# Case report: Long-term survival in synchronous double primary malignancies of lung adenocarcinomas and esophageal squamous cell carcinoma treated with definitive chemoradiotherapy and SBRT combined with anti-PD-1

**Authors:** Rui Zeng, Xiaoyun Zhou, Kexin Ou, Wei Chen, Chen Yang, Ting Wang, Yani Li, Yawen Zha, Minying Li, Jingjing Zhang

PMC · DOI: 10.3389/fimmu.2025.1548176 · 2025-02-14

## TL;DR

A patient with two primary cancers in the lung and esophagus survived over 3 years with a combination of chemotherapy, immunotherapy, and radiation therapy.

## Contribution

This case report demonstrates the effectiveness of a multi-modality treatment approach for synchronous double primary malignancies.

## Key findings

- The patient achieved complete response in esophageal lesions and partial response in lung lesions after treatment.
- Combining systemic therapy with localized radiotherapy showed acceptable safety and toxicity in thoracic double primary tumors.

## Abstract

The occurrence of multiple primary cancers has become common, and the treatment of such patients is very complex, so it is necessary to combine a variety of individualized treatment methods to achieve better treatment results.

This report describes a patient with double primary tumors of lung and esophageal cancer had more than 36 months survival with non-operation treatment. The patient diagnosed as lung adenocarcinomas (LADC) and esophageal squamous cell carcinoma (ESCC), was treated with albumin-bound paclitaxel, nedaplatin, and anti-programmed death 1 (anti-PD-1). The esophageal lesions achieved complete response (CR) after finishing two courses of induction chemotherapy combined with anti-PD-1 followed by definitive chemoradiotherapy (CRT). Radiation pneumonitis (RP) occurred one month after the completion of CRT. The pneumonia was relieved after dexamethasone and moxifloxacin treatment. Then, the lung lesion was treated with oral chemotherapy followed by stereotactic body radiation therapy (SBRT). As of July 2024, the patient has survived for more than 3 years after the above treatments, and the current efficacy evaluation is CR of esophageal lesions, PR of pulmonary lesions.

The multi-modality approach of systemic therapy combined with localized radiotherapy is an effective treatment in the patients of the double primary malignant tumors of LADC and ESCC. The safety and toxicity of radiotherapy for the thoracic double primary tumors demonstrate acceptability.

## Linked entities

- **Chemicals:** nedaplatin (PubChem CID 9796440), dexamethasone (PubChem CID 5743), moxifloxacin (PubChem CID 152946)
- **Diseases:** esophageal squamous cell carcinoma (MONDO:0005580), radiation pneumonitis (MONDO:0043919), pneumonia (MONDO:0005249)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}
- **Diseases:** primary tumors (MESH:D001932), lung lesion (MESH:D008171), RP (MESH:D017564), LADC (MESH:D000077192), toxicity (MESH:D064420), cancers (MESH:D009369), esophageal lesions (MESH:D004935), ESCC (MESH:D000077277), pneumonia (MESH:D011014), lung and esophageal cancer (MESH:D008175)
- **Chemicals:** moxifloxacin (MESH:D000077266), paclitaxel (MESH:D017239), nedaplatin (MESH:C053989), dexamethasone (MESH:D003907)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11867956/full.md

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Source: https://tomesphere.com/paper/PMC11867956