A phase 2 multicenter study of docetaxel-PM and trastuzumab-pkrb combination therapy in recurrent or metastatic salivary gland carcinomas

被引:5
作者
Lee, Jiyun [1 ]
Park, Sehhoon [1 ]
Jung, Hyun Ae [1 ]
Lee, Se-Hoon [1 ]
Seo, Seyoung [2 ]
Kim, Sung-Bae [2 ]
Kim, Ji-Won [3 ]
Lee, Keun-Wook [3 ]
Kang, Eun Joo [4 ]
Kim, Ju Won [5 ]
Choi, Yoon Ji [5 ]
Shim, Byoung-Yong [6 ]
An, Ho-Jung [6 ]
Park, Lee Chun [7 ]
Shin, Seong Hoon [7 ]
Kim, Jae-Joon [8 ]
Oh, So Yeon [8 ]
Kim, Min Kyoung [9 ]
Ahn, Myung-Ju [1 ]
机构
[1] Sungkyunkwan Univ, Samsung Med Ctr, Dept Med, Div Hematol Oncol,Sch Med, 81 Irwon Ro, Seoul 06351, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Oncol, Seoul, South Korea
[3] Seoul Natl Univ, Coll Med, Dept Internal Med, Bundang Hosp, Seongnam, South Korea
[4] Korea Univ, Dept Internal Med, Div Med Oncol, Guro Hosp, Seoul, South Korea
[5] Korea Univ, Coll Med, Dept Internal Med, Div Oncol,Anam Hosp, Seoul, South Korea
[6] Catholic Univ Korea, St Vincents Hosp, Coll Med, Dept Med Oncol, Suwon, South Korea
[7] Kosin Univ, Coll Med, Dept Internal Med, Gospel Hosp, Busan, South Korea
[8] Pusan Natl Univ, Dept Internal Med, Med Oncol & Hematol, Yangsan Hosp, Yangsan Si, Gyeongsangnam D, South Korea
[9] Yeungnam Univ Hosp, Dept Oncol Hematol, Daegu, South Korea
关键词
docetaxel-PM; head and neck cancers; HER2; salivary duct carcinoma; trastuzumab-pkrb; DUCT CARCINOMA; MALIGNANCY; OUTCOMES; CANCER;
D O I
10.1002/cncr.34892
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundSalivary duct carcinoma (SDC) is uncommon but is the most aggressive subtype of salivary gland carcinomas. The high positivity rate for human epidermal growth factor receptor 2 (HER2) led to an investigation of the efficacy of HER2-targeted agents. Docetaxel-PM (polymeric micelle) is a low-molecular-weight, nontoxic, biodegradable, and docetaxel-loaded micellar formulation. Trastuzumab-pkrb is a biosimilar to trastuzumab. MethodsThis was a multicenter, single-arm, open-label phase 2 study. Patients with HER2-positive (immunohistochemistry [IHC] score of >= 2+ and/or HER2/chromosome enumeration probe 17 [CEP17] ratio of >= 2.0) advanced SDCs were enrolled. Patients received docetaxel-PM (75 mg/m(2)) and trastuzumab-pkrb (8 mg/kg in the first cycle and 6 mg/kg in subsequent cycles) every 3 weeks. Primary end point was objective response rate (ORR). ResultsA total of 43 patients were enrolled. The best objective responses were partial response in 30 (69.8%) patients and stable disease in 10 (23.3%) patients, leading to an ORR of 69.8% (95% confidence interval [CI], 53.9-82.8) and a disease control rate of 93.0% (80.9-98.5). Median progression-free survival, duration of response, and overall survival were 7.9 (6.3-9.5), 6.7 (5.1-8.4), and 23.3 (19.9-26.7) months, respectively. Patients with HER2 IHC score of 3+ or HER2/CEP17 ratio >= 2.0 demonstrated better efficacies compared to those with HER2 IHC score of 2+. Thirty-eight (88.4%) patients experienced treatment-related adverse events (TRAE). Because of TRAE, nine (20.9%), 14 (32.6%), and 19 (44.2%) patients required temporary discontinuation, permanent discontinuation, or dose reduction, respectively. ConclusionsThe combination of docetaxel-PM and trastuzumab-pkrb demonstrated promising antitumor activity with a manageable toxicity profile in HER2-positive advanced SDC. Plain Language Summary Salivary duct carcinoma (SDC) is uncommon but is the most aggressive subtype of salivary gland carcinomas.SDC shares morphological and histological similarities with invasive ductal carcinoma of breast, which led to an investigation of hormonal receptor and human epidermal growth factor receptor 2 (HER2)/neu expression status in SDC.In this study, patients with HER2-positive SDC were enrolled and treated with combination of docetaxel-polymeric micelle and trastuzumab-pkrb.Promising antitumor activities were shown with objective response rate of 69.8%, disease control rate of 93.0%, median progression-free survival of 7.9 months, median duration of response of 6.7 months, and median overall survival of 23.3 months.
引用
收藏
页码:2966 / 2974
页数:9
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