An APP-led intake model to expedite diagnostic workup for patients with suspected lymphoma.

E Erin Taylor J Jason Westin (3Department of Lymphoma and Myeloma, MD Anderson Cancer Center, Houston, TX) S Sairah Ahmed (2Department of Lymphoma/Myeloma, MD Anderson Cancer Center, Houston, TX) A Ayushi Chauhan (2Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, United States) D Dai Chihara L Luis Fayad (1The University of Texas MD Anderson Cancer Center, Department of Lymphoma/Myeloma, Houston, United States) F Fateeha Furqan (The University of Texas MD Anderson Cancer Center) F Fredrick B. Hagemeister (The University of Texas MD Anderson Cancer Center, Houston, TX) H Hun Ju Lee (18Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX) S Swaminathan P. Iyer (2Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX) P Preetesh Jain A Anath Christopher Lionel (Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX) C Chijioke C. Nze (The University of Texas MD Anderson Cancer Center, Houston, TX) M Maria Alma Rodriguez (The University of Texas MD Anderson Cancer Center, Houston, TX) P Paolo Strati K Karen Stolar (The University of Texas MD Anderson Cancer Center, Houston, TX) F Felicia Diaz (3The University of Texas Health Science Center at Houston (UTHealth Houston), Houston, United States) C Christopher Flowers (1Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX) R Ranjit Nair

Abstract

e19111 Background: Lymphoma is a rare, heterogeneous malignancy that often presents with symptoms resembling benign, autoimmune, or other malignant conditions. At large academic centers, rapid clinical assessment is essential to improve outcomes, yet a “biopsy first” approach can delay diagnosis, heighten anxiety, and fragment care. To address this gap, we launched an Advanced Practice Provider (APP) intake clinic for patients with Suspicion of Lymphoma (SoL) to expedite workup and triage before physician evaluation. Methods: The SoL APP intake clinic launched on 10/21/24, with twice weekly sessions to prepare patients for a full diagnostic workup. Eligible patients had “Green” insurance and resided in licensed states (TX, OK, LA, FL). The APP led evaluation included labs, CT or PET imaging, and ordering core needle and/or bone marrow biopsies. Patients with benign findings but ongoing clinical concern remained under surveillance, including those with small volume, non biopsiable adenopathy or atypical lymphocytes. Confirmed lymphoma cases were classified as aggressive or indolent, and timelines to diagnosis, first physician visit, and treatment initiation were recorded. Aggressive lymphomas included Hodgkin, diffuse large B cell, mantle cell, and T cell lymphomas; indolent lymphomas included nodular lymphocyte predominate Hodgkin, marginal zone, mucosa-associated lymphoid tissue, and follicular lymphomas. Results: Between 10/21/24–1/14/26, 99 patients were evaluated (age 18–98, mean 58; 48 female, 51 male). 40 patients (40.4%) were diagnosed with lymphoma (20 aggressive, 20 indolent). One aggressive case had a prolonged 74 day diagnostic interval due to patient driven delays. Among the remaining 19 aggressive cases, median time to imaging was 1.5 days (range 1–10), to diagnosis 7 days (2–18), to physician visit 10 days (3–35), and to treatment start 19 days (5–49). For the 20 indolent cases, median time to imaging was 4 days (1–28), to diagnosis 9 days (1–25), and to physician visit 17 days (3–29). 15 indolent cases required treatment, with a median time to treatment initiation of 36 days (14–66). Conclusions: This pilot analysis shows that an APP led SoL intake clinic is feasible and accelerates lymphoma workup and treatment initiation. The model achieved shorter diagnostic timelines compared with historical physician led pathways and efficiently redirected physician resources toward confirmed malignancies while maintaining surveillance for high suspicion benign cases. Future initiatives targeting broader community engagement and clearer insurance pathways are expected to strengthen patient access and program reach. SoL Clinic Diagnosis # patients (n=99) % of total patient evaluated Lymphoma 40 40.4% Benign with high suspicion and long term follow up 24 24.2% Benign with low suspicion of lymphoma 13 13.1% Other Hematologic malignancy/disorder 11 11.1% Solid tumor 7 7.1% Sarcoidosis 4 4.0%

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 (19)

E

Erin Taylor

J

Jason Westin

3Department of Lymphoma and Myeloma, MD Anderson Cancer Center, Houston, TX

S

Sairah Ahmed

2Department of Lymphoma/Myeloma, MD Anderson Cancer Center, Houston, TX

A

Ayushi Chauhan

2Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, United States

D

Dai Chihara

L

Luis Fayad

1The University of Texas MD Anderson Cancer Center, Department of Lymphoma/Myeloma, Houston, United States

F

Fateeha Furqan

The University of Texas MD Anderson Cancer Center

F

Fredrick B. Hagemeister

The University of Texas MD Anderson Cancer Center, Houston, TX

H

Hun Ju Lee

18Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX

S

Swaminathan P. Iyer

2Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX

P

Preetesh Jain

A

Anath Christopher Lionel

Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX

C

Chijioke C. Nze

The University of Texas MD Anderson Cancer Center, Houston, TX

M

Maria Alma Rodriguez

The University of Texas MD Anderson Cancer Center, Houston, TX

P

Paolo Strati

K

Karen Stolar

The University of Texas MD Anderson Cancer Center, Houston, TX

F

Felicia Diaz

3The University of Texas Health Science Center at Houston (UTHealth Houston), Houston, United States

C

Christopher Flowers

1Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX

R

Ranjit Nair