Neoadjuvant Chemotherapy Treatment Modifications in Ovarian Carcinoma The Impact on Surgical Outcome and Progression-free Survival

被引:5
作者
Salman, Lina [1 ,2 ]
Ben-Haroush, Avi [1 ,2 ]
Raban, Oded [1 ,2 ]
Yeoshoua, Effi [1 ,2 ]
Sabah, Gad [1 ,2 ]
Jakobson-Setton, Ariella [1 ,2 ]
Tsoref, Daliah [1 ,2 ]
Eitan, Ram [1 ,2 ]
机构
[1] Helen Schneider Hosp Women, Rabin Med Ctr, Div Gynecol Oncol, Petah Tiqwa, Israel
[2] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
来源
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS | 2019年 / 42卷 / 01期
关键词
neoadjuvant chemotherapy; ovarian carcinoma; treatment modification; CLINICAL-PRACTICE; 1ST-LINE CHEMOTHERAPY; GYNECOLOGIC-ONCOLOGY; AMERICAN SOCIETY; CANCER; CARBOPLATIN; PACLITAXEL; CISPLATIN; DOCETAXEL; TRIAL;
D O I
10.1097/COC.0000000000000469
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Little is known on the impact of neoadjuvant chemotherapy (NACT) treatment modifications on surgical outcome and progression-free survival (PFS) in patients with ovarian carcinoma. We aimed to report the changes we made during NACT and to evaluate its impact on patient outcome. Methods: A retrospective cohort study of all women with advanced stage ovarian carcinoma treated with NACT followed by interval cytoreduction in one university-affiliated medical center (January 2005 to June 2017). We excluded those who were treated with NACT without any surgical intervention. NACT modifications included delay in treatment, change in chemotherapy, and dose reduction. Demographics, tumor characteristics, surgical outcome, and PFS were compared between patients exposed to NACT treatment modifications and those who received standard treatment. Results: Seventy-nine patients met inclusion criteria of whom, 59 patients received standard, nonmodified treatment and 20 patients modified NACT. There were no intergroup differences with respect to age at diagnosis (59.5 +/- 11.6 vs. 64.70 +/- 8.09, P=0.09) and stage of disease (P=0.13). Radiologic complete response rates (25.0% vs. 32.2%, P=0.545) and optimal cytoreduction rates (75.0% vs. 86.4%, P=0.23) were similar in both treatment groups. Mean PFS (in months) was comparable between patients receiving standard treatment and those who required NACT modifications (18.5 vs. 12.2, P=0.125). Conclusions: NACT treatment modifications did not affect surgical outcome and PFS. We conclude that when clinically indicated, dose alteration and scheduling can be implemented without apparent detriment to outcome.
引用
收藏
页码:17 / 20
页数:4
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