Don’t ask, don’t tell: Missing ECOGS and anticancer treatment, neutrophil-to-lymphocyte ratios, and outcomes in hospitalized patients with solid tumors.

e24071 Background: ASCO’s Choosing Wisely campaign has recommended avoiding cancer-directed therapy for patients with ECOG performance status (PS) 3–4. Hospitalized patients with solid tumor patients frequently have poor PS, yet ECOG documentation is often missing, potentially contributing to non-beneficial treatment. Caregiver-reported ECOG may offer a pragmatic alternative source of functional status information. Methods: We are enrolling hospitalized patients with solid tumors and their personal caregivers from a NYPresbyterian-affiliated (Weill, Queens, Brooklyn Methodist) Hospital (preliminary analyses on the first 21). Caregivers (e.g., spouses/partners) completed ECOG PS and sarcopenia assessments at baseline. Medical charts were reviewed for ECOG documentation, anticancer treatments, and neutrophil-to-lymphocyte ratio (NLR) values closest to baseline and 3-month follow-up. Caregiver expectations were assessed at baseline and patient survival and quality-of-life at 3 months. Results: ECOG PS was undocumented in 88% of charts within 48 hours of baseline. Caregivers rated 70% of patients as ECOG > 2. Over 80% had NLR > 4 (indicating significant inflammation). Patient sarcopenia assessments were completed by 88% of caregivers (vs. 22% of patients). Caregiver-rated patient functional impairment was substantial: 56% could not lift 10 lbs., 61% could not walk, and 41% could not transfer independently. Despite poor PS and high NLR, more than half were receiving anticancer therapy; most were offered at least one modality (chemotherapy 75%, immunotherapy 25%, targeted therapy 17%, radiation 32%, surgery 17%). Caregivers strongly endorsed treatment, with 65% wanting inpatient chemotherapy and most believing it would improve quality of life (71%) and 3-month survival (69%). At follow-up, 58% of patients had died; among survivors, 66% continued to have NLR > 4. Conclusions: Hospitalized patients with solid tumors in this cohort were acutely ill, yet ECOG PS was rarely documented. Caregivers provided feasible and clinically plausible assessments of ECOG and sarcopenia. Despite caregiver-identified poor PS and high NLR, most patients were offered and received anticancer therapy; the majority died within 3 months. Caregiver-reported ECOG may represent a scalable, underutilized clinical signal to guide more treatment decisions for hospitalized patients with solid tumor cancers.

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Publication Details

Journal
Journal of Clinical Oncology
Published
2026-05-28
DOI
https://doi.org/10.1200/jco.2026.44.16_suppl.e24071
Primary Topic
Inflammatory Biomarkers in Disease Prognosis
Type
article
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article

Don’t ask, don’t tell: Missing ECOGS and anticancer treatment, neutrophil-to-lymphocyte ratios, and outcomes in hospitalized patients with solid tumors.

Ann Rosen, Paul K. Maciejewski, Silvia C. Formenti, Lindsay Lief et al.
Journal of Clinical Oncology
Inflammatory Biomarkers in Disease Prognosis
article

Don’t ask, don’t tell: Missing ECOGS and anticancer treatment, neutrophil-to-lymphocyte ratios, and outcomes in hospitalized patients with solid tumors.

Ann Rosen, Paul K. Maciejewski, Silvia C. Formenti, Lindsay Lief, Rutika Mehta, Holly G. Prigerson, David Berlin, Rachel Ann Oshins, Madison Pavao, Julia Rebecca Sobel, Christine A. Garcia
article en

Abstract

e24071 Background: ASCO’s Choosing Wisely campaign has recommended avoiding cancer-directed therapy for patients with ECOG performance status (PS) 3–4. Hospitalized patients with solid tumor patients frequently have poor PS, yet ECOG documentation is often missing, potentially contributing to non-beneficial treatment. Caregiver-reported ECOG may offer a pragmatic alternative source of functional status information. Methods: We are enrolling hospitalized patients with solid tumors and their personal caregivers from a NYPresbyterian-affiliated (Weill, Queens, Brooklyn Methodist) Hospital (preliminary analyses on the first 21). Caregivers (e.g., spouses/partners) completed ECOG PS and sarcopenia assessments at baseline. Medical charts were reviewed for ECOG documentation, anticancer treatments, and neutrophil-to-lymphocyte ratio (NLR) values closest to baseline and 3-month follow-up. Caregiver expectations were assessed at baseline and patient survival and quality-of-life at 3 months. Results: ECOG PS was undocumented in 88% of charts within 48 hours of baseline. Caregivers rated 70% of patients as ECOG > 2. Over 80% had NLR > 4 (indicating significant inflammation). Patient sarcopenia assessments were completed by 88% of caregivers (vs. 22% of patients). Caregiver-rated patient functional impairment was substantial: 56% could not lift 10 lbs., 61% could not walk, and 41% could not transfer independently. Despite poor PS and high NLR, more than half were receiving anticancer therapy; most were offered at least one modality (chemotherapy 75%, immunotherapy 25%, targeted therapy 17%, radiation 32%, surgery 17%). Caregivers strongly endorsed treatment, with 65% wanting inpatient chemotherapy and most believing it would improve quality of life (71%) and 3-month survival (69%). At follow-up, 58% of patients had died; among survivors, 66% continued to have NLR > 4. Conclusions: Hospitalized patients with solid tumors in this cohort were acutely ill, yet ECOG PS was rarely documented. Caregivers provided feasible and clinically plausible assessments of ECOG and sarcopenia. Despite caregiver-identified poor PS and high NLR, most patients were offered and received anticancer therapy; the majority died within 3 months. Caregiver-reported ECOG may represent a scalable, underutilized clinical signal to guide more treatment decisions for hospitalized patients with solid tumor cancers.

Journal of Clinical OncologyVol. 44(16_suppl)
NewYork–Presbyterian Hospital (US), Cornell University (US), New York Hospital Queens (US), Presbyterian Hospital (US), Weill Cornell Medicine (US)
No poverty
Openalex Percentile: Top 7%
Inflammatory Biomarkers in Disease Prognosis
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