CME

International Journal of

Radiation Oncology
biology

physics

www.redjournal.org

Clinical Investigation: Lymphoma and Leukemia

Modern Radiation Therapy for Nodal Non-Hodgkin

LymphomadTarget Definition and Dose Guidelines From
the International Lymphoma Radiation Oncology Group
Tim Illidge, MD, PhD,* Lena Specht, MD,y Joachim Yahalom, MD,z
Berthe Aleman, MD, PhD,x Anne Kiil Berthelsen, MD,k Louis Constine, MD,{
Bouthaina Dabaja, MD,# Kavita Dharmarajan, MD,z Andrea Ng, MD,**
Umberto Ricardi, MD,yy and Andrew Wirth, MD,zz, on behalf of the International
Lymphoma Radiation Oncology Group
*Institute of Cancer Sciences, University of Manchester, Manchester Academic Health Sciences Centre, The Christie
National Health Service Foundation Trust, Manchester, United Kingdom; yDepartment of Oncology and Hematology,
Rigshospitalet, University of Copenhagen, Copenhagen, Denmark; zDepartment of Radiation Oncology, Memorial SloanKettering Cancer Center, New York, New York; xDepartment of Radiotherapy, The Netherlands Cancer Institute,
Amsterdam, The Netherlands; kDepartment of Radiation Oncology and PET Centre, Rigshospitalet, University of
Copenhagen, Copenhagen, Denmark; {Departments of Radiation Oncology and Pediatrics, James P. Wilmot Cancer Center,
University of Rochester Medical Center, Rochester, New York; #Division of Radiation Oncology, Department of Radiation
Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas; **Department of Radiation Oncology,
Brigham and Womens Hospital and Dana-Farber Cancer Institute, Harvard University, Boston, Massachusetts;
yy
Radiation Oncology Unit, Department of Oncology, University of Torino, Torino, Italy; and zzDivision of Radiation
Oncology, Peter MacCallum Cancer Institute, St. Andrews Place, East Melbourne, Australia
Received Nov 15, 2013, and in revised form Jan 7, 2014. Accepted for publication Jan 8, 2014.

Radiation therapy (RT) is the most effective single modality for local control of non-Hodgkin lymphoma (NHL) and is an
important component of therapy for many patients. Many of the historic concepts of dose and volume have recently been
challenged by the advent of modern imaging and RT planning tools. The International Lymphoma Radiation Oncology Group
(ILROG) has developed these guidelines after multinational meetings and analysis of available evidence. The guidelines
represent an agreed consensus view of the ILROG steering committee on the use of RT in NHL in the modern era. The roles
of reduced volume and reduced doses are addressed, integrating modern imaging with 3-dimensional planning and advanced
techniques of RT delivery. In the modern era, in which combined-modality treatment with systemic therapy is appropriate, the
previously applied extended-field and involved-field RT techniques that

Reprint requests to: Tim Illidge, MD, PhD, University of Manchester,

The Christie NHS Foundation Trust, Institute of Cancer Sciences, Manchester M20 4BX, United Kingdom. Tel: (44) 161-446-8110; E-mail:
[email protected]
NotedAn online CME test for this article can be taken at http://
astro.org/MOC.
Int J Radiation Oncol Biol Phys, Vol. 89, No. 1, pp. 49e58, 2014
0360-3016/$ - see front matter 2014 Elsevier Inc. All rights reserved.
http://dx.doi.org/10.1016/j.ijrobp.2014.01.006

This project was supported by The Connecticut Sports Foundation and

The Global Excellence Program of the Capital Region of Denmark.
Conflict of interest: none.
AcknowledgmentsdThe authors thank Ms. Jessi Shuttleworth for
coordinating the International Lymphoma Radiation Oncology Group
guidelines committee.

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Illidge et al.

International Journal of Radiation Oncology Biology Physics

targeted nodal regions have now been replaced by limiting the RT to smaller volumes based solely on detectable nodal
involvement at presentation. A new concept, involved-site RT, defines the clinical target volume. For indolent NHL, often
treated with RT alone, larger fields should be considered. Newer treatment techniques, including intensity modulated RT,
breath holding, image guided RT, and 4-dimensional imaging, should be implemented, and their use is expected to decrease
significantly the risk for normal tissue damage while still achieving the primary goal of local tumor control.
2014 Elsevier Inc.

Introduction
The purpose of these guidelines is to provide a consensus
position on the modern approach to radiation therapy (RT)
delivery in the treatment of nodal non-Hodgkin lymphoma
(NHL) and to outline a new concept of involved-site RT
(ISRT), in which reduced treatment volumes are planned
for the effective control of involved sites of disease. The
present guidelines represent a consensus viewpoint
following face to face international meetings, examination
of available evidence, and discussion within the Steering
Committee of the International Lymphoma Radiation
Oncology Group (ILROG). The guidelines are thus based
on the best available evidence and, in its absence, on the
experience and agreed consensus of ILROG members.
Radiation therapy has been widely used in the management of malignant lymphomas and was responsible for
many of the early cures (1). Radiation therapy continues to
play an important role as a single modality for some lymphomas. More recently, combination chemotherapy and
immuno-chemotherapy with the addition of rituximab has
evolved with increasing efficacy and now plays a major role
in the management of many B-cell NHLs. Radiation therapy continues to have an important place in increasing
locoregional control in combined treatment programs for
many early-stage presentations, as well as for selected
bulky and extranodal, advanced-stage, aggressive NHL
presentations (2-5). Radiation therapy serves as the sole
treatment modality in most early-stage indolent NHL (6).
With effective curative treatment regimens there is
increasing concern for the late effects of treatment and the
quality of survivorship. Therefore, it is of paramount
importance in the delivery of RT to maintain high rates of
long-term local control while minimizing radiation exposure of surrounding normal tissues. Furthermore, it is
recognized that most recurrences in patients treated for
NHL are in sites of previous involvement and that RT is
highly effective at reducing subsequent local recurrences
(7, 8). Historic guidelines for lymphoma RT predated
modern imaging techniques that identify sites of overt
(gross) disease and effective chemotherapy that sterilizes
covert (subclinical) sites. Therefore, guidelines for lymphoma RT based on involved fields defined by anatomic
landmarks and encompassing adjacent uninvolved lymph
nodes (9) are no longer appropriate for modern, morefocused RT delivery aimed at reducing normal tissue
exposure. Although we acknowledge the lack of

randomized evidence to support radiation field size reduction, there is increasing evidence to suggest effective local
control with such reduced field sizes (10, 11).
Here we have highlighted the application of advances in
the technological expertise available in the planning and
delivery of RT and provide radiation oncologists treating
NHL with guidelines on imaging, volume determination,
and treatment planning. The focus is on adult patients with
localized nodal NHL, as well as patients with bulky sites
and residual disease in advanced stages. The treatment
approaches described include both aggressive and indolent
lymphoma. Other clinical scenarios that are discussed
include the role of RT in advanced-stage NHL, recurrent
lymphoma, and palliation of nodal NHL.

Treatment Volume Principles

Modern RT planning in lymphoma incorporates the current
concepts of volume determination as outlined in the International Commission on Radiation Units and Measurements
(ICRU) report 83 (12), based on defining a gross tumor volume (GTV) and clinical target volume (CTV), which is
expanded to create a planning target volume (PTV). The PTV
is then used to define dose coverage. This approach allows
direct comparison with the diagnostic imaging, increasing
the accuracy with which lymph node localization is defined.
An important consideration in defining target volumes is
whether RT is being used as a single treatment modality or,
alternatively, whether RT is being delivered as a consolidation therapy. In patients with disease that is refractory to
chemotherapy, RT may be administered to persistent or
residual lymphomatous sites with a higher dose and larger
volume in an attempt to obtain lasting local control,
because chemotherapy has neither sterilized the identifiable
disease nor the presumed adjacent subclinical or covert
disease. Furthermore, RT is highly effective when administered to local residual or refractory lymphoma as a
treatment component preceding or following a comprehensive salvage high-dose therapy program that includes
stem cell transplantation (13, 14).

Radiation Therapy as Primary Treatment

Radiation therapy as a single modality can be curative for
patients with localized indolent lymphoma and provides
effective treatment for patients with localized aggressive

Volume 89 Number 1 2014

nodal NHL who are unsuitable for primary chemotherapy

because of serious comorbidities. Some patients with
localized disease who remain refractory to chemotherapy
may also be appropriately treated with localized RT.
In most clinical situations that require RT as the primary
modality, the GTV should be readily visualized during
treatment preparation, and it is recommended that this is
enhanced by the use of contrast. The CTV should be more
generous in this clinical situation and also encompass lymph
nodes in the vicinity that, although of normal size, might
contain microscopic disease that will not be treated when no
chemotherapy is given. The absence of effective systemic
therapy in such cases should also influence RT dose decisions.

RT as Part of a Combined-Modality Approach

Radiation therapy is often part of the treatment program for
localized aggressive nodal lymphomas and is delivered as
consolidation therapy after systemic chemotherapy. A
combined-modality approach with abbreviated chemotherapy
may be particularly relevant in elderly patients, in whom
chemotherapy is often poorly tolerated. A significant number
of these patients are unable to tolerate the full dose and number
of courses of chemotherapy, requiring significant dose,
schedule, or cycle modifications and reductions. Many of
these patients with localized disease are potentially cured with
abbreviated chemotherapy and consolidation RT. For this
group of patients the use of RT is particularly important, given
the lack of effective salvage options in relapsed disease.
Recent data suggest an important role of consolidation RT in
improving outcome for patients when delivered to sites of
initial bulky and extranodal disease, even in patients with
advanced-stage disease that achieved a complete response
after chemotherapy (2, 3). In this situation where consolidation ISRT is used, the GTV may be markedly affected by
systemic chemotherapy, and it is therefore particularly
important to review the prechemotherapy imaging and outline
the prechemotherapy volume on the simulation CT study as
prechemotherapy GTV.

Volume Definitions for Radiation Therapy

Planning of Lymphoma
Volume of interest acquisition
Planning RT for lymphoma is based on obtaining a 3dimensional (3D) simulation study using either a CT
simulator, a positron emission tomography (PET)-CT
simulator, or an MRI simulator. If PET and/or CT information has been obtained separately or before simulation, it
should be fused electronically with the CT simulation study
so original volumes of interest can be displayed on the
simulation study. Alternatively, careful manual transfer of
volumes may be carried out if electronic transfer is not
possible. Ideally, imaging studies that may provide

Modern RT for nodal NHLdILROG guidelines

51

planning information should be obtained in the treatment

position and using the planned immobilization devices.

Prechemotherapy (or presurgery) GTV

Imaging abnormalities suggestive of lymphomatous
involvement obtained before any intervention that might
have affected tumor volume should be outlined on the
simulation study, because these volumes should (in most
situations) be included in the CTV.

No chemotherapy or postchemotherapy GTV

The primary imaging of untreated lesions or postchemotherapy GTV should be outlined on the simulation
study and is always part of the CTV.

CTV determination
The CTV encompasses in principle the original (before any
intervention) GTV, even if extended beyond the involved
tissue or organ. Yet normal structures such as lungs, kidneys, and muscles that were clearly uninvolved, though
previously displaced by the GTV, should be excluded from
the CTV according to clinical judgment. In outlining the
CTV the following points should be considered: quality and
accuracy of imaging; concerns of changes in volume since
imaging; spread patterns of the disease; potential subclinical involvement; and adjacent organs constraints.
If distinct nodal volumes are involved but <5 cm apart,
they can potentially be encompassed in the same CTV.
However, if the involved nodes are >5 cm apart, they can
be treated with separate fields using the CTV-to-PTV
expansion guidelines as outlined below.

Determination of internal target volume

Internal target volume (ITV) is defined in ICRU report 62
(10) as the CTV plus a margin taking into account uncertainties in size, shape, and position of the CTV within
the patient. The ITV is mostly relevant when the target is
moving, most commonly in the chest and upper abdomen
with respiratory movements (15). The optimal way is to use
4-dimensional (4D) CT simulation to obtain the ITV margins. Alternatively, the ITV may be determined by fluoroscopy or estimated by an experienced clinician. In the
chest or upper abdomen margins of 1.5-2 cm in the superior-inferior direction may be necessary. In sites that are
unlikely to change shape or position during or in between
treatments (eg, the head and neck), outlining the ITV is not
required.

Determination of PTV
The PTV is the volume that takes into account the CTV
(and ITV, when relevant) and also accounts for setup

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Illidge et al.

uncertainties in patient positioning and alignment of the

beams during treatment planning and through all treatment
sessions.
The practice of determining the PTV varies across institutions. The clinician and/or treatment planner adds the
PTV and applies margins that depend on estimated setup
variations that are a function of immobilization device,
body site, internal organ motion, and patient cooperation.
In general, margins for uncertainties are based on probability levels. Margins should not be added linearly because
this will lead to large margins based on the most extreme
and least likely situations (16).

Determination of organs at risk

International Journal of Radiation Oncology Biology Physics

treatment position and with involvement of the radiation

oncologist.
The use of diagnostic contrast-enhanced CT is recommended to help to delineate nodal stations and differentiate
nodes from vessels. In centers where PET/CT can be done
with contrast, this can obviate the need for a separate
contrast-enhanced investigation. PET/CT scans can be done
with contrast without interfering with the attenuation
correction (18). For abdominal and pelvic locations, oral
contrast should be used. Four-dimensional CT imaging as
part of the simulation may be helpful in determining the
ITV for sites that move with respiration. Acquiring this
high-quality imaging is fundamental to high-quality RT
planning.

The organs at risk (OARs) are critical normal structures that

can manifest adverse effects from radiation, usually
dependent on the radiation dose. The OARs relevant to
treatment planning or the prescribed dose should be outlined on the simulation study. The planner should calculate
dose-volume histograms, and the plan should be evaluated
in consideration of the expected normal tissue complication
probability.

Immobilization

RT dose considerations

Treatment techniques

Historically, doses for nodal NHL have varied between 30

Gy and 55 Gy using conventional 1.8- to 2.0-Gy fractionation schedules. For aggressive NHL, radiation doses of up
to 40-55 Gy after chemotherapy have been used in clinical
trials (17). Most retrospective series on RT alone for
follicular lymphoma and marginal zone lymphoma used
doses of 35-45 Gy and 30 Gy, respectively. More recently,
differences in the relative radiosensitivity of the commonest
indolent lymphomas and aggressive lymphomas have been
recognized. A large prospective, randomized trial was undertaken in the United Kingdom comparing 24 Gy with 40
Gy in low-grade (predominantly follicular) and 30 Gy
with 40 Gy in high grade (predominantly diffuse large Bcell lymphoma). Importantly, most patients had also
received chemotherapy, and RT was given as consolidation.
More than 1000 patients were randomized, and at a median
follow-up of 5.6 years, no differences between the highand low-dose treatment arms within each lymphoma subtype were seen (6).

Radiation Treatment Planning

Role of imaging in radiation planning
Lymphoma staging and response assessment is based on 3D
imaging, with CT supplemented by functional imaging
using fluorodeoxyglucose-PET. Optimally, these images
should be acquired with the patient in the radiation

A planning CT should be taken with the patient having

appropriate immobilization. In the case of disease in the
head and neck regions, a customized thermoplastic mask
should be used. Contiguous slices with a slice thickness of
no more than 3-5 mm should be taken through the regions
of interest.

The treating radiation oncologist should make a clinical

judgment as to which treatment technique to use, based on
comparisons of treatment plans and dose-volume histograms with different techniques. In some situations, conventional anteroposterior-posteroanterior techniques may
be preferred, because the smallest volume of normal tissue
would be irradiated with this technique, albeit to the
full-prescribed dose. In other situations more-conformal
techniques, such as intensity modulated RT (IMRT), arc
therapy, or tomotherapy, may offer significantly better
sparing of critical normal structures, usually at the price of
a larger total volume of normal tissue irradiated, albeit to a
lower dose. The potential benefits and risks of proton
therapy for patients with lymphoma are not yet fully understood and require further investigation. Recommendations as to which technique to use in the individual case
cannot be made, and careful consideration must be given to
choosing the technique that the clinician considers to offer
the lowest risk of significant late toxicity for that patient.

3D planning and RT approach

The use of 3D outlining is highly recommended and is
essential for determining the CTV, PTV, and OARs. Standard 3D conformal treatment is appropriate in many cases.
However, in some clinical scenarios IMRT, inspiration
breath-hold techniques, and image guided RT may offer
significant and clinically relevant advantages and should be
used. Image guided RT verification may be indicated for

Volume 89 Number 1 2014

sites that are adjacent to critical dose-limiting normal

structures, especially in situations that entail retreatment.

Intensity modulated RT
Intensity modulated RT plans may provide improved PTV
coverage (Dmean, V95, conformity index) compared with
3D-conformal RT. In selected patients with mediastinal
involvement, IMRT reduces pulmonary toxicity predictors
(lower values for Dmean and V20) and allows for superior
protection of the heart and coronary arteries. This dosimetric gain is normally more evident in situations in which
a large PTV involves the anterior mediastinum (19, 20).
Although the advantages of IMRT include the tightly
conformal doses and steep gradient next to normal tissues,
target definition and delineation and treatment delivery
verification need even more attention than with conventional RT, to avoid the risk of tumor geographic miss and
subsequent decrease in tumor control. Image guidance may
be required to ensure that the target is optimally covered
during the administration of therapy. For IMRT in mediastinal lymphoma, the use of 4D-CT for simulation and the
adoption of strategies to deal with respiratory motion during treatment delivery may be important. The highly
conformal treatment techniques enable retreatment of relapsing patients without exceeding the tolerance of critical
normal structures such as the spinal cord (21).

Techniques to deal with tumor motion in the

thoracic region
The use of 4D imaging or deep-inspiration breath-hold
technique for disease sites that are significantly affected by
respiratory motion is encouraged. In patients with
involvement of the mediastinum, irradiation of the mediastinum is frequently indicated. Several studies have
demonstrated that treatment in inspiration enables significant sparing of lung and heart, and this technique is recommended in selected cases (22).

Dose Constraints
Previous experience comes from patients treated over the
last 5 decades, for whom extended fields and higher doses
resulted in significant risks of morbidity and mortality
(23, 24). Hence, it is important to use the ISRT treatment
technique described below and to choose the treatment plan
that is estimated to provide the lowest risk of long-term
complications for the individual patient. Consideration
should be given to factors such as gender, age, and
comorbidities.
An integral part of calculating conformal treatment
plans is the use of dose constraints for different normal
tissues. However, the dose constraints used for treatment
planning of solid tumors are in most cases not well suited
for the planning of RT for lymphomas, because the

Modern RT for nodal NHLdILROG guidelines

53

prescribed dose to the target is much lower. Radiation doses

to all normal structures should be kept as low as possible to
minimize the risk of long-term complications, but some
structures are more critical than others. Ideally, normal
tissue complication probability models for all relevant risk
organs with a special focus on the low-dose region of 20-40
Gy should be combined for each treatment plan. At present
no validated guidelines exist that allow optimization based
on weighted estimates of risks of different long-term
complications. Research into the development of methods
for this purpose, based on the available dose-response data
for different tissues and endpoints, is ongoing (25). At a
minimum, however, the doses to normal structures should
at least conform to well-documented dose constraints that
are applied to the treatment of solid tumors (26).
The risk of late RT-induced side effects should always
be balanced via multidisciplinary discussion associated
with the risks to the patient of local recurrence if RT is not
given. In many situations with aggressive nodal lymphoma,
particularly in older age groups for example, the risk and
morbidity of disease recurrence outweigh the unlikely risk
of late effects such as secondary malignancies.

Aggressive Nodal Lymphomas

Involved-site RT
The concept of ISRT is that the prechemotherapy GTV determines the CTV as discussed in more detail in the ILROG
guidelines on Hodgkin lymphoma (27). This concept assumes that chemotherapy eradicates adjacent or regional
microscopic disease, and ISRT targets the identifiable prechemotherapy disease. The irradiated volume is significantly
smaller with ISRT than with involved-field RT because all
adjacent lymph nodes that appear grossly uninvolved are not
purposely treated. However, ISRT accommodates cases in
which optimal prechemotherapy imaging, specifically highquality imaging performed in the treatment-planning position, is not available to the radiation oncologist. In these
situations it is not possible to reduce the CTV to the same
extent as with optimal imaging. In ISRT, clinical judgment in
conjunction with the best available imaging is used to contour a CTV that will accommodate the uncertainties in
defining the prechemotherapy GTV in each individual case.
For these reasons ISRT is a slightly larger irradiated volume
than involved-node RT.
In the situation in which prechemotherapy imaging (eg,
CT, PET, or MRI) of all the initially involved lymphoma
sites of disease is available, but image fusion with the
postchemotherapy planning CT scan is not possible, the
radiation oncologist will have to contour the target volume
on the planning CT scan. The prechemotherapy images are
used for contouring on the CT scan. Allowances should be
made for the uncertainty of the contouring and differences
in positioning by including a larger volume in the CTV. The

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Illidge et al.

more uncertainty there is, the larger the contoured volume

will need to be.
If no prechemotherapy imaging is available (eg, patients
presenting with neck disease but whose staging fails to
include imaging of the neck), the situation is more challenging. The radiation oncologist must gather as much
clinical information as possible concerning the pre- and
postchemotherapy location of the pathological lymph
node(s). The CTV should be contoured taking into account
all of this information, making generous allowances for the
many uncertainties in the process.

Clinical target volume

The CTV encompasses the original lymphoma volume
modified for normal tissue boundaries and expanded to
accommodate uncertainties in determining the prechemotherapy volume as outlined above.

International Journal of Radiation Oncology Biology Physics

The ITV should be added to the CTV only in situations

in which internal organ movement is of concern. The CTV
will be expanded further to create the PTV. In situations in
which RT is the primary treatment, larger margins to
encompass subclinical disease need to be applied.
Examples of ISRT CTVs are shown for aggressive nodal
lymphomas in the neck (Fig. 1), mediastinum (Fig. 2), and
axilla (Fig. 3).

Larger-field RT
The role of larger-field RT is now limited essentially to
salvage treatment in patients who fail chemotherapy and are
unable to embark upon more-intensive salvage treatment
schedules. Such salvage cases are usually addressed on a
case-by-case basis, and it is not feasible to produce guidelines given the diversity of individual cases. As such, there
are no data to support the use of extended fields that can

Fig. 1. (A-D) Patient with diffuse large B-cell lymphoma Clinical Stage (CS) 1A in the left neck. (A) Prechemotherapy CT
scan with the contoured initially involved lymphoma volume (GTVCT) in red. (B) Postchemotherapy planning CT scan with
the prechemotherapy GTVCT transferred by image fusion. (C) Postchemotherapy planning CT scan. The clinical target
volume in pink is the tissue volume that contained lymphoma initially. It is created by modifying the GTVCT to take into
account tumor shrinkage and other anatomic changes, allowing for uncertainties in contouring and differences in position. (D)
The postchemotherapy planning CT scan with the final clinical target volume, which encompasses all of the initial lymphoma
volume while still respecting normal structures that were never involved by lymphoma.

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Modern RT for nodal NHLdILROG guidelines

55

Fig. 2. (A-H) Patient with diffuse large B-cell lymphoma CS 2A with mediastinal involvement. (A) Prechemotherapy
positron emission tomography (PET)/CT scan showing the initially PET-positive volume. (B) Prechemotherapy CT part of
the PET/CT-scan with the contoured initially PET-positive involved lymphoma volume in blue. (C) Prechemotherapy CT
scan with the contoured initially involved lymphoma volume (GTVCT) in red, including both PET-positive and PET-negative
parts of the lymphoma. (D) Postchemotherapy planning CT scan with the prechemotherapy GTVCT transferred by image
fusion. (E) Postchemotherapy planning CT scan. The clinical target volume in pink is the tissue volume that contained
lymphoma initially. It is created by modifying the GTVCT to take into account tumor shrinkage and other anatomic changes,
allowing for uncertainties in contouring and differences in position. (F) Postchemotherapy planning CT scan with the final
clinical target volume, which encompasses all of the initial lymphoma volume while still respecting normal structures that
were never involved by lymphoma. (G) Coronal image. (H) Sagittal image.
cause increased normal tissue toxicity and compromise the
safety of subsequent therapy such as stem cell transplant.

Advanced-stage aggressive NHL

In patients with advanced-stage aggressive nodal NHL with
sites of original bulky disease or extranodal disease, RT may

be considered at the outset of combined-modality treatment

planning (2, 5). In this clinical situation the prechemotherapy
GTV should be considered in determining the CTV. In
contrast, in cases of isolated or solitary residual PETpositive disease, RT is often recommended after systemic
chemotherapy. In the latter situation, the CTV is defined as
residual mass(es) containing PET-positive areas on the

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International Journal of Radiation Oncology Biology Physics

Fig. 3. (A-C) A 48-year-old man with stage 2AX diffuse large B-cell lymphoma of the left axilla presented with a rapidly
growing underarm mass. (A) Baseline positron emission tomography (PET)/CT imaging shows extent of disease. (B) After 6
cycles of Rituximab-Cyclophosphamide, Adriamycin, Vincristine, Prednisolone (R-CHOP) fluorodeoxyglucose uptake
resolved, leaving residual CT abnormality only. (C) Treatment volumes are outlined on the treatment planning scan according
to International Commission on Radiation Units and Measurements guidelines; orange contour denotes postchemotherapy
gross tumor volume, red denotes prechemotherapy gross tumor volume, pink denotes clinical target volume, and light blue
denotes planning target volume.
postchemotherapy scan. A dose of 30-40 Gy to sites of residual disease is recommended.

Refractory and recurrent aggressive NHL

Despite the success of primary therapy for aggressive NHL,
a significant percentage of patients will manifest primary
refractory disease or relapse after achieving a complete
response. For this group of patients, salvage chemotherapy
followed by high-dose chemotherapy and autologous stem
cell transplantation (ASCT) is a common treatment
approach. Radiation therapy to sites of recurrent or refractory disease may enhance local disease control (28-31).
An example is shown in Figure 4. Patients with primary
refractory disease unsuitable for transplantation may
benefit from RT to doses up to 55 Gy (32-34).
Patients with primary refractory disease unsuitable for
transplantation may benefit from RT for symptom palliation
or disease control to prevent symptoms; doses will depend

on normal tissue tolerance. Patients who are candidates for

salvage therapy may benefit from irradiation either before
or immediately after ASCT to sites of dominant local
recurrence or residual disease. In patients with complete
response to salvage chemotherapy, a dose of 30-40 Gy
before or after ASCT is recommended. If given after ASCT,
there are no data to suggest the optimal timing of when the
RT should be delivered, but established practice is to
deliver RT as soon possible after the patient has recovered
from the acute side effects of ASCT, ideally within 6-8
weeks after stem cell infusion (11, 12).
For peritransplant irradiation in patients with relapsed or
refractory disease, the radiation volumes are constructed
using the guidelines provided above but determined on an
individual patient basis depending on the sites of disease at
initial diagnosis and at relapse. Consideration is given to
previous RT and to the radiosensitivity of normal tissues
and organs that would be inadvertently irradiated. Radiation therapy volumes are localized to encompass the known

Fig. 4. (A-C) A 63-year-old man with relapsed diffuse large B-cell lymphoma involving the right groin. After salvage
chemotherapy, he was referred for involved-site radiation therapy to the groin before stem cell transplant. (A) Baseline
imaging at relapse. (B) Postchemotherapy imaging and (C) simulation imaging are performed with slight differences in
patient positioning, in turn accounted for and reflected in a generously drawn clinical target volume (pink contour in C). In
(C), the orange contour denotes postchemotherapy gross tumor volume, red denotes prechemotherapy gross tumor volume,
and light blue denotes planning target volume. PET Z positron emission tomography.

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Modern RT for nodal NHLdILROG guidelines

57

Fig. 5. (A, B) A 63-year-old woman with stage 1A follicular lymphoma of the right inguinal region presented with a selfpalpated right groin mass. Diagnosis was established upon excision by a general surgeon. At simulation the patient was
placed in frog-leg position, and the scar was wired. Only CT abnormality remained (A). (B) Red contour denotes the prechemotherapy gross tumor volume, pink denotes clinical target volume, and light blue denotes planning target volume.
site(s) of disease recurrence, without prophylactic inclusion
of adjacent lymph nodal stations.

Indolent Nodal Lymphomas

Localized indolent lymphoma
For the potentially curative treatment of localized earlystage (I and II) disease, RT is used as the primary treatment
approach. The CTV must be designed to encompass suspected subclinical disease based on the preintervention
GTV imaging. The CTV should incorporate GTV and
include as a minimum adjacent lymph nodes in that site and
a generous margin dictated by the clinical situation. An
example is shown in Figure 5. For potentially curative RT
to stage IA/IIA disease a dose of 24-30 Gy in 12-15 fractions (6, 35) is recommended.

Advanced-stage indolent lymphoma

A number of retrospective cohort studies have demonstrated that patients with advanced or recurrent indolent
lymphoma treated with very low doses of only 4 Gy in 2
fractions achieve high response rates, and the treatment
provides effective palliation for localized symptomatic
disease (36-41). Initial results from a prospective, randomized trial in the United Kingdom comparing 4 Gy with
24 Gy for follicular lymphoma (41) suggest that there is
only a modest decrease in local control with the lower dose.
In some cases patients may benefit from RT to sites of
bulky disease, such as within the retroperitoneum where
monitoring clinical progression is challenging and progressive disease may lead to organ failure. These patients
require higher doses of 24-30 Gy to provide durable longterm local disease control.

Conclusion
Modern RT for nodal NHL is a highly individualized
treatment restricted to limited treatment volumes. Modern

imaging and RT techniques should be used to limit the

amount of normal tissue being irradiated, thus minimizing
the risk of long-term complications. The newly defined
concept of ISRT represents a significant reduction in the
volume included in the previously used involved-field RT.
Radiation oncologists treating NHL should be involved as
part of the multidisciplinary team in the initial management
plan and attempt to introduce imaging procedures up front
before initiation of chemotherapy. Such an integrated
collaborative multidisciplinary approach will enable the
optimal outcome for patients with nodal NHL.

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