Residual cancer burden after neoadjuvant therapy in lung cancer: A single-institution cohort.

L Leena Alhusari (1Marshall University School of Medicine - Edwards Comprehensive Cancer Center, Huntington, United States) S Samhitha Gundakaram (1Marshall University School of Medicine, Internal Medicine, Huntington, United States) M Madho Mal (4Marshall University Joan C. Edwards School of medicine, Huntington, United States) A Anthony Workman (Marshall University School of Medicine, Huntington, WV) H Hashem Rayyan (Marshall University School of Medicine, Huntington, WV) I Ihab Tahboub (1Marshall University School of Medicine - Edwards Comprehensive Cancer Center, Huntington, United States) M Moh'D Masoudi (4Marshall University School of Medicine, Hematology and Oncology, Huntington, United States) A Ahmad Mahdi (1Marshall University Joan C. Edwards School of Medicine, Internal Medicine, Huntington, United States) S Saif Ghishan (Marshall University School of Medicine, Huntington, WV) Z Zakaria Alagha (Joan C. Edwards School of Medicine, Marshall University, Huntington, WV) M Muhammad O. Jamil (Joan C. Edwards School of Medicine - Edwards Comprehensive Cancer Institute, Marshall University, Huntington, WV)

Abstract

e20050 Background: Residual cancer burden (RCB) after neoadjuvant therapy may predict recurrence and survival, but real-world data in lung cancer are limited. We evaluated RCB, clinical characteristics, and outcomes in a single-institution cohort. Methods: We retrospectively analyzed 53 patients (RCB classes pCR,1,2,3) treated with neoadjuvant therapy. Baseline demographics (age, sex, BMI, tobacco history), recurrence, and overall survival were compared across RCB classes. Cox proportional hazards models assessed the association of RCB with mortality, adjusting for age, sex, BMI, and tobacco history. Results: Baseline characteristics were similar across RCB classes. Recurrence rates increased with RCB class (pCR: 14.3%, 1: 20%, 2: 10%, 3: 25%). Mortality also trended higher with increasing RCB (pCR: 7.1%, 1: 20%, 2: 13.3%, 3: 50%). In fully adjusted Cox models, RCB 3 vs pCR showed a non-significant trend toward higher mortality (HR 4.98, 95% CI 0.49–50.7, p = 0.175). Age was independently associated with mortality (HR 1.10 per year, 95% CI 1.01–1.19, p = 0.025). Conclusions: Higher RCB may be associated with increased mortality in lung cancer, though statistical significance was not reached, likely due to small sample size. Age was an independent predictor of mortality. These findings suggest that RCB could inform post-neoadjuvant risk stratification, but larger studies are needed to confirm its prognostic value.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (11)

L

Leena Alhusari

1Marshall University School of Medicine - Edwards Comprehensive Cancer Center, Huntington, United States

S

Samhitha Gundakaram

1Marshall University School of Medicine, Internal Medicine, Huntington, United States

M

Madho Mal

4Marshall University Joan C. Edwards School of medicine, Huntington, United States

A

Anthony Workman

Marshall University School of Medicine, Huntington, WV

H

Hashem Rayyan

Marshall University School of Medicine, Huntington, WV

I

Ihab Tahboub

1Marshall University School of Medicine - Edwards Comprehensive Cancer Center, Huntington, United States

M

Moh'D Masoudi

4Marshall University School of Medicine, Hematology and Oncology, Huntington, United States

A

Ahmad Mahdi

1Marshall University Joan C. Edwards School of Medicine, Internal Medicine, Huntington, United States

S

Saif Ghishan

Marshall University School of Medicine, Huntington, WV

Z

Zakaria Alagha

Joan C. Edwards School of Medicine, Marshall University, Huntington, WV

M

Muhammad O. Jamil

Joan C. Edwards School of Medicine - Edwards Comprehensive Cancer Institute, Marshall University, Huntington, WV