“…CME is seen in various pathologies and diseases through fluorescence leakage, generally observed on fluorescein fluorescence fundus angiography due to disruption of the medial vascular retinal barrier and leakage of fluorescein out of the retinal vessels. However, CME caused by taxane-based anticancer drugs is thought to be due to toxicity to Müller cells and fluorescence leakage or fluorescence retention tends not to be observed with OCT [ 7 ]. It is assumed that the toxic taxane drugs cause intracellular fluid retention and an increase in extracellular fluid in Müller cells, resulting in the disruption of the intracellular structure of Müller cells and the formation of cysts in the outer reticular and inner granular layers, leading to the formation of CME [ 8 ].…”
Cystoid macular edema (CME) is a rare side effect associated with chemotherapy. Although the development of CME has been reported to occur following treatment with taxane drugs, such as nanoparticle albumin-bound paclitaxel (Nab-PTX), the occurrence of CME with treatment with atezolizumab has not yet been reported. Here, we report the case of a 49-year-old woman who developed CME 19 months into chemotherapy with Nab-PTX and atezolizumab. Improvement was not achieved with steroid injections into the Tenon’s sac, and Nab-PTX and atezolizumab treatments were ceased. One month later, there was subjective improvement in her symptoms. Although many reports have indicated that cessation of chemotherapy has successfully improved CME, a specific treatment for CME has not yet been established. Clinicians should be aware of the ophthalmologic side effects and offer immediate treatment if symptoms develop.
“…CME is seen in various pathologies and diseases through fluorescence leakage, generally observed on fluorescein fluorescence fundus angiography due to disruption of the medial vascular retinal barrier and leakage of fluorescein out of the retinal vessels. However, CME caused by taxane-based anticancer drugs is thought to be due to toxicity to Müller cells and fluorescence leakage or fluorescence retention tends not to be observed with OCT [ 7 ]. It is assumed that the toxic taxane drugs cause intracellular fluid retention and an increase in extracellular fluid in Müller cells, resulting in the disruption of the intracellular structure of Müller cells and the formation of cysts in the outer reticular and inner granular layers, leading to the formation of CME [ 8 ].…”
Cystoid macular edema (CME) is a rare side effect associated with chemotherapy. Although the development of CME has been reported to occur following treatment with taxane drugs, such as nanoparticle albumin-bound paclitaxel (Nab-PTX), the occurrence of CME with treatment with atezolizumab has not yet been reported. Here, we report the case of a 49-year-old woman who developed CME 19 months into chemotherapy with Nab-PTX and atezolizumab. Improvement was not achieved with steroid injections into the Tenon’s sac, and Nab-PTX and atezolizumab treatments were ceased. One month later, there was subjective improvement in her symptoms. Although many reports have indicated that cessation of chemotherapy has successfully improved CME, a specific treatment for CME has not yet been established. Clinicians should be aware of the ophthalmologic side effects and offer immediate treatment if symptoms develop.
“…It has been reported that, in 97.83% of the cases, no leakage was detected in fundus fluorescence angiography (FFA) or significant ICGA changes ( 20 , 31 ). In all T-CME cases listed here (literature review and case report), which resulted from albumin-bound paclitaxel, no or minimal leakage was identified by FFA.…”
Section: Discussionmentioning
confidence: 99%
“…Concerning treatment, the literature reviewed showed that some T-CME cases spontaneously resolved after discontinuing nab-paclitaxel without eye treatment within 1.5 weeks to 6 months (5,6,(9)(10)(11)(12)(13)(19)(20)(21). Though the mechanism of inflammatory factors is uncertain, anti-inflammatory agents (steroids or NSAIDs) were applied previously.…”
Section: Discussionmentioning
confidence: 99%
“…In these cases, the male to female ratio was 1:2.8, the mean age was 60 years (32-73 years), and almost all had bilateral eyes involvement except one. Fourteen cases were diagnosed with breast cancer (7)(8)(9)(10)(11)(12)(13)(14)(15)(16)(17)24), six with pancreatic cancer (19)(20)(21)(22)(23)(24), and the others with melanoma (5), cancer of the hypopharynx ( 18), and lung cancer (6), respectively. The treatment regimens were heterogeneous, with most patients discontinuing nab-paclitaxel with or without eye treatments, including topical nonsteroidal anti-inflammatory drugs (NSAIDs), topical corticosteroids, topical dorzolamide (DRZ), intravitreal bevacizumab (IVB), dexamethasone.…”
Angiographically silent cystoid macular edema (CME) is a rare complication from nab-paclitaxel. Here we report a 45-year-old woman with breast cancer who developed CME after several months of treatment with albumin-bound paclitaxel (nab-paclitaxel). Her visual acuity did not improve significantly with the cessation of nab-paclitaxel and intravitreal ranibizumab treatment. Then, brinzolamide eye drops were prescribed. One month later, her vision improved, with the macular edema significantly subsided. Finally, we reviewed other cases of CME induced by nab-paclitaxel that have been reported in the literature and discussed the underlying pathogenesis of nab-paclitaxel-induced CME.
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