Gianni Lorenzo, Panzini Ilaria, Li Sigui, Gelber Richard D, Collins John, Holmberg Stig B, Crivellari Diana, Castiglione-Gertsch Monica, Goldhirsch Aron, Coates Alan S, Ravaioli Alberto
Division of Oncology and Hematology, Hospital degli Infermi, Rimini, Italy.
Cancer. 2006 Feb 1;106(3):505-13. doi: 10.1002/cncr.21651.
Others have reported ocular toxicity after adjuvant chemoendocrine therapy, but this study looked at ocular toxicity in similarly treated patients from large randomized clinical trials.
Information was retrieved on incidence and timing of ocular toxicity from the International Breast Cancer Study Group (IBCSG) database of 4948 eligible patients randomized to receive tamoxifen or toremifene alone or in combination with chemotherapy (either concurrently or sequentially). Case reports of patients with ocular toxicity were evaluated to determine whether ocular toxicity occurred during chemotherapy and/or hormonal therapy. Additional information was obtained from participating institutions for patients in whom ocular toxicity occurred after chemotherapy but during administration of tamoxifen or toremifene.
Ocular toxicity was reported in 538 of 4948 (10.9%) patients during adjuvant treatment, mainly during chemotherapy. Forty-five of 4948 (0.9%) patients had ocular toxicity during hormone therapy alone, but only 30 (0.6%) patients had ocular toxicity reported either without receiving any chemotherapy or beyond 3 months after completing chemotherapy and, thus, possibly related to tamoxifen or toremifene. In 3 cases, retinal alterations, without typical aspects of tamoxifen toxicity, were reported; 4 patients had cataract (2 bilateral), 12 impaired visual acuity, 10 ocular irritation, 1 optical neuritis, and the rest had other symptoms.
Ocular toxicity during adjuvant therapy is a common side effect mainly represented by irritative symptoms due to chemotherapy. By contrast, ocular toxicity during hormonal therapy is rare and does not appear to justify a regular program of ocular examination. However, patients should be informed of this rare side effect so that they may seek prompt ophthalmic evaluation for ocular complaints.
其他人曾报道过辅助性化疗内分泌治疗后的眼部毒性,但本研究观察了大型随机临床试验中接受类似治疗患者的眼部毒性。
从国际乳腺癌研究组(IBCSG)数据库中检索了4948例符合条件患者的眼部毒性发生率及发生时间信息,这些患者被随机分配接受他莫昔芬或托瑞米芬单药治疗,或联合化疗(同时或序贯)。对眼部毒性患者的病例报告进行评估,以确定眼部毒性是否发生在化疗期间和/或激素治疗期间。对于化疗后但在服用他莫昔芬或托瑞米芬期间发生眼部毒性的患者,从参与研究的机构获取了更多信息。
在4948例(10.9%)患者的辅助治疗期间报告了眼部毒性,主要发生在化疗期间。4948例(0.9%)患者仅在激素治疗期间出现眼部毒性,但只有30例(0.6%)患者在未接受任何化疗或化疗结束后3个月以上报告了眼部毒性,因此可能与他莫昔芬或托瑞米芬有关。报告了3例视网膜改变,无典型的他莫昔芬毒性表现;4例患者有白内障(2例双侧),12例视力受损,10例眼部刺激,1例视神经炎,其余有其他症状。
辅助治疗期间的眼部毒性是一种常见的副作用,主要表现为化疗引起的刺激性症状。相比之下,激素治疗期间的眼部毒性很少见,似乎没有必要进行常规的眼部检查。然而,应告知患者这种罕见的副作用,以便他们在出现眼部不适时能及时寻求眼科评估。