ribose polymerase, PSMA prostate-specific membrane antigen

Therefore, there is need of improvement of existing therapies, development of new therapeutic agents as well as gain of a better knowledge about combining approved and upcoming therapeutic agents.

Radium-223 dosis escalation

According to the pivotal study published several years ago radium-223 is administered for 6 cycles with a dose of 55 kBq/kg in patients with bone dominant metastatic CRPC [8].

At the recent ASCO meeting, Sternberg et al. presented data of a phase II study comparing the standard radium-223 dose versus a high dose (88 kBq/kg for 6 cycles) as well as versus an increase of treatment cycles from 6 to 12 (55 kBq/kg for 12 cycles). Primary endpoint of the study was the symptomatic skeletal event-free survival. Data clearly showed after enrollment of 381 patients no difference in symptomatic skeletal event-free survival among the treatment groups. However, in both treatment arms with extended radium-223 treatment higher incidences of grade 3 treatment-related adverse events were observed [9].

Therefore, the authors concluded that the currently used doses of 55 kBq/kg up to 6 cycles remain standard of care in patients with symptomatic bone dominant metastatic CRPC without any >3 cm lymph node or visceral metastases [9].

Radium-223 plus enzalutamide

Both radium-223 [10] and the androgen receptor inhibitor enzalutamide [11, 12] are therapeutic options in patients with bone dominant metastatic CRPC.

Maughan et al. presented safety data from a phase II randomized trial of 49 patients treated with the combination of radium-223 plus enzalutamide versus enzalutamide alone. Interestingly they observed no difference in serious adverse events regardless of attribution between two arms [13].

This finding is in contrast to a phase III study (ERA 223, NCT02043678) combining radium-223 plus the CYP17 inhibitor abiraterone. Several months ago, the EMA stopped this trial because 34.7% of patients treated with radium-223/abiraterone had died so far, compared with 28.2% of patients given abiraterone monotherapy. Fractures were also occurred more frequently with the radium-223 combination than the placebo combination (26% vs. 8.1%). Until now the reasons for the increased number of deaths in the combination arm remains speculative.

PARP inhibition

In 2017 Mateo et al. reported in a phase II study that the PARP inhibitor olaparib significantly increased overall survival in patients no longer responding to standard treatments who had defects in DNA repair genes [14]. To further increase the efficacy a phase II study combining olaparib with abiraterone has been conducted whose mechanistic rationale is a previous preclinical study that PARP is involved in androgen receptor transcription [15].

At the ASCO meeting Clarke et al. reported data of 140 patients randomized either to olaparib monotherapy or to the combination olaparib/abiraterone. The primary endpoint of the study was the radiologic progression-free survival (rPFS). Fortunately, the combined treatment prolonged rPFS from 8.2 to 13.2 months (p = 0.034) with a HR of 0.65. Interestingly a subgroup analysis showed that patients without homologous recombination repair mutations also benefited from therapy. Despite highly promising response data, one must be concerned that in the combination arm significantly higher numbers of grade 3 treatment-related adverse events mainly focusing on cardiac events were observed [16].

Localized muscle-invasive bladder cancer (MIBC)

Checkpoint inhibitors in the neoadjuvant setting prior to radical cystectomy

Cisplatin-based neoadjuvant chemotherapy followed by radical cystectomy is currently the gold standard in localized MIBC according to the EAU guidelines [17]. Cisplatin-based neoadjuvant chemotherapy achieves pathological complete response (pCR) rates in about 30% [18], resulting in a median 5‑year overall survival (OS) benefit of 5–8% and a 16% reduction in mortality risk [19, 20]. Nevertheless, chemotherapy-associated toxicities, delayed cystectomy, no available biomarkers and the fact that more than 50% of patients are not eligible for cisplatin are reasons for low referral and treatment rates of neoadjuvant chemotherapy [21], although neoadjuvant chemotherapy is not associated with higher perioperative morbidity or mortality [22]. At the ASCO meeting, preliminary results of two phase II trials using atezolizumab [23] (ABACUS) and pembrolizumab [24] (PURE-01) in the neoadjuvant setting were presented. A comparison of these two trials is shown in Table 1. In summary, overall pCR rates were comparable to neoadjuvant chemotherapy, which enriched to 50% in PD-L1 positive patients, and to 90% in PD-L1 positive patients with additional DNA damage repair (DDR) or retinoblastoma (RB1) genomic alteration. Sequential biomarker analysis showed a dynamic increase in PD-L1 und CD8 expression with atezolizumab. Using pembrolizumab, T cell-inflamed signatures significantly discriminated pT0 from non-pT0 patients. In summary, neoadjuvant immunotherapy was associated with few side effects, no delayed surgery with similar pCR rates to chemotherapy, being a novel hopeful approach especially in cisplatin-unfit patients.
Table 1

Results of the phase II ABACUS and PURE-01 trial testing atezolizumab and pembrolizumab in the neoadjuvant setting prior to radical cystectomy

  

ABACUS

[23], Abstract #4506

PURE-01

[24], Abstract #4507

Phase

II

II

Study population (n)

68

43

Checkpoint inhibitor

Atezolizumab

Pembrolizumab

Number of cycles

2

3

Cisplatin-fit?

Cisplatin-unfit

Cisplatin-fit

Residual tumor after TURB

Yes

Yes

TNM for inclusion

cT2-T4aN0-N1

≤cT3bN0

pCR

Overall

29%

39.5%

PD-L1+

40% (≥5% IC)

50% (CPS score ≥ 20%)

PD-L1−

16%

PD-L1+ and DDR/RB1-GA: 90%

DDR and/or RB1-GA: 60%

Discontinuation/progression during CPI (n)

1 (1.5%)

1 (2.3%)

Most common AEs

21% fatigue

11% hyperthyroidism

Biomarkers

PD-L1

CPS Score, TMB

CD8

22-gene T‑cell inflamed panel qPCR

Genomic profiling

TURB transurethral resection of the bladder; pCR pathological complete response; CPI checkpoint inhibitor; AE adverse events; CPS combined positive score; DDR DNA damage repair; RB1-GA retinoblastoma genomic alteration; TMB tumor mutational burden

Metastatic urothelial carcinoma (mUC)

Overall survival (OS) updates of pembrolizumab and atezolizumab in the 1st line setting of cisplatin-unfit patients

Compared to the results of the EORTC 30986 trial by De Santis M et al. [25] that examined two carboplatin-based chemotherapy regimens (gemcitabine/carboplatin and methotrexate/carboplatin/vinblastine) in cisplatin-unfit patients [25], the survival update analysis of the KEYNOTE-052 [26] and IMvigor210 (cohort 1, [27]) studies presented at this ASCO meeting by Balar et al. [28] (Abstract #4523) and Vuky et al. [29] (Abstract #4524) confirmed a better median OS, 1‑year and 2‑year OS rate as shown in Table 2.
Table 2

Overview of updated survival data of the KEYNOTE-052 and IMvigor 210 (cohort 1) trial in comparison to results of the EORTC 30986

 

KEYNOTE-052

[29], Abstract #4524

IMvigor210 (Cohort 1)

[28], Abstract #4523

EORTC 30986

[25], Gemcitabine/carboplatin

Study population (n)

370

119

238

ORR (%)

28.9

24

36

CR Rate (%)

8.1

8

6.1

Median OS (months)

11.5

16.3

9.3

1-Year OS rate (%)

47.5

58

37

2-Year OS rate (%)

41

18

ORR objective response rate, OS overall survival, CR complete response

Nevertheless, according to preliminary data from the ongoing KEYNOTE-361 (NCT02853305) and IMvigor130 trial (NCT02807636) showing reduced survival with pembrolizumab and atezolizumab compared with standard chemotherapy in mUC patients who have not received prior therapy and whose tumors have low PD-L1 expression, the European Medicines Agency (EMA) restricts pembrolizumab and atezolizumab as monotherapy in the first-line setting only for cisplatin-unfit patients with high PD-L1 expression (≥5% for atezolizumab; tumoral CPS score ≥ 10% for pembrolizumab) [30, 31].

Targeted therapies in chemotherapy- and IO-refractory mUC

Previous trials have shown that responses to chemotherapy and IO vary by The Cancer Genome Atlas (TCGA) molecular subtyping in MIBC [32, 33, 34]. The luminal papillary I subtype UC is characterized by FGFR3 alterations [35], confirming no benefit from neoadjuvant chemotherapy prior to cystectomy [34] and being immunologically “cold” with no clear response to checkpoint inhibitors [32, 36]. Thus, patients with luminal I subtype may be ideal candidates for FGFR inhibitors. Results of phase I and II trials evaluating two FGFR inhibitors, rogaratinib [37] (Joerger M et al., Abstract #4513) and erdafitinib [38] (Siefker-Radtke A et al., Abstract #4503), in heavily pretreated mUC patients with FGFR alterations confirmed astonishing objective response rates in up to 40.4%, increasing to 59% in those patients with prior IO. The median OS (13.8 months) for erdafitinib was higher compared to pembrolizumab (KEYNOTE-045: 10.1 months; [39] Fradet T et al., Abstract #4521) and atezolizumab (Imvigor211: 11.1 months [40]; IMvigor210 cohort 2: 7.9 months, [28] Balar et al., Abstract #4523) in the second line setting. Thus, a phase III trial (THOR, NCT03390504) is ongoing randomizing patients for erdafitinib or pembrolizumab or chemotherapy (vinflunine, docetaxel).

Enfortumab, an antibody–drug conjugate that delivers cytostatic drugs to cells expressing nectin-4, a transmembrane cell adhesion molecule which is expressed in 83% of UC [41], showed similar results in a phase I trial (Rosenberg JE et al. [42], Abstract #4504) as erdafitinib concerning ORR and median OS (Table 3). Due to this encouraging preliminary findings, enfortumab will be evaluated in the third line setting compared to chemotherapy (vinflunine, docetaxel, paclitaxel) in a phase III trial in patients who progressed after platinum-based chemotherapy and IO therapy (NCT03474107).
Table 3

Results of novel targeted therapies using FGFR inhibitors (rogaratinib, erdafitinib) and nectin-4 monoclonal antibody (enfortumab) in heavily pretreated mUC patients

 

ROGARATINIB

[37], Abstract #4513

N = 51

ERDAFITINIB

[38], Abstract #4503

N = 99

ENFORTUMAB

[42], Abstract #4504

N = 112

Phase

I

II

I

Dosage

800 mg twice daily

8 mg daily (up to 9 mg)

1.25 mg/kg (day 1, 8, 15)

Target

FGFR1-4

FGFR1-4

Nectin-4

Inclusion criteria

≧1 line Cx

≧1 line Cx or

≧1 line Cx or

Cisplatin-unfit

Cisplatin-unfit

Prior IO allowed

Prior IO allowed

Prior IO allowed

Visceral metastasis

79%

77%

Crea Clearance < 60

53%

50%

≧2 lines systemic Cx

43%

63%

Prior IO

23%

79%

FGFR mutations

FGFR3+ 87%

FGFR3 mutation 75%

FGFR1+ 5%

FGFR2/3 fusion 25%

Dual FGFR +8%

ORR

Overall

24%

40.4%

41%

Prior IO

30%

59%

40%

Visceral metastasis

38.5%

39%

Median PFS (months)

5.5

5.4

Median OS (months)

13.8

13.6

AEs

Diarrhea (60.8%)

Hyperphosphatemia (73%)

Fatigue (54%)

Hyperphosphatemia (45.1%)

Skin disorders (49%)

Grade ≧ 3 AEs: anemia 8%, hyponatremia 7%, UTI 7%, and hyperglycemia 6%

Nail disorders (52%)

 

IO immuno-oncology, Cx chemotherapy, ORR objective response rate, FGFR fibroblast growth factor receptor, OS overall survival, PFS progression-free survival, AE adverse event, UTI urinary tract infection

Notes

Funding

Open access funding provided by University of Innsbruck and Medical University of Innsbruck.

Conflict of interest

R. Pichler, W. Horninger and I. Heidegger declare that they have no competing interests.

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© The Author(s) 2018

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  1. 1.Department of UrologyMedical University InnsbruckInnsbruckAustria

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