The University of Texas MD Anderson Cancer Center, Houston, TX
David Hui , Ishwaria M. Subbiah , David S. Hong , Jennifer Ellefson , Josue Becerra , Vera J De la Cruz , Diana L. Urbauer , Sanjay Shete , Eduardo Bruera
Background: Outpatient palliative care (PC) has been found to improve quality of life (QOL). It is not known if more frequent symptom monitoring and PC nursing contacts between clinic visits would offer additional benefits. We conducted a pilot RCT to examine the effect of a specialist PC referral with and without technology-enhancement (TEC) on symptoms in patients undergoing Phase I cancer therapies. Methods: This single-center parallel group RCT enrolled adult patients with advanced solid tumors prior to starting Phase I therapies and at least 1 Edmonton Symptom Assessment Scale (ESAS) symptom ≥4/10 and ESAS Global Distress Score (GDS) ≥20/90. Patients were randomized to PC alone or PC + TEC in a 1:1 ratio. Over the 12 w period, the PC group had in person or virtual outpatient visits with a PC physician, nurse, and as needed psychotherapist every 4 weeks; the PC + TEC group also received weekly symptom monitoring with ESAS electronically and weekly nursing phone call. The primary outcome was within-group change of GDS from baseline to 2 w; secondary outcomes included change in GDS over 4, 8, and 12 w, and change in QOL (FACIT-Sp) over 2, 4, 8 and 12 w. We estimated that a sample size of 50 patients per group would provide 90% power to detect a within-group GDS difference of 6 units with a 2-sided α of 2.5% and 20% attrition. Results: Between 12/15/2020 and 12/21/2022, 115 patients were enrolled and 101 were randomized (PC + TEC n = 57, PC n = 44). By 2 w, PC + TEC showed a significant within-group improvement in GDS (mean change -5 [95% CI -8.9, -1.2]; P= 0.01) but not PC alone (Table). PC+TEC group also had a significant improvement in GDS at 8 w and 12 w and in FACIT-SP at 2 w, 8 w and 12 w. PC alone group had a significant within-group improvement in GDS at 4 w and 12 w but no significant differences in QOL were detected. This study was not powered for between group comparison; however, FACIT-SP at 12 w was significantly higher in PC+TEC vs. PC alone (Table; mean difference 13.9; P= 0.02). Conclusions: Higher intensity of PC with closer monitoring showed within-group improvement in symptoms and QOL, while PC alone had some symptom reduction but no QOL improvement. Further studies are needed to confirm the QOL benefit of PC + TEC over PC alone. Clinical trial information: NCT04989556.
PC | PC + TEC | PC + TEC v. PC | |
---|---|---|---|
Outcome | Mean Δ (95% CI); P | Mean Δ (95% CI); P | Mean Difference (95% CI) |
GDS | |||
2 w | -2 (-5.8, 1.8); 0.29 | -5 (-8.9, -1.2); 0.01 | -3 (-8.5, 2.4) |
4 w | -5.7 (-11.2, -0.2); 0.04 | -3 (-7.3, 1.2); 0.16 | 2.6 (-4, 9.3) |
8 w | -5.7 (-13, 1.6); 0.12 | -8.1 (-14, -2.1); 0.009 | -2.3 (-11.5, 6.8) |
12 w | -8.6 (-15.3, -1.8); 0.02 | -10.2 (-17.5, -2.9); 0.008 | -1.6 (-12.2, 9) |
FACIT-SP | |||
2 w | -2.1 (-8.4, 4.2); 0.50 | 5.6 (1.2, 10); 0.01 | 1.2 (-9.9, 12.4) |
4 w | -0.3 (-8.4, 7.8); 0.94 | 3.1 (-1.4, 7.5); 0.17 | 3.4 (-5.3, 12) |
8 w | -0.5 (-9.7, 8.7); 0.92 | 7.4 (0.3, 14.5); 0.04 | 7.9 (-3.1, 18.9) |
12 w | -7.1 (-19.5, 5.3); 0.22 | 6.7 (0.9, 12.6); 0.03 | 13.9 (2.6, 25.1) |
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