Marin Abousaud, Saagar Pamulapati, Saad Rashid, Fabiola Lozano, Madeline Shepherd, Busola Fowowe, Yichun Cao, Pauline Kim, Yuan Liu, James E Bates, Mark McDonald, Soumon Rudra, William A Stokes, Jennifer Gross, Nicole C Schmitt, Mark W El-Deiry, Mihir R Patel, Anthea L Hammond, Yong Teng, Conor Steuer, Dong M Shin, Nabil F Saba
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Patients with human papillomavirus-related and unrelated disease were included. Data analysis was conducted in March 2022.</p><p><strong>Exposures: </strong>Patients received C/P or cisplatin. Most cisplatin patients received weekly cisplatin or C/P. Intensity-modulated radiotherapy was primarily used, with a median (range) total dose of 70 (66-70) Gy.</p><p><strong>Main outcomes and measures: </strong>Key efficacy end points were locoregional recurrence-free survival (LRFS), progression-free survival (PFS), distant metastasis-free survival (DMFS), overall survival (OS), and safety.</p><p><strong>Results: </strong>A total of 308 patients were included (66 female individuals [21.4%]; 60 African American individuals [19.5%], 9 Asian individuals [2.9%], 3 Hispanic individuals [1.0%], and 235 White individuals [76.3%]; median [range] age, 63 [24-89] years). Of these patients, 116 (37.7%) had never smoked, 117 (38.0%) formerly smoked, and 75 (24.4%) were active smokers. Primary sites were oropharynx (164 [53.2%]; 164 [84.7%] were human papillomavirus-positive), oral cavity (57 [18.5%]), and larynx (52 [16.9%]); a comparison of illness stage was T3/T4 (191 [62.0%]) vs T1/T2 (117 [38.0%]) and N1 to N3 (258 [83.8%]) vs N0 (50 [16.2%]). A total of 97 patients (31.5%) underwent surgery before concurrent therapy. No meaningful differences between cisplatin and C/P were observed for 3-year rates of LRFS (97.0% vs 96.2%; difference, -0.8%; 95% CI, -5.2% to 3.6%), PFS (77.5% vs 79.8%; difference, 2.3%; 95% CI, -7.4% to 12.0%), DMFS (83.4% vs 86.8%; difference, 3.4%; 95% CI, -5.3% to 12.1%), or OS (90.8% vs 92.9%; difference, 2.1%; 95% CI, -4.5% to 8.7%). C/P was associated with a higher rate of grade 3 to 4 leukopenia, anemia, and dermatitis and more feeding tube placements and hospitalizations.</p><p><strong>Conclusions and relevance: </strong>The results of this study suggest that there were no differences in LRFS, PFS, DMFS, and OS in patients with SCCHN receiving radiotherapy with C/P vs cisplatin. 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Patients with human papillomavirus-related and unrelated disease were included. Data analysis was conducted in March 2022.</p><p><strong>Exposures: </strong>Patients received C/P or cisplatin. Most cisplatin patients received weekly cisplatin or C/P. Intensity-modulated radiotherapy was primarily used, with a median (range) total dose of 70 (66-70) Gy.</p><p><strong>Main outcomes and measures: </strong>Key efficacy end points were locoregional recurrence-free survival (LRFS), progression-free survival (PFS), distant metastasis-free survival (DMFS), overall survival (OS), and safety.</p><p><strong>Results: </strong>A total of 308 patients were included (66 female individuals [21.4%]; 60 African American individuals [19.5%], 9 Asian individuals [2.9%], 3 Hispanic individuals [1.0%], and 235 White individuals [76.3%]; median [range] age, 63 [24-89] years). Of these patients, 116 (37.7%) had never smoked, 117 (38.0%) formerly smoked, and 75 (24.4%) were active smokers. 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引用次数: 0
摘要
重要性:尽管对于不适合接受顺铂的头颈部鳞状细胞癌(SCCHN)患者广泛使用卡铂/紫杉醇(C/P)联合放疗,但缺乏对C/P与顺铂的前瞻性或比较分析。目的:探讨SCCHN患者在晚期和术后接受C/P与顺铂联合放疗的临床结果。设计、环境和参与者:这项回顾性、单中心比较有效性研究纳入了2010年1月至2021年3月期间接受C/P或顺铂同步放化疗的SCCHN患者。包括与人乳头瘤病毒相关和不相关疾病的患者。数据分析于2022年3月进行。暴露:患者接受C/P或顺铂治疗。大多数顺铂患者每周接受顺铂治疗或C/P。主要采用调强放疗,中位(范围)总剂量为70 (66-70)Gy。主要结局和指标:主要疗效终点为局部无复发生存期(LRFS)、无进展生存期(PFS)、无远处转移生存期(DMFS)、总生存期(OS)和安全性。结果:共纳入308例患者,其中女性66例,占21.4%;非洲裔60例(19.5%),亚裔9例(2.9%),西班牙裔3例(1.0%),白人235例(76.3%);年龄中位数[范围]63岁[24-89]岁)。这些患者中,116例(37.7%)从未吸烟,117例(38.0%)曾经吸烟,75例(24.4%)是活跃吸烟者。原发部位为口咽部(164例,53.2%);人乳头瘤病毒阳性164例(84.7%),口腔57例(18.5%),喉部52例(16.9%);T3/T4(191例[62.0%])vs T1/T2(117例[38.0%]),N1 ~ N3(258例[83.8%])vs N0(50例[16.2%])。共有97例(31.5%)患者在接受同期治疗前接受了手术。顺铂和C/P在3年LRFS方面无显著差异(97.0% vs 96.2%;差异,-0.8%;95% CI, -5.2%至3.6%),PFS (77.5% vs 79.8%;差异,2.3%;95% CI, -7.4%至12.0%),DMFS(83.4%对86.8%;差异,3.4%;95% CI, -5.3%至12.1%)或OS (90.8% vs 92.9%;差异,2.1%;95% CI, -4.5%至8.7%)。C/P与较高的3 - 4级白细胞减少、贫血和皮炎发生率以及更多的喂食管放置和住院有关。结论及相关性:本研究结果提示,与顺铂相比,接受C/P放疗的SCCHN患者的LRFS、PFS、DMFS和OS无差异。这些结果支持在不能接受顺铂的患者中使用C/P作为替代方案。
Radiotherapy With Cisplatin vs Carboplatin Paclitaxel for Head and Neck Squamous Cell Carcinoma.
Importance: Despite the widespread use of carboplatin/paclitaxel (C/P) in concurrence with radiotherapy for patients with squamous cell carcinoma of the head and neck (SCCHN) who are ineligible to receive cisplatin, there is a lack of prospective or comparative analyses examining C/P vs cisplatin.
Objective: To examine the clinical outcomes of patients with SCCHN receiving C/P vs cisplatin in concurrence with radiotherapy in the definitive and postoperative setting.
Design, setting, and participants: This retrospective, single-center comparative effectiveness study included patients with SCCHN who received concurrent chemoradiotherapy with C/P or cisplatin from January 2010 to March 2021. Patients with human papillomavirus-related and unrelated disease were included. Data analysis was conducted in March 2022.
Exposures: Patients received C/P or cisplatin. Most cisplatin patients received weekly cisplatin or C/P. Intensity-modulated radiotherapy was primarily used, with a median (range) total dose of 70 (66-70) Gy.
Main outcomes and measures: Key efficacy end points were locoregional recurrence-free survival (LRFS), progression-free survival (PFS), distant metastasis-free survival (DMFS), overall survival (OS), and safety.
Results: A total of 308 patients were included (66 female individuals [21.4%]; 60 African American individuals [19.5%], 9 Asian individuals [2.9%], 3 Hispanic individuals [1.0%], and 235 White individuals [76.3%]; median [range] age, 63 [24-89] years). Of these patients, 116 (37.7%) had never smoked, 117 (38.0%) formerly smoked, and 75 (24.4%) were active smokers. Primary sites were oropharynx (164 [53.2%]; 164 [84.7%] were human papillomavirus-positive), oral cavity (57 [18.5%]), and larynx (52 [16.9%]); a comparison of illness stage was T3/T4 (191 [62.0%]) vs T1/T2 (117 [38.0%]) and N1 to N3 (258 [83.8%]) vs N0 (50 [16.2%]). A total of 97 patients (31.5%) underwent surgery before concurrent therapy. No meaningful differences between cisplatin and C/P were observed for 3-year rates of LRFS (97.0% vs 96.2%; difference, -0.8%; 95% CI, -5.2% to 3.6%), PFS (77.5% vs 79.8%; difference, 2.3%; 95% CI, -7.4% to 12.0%), DMFS (83.4% vs 86.8%; difference, 3.4%; 95% CI, -5.3% to 12.1%), or OS (90.8% vs 92.9%; difference, 2.1%; 95% CI, -4.5% to 8.7%). C/P was associated with a higher rate of grade 3 to 4 leukopenia, anemia, and dermatitis and more feeding tube placements and hospitalizations.
Conclusions and relevance: The results of this study suggest that there were no differences in LRFS, PFS, DMFS, and OS in patients with SCCHN receiving radiotherapy with C/P vs cisplatin. These results support the use of C/P as an alternative regimen in patients who cannot receive cisplatin.
期刊介绍:
JAMA Otolaryngology–Head & Neck Surgery is a globally recognized and peer-reviewed medical journal dedicated to providing up-to-date information on diseases affecting the head and neck. It originated in 1925 as Archives of Otolaryngology and currently serves as the official publication for the American Head and Neck Society. As part of the prestigious JAMA Network, a collection of reputable general medical and specialty publications, it ensures the highest standards of research and expertise. Physicians and scientists worldwide rely on JAMA Otolaryngology–Head & Neck Surgery for invaluable insights in this specialized field.