Hyperprogressive Disease After Immunotherapy: A Case Report of Pulmonary Enteric Adenocarcinoma

Primary pulmonary enteric adenocarcinoma (PEAC) is a rare invasive adenocarcinoma clinically similar to metastatic colorectal adenocarcinoma (MCRC). Although many studies have addressed the differential diagnosis of PEAC, few have described the treatment of PEAC, especially using immunotherapy. This...

Full description

Bibliographic Details
Published in:Frontiers in Oncology
Main Authors: Chun-Hong Hu, Shenghao Shi, Wen Dong, Lizhi Xiao, Hongjing Zang, Fang Wu
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-03-01
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2022.799549/full
_version_ 1856980990989172736
author Chun-Hong Hu
Shenghao Shi
Wen Dong
Lizhi Xiao
Hongjing Zang
Fang Wu
author_facet Chun-Hong Hu
Shenghao Shi
Wen Dong
Lizhi Xiao
Hongjing Zang
Fang Wu
author_sort Chun-Hong Hu
collection DOAJ
container_title Frontiers in Oncology
description Primary pulmonary enteric adenocarcinoma (PEAC) is a rare invasive adenocarcinoma clinically similar to metastatic colorectal adenocarcinoma (MCRC). Although many studies have addressed the differential diagnosis of PEAC, few have described the treatment of PEAC, especially using immunotherapy. This report describes a 61-year-old man who presented initially with pain in the ribs. Pathological analysis of biopsy samples shows malignant tumors of the right pleura, and next-generation sequencing of 26 genes showed a KRAS gene mutation. Positron emission tomography-computed tomography (PET-CT) found no evidence of gastrointestinal malignancy. Due to multiple metastases, the patient could not undergo radical surgery. The patient was treated with a combination chemotherapy regimen of paclitaxel plus carboplatin, along with sindilizumab immunotherapy, but, after one cycle of treatment, the tumor showed a hyperprogressive state. The patient is still being monitored regularly. These findings indicate that chemotherapy combined with immunotherapy may be ineffective in the treatment of primary PEAC with positive driver genes.
format Article
id doaj-art-eecfa5d39c6c4b23b33331bb8cf385ba
institution Directory of Open Access Journals
issn 2234-943X
language English
publishDate 2022-03-01
publisher Frontiers Media S.A.
record_format Article
spelling doaj-art-eecfa5d39c6c4b23b33331bb8cf385ba2025-08-19T19:56:57ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2022-03-011210.3389/fonc.2022.799549799549Hyperprogressive Disease After Immunotherapy: A Case Report of Pulmonary Enteric AdenocarcinomaChun-Hong Hu0Shenghao Shi1Wen Dong2Lizhi Xiao3Hongjing Zang4Fang Wu5Department of Oncology, The Second Xiangya Hospital, Central South University, Changsha, ChinaDepartment of Oncology, The Second Xiangya Hospital, Central South University, Changsha, ChinaDepartment of Oncology, The Changde First People’s Hospital, Changde, ChinaDepartment of Radiology, Second Xiangya Hospital, Central South University, Changsha, ChinaDepartment of Pathology, Second Xiangya Hospital, Central South University, Changsha, ChinaDepartment of Oncology, The Second Xiangya Hospital, Central South University, Changsha, ChinaPrimary pulmonary enteric adenocarcinoma (PEAC) is a rare invasive adenocarcinoma clinically similar to metastatic colorectal adenocarcinoma (MCRC). Although many studies have addressed the differential diagnosis of PEAC, few have described the treatment of PEAC, especially using immunotherapy. This report describes a 61-year-old man who presented initially with pain in the ribs. Pathological analysis of biopsy samples shows malignant tumors of the right pleura, and next-generation sequencing of 26 genes showed a KRAS gene mutation. Positron emission tomography-computed tomography (PET-CT) found no evidence of gastrointestinal malignancy. Due to multiple metastases, the patient could not undergo radical surgery. The patient was treated with a combination chemotherapy regimen of paclitaxel plus carboplatin, along with sindilizumab immunotherapy, but, after one cycle of treatment, the tumor showed a hyperprogressive state. The patient is still being monitored regularly. These findings indicate that chemotherapy combined with immunotherapy may be ineffective in the treatment of primary PEAC with positive driver genes.https://www.frontiersin.org/articles/10.3389/fonc.2022.799549/fullpulmonary enteric adenocarcinomachemotherapyimmunity therapyhyperprogressive diseasecase report
spellingShingle Chun-Hong Hu
Shenghao Shi
Wen Dong
Lizhi Xiao
Hongjing Zang
Fang Wu
Hyperprogressive Disease After Immunotherapy: A Case Report of Pulmonary Enteric Adenocarcinoma
pulmonary enteric adenocarcinoma
chemotherapy
immunity therapy
hyperprogressive disease
case report
title Hyperprogressive Disease After Immunotherapy: A Case Report of Pulmonary Enteric Adenocarcinoma
title_full Hyperprogressive Disease After Immunotherapy: A Case Report of Pulmonary Enteric Adenocarcinoma
title_fullStr Hyperprogressive Disease After Immunotherapy: A Case Report of Pulmonary Enteric Adenocarcinoma
title_full_unstemmed Hyperprogressive Disease After Immunotherapy: A Case Report of Pulmonary Enteric Adenocarcinoma
title_short Hyperprogressive Disease After Immunotherapy: A Case Report of Pulmonary Enteric Adenocarcinoma
title_sort hyperprogressive disease after immunotherapy a case report of pulmonary enteric adenocarcinoma
topic pulmonary enteric adenocarcinoma
chemotherapy
immunity therapy
hyperprogressive disease
case report
url https://www.frontiersin.org/articles/10.3389/fonc.2022.799549/full
work_keys_str_mv AT chunhonghu hyperprogressivediseaseafterimmunotherapyacasereportofpulmonaryentericadenocarcinoma
AT shenghaoshi hyperprogressivediseaseafterimmunotherapyacasereportofpulmonaryentericadenocarcinoma
AT wendong hyperprogressivediseaseafterimmunotherapyacasereportofpulmonaryentericadenocarcinoma
AT lizhixiao hyperprogressivediseaseafterimmunotherapyacasereportofpulmonaryentericadenocarcinoma
AT hongjingzang hyperprogressivediseaseafterimmunotherapyacasereportofpulmonaryentericadenocarcinoma
AT fangwu hyperprogressivediseaseafterimmunotherapyacasereportofpulmonaryentericadenocarcinoma