Complete response to chemoimmunotherapy with bevacizumab in synchronous multiple primary cancers: pulmonary adenocarcinoma and sarcomatoid carcinoma.
Diogo GarciaIsa MambetsarievJeremy FrickeDaniel SchmolzeMichelle AfkhamiRifat MannanPauline KimShaira Therese DingalBao NguyenRazmig BabikianYuman FongRavi SalgiaPublished in: Cold Spring Harbor molecular case studies (2023)
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.
Keyphrases
- squamous cell carcinoma
- case report
- pulmonary hypertension
- small cell lung cancer
- ejection fraction
- end stage renal disease
- gene expression
- newly diagnosed
- stem cells
- randomized controlled trial
- metastatic colorectal cancer
- prognostic factors
- peritoneal dialysis
- bone marrow
- tyrosine kinase
- mesenchymal stem cells
- subarachnoid hemorrhage
- cerebral ischemia
- chemotherapy induced
- cell therapy
- brain metastases
- brain injury
- blood brain barrier