Real-world quality of life (QOL) in patients (pts) with metastatic renal cell carcinoma (mRCC) on active surveillance (AS) in the ODYSSEY prospective observational study.

M Michael Roger Harrison (Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC) J Jesse D. Troy (Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC) B Benjamin L. Maughan (University of Utah, Salt Lake City, UT) 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) T Tian Zhang (Division of Hematology‐Oncology, Department of Internal Medicine University of Texas Southwestern Medical Center Dallas Texas USA) D Daniel J. George (Duke Cancer Institute, Duke University School of Medicine, Durham, NC)

Abstract

4553 Background: AS is a recognized strategy in select pts with mRCC to maximize QOL and delay potential toxicity of systemic therapy (ST); however, only 2 prospective studies of AS in mRCC have been published: only 1 with patient-reported outcomes (PRO) and none in the IO-TKI era. Methods: ODYSSEY is a prospective observational study of 500 US pts with mRCC. Eligible pts must have mRCC (any histology), no prior ST, age ≥19. Pts were excluded if treated for non-mRCC cancers or if not followed at a PCORnet study site. Pts completed QOL surveys at baseline, by phone every 3 months for 2 years and then every 6 months until end of follow up. 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. Here we report baseline pt characteristics in AS pts compared to ST pts, and baseline QOL differences between these cohorts. Results: As of 1/6/25, 392 pts were enrolled of whom 299 were managed with ST, and 93 pts deferred ST; of these, 53 pts (57%) were classified as AS. Pts on AS are median age 68 yrs, 66% male, 94% white, 81% clear cell, 50% favorable risk, 44% intermediate risk. Compared with ST pts, AS pts were more likely to have undergone nephrectomy (91% vs 53%), favorable risk profile (50% vs 15%), pancreatic metastasis (15% vs 5%), and longer time since RCC diagnosis (median 58 vs 3.3 months); and less likely to have bone, brain, or liver metastasis. After median 8.8 months follow-up (IQR 2.9, 16.2), 2 pts (4%) on AS had died compared with 45 pts (15%) on ST. One pt (2%) on AS started first-line therapy and 45 pts (15%) discontinued ST. Mean baseline QOL (FKSI-19 total, DRS and FACT-G) for AS and ST ODYSSEY pts is shown in the Table (higher score indicates better QOL), with RCT data for reference (NA, not assessed). ODYSSEY pts on AS had higher QOL for all measures compared with ODYSSEY pts on ST. FSKI-DRS was the same or lower for pts on AS compared to the pivotal trials, while ODYSSEY pts on ST had both lower FKSI-19 total and DRS. Conclusions: In our large prospective cohort from ODYSSEY, pts on AS had higher median QOL scores than pts on ST, but similar to those included in RCTs. These results suggest that some RCT pts could have benefitted from AS. Further follow up is needed to determine long term outcomes in pts on AS and how they respond to deferred ST. Clinical trial information: NCT04919122 . Instrument, Mean (SD) ODYSSEY AS (N=53) ODYSSEY ST (N=299) ODYSSEY Difference, AS vs ST (95% CI) CheckMate 214 (N=425) KEYNOTE 426 (N=402) CheckMate 9ER (N=323) CLEAR (N=351) FKSI-19 total 63.4 (9.2) 56.3 (12.5) 7.0(4.0, 10.1) 60.1 (9.8) NA 58.7 (10.6) NA FKSI-DRS 30.8 (4.2) 27.9 (6.0) 2.9(1.5, 4.7) 30.7 (4.5) 32 (4.2) 30.2 (5.2) 31.3 (4.4) FACT-G 87.9 (14.0) 82.4 (16.7) 5.6(1.1, 10.0) 82.6 (15.0) NA NA NA

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 4553-4553
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

M

Michael Roger Harrison

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

J

Jesse D. Troy

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

B

Benjamin L. Maughan

University of Utah, Salt Lake City, UT

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

T

Tian Zhang

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

D

Daniel J. George

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