- Research article
- Open Access
pERK, pAKT and p53 as tissue biomarkers in erlotinib-treated patients with advanced pancreatic cancer: a translational subgroup analysis from AIO-PK0104
BMC Cancer volume 14, Article number: 624 (2014)
The role of pERK, pAKT and p53 as biomarkers in patients with advanced pancreatic cancer has not yet been defined.
Within the phase III study AIO-PK0104 281 patients with advanced pancreatic cancer received an erlotinib-based 1st-line regimen. Archival tissue from 153 patients was available for central immunohistochemistry staining for pERK, pAKT and p53. Within a subgroup analysis, biomarker data were correlated with efficacy endpoints and skin rash using a Cox regression model.
Fifty-five out of 153 patients were classified as pERKlow and 98 patients as pERKhigh; median overall survival (OS) was 6.2 months and 5.7 months, respectively (HR 1.29, p = 0.16). When analysing pERK as continuous variable, the pERK score was significantly associated with OS (HR 1.06, 95% CI 1.0-1.12, p = 0.05). Twenty-one of 35 patients were pAKTlow and 14/35 pAKThigh with a corresponding median OS of 6.4 months and 6.8 months, respectively (HR 1.03, p = 0.93). Four out of 50 patients had a complete loss of p53 expression, 20 patients a regular expression and 26 patients had tumors with p53 overexpression. The p53 status had no impact on OS (p = 0.91); however, a significant improvement in progression-free survival (PFS) (6.0 vs 1.8 months, HR 0.24, p = 0.02) and a higher rate of skin rash (84% vs 25%, p = 0.02) was observed for patients with a regular p53 expression compared to patients with a complete loss of p53.
pERK expression may have an impact on OS in erlotinib-treated patients with advanced pancreatic cancer; p53 should be further investigated for its potential role as a predictive marker for PFS and skin rash.
NCT00440167 (registration date: February 22, 2007).
Despite significant efforts in clinical research in pancreatic cancer during the last decade, only moderate progress has been achieved. Main steps forward were generated with the introduction of adjuvant chemotherapy as a standard of care after curative-intent resection (yielding in a potential long-term survival or even cure in about 20% of patients resected) and more recently, with the introduction of novel combination chemotherapy regimens (e.g. FOLFIRINOX and gemcitabine/nab-paclitaxel) for the treatment of metastatic disease [1, 2]. However, several large phase III trials investigating targeted agents (in unselected patient populations) have failed with only erlotinib (in addition to standard gemcitabine) achieving a moderate gain in overall survival (OS) [3, 4].
To date, no validated tissue biomarker is available that would allow a prognostic patient stratification or even the prediction of treatment efficacy in pancreatic cancer. Several molecular predictive markers like the human equilibrative nucleoside transporter 1 (hENT1; for the efficacy of gemcitabine) and secreted protein acidic and rich in cysteine (SPARC; for nab-paclitaxel) are currently under investigation with in part inconclusive results up to now [3, 5, 6]. Regarding the use of EGFR targeting agents in advanced pancreatic cancer, the tumor KRAS status may play a role as a prognostic or even predictive biomarker: based on previous translational results from AIO-PK0104, a large randomized phase III trial comparing a treatment sequence of gemcitabine + erlotinib followed by capecitabine vs capecitabine + erlotinib followed by gemcitabine in patients with advanced disease, patients with a KRAS wildtype may have a prolonged survival compared to patients with KRAS exon 2 mutations . Other groups have confirmed these data, and the work of Kim and colleagues even suggested that KRAS may serve as a predictive biomarker for the efficacy of erlotinib [8, 9]. Based on previous analyses conducted on archival formalin fixed paraffin embedded (FFPE) tissue from AIO-PK014 no other marker besides KRAS showed a correlation with survival endpoints or objective response: data on EGFR protein expression, EGFR gene amplification, PTEN expression and on EGFR intron 1 polymorphism did not show - despite previous pre-clinical evidence - a correlation with efficacy study endpoints [10–12].
We thus decided to additionally analyze downstream targets of the EGFR pathway, namely phospho-ERK (pERK) and phospho-AKT (pAKT) as potential biomarkers in advanced pancreatic cancer. Both represent effector molecules in the EGFR downstream signalling network, pERK for the RAS/RAF/MEK cascade and pAKT is involved in the PI3K/mTOR pathway [13, 14]. Previous evidence (mainly derived from surgical series and/or in non-erlotinib treated patients) suggests a potential role of pERK and pAKT in pancreatic cancer biology and both markers additionally may represent a more appropriate way to assess EGFR pathway activation compared to single upstream markers like EGFR itself [14–17]. As increasing pre-clinical evidence from mouse models and also from genome-wide analyses revealed an important role of p53 in the pathogenesis of pancreatic cancer the investigators decided to also include this marker in the current translational analysis from AIO-PK0104 [18, 19]. This decision specifically was also based on recent data showing a potential interaction of p53 with KRAS signalling .
The aim of this retrospective translational biomarker study based on the prospective AIO-PK0104 trial thus was to determine the frequency of alterations in pERK, pAKT and p53 in erlotinib treated patients with advanced pancreatic cancer, as well as to investigate if there is a correlation of biomarker data with efficacy (progression-free survival, PFS and OS) and safety endpoints (skin rash) from the clinical data set.
Translational patient population
Adult patients (18 to 75 years) with a histologically or cytologically confirmed diagnosis of treatment-naïve, advanced exocrine pancreatic cancer (stage III and IV) were eligible for AIO-PK0104. Overall, 281 patients were randomized and 274 patients were eligible for the intention-to-treat (ITT) population; detailed results from the clinical study have been published in 2013 . Archival FFPE tissue, which was obtained during routine pre-therapeutic diagnostic procedures, was requested retrospectively from the participating centers/pathologists for the translational study. Cytological specimens were not included. FFPE histological tissue was accepted independent of its origin, e.g. surgical or biopsy specimens from primary pancreatic tumor, lymph nodes or distant metastases. The study had approval of the local ethical committees in all participating German centers (see Additional file 1: Table S1) and patients gave written informed consent prior to any study-specific procedure. This study was conducted according to GCP/ICH guidelines and according to the Declaration of Helsinki and was registered at ClinicalTrials.gov, number NCT00440167.
Analyses of molecular tissue biomarkers
The current translational analyses from AIO-PK0104 were performed at the Ludwig-Maximilians-University of Munich by SO and TK (pERK), at the Technical University of Munich by JTS, AMS and IE (pAKT and p53/TP53) as well as at the University of Tübingen by BS (p53). All available FFPE tumor blocks were checked for quality, tissue integrity and tumor content (HE staining) by a pathologist (SO) in a blinded manner. All involved pathologists that analyzed tumor tissue were blinded to the clinical study results.
Immunohistochemistry (IHC) was performed on a Ventana Benchmark XT autostainer using the XT UltraView diaminobenzidine kit (Ventana Medical Systems, Oro Valley, AZ, USA). The primary antibodies were as follows: monoclonal anti-pERK1/2 antibody (rabbit anti-phospho-p44/42 MAPK [Thr202/Tyr204] clone 20G11, Cell Signaling Technology, Danvers, MA, USA), anti-pAKT (Santa Cruz, sc-135650, 1:30, heat mediated antigen retrieval) and anti-p53 (Novocastra, DO-7, 1:200, heat mediated antigen retrieval).
For the examination of pERK IHC a scoring system analogously to a score developed for PTEN by Loupakis et al. was applied : the nuclear and cytoplasmic staining intensity (0 - no, 1 - weak, 2 - moderate, and 3 - strong staining) were added to the score for the percentage of positive cells (0 - negative, 1 - less than 25%, 2 - 25% to 50%, 3 - more than 50% positive staining cells) and finally nuclear and cytoplasmic score were summarized (score 0–12; see Additional file 2: Figure S1). Specimens were defined as pERKhigh if the total score was 6 or higher.
Cytoplasmatic and nuclear pAKT expression by IHC in tumor cells was scored analogously to the pERK score described above. If the score was 5 or higher, samples were defined as pAKThigh. Cases that exhibited no staining in stromal or inflammatory cells (as internal controls) were omitted (see Additional file 3: Figure S2, D-F).
p53 expression has been evaluated as completely lost (no reaction in tumor cells but positive internal control), variable (no to strong) nuclear expression as normal and diffusely strong as aberrant overexpression (see Additional file 3: Figure S2, A-C).
The investigators additionally selected 12 good- and poor-risk study patients based on clinical data for objective response and time-to-treatment failure for 1st-line therapy (TTF1, a pre-defined study endpoint ) in order to analyze the TP53 mutation status (exon 5 to 8) by Sanger sequencing. The following primers were used: Ex-5 F:ATC TGT TCA CTT GTG CCC TG, Ex-5R:AAC CAG CCC TGT CGT CTC TC, Ex-6 F.AGG GTC CCC AGG CCT CTG AT, Ex-6R:CAC CCT TAA CCC CTC CTC CC, Ex-7 F:CCA AGG CGC ACT GGC CTC ATC, Ex-7R:CAG AGG CTG GGG CAC AGC AGG, Ex-8 F.TTC CTT ACT GCC TCT TGC TT and Ex-8R:TGT CCT GCT TGC TTA CCT CG.
All statistical analyses for the translational study of the AIO-PK0104 trial were performed centrally at the Ludwig-Maximilians-University of Munich, Institute of Medical Informatics, Biometry and Epidemiology by RPL. Translational biomarker data were correlated with efficacy (PFS and OS) and safety study endpoints (skin rash) using univariate analyses. As appropriate, biomarker results were handled as dichotomous/categorical variables (e.g. pAKTlow vs pAKThigh, p53 expression) or as continuous variables (e.g. linear scoring system 0 to 12 for pERK). Time-to-event endpoints were analyzed with the Kaplan-Meier method; differences were compared using the log-rank test with a 2-sided p-value of ≤0.05 being regarded as statistically significant.
For the current analysis, FFPE tumor blocks were initially available from 153 of the 281 randomized patients. The ITT study population consisted of 274 eligible patients, and 153 patients were selected for the current translational patient population; detailed patient characteristics are summarized in Table 1. With regard to important baseline parameters (e.g. age, gender, stage of disease, performance status), no significant imbalances between the ITT population and the translational study population were apparent.
Frequency of alterations in pERK, pAKT and p53 and their correlation with efficacy endpoints
Within Table 2, each of the 3 analysed markers was categorized as a dichotomous variable and a correlation between selected baseline patient characteristics and molecular marker results was performed. No significant differences were obvious for the biomarker results based on clinical characteristics; of note, although the numbers were small, all 4 patients with a p53 loss had a good pre-treatment performance status and 2 of them (50%) had locally advanced disease (whereas in patients with regular p53 expression only 5% had locally advanced pancreatic cancer).
pERK IHC staining was performed on 153 samples, classifying 55 patients as pERKlow (36%) and 98 patients as pERKhigh (64%), with a median score level of 7 (range 0 to 12). pERK expression showed no correlation with KRAS status (p = 0.32), EGFR protein expression (p = 0.38) or EGFR gene amplification (p = 1.00), respectively. The pERK status had no impact on objective treatment response (p = 0.91). Median OS for patients classified as pERKlow was 6.2 months compared to 5.7 months in the pERKhigh group (HR 1.29, 95% CI 0.90-1.83; p = 0.16) (Table 3). When analysing pERK as a continuous variable, an increase in the hazard for death by a factor of 1.06 was detected for each level of the pERK expression score of 0 to 12 (HR 1.06, 95% CI 1.0-1.12; p[log rank] = 0.050, p[likelihood ratio] = 0.047). Within Figure 1, these data are illustrated graphically by showing the predicted survival probabilities (derived from a Cox model) based on 4 exemplary pERK IHC score levels.
After analysing pERK and p53, samples with an adequate amount of tumor tissue (for a usable pAKT IHC scoring) were available from 35 patients only. Of those, 21 (60%) were classified as pAKTlow and 14 (40%) as pAKThigh; the pAKT IHC score level in the analyzed subgroup ranged from 2 to 10. As shown in Table 3, the pAKT status had no significant impact on PFS or OS. Due to the lower numbers, no analysis as a continuous variable was performed for pAKT.
p53 immunohistochemistry and TP53mutational analyses
A p53 status assessment by IHC could be carried out successfully on 50 tumor samples: 4 patients (8%) had a complete loss of p53 expression, 20 patients (40%) a regular p53 expression and 26 patients (52%) a p53 overexpression, respectively. In 43 analysable patients, p53 expression did not correlate with the KRAS mutation status (wildtype vs mutation; p = 0.32). Also no significant association between p53 and the objective response rate to 1st-line treatment was obvious (p = 0.26). The p53 expression had no significant impact on OS (8.1 vs 7.0 vs 5.0 months, p[global] = 0.91; Table 3 and Figure 2B); patients with an intact p53 expression had a significantly prolonged PFS (6.0 months) compared to patients with a loss of p53 (1.8 months) or p53 overexpression (2.5 months; p[global] = 0.03) (see Table 3 and Figure 2A).
We furthermore used archival DNA samples for performing an additional post-hoc explorative analysis on TP53 gene mutations: for this post-hoc investigation, we selected 12 good- and poor-risk patients and performed TP53 sequencing of exons 5 to 8. Detailed results of these analyses are summarized within Table 4: we detected 6 missense mutations in 5 tumors, with one additional silent mutation (R248R). All patients with a prolonged disease control (TTF1 ≥ 10 months) had TP53 wildtype tumors, with 1 tumor (case no. 33) carrying the silent TP53 mutation R248R. However, we also found patients that had a rapid disease progression (e.g. case no. 98) that was classified as TP53 wildtype. One patient (case no. 99) had 2 mutations in exon 5 of p53 (T155I & V137M) and was clinically characterized by a rapid disease progression with a TTF1 of 0.5 months only (Table 4).
Correlation of biomarkers results with skin rash
Neither the pERK nor the pAKT status correlated with the occurrence of skin rash (any grade I-III): the corresponding data for each marker (analyzed as dichotomous variable) are summarized in Table 5. Patients with a loss of p53 in their tumor had a rash incidence during treatment with erlotinib of only 25%, whereas patients with a regular p53 expression had a rate for skin rash of 84% (p[global] = 0.04).
Based on translational data from controlled prospective clinical trials no prognostic or predictive tissue biomarkers have yet been defined in advanced pancreatic cancer. Some large phase III studies investigating anti-EGFR treatment strategies like erlotinib or cetuximab (in comparison to a single-agent gemcitabine control arm) were - at least up to now - not able to define prognostic or predictive biomarkers [21, 22]. Within the current translational subgroup analysis of AIO-PK0104 we thus tried to exploratively analyze if the EGFR pathway ‘downstream’ mediators pERK and pAKT could serve as biomarkers in advanced pancreatic cancer. Previous evidence from mainly small surgical series indicated that both pERK and pAKT may have a biological role in pancreatic cancer, however with in part inconclusive results on their prognostic role [15–17]. Regarding pERK, 64% of the 153 analyzed tumor samples from AIO-PK0104 were classified as pERKhigh; a significant impact on OS was found when the pERK expression score (0 to 12) was analyzed as a continuous variable (Figure 1). The observed HR of 1.06 (95% CI 1.0-1.12) reflects an increase in the hazard for death by a factor of 1.06 for each level of the pERK expression score of 0 to 12. If this association is a prognostic or a predictive phenomenon remains unclear, as all patients treated within AIO-PK0104 received an erlotinib-containing 1st-line regimen . Nevertheless, based on the fact that the pERK status had no impact on PFS or response, one might hypothesize that the observed effect on OS is rather prognostic than predictive for the efficacy of erlotinib. In contrast, the IHC expression pattern of pAKT could successfully be determined in a smaller subgroup of only 35 patients and showed no impact on survival endpoints.
The potentially most interesting and hypothesis-generating findings from the current translational analysis of AIO-PK0104 are derived from the data on p53. The role of the transcription factor p53 as a tumor suppressor in several human cancers is well known; however its role as a prognostic or predictive biomarker remains largely unclear to date . A loss of p53 is thought to stimulate tumor growth and dissemination, whereas a regular p53 expression might be associated with a more favorable disease biology. The biological role of a p53 overexpression in human tumors still is not understood entirely. Currently it also remains a matter of debate if p53 should be assessed by IHC or by mutational analysis; most authors indeed recommend combining IHC and gene-sequencing as the most reliable prognostic tool . Of the 50 samples from our study cohort assessed for p53 by IHC, 4 showed a complete loss, 20 a regular expression and 26 an overexpression. Interestingly, a loss of p53 and p53 overexpression were associated with a dismal PFS, but on the other hand had no impact on OS (Table 3 and Figure 2). Thus one might conclude (as postulated by other authors earlier) that the overexpression status of p53 might lead to a functional loss of p53 resulting in the same biological effects like the absence of p53 expression by IHC. When we looked at the association of p53 with the occurrence of skin rash (a well known side-effect of erlotinib and other anti-EGFR drugs and a predictive ‘clinical marker’ for drug efficacy) we found rash - of any grade - in 84% of the patients whose tumor carried a regular p53 expression, whereas only 25% of patients with a p53 loss developed rash during treatment with erlotinib (p = 0.02). Thus one might hypothesize a potential role for p53 as a biomarker for rash and/or as a predictive marker for the efficacy of erlotinib.
Based on the interesting p53 findings from the IHC analyses, we additionally performed Sanger sequencing of the TP53 gene (exon 5 to 8) in 12 selected good- and poor-risk AIO-PK0104 study patients (see Table 4). Simultaneous p53 IHC data were unfortunately available in 4 out of 12 patients only: two patients with TP53 wildtype had a regular p53 expression, and 2 patients with a TP53 mutation had a p53 overexpression. All patients with a prolonged disease control (TTF1 ≥ 10 months) had TP53 wildtype tumors, including one patient whose tumor carried the silent TP53 mutation R248R. These data of course should be regarded pre-liminary, but they provide early evidence of a potential important role for the p53/TP53 status as a biomarker in patients treated with anti-EGFR agents. This evidence is supported by recent data presented at the 2013 European Cancer Congress on neoadjuvant cetuximab-containing chemoradiotherapy (CRT) in locally advanced rectal cancer: translational data from a subgroup of patients (n = 144) treated within the EXPERT-C trial showed that the TP53 mutation status might serve as an independent predictive biomarker for cetuximab efficacy . In detail, for TP53 wildtype patients (48%) the addition of cetuximab to CRT was associated with a statistically significant advantage in PFS (HR 0.23, p = 0.02) and OS (HR 0.16, p = 0.02). In multivariate analyses, this interaction remained significant even after adjusting for other prognostic factors and KRAS status. In contrast, for TP53 mutant patients (52%) no improvement in survival endpoints was observed for the addition of cetuximab to neoadjuvant CRT .
The main limitation from our current retrospective translational study arises from the fact that only a subgroup of the study patients could be analyzed for the biomarkers pERK, pAKT and p53. This circumstance mainly is based on the fact that tumor samples were limited in our study collective (specifically after already having performed detailed molecular analyses on KRAS, EGFR and PTEN ), a persisting and well known hurdle for many international collaborative groups that conduct translational research in advanced pancreatic cancer . In light of the small sample size, specifically the data on pAKT and p53 should be regarded carefully and hypothesis-generating only and they clearly need prospective validation in a larger cohort of patients. Additionally one should also keep in mind that the assessment of an IHC-based scoring system may have several methodological limitations, specifically when analyzing categorical data by using predefined cut-offs (that often themselves have no clear biological rationale). We tried to overcome some of these limitations by analyzing our pERK data as continuous variable (see Figure 1); an approach that possibly better reflects the biological function of a molecular marker compared to results obtained when dichotomizing biomarker data (e.g. high vs low or positive vs negative, respectively).
The investigators are aware of the fact that the clinical value of adding erlotinib to standard gemcitabine is limited in an unselected patient population with metastatic pancreatic cancer. This specifically holds true in the context of recent phase III data on FOLFIRINOX and nab-paclitaxel, that both provide a meaningful and relevant advance in the treatment of pancreatic adenocarcinoma [26, 27]. Nevertheless, there is a subgroup of patients that derives a clinically relevant benefit of adding erlotinib to gemcitabine, namely those patients that develop skin rash during treatment. In these patients, median survival times of about 10 months can be expected - a time frame that is in the same range of the FOLFIRINOX or gemcitabine/nab-paclitaxel data [4, 7, 26, 27]. Up to now, we unfortunately are not able to molecularly define this scientifically interesting subgroup and the authors thus believe that pancreatic cancer researchers should continue their efforts to define molecular subgroups that might derive benefit from EGFR-targeting agents in this harmful disease. In this context, some novel hypothesis-generating findings could be obtained by the current translational analysis of AIO-PK0104; however, as these results will currently have no direct impact on clinical practice, a prospective scientific validation of our pre-liminary findings is recommended.
For this translational study downstream targets of the EGFR signalling network, namely pERK and pAKT, were centrally analyzed together with the tumor suppressor p53 in erlotinib-treated pancreatic cancer patients: pERK overexpression showed a negative correlation with OS. Preliminary results in 50 patients analysed for p53 expression suggested an improvement in PFS and a higher rate of skin rash in patients whose tumors had a regular p53 expression compared to patients with a complete loss of p53. Our findings thus suggest that both pERK and p53 may serve as prognostic and/or predictive biomarkers in erlotinib-treated advanced pancreatic cancer.
Verslype C, van Cutsem E, Dicato M, Arber N, Berlin JD, Büchler MW, Cervantes A, Ciardiello F, Ducreux M, Douillard JY, Grothey A, Haller D, Haustermans K, Heinemann V, Hidalgo M, Labianca R, Li J, Marshall JL, Nordlinger B, O’Reilly EM, Roth A, Rougier P, Ryan D, Schmiegel W, Seufferlein T, Schmoll HJ, Sobrero A, Tabernero J, Tempero M, van Laethem JL, Ychou M, Zalcberg J: The management of metastatic pancreatic cancer: expert discussion and recommendations from the 14th ESMO/World Congress on Gastrointestinal Cancer, Barcelona, 2012. Ann Oncol. 2013, 24 (suppl 4): iv5-iv10.
Paulson AS, Tran Cao HS, Tempero MA, Lowy AM: Therapeutic advances in pancreatic cancer. Gastroenterology. 2013, 144: 1316-1326.
Heinemann V, Haas M, Boeck S: Systemic treatment of advanced pancreatic cancer. Cancer Treat Rev. 2012, 38: 843-853.
Moore MJ, Goldstein D, Hamm J, Figer A, Hecht JR, Gallinger S, Au HJ, Murawa P, Walde D, Wolff RA, Campos D, Lim R, Ding K, Clark G, Voskoglou-Nomikos T, Ptasynski M, Parulekar W: Erlotinib plus gemcitabine compared with gemcitabine alone in patients with advanced pancreatic cancer. A phase III trial of the National Cancer Institute of Canada Clinical trials group. J Clin Oncol. 2007, 25: 1960-1966.
Poplin E, Wasan H, Rolfe L, Raponi M, Ikdahl T, Bondarenko I, Davidenko I, Bondar V, Garin A, Boeck S, Ormanns S, Heinemann V, Bassi C, Evans TR, Andersson R, Hahn H, Picozzi V, Dicker A, Mann E, Voong C, Kaur P, Isaacson J, Allen A: Randomized, multicenter, phase II study of CO-101 versus gemcitabine in patients with metastatic pancreatic ductal adenocarcinoma: including a prospective evaluation of the role of hENT1 in gemcitabine or CO-101 sensitivity. J Clin Oncol. 2013, 31: 4453-4461.
Von Hoff DD, Ramanathan RK, Borad MJ, Laheru DA, Smith LS, Wood TE, Korn RL, Desai N, Trieu V, Iglesias JL, Zhang H, Soon-Shiong P, Shi T, Rajeshkumar NV, Maitra A, Hidalgo M: Gemcitabine plus nab-paclitaxel is an active regimen in patients with advanced pancreatic cancer: a phase I/II trial. J Clin Oncol. 2011, 29: 4548-4554.
Heinemann V, Vehling-Kaiser U, Waldschmidt D, Kettner E, Märten A, Winkelmann C, Klein S, Kojouharoff G, Gauler TC, Fischer von Weikersthal L, Clemens MR, Geissler M, Greten TF, Hegewisch-Becker S, Rubanov O, Baake G, Höhler T, Ko YD, Jung A, Neugebauer S, Boeck S: Gemcitabine plus erlotinib followed by capecitabine versus capecitabine plus erlotinib followed by gemcitabine in advanced pancreatic cancer: final results of a randomised phase 3 trial of the ‘Arbeitsgemeinschaft Internistische Onkologie’ (AIO-PK0104). Gut. 2013, 62: 751-759.
Ogura T, Yamao K, Hara K, Mizuno N, Hijioka S, Imaoka H, Sawaki A, Niwa Y, Tajika M, Kondo S, Tanaka T, Shimizu Y, Bhatia V, Higuchi K, Hosoda W, Yatabe Y: Prognostic value of K-ras mutation status and subtypes in endoscopic ultrasound-guided fine-needle aspiration specimens from patients with unresectable pancreatic cancer. J Gastroenterol. 2013, 48: 640-646.
Kim ST, Lim do H, Jang KT, Lim T, Lee J, Choi YL, Jang HL, Yi JH, Baek KK, Park SH, Park YS, Lim HY, Kang WK, Park JO: Impact of KRAS mutations on clinical outcomes in pancreatic cancer patients treated with first-line gemcitabine-based chemotherapy. Mol Cancer Ther. 2011, 10: 1993-1999.
Boeck S, Jung A, Laubender RP, Neumann J, Egg R, Goritschan C, Vehling-Kaiser U, Winkelmann C, Fischer von Weikersthal L, Clemens MR, Gauler TC, Märten A, Klein S, Kojouharoff G, Barner M, Geissler M, Greten TF, Mansmann U, Kirchner T, Heinemann V: EGFR pathway biomarkers in erlotinib-treated patients with advanced pancreatic cancer: translational results from the randomised, crossover phase 3 trial AIO-PK0104. Br J Cancer. 2013, 108: 469-476.
Boeck S, Jung A, Laubender RP, Neumann J, Egg R, Goritschan C, Ormanns S, Haas M, Modest DP, Kirchner T, Heinemann V: KRAS mutation status is not predictive for objective response to anti-EGFR treatment with erlotinib in patients with advanced pancreatic cancer. J Gastroenterol. 2013, 48: 544-548.
Tzeng CW, Frolov A, Frolova N, Jhala NC, Howard JH, Vickers SM, Buchsbaum DJ, Heslin MJ, Arnoletti JP: Pancreatic cancer epidermal growth factor receptor (EGFR) intron 1 polymorphism influences postoperative patient survival and in vitro erlotinib response. Ann Surg Oncol. 2007, 14: 2150-2158.
Ng SS, Tsao MS, Nicklee T, Hedley DW: Effects of the epidermal growth factor receptor inhibitor OSI-774, Tarceva, on downstream signaling pathways and apoptosis in human pancreatic adenocarcinoma. Mol Cancer Ther. 2002, 1: 777-783.
Collisson EA, Trejo CL, Silva JM, Gu S, Korkola JE, Heiser LM, Charles RP, Rabinovich BA, Hann B, Dankort D, Spellman PT, Phillips WA, Gray JW, McMahon M: A central role for RAF→MEK→ERK signaling in the genesis of pancreatic ductal adenocarcinoma. Cancer Discov. 2012, 2: 685-693.
Yamamoto S, Tomita Y, Hoshida Y, Morooka T, Nagano H, Dono K, Umeshita K, Sakon M, Ishikawa O, Ohigashi H, Nakamori S, Monden M, Aozasa K: Prognostic significance of activated Akt expression in pancreatic ductal adenocarcinoma. Clin Cancer Res. 2004, 10: 2846-2850.
Chadha KS, Khoury T, Yu J, Black JD, Gibbs JF, Kuvshinoff BW, Tan D, Brattain MG, Javle MM: Activated Akt and Erk expression and survival after surgery in pancreatic carcinoma. Ann Surg Oncol. 2006, 13: 933-939.
Javle MM, Gibbs JF, Iwata KK, Pak Y, Rutledge P, Yu J, Black JD, Tan D, Khoury T: Epithelial-mesenchymal transition (EMT) and activated extracellular signal-regulated kinase (p-Erk) in surgically resected pancreatic cancer. Ann Surg Oncol. 2007, 14: 3527-3533.
Ardito CM, Grüner BM, Takeuchi KK, Lubeseder-Martellato C, Teichmann N, Mazur PK, Delgiorno KE, Carpenter ES, Halbrook CJ, Hall JC, Pal D, Briel T, Herner A, Trajkovic-Arsic M, Sipos B, Liou GY, Storz P, Murray NR, Threadgill DW, Sibilia M, Washington MK, Wilson CL, Schmid RM, Raines EW, Crawford HC, Siveke JT: EGF receptor is required for KRAS-induced pancreatic tumorigenesis. Cancer Cell. 2012, 22: 304-317.
Liang WS, Craig DW, Carpten J, Borad MJ, Demeure MJ, Weiss GJ, Izatt T, Sinari S, Christoforides A, Aldrich J, Kurdoglu A, Barrett M, Phillips L, Benson H, Tembe W, Braggio E, Kiefer JA, Legendre C, Posner R, Hostetter GH, Baker A, Egan JB, Han H, Lake D, Stites EC, Ramanathan RK, Fonseca R, Stewart AK, Von Hoff D: Genome-wide characterization of pancreatic adenocarcinoma patients using next generation sequencing. PLoS One. 2012, 7: e43192-
Loupakis F, Pollina L, Stasi I, Ruzzo A, Scartozzi M, Santini D, Masi G, Graziano F, Cremolini C, Rulli E, Canestrari E, Funel N, Schiavon G, Petrini I, Magnani M, Tonini G, Campani D, Floriani I, Cascinu S, Falcone A: PTEN expression and KRAS mutations on primary tumors and metastases in the prediction of benefit from cetuximab plus irinotecan for patients with metastatic colorectal cancer. J Clin Oncol. 2009, 27: 2622-2629.
Da Cunha SG, Dhani N, Tu D, Chin K, Ludkovski O, Kamel-Reid S, Squire J, Parulekar W, Moore MJ, Tsao MS: Molecular predictors of outcome in a phase 3 study of gemcitabine and erlotinib therapy in patients with advanced pancreatic cancer: National Cancer Institute of Canada Clinical Trials Group Study PA.3. Cancer. 2010, 116: 5599-5607.
Philip PA, Benedetti J, Corless CL, Wong R, O'Reilly EM, Flynn PJ, Rowland KM, Atkins JN, Mirtsching BC, Rivkin SE, Khorana AA, Goldman B, Fenoglio-Preiser CM, Abbruzzese JL, Blanke CD: Phase III study comparing gemcitabine plus cetuximab versus gemcitabine in patients with advanced pancreatic adenocarcinoma: Southwest Oncology Group-directed intergroup trial S0205. J Clin Oncol. 2010, 28: 3605-3610.
Inoue K, Kurabayashi A, Shuin T, Ohtsuki Y, Furihata M: Overexpression of p53 protein in human tumors. Med Mol Morphol. 2012, 45: 115-123.
Sclafani F, Gonzalez D, Cunningham D, Hulkki Wilson S, Peckitt C, Tabernero J, Glimelius B, Cervantes A, Brown G, Chau I: TP53 status may predict benefit from cetuximab in high-risk, locally advanced rectal cancer: Results of the EXPERT-C trial. Eur J Cancer. 2013, 49 (suppl 2): abstract #7
Tempero MA, Klimstra D, Berlin J, Hollingsworth T, Kim P, Merchant N, Moore M, Pleskow D, Wang-Gillam A, Lowy AM: Changing the way we do business: recommendations to accelerate biomarker development in pancreatic cancer. Clin Cancer Res. 2013, 19: 538-540.
Conroy T, Desseigne F, Ychou M, Bouché O, Guimbaud R, Bécouarn Y, Adenis A, Raoul JL, Gourgou-Bourgade S, de la Fouchardière C, Bennouna J, Bachet JB, Khemissa-Akouz F, Péré-Vergé D, Delbaldo C, Assenat E, Chauffert B, Michel P, Montoto-Grillot C, Ducreux M, Groupe Tumeurs Digestives of Unicancer; PRODIGE Intergroup: FOLFIRINOX versus gemcitabine for metastatic pancreatic cancer. N Engl J Med. 2011, 364: 1817-1825.
Von Hoff DD, Ervin T, Arena FP, Chiorean EG, Infante J, Moore M, Seay T, Tjulandin SA, Ma WW, Saleh MN, Harris M, Reni M, Dowden S, Laheru D, Bahary N, Ramanathan RK, Tabernero J, Hidalgo M, Goldstein D, Van Cutsem E, Wei X, Iglesias J, Renschler MF: Increased survival in pancreatic cancer with nab-paclitaxel plus gemcitabine. N Engl J Med. 2013, 369: 1691-1703.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/14/624/prepub
The authors wish to thank all patients and their families, nurses, study coordinators and investigators for their participation in the AIO-PK0104 study. Additionally, the active commitment of the pathologists providing FFPE archival tumor tissue is gratefully acknowledged because they enabled this translational study.
AIO-PK0104 was supported by unrestricted grants from Roche Pharma AG, Germany and Sturm-Stiftung, City of Munich, Germany.
Steffen Ormanns: Clovis Oncology (Travel grant)
Jens T. Siveke: None
Volker Heinemann: Roche (Honoraria for scientific presentations, Research funding, Consultant)
Michael Haas: Celgene (Honoraria for scientific presentations, Travel grant)
Bence Sipos: None
Anna Melissa Schlitter: None
Irene Esposito: None
Andreas Jung: None
Rüdiger P. Laubender: None
Stephan Kruger: None
Ursula Vehling-Kaiser: None
Cornelia Winkelmann: None
Ludwig Fischer von Weikersthal: None
Michael R. Clemens: Roche (Honoraria for scientific presentations, Research funding, Travel grants)
Thomas C. Gauler: None
Angela Märten: None
Michael Geissler: None
Tim F. Greten: None
Thomas Kirchner: Merck Serono (Honoraria for scientific presentations, Research funding), Amgen (Honoraria for scientific presentations, Research funding, Consultant), Astra Zeneca (Honoraria for scientific presentations), Roche (Honoraria for scientific presentations, Consultant), Pfizer (Consultant), Novartis (Consultant)
Stefan Boeck: Celgene (Honoraria for scientific presentations, Research funding, Consultant, Travel grants), Clovis Oncology (Research funding), Roche (Honoraria for scientific presentations, Research funding, Travel grants).
SO, JTS, VH, TK and SB were responsible for the conception and design of the study. VH, MH, SK, UVK, CW, LFvW, MRC, TCG, AM, MG, TFG and SB recruited study patients into the multicenter AIO-PK0104 trial and provided tumor tissue for translational analyses. SO, JTS, BS, AMS, IE, AJ and SB did the molecular analyses and were involved in the collection and assembly of data. SO, JTS, RPL and SB performed the statistical data analyses. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 2: Figure S1: Immunohistochemistry staining for pERK in tissue specimens from AIO-PK0104. Moderate pERK staining in pancreatic adenocarcinoma cells (score 4); B Strong pERK staining in pancreatic adenocarcinoma cells (score 9); (magnification x 200, for all figures). (ZIP 5 MB)
Additional file 3: Figure S2: Immunohistochemistry staining for p53 and pAKT in tissue specimens from AIO-PK0104. No p53 staining in pancreatic adenocarcinoma cells with positive internal control (inflammatory cells, arrows), considered as complete loss of p53; B varying expression of p53 in tumor cells, considered as regular p53 expression; C strong homogenous p53 expression, considered as p53 overexpression (corresponding to mutation in p53); D weak nuclear pAKT expression; E strong nuclear pAKT reaction in tumor cells; F strong nuclear pAKT expression with additional cytoplasmic staining; (magnification x 200, for all figures). (TIFF 6 MB)
About this article
Cite this article
Ormanns, S., Siveke, J.T., Heinemann, V. et al. pERK, pAKT and p53 as tissue biomarkers in erlotinib-treated patients with advanced pancreatic cancer: a translational subgroup analysis from AIO-PK0104. BMC Cancer 14, 624 (2014). https://doi.org/10.1186/1471-2407-14-624
- Pancreatic cancer