Real-world quality of life (QOL) for patients (pts) with metastatic renal cell carcinoma (mRCC) treated with systemic therapy (ST) in the prospective observational ODYSSEY study.

B Benjamin L. Maughan (University of Utah, Salt Lake City, UT) J Jesse D. Troy (Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC) Y Yousef Zakharia (Division of Hematology and Medical Oncology, Department of Internal Medicine Mayo Clinic Phoenix Arizona USA) E Elizabeth Marie Wulff-Burchfield (University of Kansas Medical Center, Kansas City, KS) N Nrupen Anjan Bhavsar (Department of Surgery, Duke University Health System, Durham, NC) Y Yasser Ged A Ajjai Shivaram Alva (Department of Internal Medicine, Division of Hematology and Oncology, University of Michigan, Ann Arbor, MI) P Priyanka V. Chablani (University of Pittsburgh Medical Center (UPMC), Pittsburgh, PA) B Brian Addis Costello (Division of Medical Oncology, Mayo Clinic Rochester, Rochester, MN) D Deepak Kilari (Medical College of Wisconsin, Milwaukee, WI) S Sorab Gupta (Geisinger Health System, Wilkes-Barre, PA) M Melyssa Bratton (Ochsner Health, New Orleans, LA) M Muhammad Furqan (King Edward Medical College, Lahore, punjab, Pakistan) T Tracy L. Rose S Sarah Jabusch (Duke Clinical Research Institute, Durham, NC) K Kimberly T. Ward (Duke Clinical Research Institute, Durham, NC) C Courtney Page (Duke Clinical Research Institute, Durham, NC) D Daniel J. George (Duke Cancer Institute, Duke University School of Medicine, Durham, NC) T Tian Zhang (Division of Hematology‐Oncology, Department of Internal Medicine University of Texas Southwestern Medical Center Dallas Texas USA) M Michael Roger Harrison (Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC)

Abstract

4558 Background: In the past 7 years, 4 immuno-oncology (IO) based combinations have been approved for mRCC. However, QOL data on these combinations are limited to trials in which collection and reporting was not standardized, which further limits cross trial comparisons. Real-world QOL data with multiple treatment regimens are needed to understand how these regimens are tolerated in practice. Methods: ODYSSEY is a multi-site, prospective observational study of 500 US pts with mRCC. Pts must have mRCC (any histology), no prior ST, and follow up at a PCORnet study site. Exclusion criteria include treatment for cancer except mRCC. The primary objective is to determine patterns of change in QOL and symptom burden of pts with mRCC. Minimally important differences (MID) are 3 points for FKSI-19 total score, 1 point for the FKSI-Disease Related Symptoms (DRS) subscale and 7 points for FACT-G. Results: As of 1/6/25, 392 pts were enrolled of whom 299 were managed with ST. Of pts on ST, 114 were treated with IO-IO, 108 with IO-TKI, 33 with IO alone, 27 with Other, and 18 with TKI alone. Median follow up for all pts is 8.8 months (IQR 2.9, 16.2). IO-IO pts are median age 64 yrs, 81% male, 84% white, 56% prior nephrectomy, 84% clear cell; IO-TKI pts median age 66 yrs, 76% male, 92% white, 43% prior nephrectomy, 66% clear cell; IMDC risk profiles are similar. IO-IO pts are more likely to be KPS 100; whereas, IO-TKI pts have a higher median number of metastatic sites and are more likely to have bone or liver metastasis. With median follow-up of 6.0 (IQR 1.8, 14.9) and 8.8 months (4.5, 17.8) in the IO-IO and IO-TKI cohorts, 17 (15%) and 21 (19%) pts had died with a median time to death of 5.4 (2.5, 6.4) and 5.7 months (4.4, 12.8), respectively. 20 (18%) and 16 (15%) pts on IO-IO and IO-TKI had discontinued therapy at a median of 3.0 (IQR 2.0, 4.0) and 6.4 months (2.4, 13.0), respectively. Rates of discontinuation for disease progression and toxicity are similar. Baseline PROs for pts on ST are shown in the Table (higher score indicates better QOL), with RCT data for reference (NA, not assessed). Conclusions: In our prospective multi-center ODYSSEY study, we demonstrate that real world pts treated with contemporary ST have worse baseline QOL than those enrolled on pivotal RCTs. One-third of IO-IO and IO-TKI pts died or discontinued therapy within 6 months of initiation. Our data on real world vs RCT differences in baseline QOL may partially explain the limitations of current IO combination regimens in practice and support development of alternative treatment approaches. Instrument, Mean (SD) ODYSSEYIO-IO(N=114) CheckMate214(N=425) ODYSSEYIO-TKI(N=108) KEYNOTE426(N=402) CheckMate9ER(N=323) CLEAR(N=351) FKSI-19 total 56.0 (12.5) 60.1 (9.8) 53.8 (11.8) NA 58.7 (10.6) NA FKSI-DRS 27.5 (6.3) 30.7 (4.5) 27.0 (5.8) 32 (4.2) 30.2 (5.2) 31.3 (4.4) FACT-G 82.4 (16.7) 82.6 (15.0) 78.5 (16.0) NA NA NA

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 4558-4558
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

B

Benjamin L. Maughan

University of Utah, Salt Lake City, UT

J

Jesse D. Troy

Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC

Y

Yousef Zakharia

Division of Hematology and Medical Oncology, Department of Internal Medicine Mayo Clinic Phoenix Arizona USA

E

Elizabeth Marie Wulff-Burchfield

University of Kansas Medical Center, Kansas City, KS

N

Nrupen Anjan Bhavsar

Department of Surgery, Duke University Health System, Durham, NC

Y

Yasser Ged

A

Ajjai Shivaram Alva

Department of Internal Medicine, Division of Hematology and Oncology, University of Michigan, Ann Arbor, MI

P

Priyanka V. Chablani

University of Pittsburgh Medical Center (UPMC), Pittsburgh, PA

B

Brian Addis Costello

Division of Medical Oncology, Mayo Clinic Rochester, Rochester, MN

D

Deepak Kilari

Medical College of Wisconsin, Milwaukee, WI

S

Sorab Gupta

Geisinger Health System, Wilkes-Barre, PA

M

Melyssa Bratton

Ochsner Health, New Orleans, LA

M

Muhammad Furqan

King Edward Medical College, Lahore, punjab, Pakistan

T

Tracy L. Rose

S

Sarah Jabusch

Duke Clinical Research Institute, Durham, NC

K

Kimberly T. Ward

Duke Clinical Research Institute, Durham, NC

C

Courtney Page

Duke Clinical Research Institute, Durham, NC

D

Daniel J. George

Duke Cancer Institute, Duke University School of Medicine, Durham, NC

T

Tian Zhang

Division of Hematology‐Oncology, Department of Internal Medicine University of Texas Southwestern Medical Center Dallas Texas USA

M

Michael Roger Harrison

Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC