TY - JOUR
T1 - Incidence and management of mtor inhibitor-associated pneumonitis in patients with metastatic renal cell carcinoma
AU - Albiges, L.
AU - Chamming's, F.
AU - Duclos, B.
AU - Stern, M.
AU - Motzer, R. J.
AU - Ravaud, A.
AU - Camus, P.
N1 - Funding Information:
LA: honorarium from Novartis. FC: honorarium from Novartis. BD: honoraria from Novartis, Roche, Bayer HealthCare, GlaxoSmithKline, and Sanofi-Aventis. MS: none declared. RJM: research funding from Novartis and Pfizer; consulting role for Pfizer. AR: member of Global, European and/or French Advisory Boards on urological tumours and their medical treatment for Novartis, Pfizer, Bayer Schering, GlaxoSmithKline, Roche, and Dendreon; institutional grants from Novartis and Roche. PC: none declared.
Funding Information:
This work was supported by Novartis Pharma, France.
PY - 2012/1/1
Y1 - 2012/1/1
N2 - The administration of mammalian target of rapamycin (mTOR) inhibitors can give rise to a potentially life-threatening adverse event, often referred to as 'non-infectious pneumonitis' (NIP), which is characterized by non-infectious, non-malignant, and non-specific inflammatory infiltrates. Patients usually present with cough and/or dyspnoea. We provide a brief description of the mechanism of action of mTOR inhibitors and their overall safety in patients with metastatic renal cell carcinoma (mRCC) and review the literature on mTOR inhibitor-associated NIP in patients with solid tumours. The review was used to derive questions on the diagnosis, management, and monitoring of mRCC patients with NIP, and to develop a decision tree for use in routine clinical practise. A key recommendation was the subdivision of grade 2 NIP into grades 2a and 2b, where grade 2a is closer to grade 1 and grade 2b to grade 3. This subdivision is important because it takes into account the nature and severity of clinical symptoms potentially related to NIP, either the onset of new symptoms or the worsening of existing symptoms, and thus determines the type and frequency of follow-up. It also helps to identify a subgroup of patients in whom treatment, if effective, may be continued without dose adjustment.
AB - The administration of mammalian target of rapamycin (mTOR) inhibitors can give rise to a potentially life-threatening adverse event, often referred to as 'non-infectious pneumonitis' (NIP), which is characterized by non-infectious, non-malignant, and non-specific inflammatory infiltrates. Patients usually present with cough and/or dyspnoea. We provide a brief description of the mechanism of action of mTOR inhibitors and their overall safety in patients with metastatic renal cell carcinoma (mRCC) and review the literature on mTOR inhibitor-associated NIP in patients with solid tumours. The review was used to derive questions on the diagnosis, management, and monitoring of mRCC patients with NIP, and to develop a decision tree for use in routine clinical practise. A key recommendation was the subdivision of grade 2 NIP into grades 2a and 2b, where grade 2a is closer to grade 1 and grade 2b to grade 3. This subdivision is important because it takes into account the nature and severity of clinical symptoms potentially related to NIP, either the onset of new symptoms or the worsening of existing symptoms, and thus determines the type and frequency of follow-up. It also helps to identify a subgroup of patients in whom treatment, if effective, may be continued without dose adjustment.
KW - Everolimus
KW - Mammalian target of rapamycin inhibitor
KW - Pulmonary toxicity
KW - Renal cell carcinoma
KW - Solid tumour
KW - Temsirolimus
UR - http://www.scopus.com/inward/record.url?scp=84864954263&partnerID=8YFLogxK
U2 - 10.1093/annonc/mds115
DO - 10.1093/annonc/mds115
M3 - Review article
C2 - 22689175
AN - SCOPUS:84864954263
SN - 0923-7534
VL - 23
SP - 1943
EP - 1953
JO - Annals of Oncology
JF - Annals of Oncology
IS - 8
ER -