TY - JOUR
T1 - Patient-Reported Cognitive Impairment among Women with Early Breast Cancer Randomly Assigned to Endocrine Therapy Alone Versus Chemoendocrine Therapy
T2 - Results from TAILORx
AU - Wagner, Lynne I.
AU - Gray, Robert J.
AU - Sparano, Joseph A.
AU - Whelan, Timothy J.
AU - Garcia, Sofia F.
AU - Yanez, Betina
AU - Tevaarwerk, Amye J.
AU - Carlos, Ruth C.
AU - Albain, Kathy S.
AU - Olson, John A.
AU - Goetz, Matthew P.
AU - Pritchard, Kathleen I.
AU - Hayes, Daniel F.
AU - Geyer, Charles E.
AU - Dees, E. Claire
AU - McCaskill-Stevens, Worta J.
AU - Minasian, Lori M.
AU - Sledge, George W.
AU - Cella, David
N1 - Funding Information:
Supported by the National Cancer Institute of the National Institutes of Health under the following awards to the ECOG-ACRIN Cancer Research Group: Grants No. CA189828, CA180820, CA180794, CA180790, CA180795, CA180799, C180801, CA180816, CA180821, CA180838, CA180822, CA180844, CA180847, CA180857, CA180864, CA189867, CA180868, CA189869, CA180888, CA189808, CA189859, CA190140, and CA180863; the Canadian Cancer Society Research Institute (Grants No. 015469 and 021039); the Breast Cancer Research Foundation; the Susan G. Komen This study was coordinated by the Eastern Cooperative Oncology Group and the American College of Radiology Imaging Network (ECOG-ACRIN) Cancer Research Group (Peter O’Dwyer MD; and Mitchell D. Schnall, MD, PhD, group co-chairs). We acknowledge Jeff Abrams, MD; Sheila Taube, PhD; and Ann O’Mara, PhD, National Cancer Institute, for their support of the trial at its inception and development. We thank the staff at the ECOG-ACRIN Cancer Research Group Operations Office in Boston and the Cancer Trials Support Unit. We acknowledge Mary Lou Smith, patient advocate, for her assistance with trial design and interpretation of results. We thank the late Robert L. Comis, MD, former chair of ECOG and co-chair of ECOG-ACRIN, for his leadership.
Funding Information:
Supported by the National Cancer Institute of the National Institutes of Health under the following awards to the ECOG-ACRIN Cancer Research Group: Grants No. CA189828, CA180820, CA180794, CA180790, CA180795, CA180799, C180801, CA180816, CA180821, CA180838, CA180822, CA180844, CA180847, CA180857, CA180864, CA189867, CA180868, CA189869, CA180888, CA189808, CA189859, CA190140, and CA180863; the Canadian Cancer Society Research Institute (Grants No. 015469 and 021039); the Breast Cancer Research Foundation; the Susan G. Komen
Publisher Copyright:
© 2020 by American Society of Clinical Oncology
PY - 2020/4/9
Y1 - 2020/4/9
N2 - PURPOSE Cancer-related cognitive impairment (CRCI) is common during adjuvant chemotherapy and may persist. TAILORx provided a novel opportunity to prospectively assess patient-reported cognitive impairment among women with early breast cancer who were randomly assigned to chemoendocrine therapy (CT+E) versus endocrine therapy alone (E), allowing us to quantify the unique contribution of chemotherapy to CRCI. METHODS Women with a 21-gene recurrence score of 11 to 25 enrolled in TAILORX were randomly assigned to CT+E or E. Cognitive impairment was assessed among a subgroup of 552 evaluable women using the 37-item Functional Assessment of Cancer Therapy-Cognitive Function (FACT-Cog) questionnaire, administered at baseline, 3, 6, 12, 24, and 36 months. The FACT-Cog included the 20-item Perceived Cognitive Impairment (PCI) scale, our primary end point. Clinically meaningful changes were defined a priori and linear regression was used to model PCI scores on baseline PCI, treatment, and other factors. RESULTS FACT-Cog PCI scores were significantly lower, indicating more impairment, at 3, 6, 12, 24, and 36 months compared with baseline for both groups. The magnitude of PCI change scores was greater for CT+E than E at 3 months, the prespecified primary trial end point, and at 6 months, but not at 12, 24, and 36 months. Tests of an interaction between menopausal status and treatment were nonsignificant. CONCLUSION Adjuvant CT+E is associated with significantly greater CRCI compared with E at 3 and 6 months. These differences abated over time, with no significant differences observed at 12 months and beyond. These findings indicate that chemotherapy produces early, but not sustained, cognitive impairment relative to E, providing reassurance to patients and clinicians in whom adjuvant chemotherapy is indicated to reduce recurrence risk.
AB - PURPOSE Cancer-related cognitive impairment (CRCI) is common during adjuvant chemotherapy and may persist. TAILORx provided a novel opportunity to prospectively assess patient-reported cognitive impairment among women with early breast cancer who were randomly assigned to chemoendocrine therapy (CT+E) versus endocrine therapy alone (E), allowing us to quantify the unique contribution of chemotherapy to CRCI. METHODS Women with a 21-gene recurrence score of 11 to 25 enrolled in TAILORX were randomly assigned to CT+E or E. Cognitive impairment was assessed among a subgroup of 552 evaluable women using the 37-item Functional Assessment of Cancer Therapy-Cognitive Function (FACT-Cog) questionnaire, administered at baseline, 3, 6, 12, 24, and 36 months. The FACT-Cog included the 20-item Perceived Cognitive Impairment (PCI) scale, our primary end point. Clinically meaningful changes were defined a priori and linear regression was used to model PCI scores on baseline PCI, treatment, and other factors. RESULTS FACT-Cog PCI scores were significantly lower, indicating more impairment, at 3, 6, 12, 24, and 36 months compared with baseline for both groups. The magnitude of PCI change scores was greater for CT+E than E at 3 months, the prespecified primary trial end point, and at 6 months, but not at 12, 24, and 36 months. Tests of an interaction between menopausal status and treatment were nonsignificant. CONCLUSION Adjuvant CT+E is associated with significantly greater CRCI compared with E at 3 and 6 months. These differences abated over time, with no significant differences observed at 12 months and beyond. These findings indicate that chemotherapy produces early, but not sustained, cognitive impairment relative to E, providing reassurance to patients and clinicians in whom adjuvant chemotherapy is indicated to reduce recurrence risk.
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U2 - 10.1200/JCO.19.01866
DO - 10.1200/JCO.19.01866
M3 - Article
C2 - 32271671
AN - SCOPUS:85086052712
SN - 0732-183X
VL - 38
SP - 1875
EP - 1886
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 17
ER -