TY - JOUR
T1 - Treatment of recurrent ovarian cancer with pegylated liposomal doxorubicin
T2 - a reappraisal and critical analysis
AU - Lorusso, Domenica
AU - Sabatucci, Ilaria
AU - Maltese, Giuseppa
AU - Lepori, Stefano
AU - Tripodi, Elisa
AU - Bogani, Giorgio
AU - Raspagliesi, Francesco
PY - 2019/8/1
Y1 - 2019/8/1
N2 - The vast majority of ovarian cancer relapses on front-line therapy and the optimal treatment of recurrent ovarian cancer remains controversial. This review is based on the relevant published literature indexed in PubMed on pegylated liposomal doxorubicin (PLD), either alone or in combination with other drugs, as one option in relapsed disease. PLD showed an improved pharmacokinetic profile, with a slower plasma clearance and a longer circulation time, compared to other conventional doxorubicin formulations. PLD is considered to have little potential for cardiotoxicity, even at prolonged and high cumulative doses, although there appears to be room for improvement in terms of maximal dose allowed. Notwithstanding, there remain some concerns about cardiac safety, and patient monitoring is generally advocated. No data are available on the possibility to rechallenge PLD treatment in recurrent ovarian cancer, as already known for other drugs. Optimization of treatment regimens with PLD will allow a more rational treatment in advanced ovarian cancers for which few therapeutic options are available.
AB - The vast majority of ovarian cancer relapses on front-line therapy and the optimal treatment of recurrent ovarian cancer remains controversial. This review is based on the relevant published literature indexed in PubMed on pegylated liposomal doxorubicin (PLD), either alone or in combination with other drugs, as one option in relapsed disease. PLD showed an improved pharmacokinetic profile, with a slower plasma clearance and a longer circulation time, compared to other conventional doxorubicin formulations. PLD is considered to have little potential for cardiotoxicity, even at prolonged and high cumulative doses, although there appears to be room for improvement in terms of maximal dose allowed. Notwithstanding, there remain some concerns about cardiac safety, and patient monitoring is generally advocated. No data are available on the possibility to rechallenge PLD treatment in recurrent ovarian cancer, as already known for other drugs. Optimization of treatment regimens with PLD will allow a more rational treatment in advanced ovarian cancers for which few therapeutic options are available.
KW - Anthracycline
KW - cardioprotection
KW - ovarian cancer
KW - pegylated liposomal doxorubicin
KW - personalized therapy
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U2 - 10.1177/0300891619839308
DO - 10.1177/0300891619839308
M3 - Review article
C2 - 30917765
AN - SCOPUS:85071089177
SN - 0300-8916
VL - 105
SP - 282
EP - 287
JO - Tumori
JF - Tumori
IS - 4
ER -