Clinical outcomes of frontline GemFLP in advanced urachal and non-urachal adenocarcinomas of the urinary tract: The MD Anderson Cancer Center (MDACC) experience.

Authors

Mohammad Jad Moussa

Mohammad Jad Moussa

Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX

Mohammad Jad Moussa , Adrienne H. Chen , Allison K. Grana , Jianjun Gao , Amishi Yogesh Shah , Paul Gettys Corn , Nizar M. Tannir , Sangeeta Goswami , Jianbo Wang , John C. Araujo , Ashish M. Kamat , Neema Navai , Curtis Alvin Pettaway , Mehrad Adibi , Bogdan Czerniak , Charles C. Guo , Arlene O. Siefker-Radtke , Matthew T Campbell , Omar Alhalabi

Organizations

Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, Division of Pharmacy, The University of Texas MD Anderson Cancer Center, Houston, TX, The University of Texas MD Anderson Cancer Center, Houston, TX, Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, TX, Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX

Research Funding

No funding sources reported

Background: Adenocarcinomas of the urinary tract, including urachal (UA) and non-urachal (NUA) subtypes, are rare tumors. Triplet regimens combining gemcitabine, a taxane or 5-fluorouracil (5-FU)/leucovorin (L), and cisplatin (P), have been developed. Methods: We retrospectively reviewed records of patients receiving frontline (1L)GemFLP (Gemcitabine 200 mg/m2 IV on days 1 and 5; 5-FU 200 mg/m2 IV on days 1, 2, 3, 4, 5; L 10mg/m2 IV on days 1, 2, 3, 4, 5; P 20mg/m2 IV on days 1, 2, 3, 4, 5) in advanced UA and NUA at MDACC between 2003 and 2023. Advanced disease is defined as Sheldon stages IVA/IVB in UA and TNM stage IV in NUA. Imaging-based best overall responses (BOR) were complete (CR), partial (PR), stable (SD), progressive (PD) or non-evaluable (NE). Overall response rate (ORR) covers CR + PR, while disease control rate (DCR) covers CR + PR + SD. We report overall survival (OS) and progression-free survival (PFS) from GemFLP start. Results: Baseline characteristics of UA (n=40) and NUA (n=28) are in Table. In UA, bladder dome was primary location in 39 (97.5%). NUA pts had either bladder (11, 39.3%) or urethral (17, 60.7%) origin. BOR in 1L GemFLP are shown in Table. In UA, ORR is 20% and DCR is 72.5%. Median OS (mOS) is 19.8 months (95% CI: 12.2 - 30.6) and median PFS (mPFS) is 5.3 mo (95% CI: 3.1 – 6.3). In UA, pts with CR, PR, or SD have a significantly longer mOS than pts with PD [26 mo (16.2 – 35.6) vs. 7.7 mo (2.67 – 11.9), log-rank p<0.0001]. Meanwhile, in NUA, ORR is 35.7% and DCR is 75%. mOS is 12.95 mo (95% CI: 7.1-20.2) and mPFS is 5.3 mo (1.93 – 7.6). A similar significant survival benefit is seen in NUA pts with disease control versus pts with PD [17.6 mo (12.6 – 25.9) vs. 5 mo (2.63 – 7.1), p<0.0001]. Surgical consolidation was offered for 6 UA pts (3 PR, 3 SD), 3 of whom were regional N+ only, and for 4 NUA pts (1 CR, 1 PR, 2 SD) who were all regional N+ only. All except one showed residual pathological disease. Conclusions: 1L GemFLP is an active regimen in advanced UA and NUA, with a DCR of >70%. Pts with disease control (CR, PR, or SD) have a clear survival benefit compared to non-responders. 1L GemFLP might offer chances at surgical consolidation after disease control for pts with regional node-positive only disease, with larger cohorts needed to confirm findings.

VariableUA (n=40)NUA (n=28)
Characteristics
Age at mets, median [ICR]57.3 [45.4 – 62.7]64 [59 – 67]
Race, n (%)White32 (80%)18 (64.3%)
Black6 (15%)7 (25%)
Other2 (5%)3 (10.7%)
Prior surgery for localized disease, n (%)22 (55%)7 (25%)
Visceral mets at 1L GemFLP, n (%)Any31 (77.5%)17 (60.7%)
Lung16 (40%)8 (28.6%)
Liver4 (10%)1 (3.6%)
Peritoneum15 (37.5%)1 (3.6%)
Bone3 (7.5%)6 (21.4%)
Nodal-only mets at 1L GemFLP, n (%)9 (22.5%)11 (39.3%)
Outcomes
BOR to 1L GemFLP, n (%)CR0 (0%)1 (3.6%)
PR8 (20%)9 (32.1%)
SD21 (52.5%)11 (39.3%)
PD7 (17.5%)5 (17.9%)
NE4 (10%)2 (7.1%)
Surgical consolidation after 1L GemFLP, n (%)6 (15%)4 (14.3%)

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Abstract Details

Meeting

2024 ASCO Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session B: Urothelial Carcinoma

Track

Urothelial Carcinoma

Sub Track

Therapeutics

Citation

J Clin Oncol 42, 2024 (suppl 4; abstr 630)

DOI

10.1200/JCO.2024.42.4_suppl.630

Abstract #

630

Poster Bd #

H15

Abstract Disclosures