# Case report: Sintilimab combined with anlotinib as neoadjuvant chemotherapy for metastatic bone tumor resection in patients with PSC

**Authors:** Zheming Bao, Xiuchun Yu, Kai Zheng, Kai Zhai, Haocheng Cui, Ming Xu

PMC · DOI: 10.3389/fimmu.2024.1372279 · 2024-05-02

## TL;DR

A 69-year-old man with metastatic lung cancer responded well to a combination of immunotherapy and antiangiogenic drugs before surgery, leading to successful tumor removal and limb preservation.

## Contribution

This is the first reported case of successful limb salvage in metastatic PSC using anlotinib and sintilimab as neoadjuvant therapy.

## Key findings

- The patient achieved complete response in the femur tumor and partial response in lung lesions after treatment.
- Combination therapy allowed for successful surgical resection and over 16 months of disease control.
- No significant adverse reactions were observed during the treatment period.

## Abstract

Pulmonary sarcomatoid carcinoma (PSC) is a rare subtype of non-small-cell lung cancer (NSCLC), which is resistant to chemotherapy and radiotherapy with a poor prognosis. PSC is highly malignant and is prone to recurrence even after surgery. The programmed death-ligand 1 (PD-L1) tumor cell proportion score (TPS) 5%, TERT and TP53 gene mutations were detected in this patient accompanied by multiple metastatic sites. The anlotinib is a novel multitarget tyrosine kinase inhibitor (TKI) that could be effective for advanced NSCLC and some sarcoma patients. Limited clinical trials and case reports have shown that PSC patients with gene mutations and PD-L1 expression have good responses to multitarget antiangiogenic drug and immune checkpoint inhibitors (ICIs). In this article, we reported a case with metastatic PSC diagnosed by Computed Tomography (CT)-guided needle biopsy treated with immunotherapy combined with antiangiogenic drugs as a neoadjuvant chemotherapy (NACT). PSC is controlled and the patient achieves successfully limb salvage treatment by surgical resection. Therefore, targeted therapy and immunotherapy can provide sufficient surgical opportunities for limb salvage in the treatment of metastatic PSC patients.

A 69-year-old male diagnosed with malignant bone tumor in the proximal femur was admitted to our hospital in June 2022 with recurrent fever as well as swelling and pain in the left thigh for twenty days. The initial computed tomography (CT) scan of the chest showed a pulmonary cavity (20 mm × 30 mm) and scattered lung masses. Subsequently, he underwent a CT-guided needle biopsy to distinguish the essence of osteolytic bone destruction and soft tissue mass in the left proximal femur which showed metastatic sarcomatoid carcinoma histology. Genetic testing revealed TERT c.-124C mutation (abundance 8.81%), TP53 p.R342 mutation (abundance 11.35%), tumor mutational burden (TMB) 7.09 muts/Mb, microsatellite stability (MSS), and PD-L1 (SP263) TPS 5% were also detected. The patient was tentatively treated with a combination of antiangiogenic drug and PD-1 inhibitor. After one course, the tumor volume significantly reduced in magnetic resonance imaging (MRI) and pathological fracture occurred in the femur after combined treatment. The patient received proximal femoral tumor resection and prosthesis replacement after defervescence. Sequentially sintilimab with anlotinib were administered for over 1 year. Finally, the local tumor was well controlled, and no obvious drug-related adverse reactions were observed. The lesions in the lung remained in partial response (PR) for more than 16 months and complete response (CR) of metastatic tumor in the proximal femur was observed through imaging examinations.

This is the first reported case of a metastatic PSC in femur showing a favorable response to the treatment consisting of anlotinib combined with sintilimab. This case suggests that antiangiogenic therapy combined with immunotherapy may benefit patients with metastatic PSC in the preoperative adjuvant therapy for limb salvage.

## Linked entities

- **Genes:** TERT (telomerase reverse transcriptase) [NCBI Gene 7015], TP53 (tumor protein p53) [NCBI Gene 7157]
- **Chemicals:** anlotinib (PubChem CID 25017411)
- **Diseases:** non-small-cell lung cancer (MONDO:0005233)

## Full-text entities

- **Genes:** TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, TERT (telomerase reverse transcriptase) [NCBI Gene 7015] {aka CMM9, DKCA2, DKCB4, EST2, PFBMFT1, TCS1}
- **Diseases:** tumor (MESH:D009369), NSCLC (MESH:D002289), swelling (MESH:D004487), sarcoma (MESH:D012509), PSC (MESH:D002292), pain (MESH:D010146), osteolytic bone destruction (MESH:D001847), fever (MESH:D005334), lung (MESH:D008171), femoral tumor (MESH:D005266), bone tumor (MESH:D001859), pathological fracture (MESH:D005598)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** SP263 — Homo sapiens (Human), Melanoma, Cancer cell line (CVCL_B6L0)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11096473/full.md

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Source: https://tomesphere.com/paper/PMC11096473