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Article: Novel Systemic Anticancer Treatments and Health Services Use at the End of Life Among Adults With Cancer
| Title | Novel Systemic Anticancer Treatments and Health Services Use at the End of Life Among Adults With Cancer |
|---|---|
| Authors | |
| Issue Date | 4-Jun-2025 |
| Publisher | American Society of Clinical Oncology |
| Citation | Journal of Clinical Oncology, 2025 How to Cite? |
| Abstract | PURPOSE Use of chemotherapy at the end of life (EOL) is discouraged, but evidence to guide decisions on the use of novel systemic anticancer treatment (SACT) agents is lacking. We examined trends of use among SACT types and association with health services use at the EOL.MATERIALS AND METHODS We analyzed Canadian Ontario Cancer Registry data for adults diagnosed with solid tumors or hematologic malignancies within 5 years of death who received SACT between March 2015 and March 2021. Receipt of SACT in the last 30 days of life was categorized as chemotherapy alone, chemotherapy and immunotherapy, immunotherapy alone, and targeted therapy alone. Outcomes included high health services use, including multiple (≥2) emergency department (ED) visits, multiple (≥2) hospitalizations, or any (≥1) intensive care unit admission, and hospital deaths. Segmented linear regression estimated monthly trends; multivariable logistic regression estimated adjusted odds ratios (aORs) of outcomes for various SACT types.RESULTSAmong 68,963 patients, 18,337 (26.6%) received SACT at the EOL. From March 2015 to March 2020, use of SACT at the EOL increased (0.072% per month; P <.001), mainly driven by increased use of immunotherapy alone (0.064% per month; P <.001). Adjusted odds of high health services use and hospital death were more than two-fold greater among patients receiving SACT at the EOL (vs. none); individual aORs of high health services use and hospital death were 2.20 and 2.72 for chemotherapy alone, 2.36 and 3.10 for chemotherapy and immunotherapy, 1.92 and 2.27 for immunotherapy alone, and 1.75 and 2.37 for targeted therapy alone, respectively.CONCLUSION Use of SACT at the EOL increased significantly over time, driven by increased use of immunotherapy. SACT use at the EOL, regardless of its type, was associated with high health services use and hospital death. Guidelines on the use of SACT at the EOL should include novel cancer treatments. |
| Persistent Identifier | http://hdl.handle.net/10722/358702 |
| ISSN | 2023 Impact Factor: 42.1 2023 SCImago Journal Rankings: 10.639 |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Iqbal, Javaid | - |
| dc.contributor.author | Moineddin, Rahim | - |
| dc.contributor.author | Quinn, Kieran L. | - |
| dc.contributor.author | Booth, Christopher M. | - |
| dc.contributor.author | Earle, Craig C. | - |
| dc.contributor.author | Lheureux, Stephanie | - |
| dc.contributor.author | Grant, Robert | - |
| dc.contributor.author | Lau, Jenny | - |
| dc.contributor.author | Le, Lisa W. | - |
| dc.contributor.author | Tanuseputro, Peter | - |
| dc.contributor.author | Downar, James | - |
| dc.contributor.author | Rodin, Gary | - |
| dc.contributor.author | Seow, Hsien | - |
| dc.contributor.author | Tsai, Jillian | - |
| dc.contributor.author | Fowler, Robert A. | - |
| dc.contributor.author | Hannon, Breffni | - |
| dc.contributor.author | Krzyzanowska, Monika K. | - |
| dc.contributor.author | Zimmermann, Camilla | - |
| dc.date.accessioned | 2025-08-13T07:47:31Z | - |
| dc.date.available | 2025-08-13T07:47:31Z | - |
| dc.date.issued | 2025-06-04 | - |
| dc.identifier.citation | Journal of Clinical Oncology, 2025 | - |
| dc.identifier.issn | 0732-183X | - |
| dc.identifier.uri | http://hdl.handle.net/10722/358702 | - |
| dc.description.abstract | <p>PURPOSE Use of chemotherapy at the end of life (EOL) is discouraged, but evidence to guide decisions on the use of novel systemic anticancer treatment (SACT) agents is lacking. We examined trends of use among SACT types and association with health services use at the EOL.MATERIALS AND METHODS We analyzed Canadian Ontario Cancer Registry data for adults diagnosed with solid tumors or hematologic malignancies within 5 years of death who received SACT between March 2015 and March 2021. Receipt of SACT in the last 30 days of life was categorized as chemotherapy alone, chemotherapy and immunotherapy, immunotherapy alone, and targeted therapy alone. Outcomes included high health services use, including multiple (≥2) emergency department (ED) visits, multiple (≥2) hospitalizations, or any (≥1) intensive care unit admission, and hospital deaths. Segmented linear regression estimated monthly trends; multivariable logistic regression estimated adjusted odds ratios (aORs) of outcomes for various SACT types.RESULTSAmong 68,963 patients, 18,337 (26.6%) received SACT at the EOL. From March 2015 to March 2020, use of SACT at the EOL increased (0.072% per month; P <.001), mainly driven by increased use of immunotherapy alone (0.064% per month; P <.001). Adjusted odds of high health services use and hospital death were more than two-fold greater among patients receiving SACT at the EOL (vs. none); individual aORs of high health services use and hospital death were 2.20 and 2.72 for chemotherapy alone, 2.36 and 3.10 for chemotherapy and immunotherapy, 1.92 and 2.27 for immunotherapy alone, and 1.75 and 2.37 for targeted therapy alone, respectively.CONCLUSION Use of SACT at the EOL increased significantly over time, driven by increased use of immunotherapy. SACT use at the EOL, regardless of its type, was associated with high health services use and hospital death. Guidelines on the use of SACT at the EOL should include novel cancer treatments.</p> | - |
| dc.language | eng | - |
| dc.publisher | American Society of Clinical Oncology | - |
| dc.relation.ispartof | Journal of Clinical Oncology | - |
| dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
| dc.title | Novel Systemic Anticancer Treatments and Health Services Use at the End of Life Among Adults With Cancer | - |
| dc.type | Article | - |
| dc.identifier.doi | 10.1200/JCO-24-02816 | - |
| dc.identifier.scopus | eid_2-s2.0-105008328427 | - |
| dc.identifier.eissn | 1527-7755 | - |
| dc.identifier.issnl | 0732-183X | - |
