Risk of second primary cancers in cancer patients treated with cisplatin: a systematic review and meta-analysis of randomized studies

被引:37
作者
Liang, Fei [1 ,2 ]
Zhang, Sheng [1 ,2 ,5 ]
Xue, Hongxi [3 ]
Chen, Qiang [4 ]
机构
[1] Fudan Univ, Shanghai Canc Ctr, Shanghai, Peoples R China
[2] Fudan Univ, Shanghai Med Coll, Shanghai, Peoples R China
[3] Rizhao City Hosp Tradit Chinese Med, 35 Wanghai Rd, Rizhao, Peoples R China
[4] Taishan Med Univ, Sch Publ Hlth, Dept Clin Biochem, Taishan, Peoples R China
[5] Fudan Univ, Shanghai Canc Ctr, Med Oncol, 270 Dongan Rd, Shanghai 200032, Peoples R China
关键词
Second cancer; Cisplatin; Randomized controlled trials; SQUAMOUS-CELL CARCINOMA; COOPERATIVE-ONCOLOGY-GROUP; ADVANCED OVARIAN-CARCINOMA; PHASE-III TRIAL; COMBINATION CHEMOTHERAPY; INDUCTION CHEMOTHERAPY; TESTICULAR NONSEMINOMA; ADJUVANT CHEMOTHERAPY; BREAST-CANCER; BRAIN-TUMORS;
D O I
10.1186/s12885-017-3902-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Case reports, retrospective analyses, and observational studies have linked the use of cisplatin to increased risk of second cancers, especially life-threatening secondary leukemia. We therefore performed a systematic review and meta-analysis to evaluate the risk of second cancers associated with receipt of cisplatin-based chemotherapy in randomized controlled trials (RCTs). Methods: We searched MEDLINE, Embase, the Cochrane Central Register of Controlled Trials, trial registers, conference proceedings, review articles, and reference lists of trial publications for all relevant RCTs comparing cisplatin-versus noncisplatin-containing chemotherapy with data on second cancers. We extracted data about study characteristics and second cancers, especially leukemia/myelodysplasia. The primary and secondary outcomes were the odds ratios (ORs) for all second cancers and for secondary leukemia/myelodysplasia, respectively. Results: We identified 28 eligible trials with 7403 patients. Second cancers were reported in 143 patients, including 75 patients in the cisplatin arm and 68 in the non-cisplatin arm (raw event rates of 1.91 and 1.96%, respectively). The pooled OR for risk of all second cancers associated with cisplatin-based chemotherapy was 0.95 (95% confidence interval (CI): 0.67-1.33, P = 0.76). Secondary leukemia/myelodysplasia was reported in 14 patients on cisplatin arms and in 6 patients on non-cisplatin arms of 11 eligible RCTs with 2629 patients (raw event rates of 1.09 and 0.45%, respectively; pooled OR = 2.34, 95% CI 0.97-5.65, P = 0.06). Conclusion: Cisplatin was not associated with a significantly increased risk of second cancers compared with noncisplatin- based chemotherapy. There is a non-significant trend to increased risk of leukemia/myelodysplasia and the absolute risk was low. The concern about risk of second cancers should not influence decisions to use an efficacious regimen containing cisplatin.
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页数:12
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