multiple primary malignancies

多发性原发性恶性肿瘤
  • 文章类型: Case Reports
    背景:多原发恶性肿瘤(MPMNs)的患病率与恶性肿瘤的发病率同时增加,诊断模型的持续改进,延长肿瘤患者的寿命,尤其是那些消化系统。然而,MPMNs与十二指肠腺癌(DA)并存的报道很少.此外,缺乏关于多组学和肿瘤微环境(TME)的MPMNs的综合分析。
    方法:在本文中,我们报告一例56岁的男性,主诉胸部不适和腹胀。患者在肿瘤科诊断为异时食管鳞状细胞癌和DA。他接受了食管肿瘤的根治性切除和化疗,以及化疗联合程序性死亡-1抑制剂治疗十二指肠肿瘤。总生存期为16.6mo。对原发性和转移性肿瘤的多组学和微环境特征进行了广泛评估,以:(1)确定在这种情况下导致不良预后和治疗耐药性的原因;(2)为MPMNs提供新的诊断和治疗方法。这种情况表明,第二种恶性肿瘤的发展可能与第一种肿瘤的位置无关。因此,为了准确诊断MPMNs,应将肿瘤复发(包括转移)与第二原发灶区分开来.
    结论:多组学特征和TME可能有助于治疗选择,提高疗效,并辅助预测预后。
    BACKGROUND: The prevalence of multiple primary malignant neoplasms (MPMNs) is increasing in parallel with the incidence of malignancies, the continual improvement of diagnostic models, and the extended life of patients with tumors, especially those of the digestive system. However, the co-existence of MPMNs and duodenal adenocarcinoma (DA) is rarely reported. In addition, there is a lack of comprehensive analysis of MPMNs regarding multi-omics and the tumor microenvironment (TME).
    METHODS: In this article, we report the case of a 56-year-old man who presented with a complaint of chest discomfort and abdominal distension. The patient was diagnosed with metachronous esophageal squamous cell carcinoma and DA in the Department of Oncology. He underwent radical resection and chemotherapy for the esophageal tumor, as well as chemotherapy combined with a programmed death-1 inhibitor for the duodenal tumor. The overall survival was 16.6 mo. Extensive evaluation of the multi-omics and microenvironment features of primary and metastatic tumors was conducted to: (1) Identify the reasons responsible for the poor prognosis and treatment resistance in this case; and (2) Offer novel diagnostic and therapeutic approaches for MPMNs. This case demonstrated that the development of a second malignancy may be independent of the location of the first tumor. Thus, tumor recurrence (including metastases) should be distinguished from the second primary for an accurate diagnosis of MPMNs.
    CONCLUSIONS: Multi-omics characteristics and the TME may facilitate treatment selection, improve efficacy, and assist in the prediction of prognosis.
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  • 文章类型: Case Reports
    乳腺癌和非霍奇金淋巴瘤的同时发生是一种罕见的疾病,具有诊断和治疗挑战。先前尚未描述滤泡性淋巴瘤(FL)和三阴性乳腺癌(TNBC)的共存。
    一个46岁的女人,已经遭受了未经治疗的历史,高级阶段,高肿瘤负荷FL,因快速进展的右乳房肿块入院。超声检查显示右乳有8.3×3.6×4.1cm的基底肿块,双侧腋窝淋巴结肿大(LNs)。PET-CT显示右乳腺肿块18F-FDG活性增加,隔膜两侧的LN,脾脏肿大,还有骨髓.右侧乳腺肿块活检显示TNBC。患者接受了R-CHOP的新辅助治疗,并获得了乳腺肿瘤的部分缓解。然而,TNBC在R-CHOP三个周期后进展。根据对乳腺肿块的下一代测序(NGS)分析,同源重组修复(HRR)缺陷(HRD)评分为72,新辅助方案改为利妥昔单抗加nab-紫杉醇和顺铂(R-TP),并导致明显的肿瘤消退。然后,患者接受了右乳房切除术,并进行了腋窝LN解剖。手术后,对患者进行定期监测,并给予R-TP和放疗辅助治疗.
    FL和HRD阳性TNBC的共存带来了诊断和治疗的挑战。基于多学科团队(MDT)讨论和NGS的有充分依据的新辅助策略在这种情况下保证了良好的结果。
    UNASSIGNED: Co-occurrence of breast cancer and non-Hodgkin\'s lymphoma is a rare condition with diagnostic and therapeutic challenges. The coexistence of follicular lymphoma (FL) and triple-negative breast cancer (TNBC) has not been described previously.
    UNASSIGNED: A 46-year-old woman, already suffering a history of untreated, advanced-stage, high tumor burden FL, was admitted for a rapidly progressing right breast mass. Ultrasonography showed an 8.3 × 3.6 × 4.1 cm fungating mass in the right breast with enlarged lymph nodes (LNs) in bilateral axillae. PET-CT demonstrated increased 18F- FDG activity in right breast mass, LNs on both sides of the diaphragm, enlarged spleen, and bone marrow. Biopsy of the right breast mass revealed TNBC. The patient underwent neoadjuvant therapy with R-CHOP and achieved partial response of breast tumor. However, TNBC progressed after three cycles of R-CHOP. According to the next-generation sequencing (NGS) assay on breast mass showing a homologous recombination repair (HRR) deficiency (HRD) score of 72, the neoadjuvant regimen was changed to rituximab plus nab-paclitaxel and cisplatin (R-TP) and resulted in significant tumor regression. The patient then underwent right mastectomy with an axillary LN dissection. After the surgery, she was regularly monitored and given adjuvant therapy with R-TP and radiotherapy.
    UNASSIGNED: The coexistence of FL and HRD-positive TNBC poses diagnostic and treatment challenges. Well-founded neoadjuvant strategy based on multidisciplinary team (MDT) discussion and NGS warranted a good outcome in this case.
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  • 多发性原发性恶性肿瘤合并SWI/SNF复合物缺陷型胃癌是一种罕见的临床实体,文献报道很少。在此,我们报告了在我院接受治疗的一名81岁男性患者中的一例这种疾病。在确定异时多原发恶性肿瘤的诊断之前,患者接受左下叶切除术治疗左肺占位性肿块,经术后病理证实为早期肺癌。随后通过胃镜检查发现SWI/SNF复合物缺乏伴转移的胃癌,高通量测序鉴定了肿瘤组织中的ARID1A和TMB-H基因突变。患者接受了化疗联合免疫疗法,但对治疗无效,13个月后去世.我们进行了文献回顾并分析了发生的情况,病理和免疫组织化学特征,诊断,本病的治疗和预后。
    Multiple primary malignancies combined with SWI/SNF complex-deficient gastric cancer is a rare clinical entity and poorly documented. Herein we report a case of this disease in an 81-year-old male patient treated in our hospital. Before the established diagnosis of metachronous multiple primary malignancies, the patient received left lower lobectomy for a spaceoccupying mass in the left lung, which was confirmed by postoperative pathology as early stage lung cancer. SWI/SNF complex-deficiency gastric cancer with metastasis was subsequently detected by gastroscopy, and high-throughput sequencing identified ARID1A and TMB-H gene mutations in the tumor tissues. The patient received chemotherapy combined with immunotherapy but failed to respond to the treatment, and died 13 months later. We conducted a literature review and analyzed the occurrence, pathological and immunohistochemical characteristics, diagnosis, treatment and prognosis of this disease.
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  • 文章类型: Case Reports
    随着癌症诊断工具和治疗方式的重大进展,在过去的几十年中,多原发恶性肿瘤(MPM)的发病率有所增加。治疗选择随着免疫检查点抑制剂(ICIs)的出现而改变,提高了广谱肿瘤的存活率。然而,关于疗效的信息很少,阻力,以及ICI的潜在机制。
    一名67岁女性被诊断为肺肉瘤样癌(PSC),有肝细胞癌(HCC)和病毒性乙型肝炎病史。她接受了Camrelizumab的治疗,抗程序性细胞死亡蛋白1单克隆抗体,结合化疗,PSC和HCC均获得部分缓解。经过9个月的疗程,PSC病变仍然缩小,虽然HCC被评估为一种进行性疾病,肝脏肿瘤的直径增加,甲胎蛋白升高,和腹部淋巴结肿大。然后,加上腹部转移的放射治疗,肺部病变持续缩小。同时,肝肿瘤和腹部淋巴结未见明显肿大。
    Camrelizumab联合治疗可持续受益于PSC和HCC的MPM患者,对于MPM患者来说,这可能是一个有希望的选择。
    UNASSIGNED: With significant advances in the diagnostic tools and treatment modalities of cancer, the incidence of multiple primary malignancies (MPMs) has increased in the last decades. The therapeutic option changed with the arising of immune checkpoint inhibitors (ICIs), which have improved the survival of a broad spectrum of tumors. However, little information is available when it comes to the efficacy, resistance, and underlying mechanisms of ICIs.
    UNASSIGNED: A 67-year-old woman was diagnosed with pulmonary sarcomatoid carcinoma (PSC) with a history of hepatocellular carcinoma (HCC) and viral hepatitis B. Following the lack of response to systemic chemotherapy, she was treated with camrelizumab, an anti-programmed cell death protein 1 monoclonal antibody, in combination with chemotherapy, and a partial response was obtained both in PSC and HCC. After a course of 9-month treatment, the PSC lesion shrank still, while HCC was evaluated as a progressive disease with an increase in the diameter of liver neoplasm, elevated alpha-fetoprotein, and enlarged abdominal lymph nodes. Then, with the addition of radiotherapy for abdominal metastasis, the lung lesion was continuously shrinking. In the meantime, the liver neoplasm and abdominal lymph nodes showed no significant enlargement.
    UNASSIGNED: Camrelizumab combination therapy could consistently benefit the MPM patients with PSC and HCC, which may be a promising option for patients with MPMs.
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  • 文章类型: Case Reports
    同一患者的多发性原发性恶性肿瘤(MPM)很少见。在过去的十年里,MPM的发病率正在增加。一般人群的患病率为0.7-11.7%,在老年人中发病率较高。发病率的增加可以归因于寿命的延长,环境因素,早期慢性病/癌症筛查,和先进的治疗导致更多的化生。由于放化疗的致癌作用,癌症患者的机会更高。这里,我们介绍了一名79岁的女性,有27年的吸烟史,没有任何明显的遗传倾向,他们在2017年发展了四种不同的原发性恶性肿瘤,包括(1)慢性淋巴细胞白血病(I期改良Rai),CD23和CD5阳性,不需要治疗;(2)2019年切除后左颊原位黑色素瘤;(3)分子研究阴性的肺腺癌(表皮生长因子受体(EGFR)/ROS原癌基因,受体酪氨酸激酶(ROS)/v-Raf鼠肉瘤病毒癌基因同源物B1(BRAF)/间变性淋巴瘤激酶(ALK))和阴性程序性细胞死亡配体1(PDL-1)在2020年接受了卡铂治疗,培美曲塞,和pembrolizumab;(4)监测CT扫描的左下极肾肿块,高度怀疑原发性恶性肿瘤而不是转移,为此,她接受了根治性肾切除术和透明细胞肾癌活检阳性。关于这些多原发癌,考虑了种系突变的想法。但是由于她没有恶性肿瘤的家族史,根据遗传咨询师,不需要进行基因检测。随着肿瘤检测和治疗的进步,患者被诊断为MPM。随着治疗的进步,癌症存活率正在改善。鉴于没有大型研究,我们认为,MPM的治疗方式应以个案为基础,需要采用多学科方法来应对治疗挑战并提供根治性治疗.
    Multiple primary malignancies (MPMs) in the same patient are rare. Over the past decade, the incidence of MPMs is increasing. The prevalence in the general population is 0.7-11.7%, with a higher incidence in the elderly. This increase in incidence can be attributed to advanced lifespan, environmental factors, early chronic disease/cancer screening, and advanced treatment leading to more metaplasia. The chances are higher in cancer patients due to the carcinogenic effect of chemoradiotherapy. Here, we present a 79-year-old female with a 27 pack-year smoking history without any significant genetic predisposition, who developed four different primary malignancies including (1) chronic lymphocytic leukemia in 2017 (stage I modified Rai), positive for CD23 and CD5, which did not require treatment; (2) melanoma in situ on the left cheek in 2019 status post excision; (3) lung adenocarcinoma with negative molecular study (epidermal growth factor receptor (EGFR)/ROS proto-oncogene, receptor tyrosine kinase (ROS)/v-Raf murine sarcoma viral oncogene homolog B1 (BRAF)/anaplastic lymphoma kinase (ALK)) and negative programmed cell death ligand 1 (PDL-1) in 2020 for which she received treatment with carboplatin, pemetrexed, and pembrolizumab; and (4) left lower pole renal mass on surveillance CT scan, which was highly suspicious for primary malignancy as opposed to metastasis, for which she underwent radical nephrectomy and biopsy positive for clear cell renal cancer. Regarding these multiple primary cancers, the thought of germline mutation was considered. But as she did not have a family history of malignancy, genetic testing was not needed as per the genetic counselor. Patients are being diagnosed with MPMs as there is more advancement in tumor detection and treatment. With the advancement in the treatment, cancer survivorship is improving. Given that there are no large studies, we believe that treatment modality for MPMs should be on a case-to-case basis and needs a multidisciplinary approach to tackle therapeutic challenges and provide radical treatment.
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  • 文章类型: Journal Article
    UNASSIGNED: Multiple primary malignancy (MPM) is defined as occurrence of two or more synchronous or metachronous primary malignancies. With the rise in cancer burden and meticulous screening of index primary malignancy (IPM) during treatment, increased incidence of second primary malignancy (SPM) is expected. This study was undertaken with an attempt to analyze the incidence, commonest associations, management strategies, and clinical outcomes of MPM.
    UNASSIGNED: This is an observational retrospective study carried out in a single institute with patients registered between 1st January 2015 and 31st August 2019. The International Association of Cancer Registries and International Agency for Research on Cancer (IACR/IARC) definition was used for identification of IPM and SPM. Synchronous SPM was defined as malignancy occurring within 6 months from the diagnosis of IPM.
    UNASSIGNED: Out of 16,461 registered patients during the study interval, 44 (0.26%) cases were found to have MPM. A total of 31 (70.5%) cases were women and 13 (29.5%) cases were men. Median age at presentation of IPM was 48 years and of SPM was 56 years, with median duration between two primaries being 38 months. Seven patients (15.9%) had synchronous malignancies. Gynecological tumors were the most common site of IPM presentation (n = 14, 31.8%) followed by breast (n = 09, 20.5%) and head and neck tumors (n = 07, 15.9%), respectively. The most common SPM was gynecological tumors (n = 12, 27.3%) followed by gastrointestinal malignancies (n = 10, 23.3%). Curative treatment was offered to 88% of patients with IPM and 70% patients with SPM. At a median follow-up of 365 days, 21 (47.72%) patients were disease free, six (13.6%) died of disease and nine (20.5%) were lost to follow-up.
    UNASSIGNED: The study emphasizes the importance of detecting SPM as a result of improved diagnostic and screening procedures. Clinicians should be aware of it and offer multidisciplinary management.
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  • 文章类型: Journal Article
    Multiple primary malignancies (MPM) are rare. In particular, synchronous gallbladder and gastric malignancies are extremely rare, are associated with a concealed onset and atypical symptoms, and are highly likely to be overlooked or misdiagnosed. The clinical data of two patients with synchronous gallbladder and gastric malignancies are herein reported and integrated with the relevant literature to retrospectively analyze and summarize the pathogenesis and clinical characteristics of MPM. Case 1 was a male 46-year-old patient who underwent laparoscopic cholecystectomy, and succumbed to extensive tumor metastasis 2 months after the operation. Case 2 was an 80-year-old female patient who was treated with distal gastrectomy for gastric cancer, cholecystectomy, gastrojejunostomy and dissection of 5 suprapyloric, 6 subpyloric, 7 left gastric and 8 common hepatic artery lymph nodes, and succumbed to multiple organ failure induced by extensive tumor invasion within 1 week after the operation. Clinical physicians must pay closer attention to early symptoms of MPM in order to make an accurate diagnosis, perform timely radical surgical treatment and achieve favorable therapeutic outcomes, in terms of significantly increasing long-term patient survival rates.
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    文章类型: Case Reports
    A pathological complete response in a patient affected by multiple synchronous, breast and lung primary malignancies is reported. A 63-year-old woman presented with an invasive ductal carcinoma of the breast and a lung adenocarcinoma. After multidisciplinary discussion, the patient underwent pulmonary left lower lobectomy followed by radio-chemotherapy with cisplatin and vinorelbine and started hormone therapy with letrozole. Ten months later, a left mastectomy with axillary lymph nodes dissection was performed. Histologically, a pathological complete response (pCR) was documented. With a review of the Literature, we discuss the issue of multiple primary malignancies, with its diagnostic and therapeutic implications. In cases of multiple synchronous malignancies it has been highlighted the importance of the choice of the best therapeutic approach for both the malignancies, reducing collateral individual effects.
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