Editorial
Copyright copy;2010 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Gastroenterol. Oct 21, 2010; 16(39): 4883-4887
Published online Oct 21, 2010. doi: 10.3748/wjg.v16.i39.4883
Neoadjuvant treatment for resectable pancreatic cancer: Time for phase III testing?
Michele Reni
Michele Reni, Medical Oncology Unit, Department of Oncology, San Raffaele Scientific Institute, 20132-Milan, Italy
Author contributions: Reni M is the sole contributor to this paper.
Correspondence to: Michele Reni, MD, Medical Oncology Unit, Department of Oncology, San Raffaele Scientific Institute, Via Olgettina 60, 20132-Milan, Italy. reni.michele@hsr.it
Telephone: +39-2-26437644 Fax: +39-2-26437625
Received: April 26, 2010
Revised: June 1, 2010
Accepted: June 8, 2010
Published online: October 21, 2010

Abstract

This paper discusses the rationale for phase III testing of neoadjuvant therapy in patients affected by resectable pancreatic adenocarcinoma. The therapeutic management of patients affected by resectable pancreatic cancer is particularly troublesome due to the aggressiveness of the disease and to the limited efficacy and sometimes unfavourable risk-benefit ratio of the available therapeutic tools. Conflicting data on the role of adjuvant chemoradiation have been reported, while adjuvant single-agent chemotherapy significantly improved overall survival (OS) when compared to surgery alone. However, the OS figures for adjuvant chemotherapy remain disappointing. In effect, pancreatic cancer exhibits a prominent tendency to recur after a brief median time interval from surgery and extra-pancreatic dissemination represents the predominant pattern of disease failure. Neoadjuvant treatment has a strong rationale in this disease but limited information on the efficacy of this approach is available from single arm trials with low levels of evidence. Thus, in spite of two decades of investigation there is currently no evidence to support the routine use of pre-surgical therapy in clinical practice. To foster knowledge on the optimal management of this disease, and to produce evidence-based treatment guidelines, there is no alternative to well designed randomized trials. Systemic chemotherapy is a candidate for testing because it is supported by a more robust rationale than chemoradiation. Combination chemotherapy regimens with elevated activity in advanced disease warrant investigation. Caution would suggest the running of an exploratory phase II randomized trial before embarking on a large phase III study.

Key Words: Pancreatic cancer, Neoadjuvant therapy, Phase III trial, Chemotherapy



INTRODUCTION

Pancreatic cancer represents the fourth most common cause of cancer death, bears the worst prognosis among solid tumors and has seen very limited progress over the last 30 years. Due to intrinsic chemo- and radio-resistance, surgical resection is considered the only therapy that may have an impact on the natural history of the disease and may increase chance for cure. However, 5-year overall survival (OS) rates of less than 20% can be expected even after a curative resection, which is related to a non-negligible risk of mortality and morbidity. Therefore, the therapeutic management of patients affected by resectable pancreatic cancer is particularly troublesome due to the aggressiveness of the disease and to the limited efficacy and, sometimes, unfavourable risk-benefit ratio of the available therapeutic tools.

STANDARD TREATMENT IN RESECTABLE PANCREATIC CANCER

Adjuvant fluorouracil-based chemoradiation followed[1,2] or not[3] by maintenance systemic chemotherapy with 5-fluorouracil has been tested against surgery alone in a few phase III trials with conflicting results, ranging from a significant improvement[1] to a detrimental impact on OS[2]. Accordingly, the use of this strategy is a highly controversial topic in the management of patients with resected pancreatic adenocarcinoma.

More recently, randomized trials have suggested that both adjuvant 5-fluorouracil and gemcitabine may obtain an improvement in median survival of 2.6-4.5 mo and in 2-year OS of 6%-10% over pancreatic resection alone[2,4], with no significant difference between the two drugs[5,6].

It is noteworthy that the OS benefit achieved by adjuvant chemotherapy, in addition to being modest, does not apply to the whole population of patients submitted to pancreatic resection. In fact, up to 25% of patients have a complicated course after surgery and are unable to receive the planned treatment in due time[3,7]. Also, patients with evidence of persistent local disease or metastatic disease at the first post-operative radiological assessment are ineligible for prospective trials on adjuvant chemotherapy, whose results are, consequently, not fully generalizable.

PATTERN OF DISEASE RECURRENCE AFTER STANDARD TREATMENT

In the subset of patients receiving postoperative treatment, pancreatic cancer exhibits a prominent tendency to recur locally and to metastasize after a brief median time interval of about 13 mo from surgery[4]. Early relapse after curative surgery may be explained by the presence of micro-metastases or minimal residual disease not detectable at the time of surgery, or by the spread of cancer cells into the portal vein, lymphatic vessels, and the peritoneal cavity due to surgical manipulation of the tumor. In spite of adjuvant systemic chemotherapy, extra-pancreatic dissemination represents the predominant pattern of disease failure, affecting 63%-83% of patients, and occurs earlier than isolated local failure, which can be observed in 17%-37% of cases[2,4-6,8,9].

RATIONAL FOR NEOADJUVANT THERAPY

In this scenario, the administration of neoadjuvant systemic chemotherapy may offer several theoretical advantages. Firstly, micro-metastatic disease may be immediately treated, thus avoiding the harmful delay of at least 2 mo which occurs for patients submitted to upfront surgery. Second, a larger proportion of patients may receive an active systemic treatment compared with the adjuvant setting. Third, the treatment itself may be better tolerated, resulting in a higher rate of treatment compliance and improved dose-intensity. Fourth, neoadjuvant chemotherapy potentially reduces intraoperative tumor spillage. Fifth, the delivery of treatment before surgical manipulation may be favored by better tissue oxygenation, facilitating the distribution of chemotherapy agents into the tumor, and increasing normal tissue tolerance. Moreover, the administration of chemotherapy before surgery allows an in vivo assessment of tumor chemo-sensitivity. Finally, neoadjuvant chemotherapy may also lead to more definitive surgical resections by reducing the risk of tumoral infiltration of lymph nodes and of resection margins in the surgical specimen.

On the other hand, the neoadjuvant approach is subject to hypothetical risks such as (1) inaccurate staging and the consequent overtreatment of very early disease; (2) erroneous histology; (3) diagnostic inaccuracy due to difficulties in distinguishing between intra-pancreatic bile duct adenocarcinoma and pancreatic adenocarcinoma; (4) increase in operative morbidity and mortality; and (5) the possibility that the disease might metastasize or become unresectable during the course of induction therapy. The first topic appears to be of little relevance in pancreatic cancer since systemic treatment administration is warranted at virtually any stage of disease, aside from, perhaps, stage I, which is exceedingly rare. Similarly, the risk of yielding an inaccurate pathological diagnosis is limited as the widespread and systematic use of endoscopic ultrasound and fine needle aspiration considerably reduces the possibility of errors. As regards surgical complications, no increase in morbidity or mortality after neoadjuvant therapy has been reported in prior trials[10-12]. Conversely, the topic of disease progression during pre-surgical treatment is of considerable concern because, among patients whose disease was deemed resectable at the time of trial enrolment, only 45%-74% were actually submitted to surgical resection after induction chemoradiation[12-16] and 38%-70% after induction chemotherapy followed[10] or not[11] by chemoradiation. Proponents of neoadjuvant therapy consider these figures another advantage of this strategy, claiming that patients who experience disease progression during induction treatment suffer from an extremely aggressive tumor, which cannot be cured by extensive surgery. In fact, avoiding the risk of surgical mortality and morbidity in this subset of patients may be appealing. However, this is not necessarily true for patients who experience only local progression during neoadjuvant therapy, and in any case, no comparative information from randomized trials on the impact of the different management strategies is available in order to rule out a detrimental impact of delaying surgery. Furthermore, the proper aim for pre-surgical therapy should be that of downstaging disease and of improving both disease control and, ultimately, cure rate, rather than improving patient selection for surgery. Overall, the balance between the theoretical advantages and disadvantages of neoadjuvant therapy in pancreatic cancer appears uncertain.

PRIOR EXPERIENCE WITH NEOADJUVANT THERAPY

There have been no large randomised controlled studies on the use of neoadjuvant therapy in resectable pancreatic cancer and the sample size of prospective series has usually been limited. In addition to the abovementioned disappointing resection rates, reported median OS and 2-year OS in this single arm selected series ranged from 8 to 23 mo and from 27% to 40%[10-17]. Altogether, these figures do not appear to represent a remarkable improvement when compared to those of patients submitted to surgery alone (median OS 11-17 mo; 2-year OS 15%-31%)[1-3], or to compare favorably with those of adjuvant therapy (median OS 14-25 mo; 2-year OS 29%-55%)[1-4,6,7]. It is noteworthy that prior experiences with adjuvant combination chemotherapy reported more promising results (median OS 27-44 mo; 2-year OS 53%-58%)[9,18,19]. However, inter-trial comparisons, which already have several limitations, are in this case subject to an additional bias due to the different enrolment timing. In fact, the typical population enrolled in a prospective adjuvant trial is better selected than the typical population enrolled in a neoadjuvant trial because it does not include patients with intraoperative or postoperative detection of metastases, patients who die due to surgical complications or those who experience severe morbidity and delayed surgical recovery.

Thus, in spite of two decades of investigation of neoadjuvant therapy in resectable pancreatic cancer, there is currently no evidence to support its routine use in clinical practice, and even a detrimental effect on outcome cannot be ruled out.

TRIAL DESIGN TO ASSESS THE ROLE OF NEOADJUVANT THERAPY

Single arm trials with historical or literature comparison, and divergent study designs and entry criteria have produced modest therapeutic progress and do not allow a proper assessment of the role of neoadjuvant therapy in resectable pancreatic cancer. To foster knowledge regarding the optimal management of this disease and to produce evidence-based treatment guidelines, there is no alternative to well designed randomized trials. Since timing and sequencing of treatments appears to be a crucial and as yet unanswered issue, patients in the ideal trial should be randomly allocated to receive exactly the same treatment for the same period of time before and after surgery. Otherwise, the attribution of any potential outcome improvement to treatment type, timing or duration will be irremediably confounded and trial interpretation inconclusive.

CANDIDATES FOR PROSPECTIVE ASSESSMENT

As mentioned above, pancreatic cancer has an elevated risk of both local and systemic failure after surgery. In this perspective, local therapy represents a poor chance of considerably improving cure rates while the concomitant administration of radiotherapy and systemic chemotherapy may simultaneously address both troubles. The main radio-sensitizing antitumor agents available for pancreatic cancer are gemcitabine and 5-fluorouracil. Unfortunately, gemcitabine has to be administered at suboptimal doses which are unlikely to achieve any effect against systemic disease, due to the overlapping toxicity with radiotherapy and both drugs yield scarce activity. In fact, gemcitabine and 5-fluorouracil obtained objective response rates around 10% in advanced disease[20-26]. Any chemotherapy with a low rate of tumor shrinkage is clearly unable to provide any major advantage in terms of either micro-metastatic or local disease control for the majority of patients and may therefore be assumed to have a limited role in the neoadjuvant setting. More active combination chemotherapy regimens appear to be more promising candidates for testing but have feasibility limitations with concomitant irradiation. Furthermore, the value of radiotherapy in this disease is controversial and, at the moment, does not represent the most burning question, while the rational endorsement of the assessment of the role of combination chemotherapy as pre-surgical therapy is more convincing. Among several regimens with conventional or target agents that have been assessed for use against advanced pancreatic cancer, objective response rates over 20% have rarely been reported, while gemcitabine-cisplatin and gemcitabine-oxaliplatin doublets obtained a response rate of 26%[22] and 28%[23], respectively. Unfortunately, these figures were not reproduced in larger trials where partial plus complete response rate was in the range of 10% to 13% with gemcitabine-cisplatin[24,25] and 9% with gemcitabine-oxaliplatin[26]. Response rates with triplets including gemcitabine, a fluoropyrimidin and either a platinating agent (18%-33%)[27-29] or docetaxel (29%)[30], FOLFOXIRI (5-fluorouracil-oxaliplatin-irinotecan; 26%)[31] and G-FLIP (gemcitabine-5-fluorouracil-irinotecan-cisplatin; 26%)[32] regimens have shown promise in single phase II series, but no phase III or confirmatory trials are available. A PEFG (cisplatin, epirubicin, 5-fluorouracil, gemcitabine) regimen was proven, in a phase III trial, to be both clinically and statistically more effective than single agent gemcitabine as upfront treatment in advanced pancreatic cancer[33]. It is noteworthy that this combination chemotherapy had manageable toxic effects and the significant survival improvement was not achieved at the cost of impaired quality of life[34]. Four consecutive trials with the PEFG regimen and its variants reproduced a radiological response rate in the range of 38.5%-51%[33,35-37]. The substitution of infusional 5-fluorouracil by oral capecitabine originated the PEXG regimen that further confirmed the activity figures[38] and rendered the schedule more suitable for clinical use. The reliability of the response rate was also endorsed by the biochemical response rate. In effect, a major biochemical response (i.e. CA19.9 reduction at nadir relative to baseline value reduction ≥ 90%) was observed in 30% of patients treated with quadruplets vs 7% with single agent gemcitabine[39]. The superiority of this four-drug combination over other regimens was also suggested by a recent survey on treatment trends and outcomes of 650 patients with stage III pancreatic adenocarcinoma[40]. Based on these data and considerations, the PEXG regimen appears to be the most deserving candidate for a prospective assessment in the neoadjuvant setting.

CONCLUSION

The topic of treatment sequencing for patients affected by resectable pancreatic adenocarcinoma is of paramount importance and warrants further investigation. Time is mature for the running of a randomized prospective study, which is the only approach capable of providing evidence-based answers. To date, on the basis of activity data from trials on advanced pancreatic cancer, the most robust candidate for testing is the PEXG regimen. However, the lack of a large randomized trial confirming survival improvement over single agent gemcitabine in advanced disease suggests caution before embarking on a phase III study in the neoadjuvant setting. An exploratory phase II randomized trial seems to embody the optimal approach to avoid the risk of wasting resources and time. Accordingly, a clinical trial involving more than 20 Italian institutions has been designed as a three-arm calibrated study[41] and is currently underway. Patients are randomly allocated to receive either an adjuvant treatment with gemcitabine for 6 mo (calibration arm) or an adjuvant treatment with PEXG for 6 mo or a peri-operative treatment (3 mo before and 3 mo after surgery) with PEXG. After completion of recruitment for the phase II part of the study, an analysis of the results will be performed to decide whether to continue to the subsequent phase III part of the study. It is hoped that this trial will contribute to an expansion of knowledge on the optimal therapeutic management of resectable pancreatic cancer.

Footnotes

Peer reviewer: Dr. Joseph J Cullen, MD, Professor, Department of Surgery, University of Iowa Carver College of Medicine, 4605 JCP, University of Iowa Hospitals and Clinics, 200 Hawkins Drive, Iowa City, IA 52242, United States

S- Editor Wang YR L- Editor O’Neill M E- Editor Zheng XM

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