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Published in: Medical Oncology 3/2012

01-09-2012 | Letter to the Editor

Fatal pneumonitis after treatment with pegylated liposomal doxorubicin in a patient with metastatic breast cancer in complete remission

Authors: Michael Mark, Beat Thürlimann

Published in: Medical Oncology | Issue 3/2012

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Excerpt

This case describes a 70-year-old female with right-sided breast cancer diagnosed in 1976. The patient was treated with a Halsted operation followed by adjuvant radiotherapy. In 1991, the patient had a left-side modified radical mastectomy followed by adjuvant chemotherapy with 6 cycles of cyclophosphamide/methotrexate/5-fluorouracil and adjuvant endocrine therapy with tamoxifen for 5 years due to invasive ductal breast cancer. In 2003, systemic relapse with cytologically confirmed malignant right-sided pleural effusion was diagnosed. Tumor marker CA 15-3 was slightly elevated, 49 kU/l (norm < 27 kU/l). Staging procedures showed no other sites of tumor recurrence. In November 2009, after 6½ years of tumor stabilization with letrozole followed by tamoxifen palliative chemotherapy with pegylated liposomal doxorubicin (PLD) 20 mg/m2 every 2 weeks was started due to progressive right-sided pleural effusion. After 4 months of therapy, CT examination confirmed almost complete regression of the pleural effusion. Chemotherapy was at this stage paused. Following 3 months of endocrine maintenance therapy with fulvestrant palliative chemotherapy with weekly paclitaxel was initiated due to increasing right-sided pleural effusion and radiologically bilateral nodular lung lesions. No other tumor lesions were noted at this time. Intractable myalgia after the first application of paclitaxel led to the request of the patient for another type of chemotherapy. The previously well-tolerated treatment with PLD was resumed in October 2010 leading to a radiologically partial remission after 3 months of therapy. The CT scan showed regression of the pulmonary nodular lesions. However, several discrete asymptomatic unilateral pulmonary ground-glass findings were observed. After 6 weeks of continued therapy with PLD, the patient was hospitalized in February 2011 complaining of progressive shortness of breath. The patient was afebrile, with a laboratory finding of an elevated C-reactive protein of 101 mg/l (norm < 8 mg/l). The CT scan at this time showed bilaterally pronounced alveolitic changes. No signs of cardiac failure or pulmonary embolism were found. The bronchioalveolar lavage revealed no malignant cells but nonspecific inflammatory changes: lymphocytes 26%, neutrophil granulocytes 26%, and macrophages 48%. No evidence for opportunistic infection was found, and normal proportion of siderophages was observed. …
Literature
1.
2.
go back to reference Huober J, Schoch O, Templeton A, Spirig C, Thürlimann B. Interstitial pneumonitis after treatment with bevacizumab and pegylated liposomal doxorubicin in a patient with metastatic breast cancer. Chemotherapy. 2010;56(1):69–70.PubMedCrossRef Huober J, Schoch O, Templeton A, Spirig C, Thürlimann B. Interstitial pneumonitis after treatment with bevacizumab and pegylated liposomal doxorubicin in a patient with metastatic breast cancer. Chemotherapy. 2010;56(1):69–70.PubMedCrossRef
3.
go back to reference Mirza MR, et al. A phaseII study of combination chemotherapy in early relapsed epithelial ovarian cancer using gemcitabine and pegylated liposomal doxorubicin. Gynecol Oncol. 2010;119(1):26–31.PubMedCrossRef Mirza MR, et al. A phaseII study of combination chemotherapy in early relapsed epithelial ovarian cancer using gemcitabine and pegylated liposomal doxorubicin. Gynecol Oncol. 2010;119(1):26–31.PubMedCrossRef
Metadata
Title
Fatal pneumonitis after treatment with pegylated liposomal doxorubicin in a patient with metastatic breast cancer in complete remission
Authors
Michael Mark
Beat Thürlimann
Publication date
01-09-2012
Publisher
Springer US
Published in
Medical Oncology / Issue 3/2012
Print ISSN: 1357-0560
Electronic ISSN: 1559-131X
DOI
https://doi.org/10.1007/s12032-011-0002-1

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