A Population-based Assessment of Curative Intended Multimodal Treatment in Patients With Oligometastatic Pancreatic Cancer, Responsive to Neoadjuvant Chemotherapy - ScanPan 1 - A Scandinavian Prospective Multicenter Study
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 64
- 试验地点
- 2
- 主要终点
- Feasibility of treatment
研究概览
简要总结
Dissemination from pancreatic ductal adenocarcinoma (PDAC) occurs in clinical practice either in the form of recurrence after initial treatment with curative intent resection (metachronous) or more frequently prevails already at the time of diagnosis (synchronous). Traditionally, metastatic pancreatic cancer (mPDAC) is considered not to be eligible for meaningful aggressive therapies to be implemented. However, with the development of local as well as more effective systemic therapeutic regimens a variety of clinical situations have to be reevaluated. For instance, recent reports have indicated an option for maintained or even prolonged survival after resections and/or ablations of oligometastatic pancreatic cancer (OMDPDAC), as represented by a single or few liver metastasis (es). These reports are burdened by methodological weaknesses such as being retrospective, single institution and reporting only from highly selected case series.
A common denominator of acceptable outcome is, however, that all metastatic lesions have been preoperatively treated and responded to chemotherapy, indicating an advantageous tumor biology.
Hence an unbiased approach, including neo-adjuvant chemotherapy before any aggressive local treatment must be explored to the updated management opportunities in terms of assessing the prevalence, safety, feasibility, tolerability and possible disease control options.
Primary objective (clinical): To prospectively investigate (on an intention to treat basis) the safety, feasibility, tolerability and clinical outcomes of all patients with PDAC presenting with limited metastatic disease, where a treatment option can be launched with the ambition of local disease control and eventually better survival.
The cohorts to be included are:
Primary cohort: Patients with liver limited (metachronous and synchronous) metastasis(es) due to PDAC. This cohort is further subdivided to:
Limited liver disease. Extended liver disease. Secondary cohort: Patients with OMDPDAC and at least one extrahepatic manifestation of PDAC.
Secondary objective (translational) is to improve the understanding of PDAC liver metastases biology by studying the mechanistic aspects of metastases invasion as well as intra- and peri-tumoral liver metastatic niche, and by charting the cellular composition of liver metastases on single cell level with a focus on the impact of cellular interactions on tumor cell growth and differentiation. Furthermore, the study aims to identify blood-based biomarkers of response to oncologic/surgical treatment.
详细描述
Dissemination from pancreatic ductal adenocarcinoma (PDAC) occurs in clinical practice either in the form of recurrence after initial treatment with curative intent or more frequently is manifested already at the time of diagnosis. Traditionally corresponding disease states are considered not to be eligible for meaningful aggressive therapies to be implemented. Instead, palliative therapies are instituted with a very limited survival. However, with the development of local as well as more effective systemic therapeutic regimens, a variety of clinical situations must be reevaluated.
In PDAC, disseminated to the liver, the traditional view as that the corresponding lesions are non-treatable by aggressive chemotherapy followed by surgical interventions and generally, surgery has been considered obsolete in this patient cohort5. Despite these early discouraging results there are some reports, from selected cohorts, indicating more promising survival rates after resection of metastasis(es) than ever earlier described6. Moreover, during recent years there has been significant improvement in the efficacy of chemotherapy regimens available for patients with localized as well as disseminated PDAC that may enhance the effect of surgical removal of macroscopic tumor manifestations.
The same may be true for alternative limited manifestations of metastatic PDAC disease. Hence an unbiased approach must be explored to the updated management opportunities in terms of assessing the incidence, safety, feasibility, tolerability and possible disease control options.
According to the Swedish and Danish pancreatic cancer registry the overall median survival (OS) of patients with pancreatic cancer is about 6-7 months while studies demonstrate 9-15 months median survival when palliative chemotherapy is used7, 8.
Hitherto, no prospective, population-based study, with intention to treat design, has been presented to define the role of aggressive oncological regimens with successive macroscopic eradication of tumor lesions as exemplified by surgery in disseminated PDAC. The evidence at hand comes from retrospectively collected and selected cohorts where comparison is often made to surgical palliation alone (intestinal bypass surgery) or best supportive care. The reported median survival after surgery varies widely from 7.6 months to as long as 56 months9. A recent case matched study suggested that in selected cases, surgery may improve median survival from about 1 to 2 years10. Corresponding data just reflect the large impact of selection on either the intervention and/or the control group. The main drawback of the available literature is the general lack of population based, intention to treat data and lack of clear definition of disease stages that severely limit the usefulness of these results in clinical decision making.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Confirmed PDAC with synchronous or metachronous dissemination isolated in the liver (primary cohort) or other dissemination as described in chapter 7.
- •where the local tumour board find indication for curative treatment attempt.
- •The confirmation of PDAC before chemotherapy is not regulated by the protocol but EUS guided biopsies directed to the primary tumour or a site of recurrence/dissemination is recommended whereas a percutaneous approach towards liver lesion(s) can be an alternative diagnostic approach; radiology and elevated serum tumor markers may guide diagnosis in exceptional cases, for which, e.g., pathological sampling fails.
- •Metastases are defined as synchronous when liver tumors are detected simultaneously with the primary tumor or within the first 6 months thereafter. All other tumors are regarded as metachronous metastases or locally recurrent disease (when applicable).
- •The same definition applies to localized lesions detected intra- as well as extra-abdominally.
- •Patients treated due to the radiological appearance and or elevated CA-19.9 levels despite negative biopsies are accepted for inclusion into the study
- •To be included in "Limited liver desease":
- •Up to 4 liver metastases treatable with liver resections (without volume expansion of the future liver remnant)/thermal ablations/RFA/IRE (largest diameter < 5 cm and for ablative techniques < 2 cm).
- •Age 18 years or older ECOG 0-1 Any resectable (including borderline resectable, but without need for arterial reconstruction) (before or after neoadjuvant treatment) PDAC Patient can understand verbal and written information
排除标准
- •Age less than 18 years ECOG >2 Patient is not able to understand the verbal and written information Progression of tumor (RECIST 1.1) during or after chemotherapy Distant metastases outside the liver (applies only to the primary cohort) Other malignancy within 2 years, the prognosis of which may affect the evaluation of the therapeutic outcome.
- •Major non-pancreatic surgery within 4 weeks prior to study treatment start, or lack of complete recovery from the effects of major surgery Uncontrolled (bacterial or fungal) infections Significant concomitant diseases preventing the safe administration of study drugs or likely to interfere with study assessments Uncontrolled angina pectoris; cardiac failure or clinically significant arrhythmias Continuous use of immunosuppressive agents (Corticoids are allowed) Neuropathy >grade 1 (CTCAE, v 5.0) Pregnancy or breast feeding Patients (M/F) with reproductive potential not implementing adequate contraceptive measures Pre-defined need for arterial reconstruction to resect primary tumor
结局指标
主要结局
Feasibility of treatment
时间窗: 3 years
Measured as the proportion of patients starting neoadjuvant chemotherapy that finally get invasive treatment for their liver metastases
Safety of surgery
时间窗: Up to 90 days after surgery
Safety of liver metastases treatment with surgery or ablation as measured by the proportion of patients experiencing severe complications (defined by the Clavien-Dindo classification)
次要结局
- Histological tumor response(3 years)
- Progression free survival(5 years)
- Chemotherapy associated morbidity(3 years)
- Surgical morbidity according to the Clavien-Dindo classification(90 days after surgery)
- Quality of life after surgery(5 years)
- R0 resection rate of liver metastasis(3 yeras)
- Overall survival(5 years)
- Surgical morbidity according to the CCI (comprehensive complication index)(90 days post operatively)
- Pos operative pancreatic fistula (POPF)(90 days post operatively)
- Post pancreatectomy hemorrhage (PPH)(90 days post operatively)
- Delayed gastric emptying (DGE)(90 days post operatively)
- Disease free survival(5 years)
研究者
Bergthor Björnsson
Associate Professor
Linkoeping University