LBPO.CL04 · 临床研究 · Late-Breaking

Impact of severe liver metastases on clinical response to immunotherapy in solid tumors

海报缩略图:Impact of severe liver metastases on clinical response to immunotherapy in solid tumors
编号 LB429 展板 19 时间 4/22 09:00–12:00 区域 Section 51 主讲 Aung Naing, MD
分会场 Late-Breaking Research: Clinical Research 4
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作者与单位

Jibran Ahmed1, Bettzy Stephen1, Evan Kwiatkowski2, Marcus R. Anderson1, Mohamed H. Derbala1, Israa Salih1, Lilibeth Castillo1, Yali Yang1, Serdar A. Gurses1, Hao Yan2, Joann T. Lim1, Albert R. Klekers1, Hung Le1, Lei Kang1, Mingxuan Xu1, Harold N. Tan1, Stephane Champiat1, Tin-Yun Tang1, Ecaterina E. Dumbrava1, Sarina A. Piha-Paul1, Jordi Rodon Ahnert1, Apostolia M. Tsimberidou1, Timothy A. Yap1, Siqing Fu1, David S. Hong1, Funda Meric-Bernstam1, Priya R. Bhosale1, Aung Naing1

1The University of Texas MD Anderson Cancer Center, Houston, TX,2UT Health Houston, Houston, TX

摘要 Abstract

Background: The presence of liver metastases negatively influences immunotherapy response across solid tumors by promoting an immunosuppressive microenvironment. However, it remains unclear whether a specific threshold of liver metastases, defined by lesion size and number, is associated with progressively worse response to immunotherapy-based regimens. Methods: We retrospectively analyzed clinical and radiologic data from 594 patients with advanced solid tumors treated on immunotherapy-based clinical trials at the University of Texas MD Anderson Cancer Center between 3/2016 and 2/2022 (IRB-approved protocol PA15-0315). Baseline imaging categorized liver metastases as 1) absent; 2) mild (<5 lesions, all <3 cm); 3) moderate (<5 lesions with ≥1 lesion ≥3 cm); or 4) severe (≥5 lesions of any size). Tumor response was assessed by RECIST v1.1. Responders were defined as complete response, partial response, or stable disease (SD) lasting ≥6 months; non-responders included SD <6 months, progressive disease, or clinical progression. Odds ratios (ORs) and 95% confidence intervals (CI) for response were estimated using logistic regression. Results: Of the 594 patients, 52% were female, 79% were white, 90% had an ECOG performance status of 1. The most common tumor types were gastrointestinal (18%) and gynecologic (14%) malignancies. A total of 537 were evaluable for response. Liver metastases were present in 213 (mild n=40, moderate n=34, severe n=139) and absent in 324 patients. The presence of liver metastases was significantly associated with lower response rates (p<0.001). Patients with severe liver metastases had lower odds of response compared to those with mild/moderate liver metastases, though the difference did not reach statistical significance (OR 0.69, 95% CI 0.30-1.58; p=0.39). The odds of response were significantly lower in patients with mild/moderate liver metastases than in patients without liver metastases (OR 0.46, 95% CI 0.23-0.90; p=0.024). Severe liver metastasis was associated with significantly lower odds of response compared to none or mild/moderate disease (OR 0.36, 95% CI 0.20-0.64; p=0.0004). Conclusions: The presence of liver metastases is associated with lower response rate to immunotherapy-based regimen. Patients with severe liver metastases demonstrated significantly lower odds of response compared to those with no or mild/moderate metastases. Therefore, severe liver metastases may represent a clinically meaningful threshold for worse response and may inform risk stratification and clinical trial eligibility.
利益披露 Disclosure
J. Ahmed, NCI Employment, However, Dr. Ahmed participated in this work described in the abstract during his employment at The University of Texas MD Anderson Cancer Center. B. Stephen, The University of Texas MD Anderson Cancer Center Employment. E. Kwiatkowski, UT Health Houston Employment. M. R. Anderson, The University of Texas MD Anderson Cancer Center Employment. M. H. Derbala, The University of Texas MD Anderson Cancer Center Employment. I. Salih, The University of Texas MD Anderson Cancer Center Employment. L. Castillo, The University of Texas MD Anderson Cancer Center Employment. Y. Yang, The University of Texas MD Anderson Cancer Center Employment. S. A. Gurses, The University of Texas MD Anderson Cancer Center Employment. H. Yan, None. J. T. Lim, The University of Texas MD Anderson Cancer Center Employment. A. R. Klekers, The University of Texas MD Anderson Cancer Center Employment. H. Le, The University of Texas MD Anderson Cancer Center Employment. L. 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Society for the Immunotherapy of Cancer (SITC); Telperian Travel, Other, Accommodations; Expenses. 280 Bio; Acuta Capital Partners LLC; Alpha Insights; Amgen; Bain Capital; Bayer; BluePrint Medicine; BlueStar; Boxer Capital; Breakthrough Bio; Children’s Oncology Group; COR2ed; Cowen Group Inc; Other, Consulting; Speaker; or Advisory Role. Crossbridge Bio; Ecor1 Capital; Erasca; Gerson Lehrman Group Inc.; Group H; Guidepoint; Immunogenesis; Janssen Pharmaceuticals; Kestrel Therapeutics; Medacorp; Medscape; Orbi Capital; Pfizer; Other, Consulting; Speaker; or Advisory Role. PharmaResearch; Remedy Inc; Revolution Medicines; Stipple Bio;T-Knife; TouchEd; Travistock Group; Xencor; WebMD Other, Consulting; Speaker; or Advisory Role. Molecular Match (Advisor); OncoResponse (Founder; Advisor); Telperian (Founder; Advisor); CrossBridge Bio (Advisor) Other, Other ownership interests. F. Meric-Bernstam, The University of Texas MD Anderson Cancer Center Employment. 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Cholangiocarcinoma Foundation; Dava Oncology; European Organisation for Research and Treatment of Cancer (EORTC); European Society for Medical Oncology (ESMO); Physician Education Resource (PER) Travel, Travel-related support. P. R. Bhosale, The University of Texas MD Anderson Cancer Center Employment. A. Naing, The University of Texas MD Anderson Cancer Center Employment. NCI; EMD Serono; MedImmune; Healios Onc. Nutrition; Atterocor/Millendo; Amplimmune; ARMO BioSciences; Karyopharm Therapeutics; Incyte; Novartis; Regeneron; Merck; Bristol-Myers Squibb; Pfizer; ). CytomX Therapeutics; Neon Therapeutics; Calithera Biosciences; TopAlliance Biosciences; Eli Lilly; Kymab; PsiOxus; Arcus Biosciences; NeoImmuneTech; Immune-Onc Therapeutics; Surface Oncology; ). Monopteros Therapeutics; BioNTech SE; Seven & Eight Biopharma; and SOTIO Biotech AG; GV 20 Therapeutics ). 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