標的がん治療に関連する重篤感染リスクを特定(UC Irvine Study Identifies Serious Infection Risks Linked to Targeted Cancer Therapies)

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2026-06-02 カリフォルニア大学アーバイン校(UCI)

米国カリフォルニア大学アーバイン校(UCI)の研究チームは、分子標的がん治療薬の使用に伴う重篤な感染症リスクを大規模解析により明らかにした。近年、分子標的薬は従来の化学療法に比べ副作用が少ないと考えられてきたが、本研究では複数の標的治療薬が細菌、ウイルス、真菌などによる重篤な感染症の発症リスクを高める可能性が示された。研究では臨床試験データや患者情報を統合解析し、特定のシグナル伝達経路や免疫関連分子を標的とする薬剤で感染症リスクが顕著に上昇することを確認した。これは、腫瘍細胞の増殖を抑制する一方で、免疫機能にも影響を及ぼし、病原体への防御能力を低下させるためと考えられる。研究チームは、分子標的薬の有効性を損なうことなく安全性を高めるため、治療前の感染症リスク評価や予防措置、治療中の継続的なモニタリングの重要性を強調している。本研究は、がん患者の支持療法や個別化医療の改善に向けた重要な知見を提供するものであり、今後の治療ガイドラインにも影響を与える可能性がある。

<関連情報>

抗体薬物複合体に関連する臨床的に重要な好中球減少症および合併症の発生率:カリフォルニア大学における実臨床研究 Incidence of Clinically Significant Neutropenia and Complications Related to Antibody-Drug Conjugates: A Real-World Study at the University of California

Tiffany Jan,Miranda Chen,Fan-Ying Chan,Nicole Kuderer and Alexandre Chan
Cancers  Published: 12 May 2026
DOI:https://doi.org/10.3390/cancers18101563

標的がん治療に関連する重篤感染リスクを特定(UC Irvine Study Identifies Serious Infection Risks Linked to Targeted Cancer Therapies)

Simple Summary

Antibody-drug conjugates are cancer treatments that deliver powerful chemotherapy directly to tumor cells, reducing harm to healthy tissue. While these drugs can be more effective and safer than traditional chemotherapy, they can still cause serious side effects, in particular low white blood cell counts, which increase infection risk and hospital visits. In this study, we analyzed real-world data from 3511 patients across six University of California hospitals to understand how often these blood-related complications occur with different antibody-drug conjugates. We found that the risk of serious infections and low white blood cells varied widely depending on the drug, and certain conditions, like anemia or weakened immunity, increased the risk. These findings can help doctors better monitor and manage side effects and provide insights for researchers developing safer and more effective targeted cancer therapies.

Abstract

Background/Objectives: Using real-world data, this study evaluates the use of ADCs over a decade across six University of California (UC) medical centers, focusing on the incidence of neutropenia-related adverse effects and associated clinical outcomes. Methods: A real-world retrospective study utilizing UC Health Data Warehouse records of patients receiving at least one dose of the ten most-used ADCs at one of the 6 UC hospitals between 2012 and 2024. The outcomes evaluated in this study were grade 3+ neutropenia and febrile neutropenia (FN) during any treatment cycle, and healthcare utilization outcomes including G-CSF prophylaxis, hospital and ICU admission, and mortality. Multivariate logistic regression was conducted to identify predictors for neutropenia-related events after the first dose of ADC.
Results: Data from 3511 patients (mean ± SD age: 56.7 ± 17.6 years) were analyzed. The most commonly observed cancer types were breast cancer (43.4%), lymphoid, hematopoietic (41.8%), and urinary tract cancer (13.4%). The top three most commonly prescribed ADCs were fam-trastuzumab deruxtecan (22.6%), ado-trastuzumab emtansine (19.4%), and brentuximab vedotin (18.1%). Their respective all-cycle rates of FN were 5.4%, 1.2%, and 10.4%, while grade 3+ neutropenia rates were 16.4%, 5.1%, and 40.1%. Gemtuzumab ozogamicin and inotuzumab ozogamicin were associated with the highest rates of FN (both 18.1%), and inotuzumab ozogamicin was associated with the highest rates of hospital admissions (27.1%), ICU admissions (3.8%), and deaths (5.2%). Anemia and immunodeficiency disorders were identified as predictors for first-dose FN among patients receiving ADCs.
Conclusions: Real-world data from this large multi-center cohort showed substantial variation in neutropenia-related events across ADCs. As ADC use continues to grow, these findings highlight the need for vigilant monitoring and proactive supportive care.

 

 

医療・健康
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