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. 2022 Jun 13;14(12):2905.
doi: 10.3390/cancers14122905.

Cancer-of-Unknown-Primary-Origin: A SEER-Medicare Study of Patterns of Care and Outcomes among Elderly Patients in Clinical Practice

Affiliations

Cancer-of-Unknown-Primary-Origin: A SEER-Medicare Study of Patterns of Care and Outcomes among Elderly Patients in Clinical Practice

Linda Mileshkin et al. Cancers (Basel). .

Abstract

Knowledge of contemporary patterns of cancer-of-unknown-primary-origin (CUP) diagnostic work-up, treatment, and outcomes in routine healthcare is limited. Thus, we examined data from elderly patients diagnosed with CUP in real-world US clinical practice. From the Surveillance, Epidemiology, and End Results-Medicare-linked database, we included patients ≥ 66 years old with CUP diagnosed between 1 January 2013 and 31 December 2015. We analyzed baseline demographics, clinical characteristics, methods of diagnostic work-up (biopsy, immunohistochemistry, imaging), treatment-related factors, and survival. CUP diagnosis was histologically confirmed in 2813/4562 patients (61.7%). Overall, 621/4562 (13.6%) patients received anticancer pharmacotherapy; among these, 97.3% had a histologically confirmed tumor and 83.1% received all three procedures. Among those with a histologically confirmed tumor, increasing age, increasing comorbidity score, not receiving all three diagnostic measures, and having a not-further specified histologic finding of only 'malignant neoplasm' were all negatively associated with receipt of anticancer pharmacotherapy. Median overall survival was 1.2 months for all patients. Median time between CUP diagnosis and treatment initiation was 41 days. Limited diagnostic work-up was common and most patients did not receive anticancer pharmacotherapy. The poor outcomes highlight a substantial unmet need for further research into improving diagnostic work-up and treatment effectiveness in CUP.

Keywords: Medicare Part A; Medicare Part B; SEER program; diagnostic tests and procedures; drug therapy; neoplasms; registries; survival analysis; unknown primary.

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Conflict of interest statement

L.M. reports travel/accommodation expenses from F. Hoffmann-La Roche Ltd. and BeiGene. T.B. works as a study oncologist for the CUPISCO trial, which is sponsored by F. Hoffmann-La Roche Ltd. and has received coverage for study-related travel and study-related work in the molecular tumor board for the benefit of his employer. G.G. received compensation from F. Hoffmann-La Roche Ltd. for a meeting in Zurich in June 2019. R.K. declares equity interests for CureMatch, Inc., CureMetrix Inc., and IDbyDNA, has had consulting, speaker, or advisory roles for Actuate Therapeutics, AstraZeneca, Bicara Therapeutics, Biological Dynamics, Eisai Co., Ltd., EOM Pharmaceuticals, Inc., F. Hoffmann-La Roche Ltd., Iylon, Merck, NeoGenomics, NeoMed, Pfizer, Prosperdtx, TD2/Volastra, Turning Point Therapeutics, and X-Biotech, has received research funding from Biological Dynamics, Boehringer Ingelheim, Debiopharm, Foundation Medicine, Genentech, Grifols, Guardant Health, Incyte, Konica Minolta, Medimmune, Merck Serono, OmniSeq, Pfizer, Sequenom, Takeda, and TopAlliance, is a co-founder of CureMatch, Inc., and is a board member for CureMatch, Inc. and CureMetrix Inc. A.B. is an employee of F. Hoffmann-La Roche Ltd. M.M.-O. is an employee of, and holds stock options in, F. Hoffmann-La Roche Ltd. A.S. is an employee of Genesis Research, which receives consulting fees from F. Hoffmann-La Roche Ltd. C.P. is an employee of F. Hoffmann-La Roche Ltd. M.T. is an employee of, and holds stock options in, F. Hoffmann-La Roche Ltd. A.G. is an employee of, and holds stock options in, F. Hoffmann-La Roche Ltd. A.K. has received self-honoraria from F. Hoffmann-La Roche Ltd. and Daiichi Sankyo, institutional honoraria from F. Hoffmann-La Roche Ltd. and Bayer, has performed an advisory/consulting role for F. Hoffmann-La Roche Ltd., Daiichi Sankyo, BMS, and AbbVie, has a leadership role in F. Hoffmann-La Roche Ltd., has received institutional research funding from Bayer and Merck, and has received travel/accommodation expenses from F. Hoffmann-La Roche Ltd., Celgene, and Daiichi Sankyo. All authors received research support of writing assistance for this manuscript, furnished by Martin Cadogan, was provided by F. Hoffmann-La Roche Ltd.

Figures

Figure 1
Figure 1
Trends in the number of diagnosticsa performed among treated (n = 621; closed circles) and untreated patients (n = 3941; open circles) with CUP. B, biopsy; CUP, cancer-of-unknown-primary-origin; IHC, immunohistochemistry; IM, imaging. a Record of claim for a biopsy, immunohistochemistry, or imaging modality (computed tomography, positron emission tomography, magnetic resonance imaging) for any reason.
Figure 2
Figure 2
Survival of patients with CUP who were (A) untreated, overall and by histologic confirmation status, (B) treated without pharmacotherapy, and (C) treated alongside pharmacotherapy. * Suppressed data based on NCI guidelines for confidentiality. CUP, cancer-of-unknown-primary-origin; NCI, National Cancer Institute. See Table S4 for further data on patient survival.

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