mTOR inhibitor-induced interstitial lung disease in cancer patients: Comprehensive review and a practical management
Annelieke E C A B Willemsen1, Jan C Grutters2,3, Winald R Gerritsen1
1Department of Medical Oncology, Radboud university medical center, Nijmegen, The Netherlands.
Abstract:
Mammalian target of rapamycin inhibitors (mTORi) have clinically significant activity against various malignancies, such as renal cell carcinoma and breast cancer, but their use can be complicated by several toxicities. Interstitial lung disease (ILD) is an adverse event of particular importance. Mostly, mTORi-induced ILD remains asymptomatic or mildly symptomatic, but it can also lead to severe morbidity and even mortality. Therefore, careful diagnosis and management of ILD is warranted. The reported incidence of mTORi-induced ILD varies widely because of a lack of uniform diagnostic criteria and active surveillance. Because of the nonspecific clinical features, a broad differential diagnosis that includes (opportunistic) infections should be considered in case of suspicion of mTORi-induced ILD. The exact mechanism or interplay of mechanisms leading to the development of ILD remains to be defined. Suggested mechanisms are either a direct toxic effect or immune-mediated mechanisms, considering mTOR inhibitors have several effects on the immune system. The clinical course of ILD varies widely and is difficult to predict. Consequently, the discrimination between when mTOR inhibitors can be continued safely and when discontinuation is indicated is challenging. In this review, we give a comprehensive review of the incidence, clinical presentation and pathophysiology of mTORi-induced ILD in cancer patients. We present newly developed diagnostic criteria for ILD, which include clinical symptoms as well as basic pulmonary function tests and radiological abnormalities. In conjunction with these diagnostic criteria, we provide a detailed and easily applicable clinical management algorithm.
Insights
Mammalian target of rapamycin inhibitors (mTORi) can cause interstitial lung disease (ILD) in cancer patients. This review details mTORi-induced ILD diagnosis, pathophysiology, and management strategies for improved patient outcomes.
Area of Science:
- Oncology
- Pulmonology
- Pharmacology
Background:
- Mammalian target of rapamycin inhibitors (mTORi) are effective cancer treatments but can cause toxicities.
- Interstitial lung disease (ILD) is a significant adverse event associated with mTORi therapy, ranging from asymptomatic to fatal.
- The incidence and management of mTORi-induced ILD are challenging due to variable diagnostic criteria and nonspecific clinical features.
Purpose of the Study:
- To provide a comprehensive review of the incidence, clinical presentation, and pathophysiology of mTORi-induced ILD in cancer patients.
- To introduce newly developed diagnostic criteria for ILD, incorporating clinical symptoms, pulmonary function tests, and radiological findings.
- To present a detailed and applicable clinical management algorithm for mTORi-induced ILD.
Main Methods:
- Literature review focusing on mTORi-induced ILD in cancer patients.
- Analysis of reported incidence, clinical features, and proposed pathophysiological mechanisms.
- Development of novel diagnostic criteria and a clinical management algorithm.
Main Results:
- The incidence of mTORi-induced ILD is highly variable due to a lack of standardized diagnostic criteria.
- Differential diagnosis must consider opportunistic infections due to nonspecific clinical presentations.
- Proposed mechanisms include direct toxicity and immune-mediated effects of mTOR inhibitors.
Conclusions:
- Accurate diagnosis and management of mTORi-induced ILD are crucial due to potential severe morbidity and mortality.
- Newly proposed diagnostic criteria and a management algorithm aim to standardize and improve patient care.
- Further research is needed to fully elucidate the mechanisms underlying mTORi-induced ILD.
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