Improved survival with chemoradiotherapy > 40 Gy after systemic treatment
verfasst von:
Sebastian Bachmayer, M.D., Gerd Fastner, M.D., Andrea Vaszi, M.D., Wolfgang Iglseder, M.D., Peter Kopp, Ph.D., Josef Holzinger, M.D., Adam Dinnewitzer, M.D., Gabriel Rinnerthaler, M.D., Simon Peter Gampenrieder, M.D., Klaus Emmanuel, M.D., Richard Greil, M.D., Felix Sedlmayer, M.D., Franz Zehentmayr, M.D., M.Sc.
The role of radiotherapy (RT) for nonmetastatic pancreatic cancer is still a matter of debate since randomized control trials have shown inconsistent results. The current retrospective single-institution study includes both resected and unresected patients with nonmetastasized pancreatic cancer. The aim is to analyze overall survival (OS) after irradiation combined with induction chemotherapy.
Patients and methods
Of the 73 patients with nonmetastatic pancreatic cancer eligible for the present analysis, 42 (58%) patients had adjuvant chemoradiotherapy (CRT), while 31 (42%) received CRT as primary treatment. In all, 65 (89%) had chemotherapy at any time before, during, or after RT, and 39 (53%) received concomitant CRT. The median total dose was 50 Gy (range 12–77 Gy), while 61 (84%) patients received >40 Gy.
Results
With a median follow-up of 22 months (range 1.2–179.8 months), 14 (19%) are still alive and 59 (81%) of the patients have died, whereby 51 (70%) were cancer-related deaths. Median OS and the 2‑year survival rate were 22.9 months (1.2–179.8 months) and 44%, respectively. In addition, 61 (84%) patients treated with >40 Gy had a survival advantage (median OS 23.7 vs. 17.3 months, p = 0.026), as had patients with 4 months minimum of systemic treatment (median OS 27.5 vs. 14.3 months, p = 0.0004).
Conclusion
CRT with total doses >40 Gy after induction chemotherapy leads to improved OS in patients with nonmetastatic pancreatic cancer.
European Organisation for Research and Treatment of Cancer
ESPAC
European Study Group for Pancreatic Cancer
EQD2
Biologically equivalent dose in 2 Gy fractions
GERCOR
Groupe Coopérateur Multidisciplinaire en Oncologie
GITSG
Gastrointestinal Tumor Study Group
HR
Hazard ratio
IMRT
Intensity-modulated radiotherapy
IOERT
Intraoperative radiotherapy with electrons
LAPC
Locally advanced pancreatic cancer
mOS
Median overall survival
mRT‑dose
Median radiation dose
MVA
Multivariate analysis
NCDB
National Cancer Database
NR
Not reported
NS
Not significant
OS
Overall survival
RT
Radiotherapy
UICC
Union Internationale Contre le Cancer
Introduction
In Europe, a total of 87,400 deaths due to pancreatic cancer were predicted for 2017, which amounts to approximately 6% of all cancer deaths [1]. These numbers indicate the aggressiveness of this disease and its dismal prognosis. Surgery is still the cornerstone of curative treatment. Unfortunately, only 20% of the patients are resectable at the time of diagnosis, 30% present with unresectable locally advanced disease, and 50% of the patients already have distant metastases [2].
While adjuvant chemotherapy (CT) is undisputed, the addition of radiotherapy is recommended only for subgroups of patients. According to the ASCO guidelines, it should be offered to patients with N1 and/or R1 status [3, 4], whereas in Germany adjuvant chemoradiotherapy (CRT) is restricted to clinical trials only [5]. The prospective studies that informed this conceptual framework were conducted between 1985 [6] and 2004 [7]. Based on an outdated radiation treatment schedule—40 Gy split course— the European Study Group for Pancreatic Cancer (ESPAC) came to the conclusion that CRT is not only inferior to CT but detrimental with respect to overall survival (OS). In the latest study, 50.4 Gy total dose in the CRT arm were administered, which resulted in OS rates similar to CT alone [8].
Anzeige
For the treatment of locally advanced pancreatic cancer (LAPC) guidelines recommend initial CT followed by CRT only for those patients without systemic progression [3, 4]. The prospective randomized control trials in the field published in the past decade [9‐11] were conducted with radiation doses of 46 to 60 Gy. The study design of the latest of these three studies included a period of 4 months of CT before CRT with 54 Gy. The two treatment regimens were iso-effective with respect to OS but locoregional control and time to retreatment was significantly better in the CRT arm [11].
Taken together, the role of radiotherapy both for resectable and unresectable pancreatic cancer is still under investigation. Due to a probability of 30% for micrometastases at the time of diagnosis [12] patients with nonmetastasized pancreatic cancer may progress early at distant sites, which impairs clinical outcome. Simultaneously, locoregional recurrence may also lead to death [13].
The current study includes both resected and unresected patients with nonmetastasized pancreatic cancer. Its aim is to analyze OS following irradiation combined with induction chemotherapy in the therapeutic setting of a European tertiary referral center.
Materials and methods
Patients
Between 1982 and 2016, 150 patients with pancreatic and periampullary cancer were referred to our department for radiation therapy. In all, 77/150 (51%) patients were excluded from the present analysis mainly for distant metastasis at the time of diagnosis. For the current analysis we included 73 patients who were referred since 1998, when intraoperative radiotherapy with electrons (IOERT) as well as 3D CRT were fully implemented. The primary endpoint was overall survival (OS).
Anzeige
Patients’ characteristics are described in Table 1. Patients were staged according to the 6th edition of the TNM system before 2010. When reviewing the charts in 2016 we used the 7th edition as a reference knowing that the two systems were identical with respect to pancreatic cancer. The majority of patients were classified as T3 (55%) and T4 (38%), respectively. Out of T4 tumors, 14 (19%) patients presented with involvement of duodenum, spleen or adrenal glands. In total, 66/73 (90%) patients presented with Union internationale contre le cancer (UICC) stages IIB or III. In 47/73 (64%) cases, the primary tumor was located in the head of the pancreas or the uncinate process, in 4/73 (6%) the papilla of vater and in 19/73 (26%) in the body or tail. In addition, 3/73 (4%) were found in the neck of the pancreas. At the start of radiation treatment, 19/73 (26%) patients presented with local progression after induction CT. Disease progression was diagnosed by imaging (computed tomography, MRI or PET-CT scans) with histological confirmation at the discretion of the treating physician.
Table 1
Patient characteristics
Patient characteristics at baseline N = 73
Sex (n)
Male
37
51%
Female
36
49%
Age at diagnosis (years)
Median
66.9
–
Range
45.6–83.7
–
Pathological confirmation
Yes
64
88%
No
9
12%
Tumor location (n)
Papilla of vater
4
6%
Head or uncinate process
47
64%
Body or tail
19
26%
Neck
3
4%
T (n)
T1
1
1%
T2
4
5%
T3
40
55%
T4
28
38%
N (n)
N0
21
29%
N1
52
71%
M (n)
M0
72
99%
Mx
1
1%
Involvement of either duodenum, spleen or adrenal glands (n)
Yes
14
19%
No
59
81%
Histologic type (n)
Papilla of vater
4
5%
Adenocarcinoma
57
78%
Neuroendocrine tumor
2
3%
Unknown
10
14%
Grading (n)
G1
3
4%
G2
38
52%
G3
18
25%
Gx
14
19%
UICC stage (n)
IA
1
1%
IB
1
1%
IIA
7
10%
IIB
36
49%
III
28
38%
Karnofsky performance score (n)
≥70
57
78%
<70
16
22%
Local progression during CT
before RT (n)
Yes
19
26%
No
54
74%
CT chemotherapy, RT radiotherapy
Treatment
In resectable patients (42/73, 58%), CRT was applied as adjuvant treatment, while being the primary approach for the 31/73 (42%) patients who presented with locally advanced disease deemed to be unresectable. Treatment characteristics are summarized in Table 2.
Surgery was performed in curative intention and resulted in 20/42 (48%) histologically complete (R0) and 21/42 (50%) incomplete (R1) resections. In 1/42 (2%) patient surgery was macroscopically incomplete (R2). Pathology reports were re-evaluated and—in accordance with Verbeke et al.—resection was regarded as incomplete if tumor cells were found within 1 mm of the resection margin [14].
Radiotherapy was performed as intraoperative radiotherapy with electrons (IOERT) and/or external beam treatment. IOERT was delivered by means of a standard LINAC (median 8 MeV, range 6–18 MeV). The energy was chosen according to dose depth (median 2.2 cm, range 0.9–4 cm) determined by ultrasound. The tube diameter was adjusted to tumor bed dimensions (median 3.7 cm, range 2.0–5.5 cm). The median 90% isodose was 9 Gy (range 7–18 Gy). A total of 18/73 (24%) patients received single fraction IOERT during surgery, and out of these, 3 patients in the course of explorative laparotomies. The median IOERT dose (Dmax) was 10 Gy (range 8–20 Gy), resulting in a median total equivalent dose (EQD2) of 17 Gy (range 12–49 Gy) in the tumor bed.
EBRT was usually performed with 15 MV photons (range 15–25 MV) in conventional 3D-box technique (three or four portals). The median single dose was 1.8 Gy (range 1.6–2 Gy). The dose–volume constraints were set at the usual levels with maximum doses of small intestine as well as myelon at 45 Gy, the stomach at 50 Gy, V50 for the kidney <30% [15]. A total of 61/73 (84%) patients received EBRT, one of these was treated with IMRT. In 43/73 (59%) patients, the planning target volume included the regional lymphatic drain. The median total EQD2 (EBRT + IOERT) for all patients was 50 Gy (range 12–77 Gy); 61/73 (84%) patients received more than 40 Gy EQD2 (median 50 Gy, range 44–77 Gy).
The chemotherapeutic regimens were based on 5‑FU (or capecitabine) or gemcitabine. In all, 26/42 resected patients received CT before RT in two possible therapy sequences: CT + surgery + (C)RT (n = 2) or surgery + CT + (C)RT (n = 24). Thus, induction chemotherapy in the strict sense was applied in 2 cases with the intention to achieve operability. A total of 18 patients had gemcitabine mono (1000 mg/m2 on day 1, 3 out of 4 weeks), 3 GEMOX (gemcitabine 1000 mg/m2, oxaliplatin 100 mg/m2, every 2 weeks), 3 FOLFIRINOX (oxaliplatin 85 mg/m2, irinotecan 180 mg/m2, leucovorin 400 mg/m2, 5‑FU bolus 400 mg/m2, 5‑FU continuous 2400 mg/m2 over 46 h, every 2 weeks), one patient had 5‑FU/leucovorin (425 mg/m2, 20 mg/m2, weekly) and another one EVANS (doxorubicin 50 mg/m2 on day 1, cyclophosphamide 1000 mg/m2 on day 1, cisplatin 25 mg/m2 on days 1–5, etoposide 50 mg/m2 on days 1–5, every 3 weeks). The median number of cycles was 6 (range 1–17). In the group of unresected patients 27/31 had CT before RT: 6 gemcitabine mono, 10 GEMOX, 10 FOLFIRINOX and one EVANS. The median number of cycles was 4 (range 3–11).
CRT was administered to 39/73 (54%) patients, while 65/73 (89%) patients had chemotherapy at any time (prior, following or concomitant to irradiation).
Equivalent total dose in 2 Gy fractions (EQD2)
The generally accepted α/β values for gastrointestinal tissues range from 6–13 Gy [16, 17]. A recent publication by Unkel et al. analyzed clonogenic assays in nine pancreatic cancer cell lines. The median α/β value extrapolated from these experiments was 9.4 Gy (range 1.85–191.58 Gy; [18]). Taking into account the considerable heterogeneity of these numbers EQD2 in the current study was calculated with an α/β value of 10.
Anzeige
Statistics
OS was defined as the time from diagnosis until death or last follow-up and estimated by the Kaplan–Meier method. The patient cohort was divided into groups according to EQD2: dose splits were set at 40 Gy, 45 Gy, 50 Gy, and 55 Gy. These subgroups were compared by log-rank testing. In order to detect patient-related factors that are prognostically relevant with respect to OS, multivariate analyses (MVA) were performed by Cox regression (forward likelihood ratio). MVA models were calculated for resected and unresected patients separately. They included the following variables: sex, age at diagnosis, tumor location, T‑stage, N‑stage, involvement of adjacent structures (i.e., duodenum, spleen, adrenal glands), histology, grading, UICC stage, Karnofsky performance score, local progression before RT. P-values of 0.05 with a 95% confidence interval were regarded as statistically significant. Data were analyzed with SPSS™ for Windows v 21.0.0.1.
Results
With a median follow-up of 22 months (range 1.2–179.8 months), 59/73 (81%) of the patients died and 14/73 (19%) are still alive. There were 51/73 (70%) cancer-related deaths, 1/73 (1%) patient died for septic multiple organ failure and 2/73 (2%) died for cardiac reasons. In 5/73 (7%) patients, the medical charts were incomplete and no information could be obtained so that the cause of death remained unknown. The median OS for the whole patient cohort was 22.9 months, with 2‑ and 5‑year survival rates of 44 and 16%, respectively (Fig. 1). In the subgroup of resected patients, the corresponding numbers were 25.5 months, 52 and 20%, while in unresected patients median survival was 20.4 months, 2‑year and 5‑year survival rates were 34 and 13%, respectively (log-rank p = 0.154).
×
Based on EQD2, patients were grouped into two dose bins with a threshold dose below (group 1) or above 40 Gy (group 2), respectively. Fig. 2 shows the comparison of 61/73 (84%) patients in group 1 who were treated with at least 40 Gy EQD2 (median 50 Gy, range 44–77 Gy) compared to 12/73 (16%) individuals (group 2) who received less than 40 Gy (median 17 Gy, range 12–37 Gy) for one of the following reasons: postsurgery complications (5), lack of compliance (2), M1 during chemotherapy (3), multiorgan failure due to infection (1). Additionally, one patient received previous irradiation for seminoma 26 years before he was diagnosed with pancreatic cancer. In group 1, the median OS was 23.7 months, and the 2‑ and 5‑years survival rates amounted to 47 and 19%, while in group 2 the respective numbers were 17.3 months, 19 and 0% (p = 0.026). Of note, this difference remained significant within the cohort of the 42 patients who had received surgery: when treated with doses >40 Gy, the median survival time, as well as the 2‑ and 5‑year survival rates amounted to 27.5 months, 56 and 20%, respectively, compared to 19.3 months, 23 and 0% in those patients with the lower dose (p = 0.028). For the 31 unresected patients no significant difference could be detected (p = 0.073): patients with >40 Gy had a median, 2‑ and 5‑years survival of 20.4 months, 37 and 14%, compared to 4.2 months, 0% for those with lower doses.
×
We also compared survival between patients with 4 months of chemotherapy to those without. Patients with at least 4 months of systemic treatment lived significantly longer than those who had less (>4 months: median OS 27.5 months, 2 year 54%, 5 year 24%; <4 months: median OS 14.3 months, 2 year 25%, 5 year 4%; p = 0.0004, Fig. 3). This significant difference persisted in resected patients (p = 0.003, supplementary Fig. 1) as well as in unresected patients (p = 0.023, supplementary Fig. 2).
×
Anzeige
A comparison of combined treatment modalities showed that patients who received >4 months of systemic treatment followed by >40 Gy radiation therapy had an overall survival advantage (median OS 28.3 months versus 14.3 months, p = 0.0002, Fig. 4). Again, the difference persisted both in resected (p = 0.003) and unresected patients (p = 0.020).
×
Prognostically relevant parameters for overall survival were analyzed separately for resected and unresected patients (Table 3). In resected patients involvement of either duodenum, spleen or adrenal glands was a significant factor in univariate analysis (p = 0.046) but no longer in the MVA model. In unresected patients, local progression was found to be a significant prognosticator in both models (UVA: p = 0.014; MVA: HR = 4.132, 95% CI 1.217–14.030, p = 0.023).
Table 3
Prognostic factors for overall survival
Prognostic factors
Resected patients
Unresected patients
UVA
MVA
UVA
MVA
Sex
0.091
n.s.
0.376
n.s.
Age at diagnosis
0.974
n.s.
0.660
n.s.
Tumor location
0.287
n.s.
0.846
n.s.
T
0.269
n.s.
0.992
n.s.
N
0.226
n.s.
0.162
n.s.
Involvement of either duodenum, spleen or adrenal glands
0.046
n.s.
0.778
n.s.
Histologic type
0.127
n.s.
0.634
n.s.
Grading
0.051
n.s.
0.300
n.s.
UICC stage
0.088
n.s.
0.634
n.s.
Karnofsky performance score
0.629
n.s.
0.737
n.s.
Local progression during induction chemotherapy
0.726
n.s.
0.014
0.023
UVA univariate analysis, MVA multivariate analysis, n.s. not significant
Toxicity was mild and well manageable: 67/73 (92%) patients had no major adverse effects reported, while 6/73 (8%) patients suffered from radiation induced inflammatory reactions (gastritis, duodenitis, colitis, inflammation of anastomosis).
Discussion
In this retrospective analysis we could demonstrate that following a minimum of 4 months of systemic treatment, the administration of a total dose higher than 40 Gy improves OS in patients with nonmetastatic pancreatic cancer.
Anzeige
A total of 40 Gy was selected as cutoff since practice changing studies conducted by ESPAC [7], the European Organisation for Research and Treatment of Cancer (EORTC) [19] and the Gastrointestinal Tumor Study Group (GITSG) [6] used this regimen (40 Gy in 2 Gy fractions, split course). This amounts to an EQD2 of 32 Gy assuming a daily loss of 0.6 Gy during the 2‑week break. The median dose of the study published by the Groupe Coopérateur Multidisciplinaire en Oncologie (GERCOR) was 50.4 Gy conventional RT [8]. With the radiation regimens implemented in these trials, median OS ranges between 159 [7] and 243 [8] months were achieved. In retrospective series and population-based cohort studies, the highest reported median OS was 39.9 months with CRT at median total doses of 50.4 Gy [20‐30]. A National Cancer Database (NCDB) analysis revealing a median OS of 21 months concluded that the optimal dose range for adjuvant RT is possibly between 50 and 55 Gy, while doses <40 Gy lead to worse survival [24]. In the current study 31/42 (74%) of the resected patients received >40 Gy. With this treatment schedule, a median OS of 25.5 months was achieved, which is on the upper edge of the published results for CRT arms of prospective studies [6‐8, 19]. Except for the GERCOR trial, these studies applied radiation in split course to potentially large volumes without a centralized quality audit. Apart from the RT concepts, these studies were frequently criticized for their design and statistical analyses so that their results remain disputed.
Adjuvant CT trials report mOS between 22.1 and 28 months [31‐34]. Except for one outlier of 48 months [35] this is well in line with our results. A re-analysis of the ESPAC-3 data concluded that the administration of six cycles of adjuvant CT is more important in terms of OS than an early start after surgery in order to allow for complete recovery [36]. On average the resected patients in our cohort received six cycles of adjuvant CT and therefore fulfill this prerequisite for the best possible outcome.
A recent comprehensive review including four meta-analyses [37‐40] stated that despite of the inconclusiveness of prospective and retrospective studies, adjuvant CRT should be offered to patients with N1 and/or R1 situation after 4–6 months of chemotherapy [4, 30]. Our data corroborate the idea that 4 months of CT prior to RT improves OS (Fig. 3), whereas neither resection nor lymph node status were significant prognosticators in our cohort. A point of criticism in the above mentioned meta-analyses [37‐40] is the disregard for improved local control by CRT. Of note, especially in primarily resectable patients who received adjuvant CT after surgery, the rate of isolated local relapses lies between 18 and 28% [33‐35]. This is also true for the CT arm of the EORTC-40013-22012/FFCD 9203/GERCOR study with 24% isolated local relapses reported, compared to 11% in the CRT arm [8]. This underlines the importance of RT as an effective adjunct local treatment, which reduces the rate of local relapses and their consequences (pain, lower quality of life, higher rate of retreatment) by a factor of 2. When considering also patients with synchronous distant metastases, the percentage of patients who experience a local relapse is even higher (34 to 82%; [31, 33, 34]). These figures clearly challenge the widely spread notion that CRT should not play a role in resectable pancreatic cancer. In contrast to this assumption, we strongly advocate RT as a powerful tool for the prevention of a local regrowth.
In LAPC patients the mOS in the present analysis was roughly 20 months, which seems to be superior to the mOS rates reported in the majority of clinical trials (8.3–17.4 months; [9‐12, 41‐43]). Being aware of the fact that a comparison with prospectively collected data is indirect (supplementary Table 2) a critical discussion of our findings has to consider patient selection as well as therapy regimens and toxicity. Reportedly, up to 30% of the patients develop metastases during induction CT and are therefore considered as unsuitable for subsequent combined CRT [12]. In trials without preceding CT, these patients are however included in the CRT group, which may compromise mOS [9, 10]. In our cohort of unresected patients, 27/31 (90%) received systemic treatment before CRT, thus selecting those patients who would potentially benefit most from RT.
CRT was administered in 19 cases mostly as single agent therapy (either gemcitabine or 5‑FU). Therefore, toxicity might be higher in prospective studies that apply CT doublets concomitant to irradiation. For example, in the FFCD/SFRO study only 40% of the patients received CRT as planned. The mOS was 13 months with gemcitabine mono versus 8.6 months with 60 Gy plus 5‑FU/cisplatinum [9]. Hence, the differences between the current study and prospective trials may—on the one hand—be due to the effectiveness of systemic treatment before CRT, which selects those patients who are most suitable for locoregional treatment. On the other hand, single agent CRT entails a lower rate of toxicity related treatment interruptions. Hence, in terms of mOS, a less aggressive strategy might be of advantage in this generally frail patient population.
The LAP07 study is the latest prospective randomized control trial on LAPC [11]. After the first randomization 223 patients received gemcitabine weekly and 219 patients the same CT combined with erlotinib. The second randomization step allocated those patients without tumor progression either continue the same systemic treatment (136 patients) or to receive 54 Gy CRT with capecitabine (133 patients). Median OS, which was the primary endpoint, did not differ significantly between the CRT and the CT arm (15.2 and 16.5 months; [11, 44]). In the current study, 30/31 (97%) patients with unresectable LAPC received >40 Gy, which results in a median OS of 20.4 months and 2‑year survival rates of 34%. At first sight, our findings seem to be in contrast to the results of the LAP07 study, where no survival difference was noted between patients receiving CRT with 54 Gy versus CT only. However, LAP07—like similar studies listed in supplementary Table 2—tested CRT versus CT alone, whereas the current retrospective analysis compares different dose levels (> vs. <40 Gy) within a cohort treated with RT. Thus, since the treatment characteristics of patient groups are different in these analyses, a direct comparison is—to our mind—hardly possible.
The current study is limited by its retrospective nature and the small sample size with 73 patients included between 1998 and 2016. The number of CRT patients in prospective studies is generally small compared to CT trials both in resectable and unresectable situations. In trials with postoperative CRT it is between 21 and 145 patients [6‐8, 19] (supplementary Table 1). In 2/4 (50%) of these studies [6, 8] the number of CRT patients included is smaller than in the current cohort. Considering only resected patients in our cohort (n = 42), there is still one study that is smaller [6] and another one with only three patients more than in our collective [8]. In prospective LAPC studies the total number of patients is 23 to 109, 6/8 (75%) studies include less than the current study. The number of unresected patients in our cohort is 31, in 2/8 (25%) of the mentioned prospected LAPC trials it is lower ([9‐12, 42, 43, 45, 46]; supplementary Table 2). Admittedly, a downside of the current analysis is that the group sizes are not well balanced, which reflects daily clinical practice.
Due to the inherent selection bias in retrospective studies disproportionate group sizes may lead to statistical inaccuracies so the results have to be interpreted with caution. The statistics should be understood as largely descriptive of a heterogeneous patient population and cannot be taken as a basis to draw firm conclusions. In addition, patients were treated with a variety of CRT schedules, which reflects clinical practice. Also, there are no clear cutoff criteria for more or less than 4 months of systemic treatment before CRT. This decision was left at the discretion of the treating medical oncologist and discussed in the tumor board. The retrospective application of a 4-month cutoff in our cohort was based on published literature rather than on a strict study design per se [11].
Despite these shortcomings our data confirm that CRT with threshold doses >40 Gy after at least 4 months of CT is beneficial both for resected and unresected patients with nonmetastasized pancreatic cancer.
Compliance with ethical guidelines
Conflict of interest
S. Bachmayer, G. Fastner, A. Vaszi, W. Iglseder, P. Kopp, J. Holzinger, A. Dinnewitzer, G. Rinnerthaler, S.P. Gampenrieder, K. Emmanuel, R. Greil, F. Sedlmayer and F. Zehentmayr declare that they have no competing interests.
Ethical standards
All procedures performed in the study involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. For this type of study formal consent is not required. This article does not contain any studies with animals performed by any of the authors.
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
Mit e.Med Radiologie erhalten Sie Zugang zu CME-Fortbildungen des Fachgebietes Radiologie, den Premium-Inhalten der radiologischen Fachzeitschriften, inklusive einer gedruckten Radiologie-Zeitschrift Ihrer Wahl.
Bis 11. April 2024 bestellen und im ersten Jahr 50 % sparen!
Nonmetastatic pancreatic cancer Improved survival with chemoradiotherapy > 40 Gy after systemic treatment
verfasst von
Sebastian Bachmayer, M.D. Gerd Fastner, M.D. Andrea Vaszi, M.D. Wolfgang Iglseder, M.D. Peter Kopp, Ph.D. Josef Holzinger, M.D. Adam Dinnewitzer, M.D. Gabriel Rinnerthaler, M.D. Simon Peter Gampenrieder, M.D. Klaus Emmanuel, M.D. Richard Greil, M.D. Felix Sedlmayer, M.D. Franz Zehentmayr, M.D., M.Sc.