Table of Contents Table of Contents
Previous Page  489 656 Next Page
Information
Show Menu
Previous Page 489 656 Next Page
Page Background

these criteria are not followed, TMT outcomes will appear

worse. Second, the actual indication for TMT is not specified

and may be a ‘‘last ditch effort’’ for sicker patients, again

potentially biasing towards worse TMT outcomes. Third, the

NCDB lacks granular data points such as type of chemothera-

py or number of cycles administered, in addition to indicators

for why complete chemotherapy regimens were not

completed (ie, renal function, performance status). Ideally,

chemotherapy for TMT should be a cisplatin-based regimen

[6]

. Additionally, timing of chemotherapy (ie, neoadjuvant vs

adjuvant vs concomitant) is not specified in the database,

only whether ‘‘single or multiagent chemotherapy was

administered as first course therapy.’’ Thus, whether patients

received ‘‘complete TMT’’ is speculative. Finally, OS was the

end-point used in the current study, since disease-specific

survival (DSS) outcomes are not feasible in the NCDB.

Arguably, OS is an ‘‘all-encompassing’’ and clinically relevant

endpoint; however, when comparing efficacy of two

treatment approaches head-to-head for superiority, evaluat-

ing DSS may be considered a more appropriate outcome that

provides more convincing conclusions.

While we agree with the authors that in a perfect world

randomized control trials comparing TMT with RC would be

ideal, the likelihood of accruing to and completing such a trial

will be difficult, particularly if superiority is not the ultimate

study goal. With these shortcomings in mind, there are two

institutional studies that have compared outcomes of TMT to

RC using propensity score matching analysis. Our group at

the University of Toronto recently matched 56 TMT patients

(of 59 eligible) to RC patients using propensity scores

[9]

. Included in the matching were cT and cN-stage, Eastern

Cooperative Oncology Group score, comorbidity, extent of CIS

and hydronephrosis, and year of therapy. These granular

details allowed for a robust comparison of RC versus TMT

outcomes, where the latter was given as a bladder-preserving

curative treatment. After a median 4.5 yr of follow-up, there

was no significant difference in DSS between the two groups

(HR for TMT: 0.92, 95% CI: 0.41–2.04). Authors from South

Korea recently published a cohort of 29 TMT patients who

were propensity score matched to 50 patients undergoing RC

[10]

, noting comparable 5-yr DSS between the two groups

(RC 69% vs TMT 63%; HR: 0.96, 95% CI: 0.38–2.47). Albeit

smaller institutional studies, these analyses ensure strict TMT

selection criteria adherence, demonstrating no difference

between TMT and RC in highly selected MIBC patients.

Ultimately, in the absence of randomized control trials,

we must rely on methodologically sound observational

studies with granular data to help guide treatment decisions.

Undoubtedly, RC remains the surgical gold-standard for

localized MIBC. However, patients who are candidates for

both treatment modalities should at least be engaged in a

discussion about the merits of both approaches. With sound

clinical judgement to appropriately select patients and

judicious informed consent discussions, patients with

localized MIBC may actually have a second treatment option

beyond our traditional gold standard.

Conflicts of interest:

The authors have nothing to disclose.

References

[1]

Shabsigh A, Korets R, Vora KC, et al. Defining early morbidity of radical cystectomy for patients with bladder cancer using a stan- dardize reporting methodology. Eur Urol 2009;55:164–74.

[2]

Izquierdo L, Peri L, Leon P, et al. The role of cystectomy in elderly patients—a multicenter analysis. BJU Int 2015;116:73–9

.

[3]

Garde H, Ciappara M, Galante I, et al. Radical cystectomy in octoge- narian patients: a difficult decision tomake. Urol Int 2015;94:390–3

.

[4]

Gore JL, Litwin MS, Lai J, et al. Use of radical cystectomy for patients with invasive bladder cancer. J Natl Cancer Inst 2010;102:802–11

.

[5]

Russel CM, Lebastchi AH, Borza T, Spratt DE, Morgan TM. The role of transurethral resection in trimodal therapy for muscle-invasive bladder cancer. Bladder Cancer 2016;2:381–94

.

[6]

Chen RC, Shipley WU, Efstathiou JA, Zietman AL. Trimodality blad- der preservation therapy for muscle-invasive bladder cancer. J Natl Compr Canc Netw 2013;11:952–60

.

[7]

Seisen T, Sun M, Lipsitz SR, et al. Comparative effectiveness of trimodal therapy versus radical cystectomy for localized muscle- invasive urothelial carcinoma of the bladder. Eur Urol 2017;72:483–7

.

[8]

Efstathiou JA, Spiegel DY, Shipley WU, et al. Long-term outcomes of selective bladder preservation by combined-modality therapy for invasive bladder cancer: The MGH experience. Eur Urol 2012;61:705–11

.

[9]

Kulkarni GS, Hermanns T, Wei Y, et al. Propensity score analysis of radical cystectomy versus bladder-sparing trimodal therapy in the setting of a multidisciplinary bladder cancer clinic. J Clin Oncol 2017;35:2299–305

.

[10] Kim YJ, Byun SJ, Ahn H, et al. Comparison of outcomes between

trimodal therapy and radical cystectomy in muscle-invasive blad-

der cancer: a propensity score matching analysis. Oncotarget. In

press.

http://dx.doi.org/10.18632/oncotarget.16576

.

http://dx.doi.org/10.1016/j.eururo.2017.04.028

Platinum Priority

Reply from Authors re: Girish S. Kulkarni,

Zachary Klaassen. Trimodal Therapy is Inferior to

Radical Cystectomy for Muscle-invasive Bladder

Cancer

[34_TD$DIFF]

using Population-level Data: Is There Evidence in

the (Lack of) Details? Eur Urol 2017;72:488–9

Using the National Cancer Data Base to Compare Treat-

ment Modalities for Localized Muscle-invasive Bladder

Cancer

Thomas Seisen, Alexander P. Cole, Quoc-Dien Trinh

*

Division of Urological Surgery and Center for Surgery and Public Health,

Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA

DOIs of original articles:

http://dx.doi.org/10.1016/j.eururo.2017.04.028

,

http://dx.doi.org/10.1016/j.eururo.2017.03.038

.

* Corresponding author. Division of Urological Surgery, Brigham and

Women’s Hospital, 45 Francis Street, Boston, MA 02115, USA.

Tel. +1 617 5257350; Fax: +1 617 5256348.

E-mail address:

qtrinh@bwh.harvard.edu

(Q.-D. Trinh).

E U R O P E A N U R O L O G Y 7 2 ( 2 0 1 7 ) 4 8 8 – 4 9 1

489