First-Line Anlotinib Combined with Stereotactic Body Radiation Therapy for an Octogenarian with Pulmonary Carcinosarcoma.

Pulmonary carcinosarcoma (PC) is a rare and highly malignant type of non-small cell lung cancer (NSCLC) that is insensitive to radiotherapy and chemotherapy and has a poor prognosis. Here, we report a case of an 88-year-old patient with inoperable PC and a history of cerebral infarction who was treated with first-line anlotinib combined with stereotactic body radiation therapy (SBRT). The therapeutic response has sustained for 10 months. Our work suggests that SBRT combined with anlotinib may be a safe and effective treatment strategy for octogenarians with PC.

Introduction

The World Health Organization classifies pulmonary carcinosarcoma (PC) as a subtype of sarcomatoid carcinoma with poor cell differentiation. It partially contains or completely lacks conventional components of non-small cell lung cancer (NSCLC),1 PC is very rare and highly invasive in clinical practice, also has a poor prognosis. Identification of effective and safe treatments for patients with advanced PC is an urgent clinical problem. We report an octogenarian patient with inoperable PC and a history of cerebral infarction who achieved a partial response (PR) after receiving local stereotactic body radiation therapy (SBRT) combined with first-line anlotinib.

Case Report

An 88-year-old male patient with a 60 pack-year history of smoking suffered cerebral infarction in August 2020. Computed tomography (CT) scans showed an 11.0 cm × 5.6 cm left upper lobe lesion, and necrosis was visible in the pleura (Figure 1). Histological examination showed squamous cell carcinoma and osteosarcoma, suggesting carcinosarcoma. Immunohistochemistry (IHC) showed heteroepithelial nests that were positive for P40, PCK, CK5/6, SATB2, SMA (partial), and negative for TTF-1, CK7, Dcsmin, CD34, STAT6, ALK-V, and ROS-1. Our gene detection method showed that EGFR, ALK, ERBB2, BRAF, MET, ROS1, RET, and KRAS were all wild-type and unamplified. So the diagnosis was left upper lobe pulmonary carcinosarcoma (cT4N0M0 stage II AJCC 8th).

Figure 1

Chest CT scans demonstrating a left upper lung lobe lesion, (A and B) at diagnosis, (C and D) following 3 months of anlotinib treatment, and (E and F) following 9 months of anlotinib treatment.

The patient was deemed inoperable after being reviewed by the Institutional MDT group. In October 2020, he was treated with 10 mg anlotinib per day orally, combined with SBRT at the same time. The maximum intensity projection of gross lesion was defined as gross tumor volume (GTV). The planning target volume (PTV) was determined based on the GTV2 with a margin of 5 mm, GTV1 has no PTV.Treatment was delivered using volumetric modulated arc therapy (VMAT). Simultaneously integrated boost radiotherapy(SIB) was used on the target area (Figure 2), which approach to the hypoxic center of a tumor may have benefits for treating resistant clones while also allowing for lower radiation doses that are safe for normal tissues.2 GTV1= 65.5 Gy/10F [biologic equivalent dose (BED) =109.4 Gy]. GTV2=50 Gy/10F (BED=75 Gy). The SBRT plan was optimized to achieve a D95 PTV (dose received by 95% volume) of 100%. The mean bilateral lung dose was 8.3 Gy. The portion of lung receiving a dose of 5 Gy (V5) was 46.8%, 10 Gy (V10) was 35.3%, and 20 Gy (V20) was 11.8%. The maximum dose to the spinal cord was 6.9 Gy. The patient tolerated the therapy well without grade 2–5 toxicities throughout the treatment period. The lesion was decreased on chest CT scans 3 and 9 months later, and the response evaluation was PR (Figure 1). Anlotinib treatment was ongoing, and during this period the patient presented with Common Terminology Criteria for Adverse Events grade 2 elevated blood pressure, constipation, and other discomfort. Imaging showed PR with no grade ≥3 adverse effects.

Figure 2

Treatment planning: image of GTV for the SIB technique; the internal area is GTV1 with dose at the level of 65.5 Gy (red), and the peripheral area is GTV2 shown at the level of 50 Gy (pink).

Discussion

Pulmonary carcinosarcoma is composed of both NSCLC (especially squamous cell carcinoma or adenocarcinoma) and heterogeneous sarcoma components (such as rhabdomyosarcoma and chondrosarcoma). It accounts for less than 1% of malignant thoracic tumors.3 In one study using the SEER database, 411 patients with PC were analyzed from 1973 to 2012. The median age was 67 years, and the overall survival (OS) for patients with localized disease compared to patients with non-localized disease was 31 months vs 6 months, respectively,4 suggesting that the prognosis of patients with advanced carcinosarcoma is extremely poor. For patients with advanced or inoperable pulmonary carcinosarcomas, the standard treatment strategy has not yet been well defined,3 especially for elderly patients.

Due to the rarity of PC, there have been no large-scale randomized clinical trials for genetic testing and targeted therapy. However, several individual reports using anti-tumor angiogenesis treatment have shown some efficacy. Tanimoto et al reported a metastatic case treated with pazopanib with 6 months of progression-free survival (PFS).5 Furthermore, another case report used apatinib combined with endostatin in PC, and the PFS was up to 6 months.6 At present, anti-tumor angiogenesis therapy for lung sarcoma is mainly used as a second-line treatment or beyond. It shows clinical benefits, but PFS is limited. In this case, the patient was treated with first-line anlotinib in combination with SBRT, and the PFS was longer than that reported for anti-tumor angiogenesis therapy. Anlotinib is a small-molecule, multi-target tyrosine kinase inhibitor for tumor angiogenesis and growth. The ALTER0303 study reported that third-line anlotinib for advanced refractory NSCLC resulted in significantly longer OS (9.6 months vs 6.3 months) and PFS (5.4 months vs 1.4 months) compared with the placebo.7

The patient reported here could not be treated surgically due to age and a history of cerebral infarction. Over the past decade, SBRT has become an effective treatment for inoperable lung cancer. It has been demonstrated to provide survival benefits superior to conventional fractionated radiotherapy, especially for elderly oligometastatic patients.8–10 There are some reports demonstrates that SBRT might be safe and effective for soft tissue sarcoma.11–13 Huang et al reported a case of an octogenarian with PC treated with SBRT, at a dose of 60 Gy in eight fractions (7.5 Gy per fraction). The treatment was evaluated as PR and lasted for 2 years.14 Therefore, SBRT is an effective local treatment for medically inoperable PC patients.

The most common adverse effects of anlotinib include hypertension, hand-foot syndrome (HFSR), fatigue, diarrhea, and anorexia.15 In this case, there were no adverse events that required discontinuation or dose reduction, indicating that anlotinib is safe for elderly patients.

In summary, carcinosarcoma (including squamous cell carcinoma and osteosarcoma components) is a rare subtype of NSCLC, and there are difficulties and limitations in diagnosis and treatment. In the current case, despite advanced age and cerebral infarction, the use of SBRT combined with oral anlotinib was effective and safe. PFS has sustained for 10 months, and the treatment did not cause serious adverse reactions. Large-scale clinical studies are required to confirm our findings.