Department of Obstetrics and Gynecology and CCC Munich LMU University Hospital, Ludwig Maximilians University (LMU), Munich, Germany.
Department of Internal Medicine III and CCC Munich LMU, University Hospital, Ludwig Maximilians University (LMU), Munich, Germany.
Arch Gynecol Obstet. 2021 May;303(5):1331-1345. doi: 10.1007/s00404-020-05881-z. Epub 2020 Dec 4.
Comprehensive genomic profiling identifying actionable molecular alterations aims to enable personalized treatment for cancer patients. The purpose of this analysis was to retrospectively assess the impact of personalized recommendations made by a multidisciplinary tumor board (MTB) on the outcome of patients with breast or gynecological cancers, who had progressed under standard treatment. Here, first experiences of our Comprehensive Cancer Center Molecular Tumor Board are reported.
All patients were part of a prospective local registry. 95 patients diagnosed with metastatic breast cancer or gynecological malignancies underwent extended molecular profiling. From May 2017 through March 2019, the MTB reviewed all clinical cases considering tumor profile and evaluated molecular alterations regarding further diagnostic and therapeutic recommendations.
95 patients with metastatic breast or gynecological cancers were discussed in the MTB (68% breast cancer, 20% ovarian cancer, 5% cervical cancer, 3% endometrial cancer and 4% others). Genes with highest mutation rate were PIK3CA and ERBB2. Overall, 34 patients (36%) received a biomarker-based targeted therapy recommendation. Therapeutic recommendations were implemented in nine cases; four patients experienced clinical benefit with a partial response or disease stabilization lasting over 4 months.
In the setting of a multidisciplinary molecular tumor board, a small but clinically meaningful group of breast and gynecological cancer patients benefits from comprehensive genomic profiling. Broad and successful implementation of precision medicine is complicated by patient referral at late stage disease and limited access to targeted agents and early clinical trials.
284-10 (03.05.2018).
全面的基因组分析确定可行的分子改变旨在为癌症患者提供个性化治疗。本分析的目的是回顾性评估多学科肿瘤委员会(MTB)提出的个性化建议对标准治疗后进展的乳腺癌或妇科癌症患者结局的影响。在此,报告了我们综合癌症中心分子肿瘤委员会的初步经验。
所有患者均为前瞻性本地登记处的一部分。95 名诊断为转移性乳腺癌或妇科恶性肿瘤的患者接受了扩展的分子分析。从 2017 年 5 月到 2019 年 3 月,MTB 审查了所有考虑肿瘤谱的临床病例,并评估了分子改变,以提出进一步的诊断和治疗建议。
95 名患有转移性乳腺癌或妇科癌症的患者在 MTB 中进行了讨论(68%乳腺癌,20%卵巢癌,5%宫颈癌,3%子宫内膜癌和 4%其他)。突变率最高的基因是 PIK3CA 和 ERBB2。总体而言,34 名患者(36%)接受了基于生物标志物的靶向治疗建议。在 9 例中实施了治疗建议;4 名患者经历了部分缓解或疾病稳定超过 4 个月的临床获益。
在多学科分子肿瘤委员会的设置下,一小部分但具有临床意义的乳腺癌和妇科癌症患者受益于全面的基因组分析。精准医学的广泛和成功实施受到患者在晚期疾病时的转介、靶向药物和早期临床试验的有限获得的限制。
284-10(2018 年 3 月 3 日)。