Complete response to chemoimmunotherapy with bevacizumab in synchronous multiple primary cancers: pulmonary adenocarcinoma and sarcomatoid carcinoma.

IF 1.8 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Diogo Garcia, Isa Mambetsariev, Jeremy Fricke, Daniel Schmolze, Michelle Afkhami, Rifat Mannan, Pauline Kim, Shaira Therese Dingal, Bao Nguyen, Razmig Babikian, Yuman Fong, Ravi Salgia
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引用次数: 0

Abstract

A small percentage of patients have multiple synchronous primary cancers at presentation. In the last five years, many regimens associated with immunotherapy and chemotherapy were approved for first-line metastatic non-small-cell lung cancer (NSCLC) and other solid tumors, but the study of immunotherapy when multiple cancers are present in one patient remains incomplete. Next-generation sequencing biomarkers and immunotherapy markers including PD-L1 can be effectively utilized in the diagnosis and treatment plan for multiple synchronous primary cancers. Immune biomarkers and PD-L1 expression warrant individualized treatments in synchronous primary adenocarcinoma and pulmonary sarcomatoid carcinoma. We describe the case of a patient with pulmonary sarcomatoid carcinoma and lung adenocarcinoma, metastatic to brain de novo. The patient achieved a complete response after only three cycles of carboplatin, paclitaxel, bevacizumab, and atezolizumab and remains free of any evidence of disease after 18 mo of maintenance therapy.

Abstract Image

Abstract Image

贝伐单抗化疗免疫治疗同步多发性原发癌症的完全缓解:肺腺癌和肉瘤样癌。
一小部分患者在发病时伴有多发原发癌。在过去的五年中,许多与免疫治疗和化疗相关的方案被批准用于一线转移性非小细胞肺癌(NSCLC)和其他实体肿瘤,但是当一个患者出现多种癌症时,免疫治疗的研究仍然不完整。包括PD-L1在内的新一代测序生物标志物和免疫治疗标志物可有效用于多种同步原发癌症的诊断和治疗方案。免疫生物标志物和PD-L1表达支持同步原发性腺癌和肺肉瘤样癌的个体化治疗。我们报告一例合并肺肉瘤样癌及肺腺癌,转移至脑部的病例。患者仅在卡铂、紫杉醇、贝伐单抗和阿特唑单抗三个周期后就获得了完全缓解,并且在18个月的维持治疗后仍无任何疾病迹象。
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来源期刊
Cold Spring Harbor Molecular Case Studies
Cold Spring Harbor Molecular Case Studies MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.20
自引率
0.00%
发文量
54
期刊介绍: Cold Spring Harbor Molecular Case Studies is an open-access, peer-reviewed, international journal in the field of precision medicine. Articles in the journal present genomic and molecular analyses of individuals or cohorts alongside their clinical presentations and phenotypic information. The journal''s purpose is to rapidly share insights into disease development and treatment gained by application of genomics, proteomics, metabolomics, biomarker analysis, and other approaches. The journal covers the fields of cancer, complex diseases, monogenic disorders, neurological conditions, orphan diseases, infectious disease, gene therapy, and pharmacogenomics. It has a rapid peer-review process that is based on technical evaluation of the analyses performed, not the novelty of findings, and offers a swift, clear path to publication. The journal publishes: Research Reports presenting detailed case studies of individuals and small cohorts, Research Articles describing more extensive work using larger cohorts and/or functional analyses, Rapid Communications presenting the discovery of a novel variant and/or novel phenotype associated with a known disease gene, Rapid Cancer Communications presenting the discovery of a novel variant or combination of variants in a cancer type, Variant Discrepancy Resolution describing efforts to resolve differences or update variant interpretations in ClinVar through case-level data sharing, Follow-up Reports linked to previous observations, Plus Review Articles, Editorials, and Position Statements on best practices for research in precision medicine.
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