European Urology
The Shifting Landscape of Genitourinary Oncology During the COVID-19 Pandemic
and how Italian Oncologists Reacted: Results from a National Survey
--Manuscript Draft--
Manuscript Number: EURUROL-D-20-00508
Article Type: Research Letter
Keywords: COVID-19; genitourinary cancers; immunotherapy; Medical Oncology; patient
management
Corresponding Author: Laura Marandino
Fondazione IRCCS Istituto Nazionale dei Tumori
ITALY
First Author: Laura Marandino, M.D.
Order of Authors: Laura Marandino, M.D.
Massimo Di Maio, Prof.
Giuseppe Procopio
Saverio Cinieri
Giordano Domenico Beretta
Andrea Necchi, M.D.
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The authors listed below have made substantial contributions to the intellectual content of
the paper in the various sections described below.
(list appropriate author next to each section – each author must be listed in at least 1 field.
More than 1 author can be listed in each field.)
_ conception and design Laura Marandino, Massimo Di Maio, Andrea Necchi
_ acquisition of data All authors
_ analysis and interpretation of data Laura Marandino, Massimo Di Maio, Andrea Necchi
_ drafting of the manuscript Laura Marandino, Massimo Di Maio, Andrea Necchi
_ critical revision of the manuscript for
important intellectual content All authors
_ statistical analysis Laura Marandino, Massimo Di Maio, Andrea Necchi
_ obtaining funding Not applicable
_ administrative, technical, or
material support Not applicable
_ supervision Andrea Necchi, Massimo Di Maio
_ other (specify) Not applicable
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None of the contributing authors have any conflicts of interest, including specific financial
interests and relationships and affiliations relevant to the subject matter or materials
discussed in the manuscript.
OR
I certify that all conflicts of interest, including specific financial interests and relationships
and affiliations relevant to the subject matter or materials discussed in the manuscript (eg,
employment/ affiliation, grants or funding, consultancies, honoraria, stock ownership or
options, expert testimony, royalties, or patents filed, received, or pending), are the following:
(please list all conflict of interest with the relevant author’s name):
Massimo Di Maio received advisory board or consultant fees from Merck Sharp & Dohme,
Bristol Myers Squibb, Eisai, Janssen, Astellas, AstraZeneca, Pfizer, Takeda and institutional
research grant from Tesaro.
Giuseppe Procopio received advisory board or consultant fees from AstraZeneca, Bayer,
Bristol Myers Squibb, Janssen, Ipsen, Merck Sharp & Dohme, Novartis, Pfizer.
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and/or work are clearly identified in the manuscript.
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material in the study are also listed below:
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any, are clearly identified hereunder:
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Design and conduct of the study
Collection of the data
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Analysis
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Preparation
Review
Approval of the manuscript
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No funding or other financial support was received.
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The Shifting Landscape of Genitourinary Oncology During the COVID-19 Pandemic
and how Italian Oncologists Reacted: Results from a National Survey
Laura Marandino a,
*, Massimo Di Maio b
, Giuseppe Procopio a
, Saverio Cinieri c
, Giordano
Domenico Beretta d
, Andrea Necchi a
The outbreak of the novel coronavirus disease-19 (COVID-19) caused by severe acute
respiratory syndrome corona virus 2 (SARS-CoV-2) suddenly revolutionized the way we take
care of patients with cancer. This situation was dramatically felt in geographic regions where
the spread of the infection, qualified as a pandemic by the World Health Organization on
March 11, 2020, was causing an emergency health care situation. After the original outbreak
in Wuhan City, Hubei Province, China, the infection rapidly spread throughout the world in
more than 199 countries (www.worldometers.info/coronavirus). At the time of writing, Italy,
and the Lombardy region in particular, was ranked first in terms of COVID-19-associated
deaths, making this region one of the most critical hotspots of the COVID-19 outbreak [1]. In
Italy, a total of 10 779 deaths had been reported by the health care authorities and 3906
patients required intensive care unit (ICU) admittance at the time of writing.
Patients diagnosed with cancer have a higher risk of developing serious complications and
dying from COVID-19 [2,3]. Besides this consideration, a number of critical dilemmas have
emerged regarding indications for cancer therapies and management of associated side
effects. General clinical recommendations for patients with genitourinary cancers have
already been published, obviously biased by the lack of actual data for most of the guidelines
[4].
It is important to anticipate the shifting landscape that will probably occur in the management
of patients with cancer to better prepare health care providers and systems for future needs. In
March 2020 we therefore carried out a nationwide survey among Italian medical oncologists
that focused on the management of patients with genitourinary malignancies.
The survey was endorsed by and conducted through the Associazione Italiana di Oncologia
Medica (AIOM) network, and took the form of an online questionnaire sent to all AIOM
members.
A total of 72 physicians provided feedback; their general characteristics are shown in
Supplementary Table 1. The questions and corresponding results are shown in Figure 1. In
general, there was consensus among oncologists to pursue treatment, possibly without delays
or interruptions, for patients with locally advanced or metastatic disease for which an
induction or first-line therapy option is indicated in guidelines, particularly for patients
suffering from prognostically aggressive disease requiring timely treatment (Fig. 1A–H). A
higher proportion of physicians were willing to consider delays or interruption for clinical
settings characterized by more indolent disease or treatments associated, on average, with
clinical benefit of lower magnitude. Of note, despite the public health care emergency, Italian
oncologists were still in favor of close adherence to guidelines regarding administration of
perioperative therapies, such as neoadjuvant chemotherapy in patients with clinical T3–
4N0M0 urothelial bladder cancer (Fig. 1C,D) and adjuvant therapy in high-risk, clinical stage
I germ-cell tumors (Fig. 1F,G). Overall, although the main factor taken into account for
treatment decisions was its proven survival benefit, the number of hospital visits ranked
second, ahead of other factors usually considered important in clinical decisions.
Lastly, two important notions emerged from this survey. First, Italian oncologists are still in
favor of considering delivery of the best treatment option for genitourinary cancer patients
through inclusion in clinical trials (61%), although most of them (54%) underlined the
unavoidable more stringent selection and the need to face severe logistic difficulties, as
Manuscript
indicated in Fig. 1I. Second, although the risks associated with immune checkpoint inhibitors
in the present pandemic context are not well defined, most of the respondents would justify
interruption of therapy only after case-by-case discussions with patients with a sustained
response during treatment, or would consider skipping some doses to reduce the number of
hospital visits (Fig. 1M).
Implementation of telemedicine will be critical in managing follow-up visits and oral drug
delivery, as is currently done in several institutions nationwide.
This survey provides a snapshot of the opinion of Italian oncologists regarding the
management of patients with genitourinary malignancies. Similar considerations would
probably apply to other solid tumors. In our opinion, the main message is that in spite of huge
sudden changes in a geographic area representing an epicenter of the COVID-19 pandemic,
oncologists are still determined to achieving treatment delivery as close as possible to clinical
guidelines or routine clinical practice, at least for treatments supported by evidence of a
clinically relevant gain in life expectancy. In the setting of advanced disease without curative
intent, a non-negligible number of oncologists would delay treatment initiation (or consider
interruption) in the second or further lines of treatment associated with a lower clinical
benefit. For patients who deserve a systemic treatment with curative intent, we should still
rely on the multidisciplinary approach among several other specialists. This continuing
collaboration will require profound organizational changes, primarily related to the obvious
delays in biopsies or radical surgical interventions that were promptly outlined by Italian
urologists [5].
Conflicts of interest: Massimo Di Maio has received advisory board or consultant fees from
Merck Sharp & Dohme, Bristol Myers Squibb, Eisai, Janssen, Astellas, AstraZeneca, Pfizer,
and Takeda and an institutional research grant from Tesaro. Giuseppe Procopio has received
advisory board or consultant fees from AstraZeneca, Bayer, Bristol Myers Squibb, Janssen,
Ipsen, Merck Sharp & Dohme, Novartis, and Pfizer. The remaining authors have nothing to
disclose.
References
1. Grasselli G, Pesenti A, Cecconi M. Critical care utilization for the COVID-19 outbreak in
Lombardy, Italy: early experience and forecast during an emergency response. JAMA. In
press. https://doi.org/10.1001/jama.2020.4031
2. Liang W, Guan W, Chen R, et al. Cancer patients in SARS-CoV-2 infection: a nationwide
analysis in China. Lancet Oncol 2020;21:335–7.
3. Zhang L, Zhu F, Xie L, et al. Clinical characteristics of COVID-19-infected cancer
patients: a retrospective case study in three hospitals within Wuhan, China. Ann Oncol. In
press. https://doi.org/10.1016/j.annonc.2020.03.296
4. Gillessen Sommer S, Powles T. Advice regarding systemic therapy in patients with
urological cancers during the COVID-19 pandemic. Eur Urol. In press.
5. Naspro R, Da Pozzo LF. Urology in the time of corona. Nat Rev Urol. In press.
https://doi.org/10.1038/s41585-020-0312-1
Fig. 1 – Questions and corresponding answers collected during the survey.
a
Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori,
Milan, Italy
b
Department of Oncology, University of Turin, Azienda Ospedaliera Ordine Mauriziano,
Turin, Italy
c
Medical Oncology & Breast Unit, Antonio Perrino Hospital, Brindisi, Italy
d
Medical Oncology Department, Humanitas Gavazzeni Clinic, Bergamo, Italy
* Corresponding author. Department of Medical Oncology; Fondazione IRCCS Istituto
Nazionale dei Tumori, Via G. Venezian 1, 20133 Milan, Italy. Tel. +39 02 23902402; Fax:
+39 02 23903150.
E-mail address: laura.marandino@istitutotumori.mi.it (L. Marandino).
RENAL CELL CARCINOMA
• Do you consider it appropriate to evaluate a delay in
treatment initiation in these clinical settings?
56
26
9
35
16
44
62
36
0% 20% 40% 60% 80% 100%
Metastatic renal cell carcinoma –
Third and further lines
Metastatic renal cell carcinoma -
Second Line
Metastatic renal cell carcinoma –
First Line; Intermediate/Poor risk
Metastatic renal cell carcinoma –
First Line; Favorable risk
Yes
No
Figure 1A
figure one
RENAL CELL CARCINOMA
• Do you consider it appropriate to evaluate interruption
of treatment in these clinical settings?
44
55
22
33
3
27
16
49
37
68
0% 20% 40% 60% 80% 100%
Metastatic renal cell carcinoma –
Long responders to
Antiangiogenic Drugs
Metastatic renal cell carcinoma –
Long responders to Immunotherapy
Metastatic renal cell carcinoma –
Second and further Lines,
Antiangiogenic Drugs
Metastatic renal cell carcinoma -
Second and further Lines,
Immunotherapy
Metastatic renal cell carcinoma –
First Line
Yes
No
Figure 1B
UROTHELIAL CANCER
• Do you consider it appropriate to evaluate NOT starting
a systemic treatment in these clinical settings?
38
15
10
38
33
56
61
33
0% 20% 40% 60% 80% 100%
Muscle-invasive bladder cancer–
Adjuvant therapy
Muscle-invasive bladder cancer–
Neoadjuvant therapy, in case of
long waiting list for radical surgery
Muscle-invasive bladder cancer
cT3-4N0 – Neoadjuvant therapy
Muscle-invasive bladder cancer
cT2N0 – Neoadjuvant therapy
Yes
No
Figure 1C
UROTHELIAL CANCER
• Do you consider it appropriate to evaluate a delay
in treatment initiation in these clinical settings?
58
38
8
15
13
33
63
56
0% 20% 40% 60% 80% 100%
Metastatic Urothelial Cancer -
Second and further lines
Metastatic Urothelial Cancer- First
Line, in patients without visceral
disease or rapid progression
Metastatic Urothelial Cancer- First
Line, all cases
Locally advanced disease N+
Yes
No
Figure 1D
UROTHELIAL CANCER
• Do you consider it appropriate to evaluate interruption
of treatment in these clinical settings?
58
37
51
61
4
11
35
20
10
66
0% 20% 40% 60% 80% 100%
Metastatic Urothelial Cancer - Second and
further lines, long responders to
immunotherapy
Metastatic Urothelial Cancer - Second and
further lines, immunotherapy regardless of
the number of cycles administered
Metastatic Urothelial Cancer - Second and
further lines, chemotherapy
Metastatic Urothelial Cancer - First Line,
after 4 cycles of platinum-based
chemotherapy
Metastatic Urothelial Cancer - First Line,
regardless of the number of cycles
administered
Yes
No
Figure 1E
GERM CELL TUMOURS
• Do you consider it appropriate to evaluate NOT starting
a systemic treatment in these clinical settings?
34
16
25
38
31
53
43
30
0% 20% 40% 60% 80% 100%
In all these cases, I would request an
opinion from a referral center
Stage I non seminoma - adjuvant
therapy; in case of vascular invasion
Stage I non seminoma - adjuvant
therapy; all cases
Stage I seminoma - adjuvant therapy
Yes
No
Figure 1F
GERM CELL TUMOURS
• Do you consider it appropriate to evaluate a delay in
treatment initiation in these clinical settings?
35
22
5
9
25
28
49
66
60
46
0% 20% 40% 60% 80% 100%
In all these cases I would request an
opinion from a referral center
Advanced disease - Second Line
Advanced disease - Poor prognosis
risk group
Advanced disease - Intermediate
prognosis risk group
Advanced disease - Good prognosis
risk group
Yes
No
Figure 1G
PROSTATE CANCER
• Do you consider it appropriate to evaluate a delay in
treatment initiation in these clinical settings?
50
56
15
25
21
15
56
47
0% 20% 40% 60% 80% 100%
Metastatic castration-resistant prostate
cancer – Second and further lines
Metastatic castration-resistant prostate
cancer – First Line, absence of visceral
disease and asymptomatic patient
Metastatic castration-resistant prostate
cancer – First Line, regardless of
disease characteristics
Newly diagnosed hormone-sensitive
metastatic prostate cancer – high
volume
Yes
No
Figure 1H
CLINICAL TRIALS
• Do you consider it appropriate to enrol patients in clinical
trials during the emergency period?
28, 39%
5, 7%
39, 54%
No, due to concerns
about logistics and
human resources
Yes, in all cases where
clinical trials are
available
Yes, for selected
patients and in case of
favourable logistics
Figure 1I
ORAL ANTICANCER THERAPY
• How are you managing patients receiving oral anticancer
drugs during this emergency period?
20
27
30
52
14
Drug interruption for patients who report toxicity at
telephone interview/mail conversation and update
through telephone interview/mail
Physical examination for patients who report toxicity at
telephone interview/mail conversation
Drug dispensation for more than one cycle of treatment
Telephone interview/Mail conversation + blood tests in
a lab near patient’s residence and drug dispensation
directly in the hospital pharmacy/home delivery
My clinical practice has not changed
0 10 20 30 40 50 60
Figure 1L
(20%)
(73%)
(42%)
(38%)
(28%)
Respondents
IMMUNOTHERAPY
• Do you consider it appropriate to evaluate treatment
interruption for patients receiving immunotherapy
during the emergency period?
7, 10%
2, 3%
6, 8%
33, 46%
20, 28%
4, 5% Yes, in case of prolonged complete
response
Yes, in case of prolonged partial
response
Yes, in case of prolonged complete
or partial response
Yes, but only evaluating case by
case in case of prolonged complete
or partial response
No, but I consider to «skip» some
cycle to reduce hospital visits
No, due to the lack of solid
evidence
Figure 1M
CHOICE OF TREATMENT
• What are the main factors that you consider in the choice
of treatment during this emergency period? (max 2
choices)
22
16
13
18
11
53
Number of required visits in the hospital
Route of administration (ev/os)
Toxicity
Quality of life benefit
Progression free survival benefit
Proven overall survival benefit
0 20 40 60
(31%)
(22%)
(18%)
(25%)
(15%)
(74%)
Figure 1N Respondents
FOLLOW-UP
• How are you managing follow-up of off-treatment
patients during this emergency period?
2, 3%
6, 8%
62, 86%
2, 3%
Follow-up visits are
continuing
Follow-up visits have been
reduced
Follow-up visits have been
cancelled and they are
carried out through
telephone/mail
Follow-up visits have been
cancelled and we are still
unable to carry follow-up in
an alternative way
Figure 1O
CHANGE IN CLINICAL PRACTICE
• To what extent has the public health emergency changed
your clinical practice? (0 = minimum; 10 = maximum)
0 0 0
1
4
7
12
17
21
10
1 2 3 4 5 6 7 8 9 10
0
5
10
15
20
25
Figure 1P
For TS.
Figures.
Please use sentence case throughout (no change to acronyms).
Ensure all data are legible/visible.
Change ‘max 2 choices’ to ‘max. two choices’.
Ensure one space between digits and opening bracket.
INSTRUCTION TO TYPE SETTER
Supplementary Table 1
Click here to access/download
Supplementary file
RLE-D-20-00508_Suppl Table
1_compuscript_mk_edited.docx

The Shifting Landscape of Genitourinary Oncology During the Covid-19 Pandemic and How Italian Oncologist Reacted

  • 1.
    European Urology The ShiftingLandscape of Genitourinary Oncology During the COVID-19 Pandemic and how Italian Oncologists Reacted: Results from a National Survey --Manuscript Draft-- Manuscript Number: EURUROL-D-20-00508 Article Type: Research Letter Keywords: COVID-19; genitourinary cancers; immunotherapy; Medical Oncology; patient management Corresponding Author: Laura Marandino Fondazione IRCCS Istituto Nazionale dei Tumori ITALY First Author: Laura Marandino, M.D. Order of Authors: Laura Marandino, M.D. Massimo Di Maio, Prof. Giuseppe Procopio Saverio Cinieri Giordano Domenico Beretta Andrea Necchi, M.D. Powered by Editorial Manager® and ProduXion Manager® from Aries Systems Corporation
  • 2.
    EUROPEAN UROLOGY AUTHORSHIPRESPONSIBILITY, FINANCIAL DISCLOSURE, AND ACKNOWLEDGMENT FORM. By completing and signing this form, the corresponding author acknowledges and accepts full responsibility on behalf of all contributing authors, if any, regarding the statements on Authorship Responsibility, Financial Disclosure and Funding Support. Any box or line left empty will result in an incomplete submission and the manuscript will be returned to the author immediately. Authorship Responsibility By signing this form and clicking the appropriate boxes, the corresponding author certifies that each author has met all criteria below (A, B, C, and D) and hereunder indicates each author’s general and specific contributions by listing his or her name next to the relevant section. A. This corresponding author certifies that: • the manuscript represents original and valid work and that neither this manuscript nor one with substantially similar content under my authorship has been published or is being considered for publication elsewhere, except as described in an attachment, and copies of closely related manuscripts are provided; and • if requested, this corresponding author will provide the data or will cooperate fully in obtaining and providing the data on which the manuscript is based for examination by the editors or their assignees; • every author has agreed to allow the corresponding author to serve as the primary correspondent with the editorial office, to review the edited typescript and proof. B. Each author has given final approval of the submitted manuscript. C. Each author has participated sufficiently in the work to take public responsibility for all of the content. D. Each author qualifies for authorship by listing his or her name on the appropriate line of the categories of contributions listed below. Disclosure
  • 3.
    The authors listedbelow have made substantial contributions to the intellectual content of the paper in the various sections described below. (list appropriate author next to each section – each author must be listed in at least 1 field. More than 1 author can be listed in each field.) _ conception and design Laura Marandino, Massimo Di Maio, Andrea Necchi _ acquisition of data All authors _ analysis and interpretation of data Laura Marandino, Massimo Di Maio, Andrea Necchi _ drafting of the manuscript Laura Marandino, Massimo Di Maio, Andrea Necchi _ critical revision of the manuscript for important intellectual content All authors _ statistical analysis Laura Marandino, Massimo Di Maio, Andrea Necchi _ obtaining funding Not applicable _ administrative, technical, or material support Not applicable _ supervision Andrea Necchi, Massimo Di Maio _ other (specify) Not applicable Financial Disclosure None of the contributing authors have any conflicts of interest, including specific financial interests and relationships and affiliations relevant to the subject matter or materials discussed in the manuscript. OR I certify that all conflicts of interest, including specific financial interests and relationships and affiliations relevant to the subject matter or materials discussed in the manuscript (eg, employment/ affiliation, grants or funding, consultancies, honoraria, stock ownership or options, expert testimony, royalties, or patents filed, received, or pending), are the following: (please list all conflict of interest with the relevant author’s name):
  • 4.
    Massimo Di Maioreceived advisory board or consultant fees from Merck Sharp & Dohme, Bristol Myers Squibb, Eisai, Janssen, Astellas, AstraZeneca, Pfizer, Takeda and institutional research grant from Tesaro. Giuseppe Procopio received advisory board or consultant fees from AstraZeneca, Bayer, Bristol Myers Squibb, Janssen, Ipsen, Merck Sharp & Dohme, Novartis, Pfizer. Funding Support and Role of the Sponsor I certify that all funding, other financial support, and material support for this research and/or work are clearly identified in the manuscript. The name of the organization or organizations which had a role in sponsoring the data and material in the study are also listed below: All funding or other financial support, and material support for this research and/or work, if any, are clearly identified hereunder: The specific role of the funding organization or sponsor is as follows: Design and conduct of the study Collection of the data Management of the data Analysis Interpretation of the data Preparation Review Approval of the manuscript OR No funding or other financial support was received.
  • 5.
    Acknowledgment Statement This correspondingauthor certifies that: • all persons who have made substantial contributions to the work reported in this manuscript (eg, data collection, analysis, or writing or editing assistance) but who do not fulfill the authorship criteria are named with their specific contributions in an Acknowledgment in the manuscript. • all persons named in the Acknowledgment have provided written permission to be named. • if an Acknowledgment section is not included, no other persons have made substantial contributions to this manuscript. After completing all the required fields above, this form must be uploaded with the manuscript and other required fields at the time of electronic submission.
  • 6.
    The Shifting Landscapeof Genitourinary Oncology During the COVID-19 Pandemic and how Italian Oncologists Reacted: Results from a National Survey Laura Marandino a, *, Massimo Di Maio b , Giuseppe Procopio a , Saverio Cinieri c , Giordano Domenico Beretta d , Andrea Necchi a The outbreak of the novel coronavirus disease-19 (COVID-19) caused by severe acute respiratory syndrome corona virus 2 (SARS-CoV-2) suddenly revolutionized the way we take care of patients with cancer. This situation was dramatically felt in geographic regions where the spread of the infection, qualified as a pandemic by the World Health Organization on March 11, 2020, was causing an emergency health care situation. After the original outbreak in Wuhan City, Hubei Province, China, the infection rapidly spread throughout the world in more than 199 countries (www.worldometers.info/coronavirus). At the time of writing, Italy, and the Lombardy region in particular, was ranked first in terms of COVID-19-associated deaths, making this region one of the most critical hotspots of the COVID-19 outbreak [1]. In Italy, a total of 10 779 deaths had been reported by the health care authorities and 3906 patients required intensive care unit (ICU) admittance at the time of writing. Patients diagnosed with cancer have a higher risk of developing serious complications and dying from COVID-19 [2,3]. Besides this consideration, a number of critical dilemmas have emerged regarding indications for cancer therapies and management of associated side effects. General clinical recommendations for patients with genitourinary cancers have already been published, obviously biased by the lack of actual data for most of the guidelines [4]. It is important to anticipate the shifting landscape that will probably occur in the management of patients with cancer to better prepare health care providers and systems for future needs. In March 2020 we therefore carried out a nationwide survey among Italian medical oncologists that focused on the management of patients with genitourinary malignancies. The survey was endorsed by and conducted through the Associazione Italiana di Oncologia Medica (AIOM) network, and took the form of an online questionnaire sent to all AIOM members. A total of 72 physicians provided feedback; their general characteristics are shown in Supplementary Table 1. The questions and corresponding results are shown in Figure 1. In general, there was consensus among oncologists to pursue treatment, possibly without delays or interruptions, for patients with locally advanced or metastatic disease for which an induction or first-line therapy option is indicated in guidelines, particularly for patients suffering from prognostically aggressive disease requiring timely treatment (Fig. 1A–H). A higher proportion of physicians were willing to consider delays or interruption for clinical settings characterized by more indolent disease or treatments associated, on average, with clinical benefit of lower magnitude. Of note, despite the public health care emergency, Italian oncologists were still in favor of close adherence to guidelines regarding administration of perioperative therapies, such as neoadjuvant chemotherapy in patients with clinical T3– 4N0M0 urothelial bladder cancer (Fig. 1C,D) and adjuvant therapy in high-risk, clinical stage I germ-cell tumors (Fig. 1F,G). Overall, although the main factor taken into account for treatment decisions was its proven survival benefit, the number of hospital visits ranked second, ahead of other factors usually considered important in clinical decisions. Lastly, two important notions emerged from this survey. First, Italian oncologists are still in favor of considering delivery of the best treatment option for genitourinary cancer patients through inclusion in clinical trials (61%), although most of them (54%) underlined the unavoidable more stringent selection and the need to face severe logistic difficulties, as Manuscript
  • 7.
    indicated in Fig.1I. Second, although the risks associated with immune checkpoint inhibitors in the present pandemic context are not well defined, most of the respondents would justify interruption of therapy only after case-by-case discussions with patients with a sustained response during treatment, or would consider skipping some doses to reduce the number of hospital visits (Fig. 1M). Implementation of telemedicine will be critical in managing follow-up visits and oral drug delivery, as is currently done in several institutions nationwide. This survey provides a snapshot of the opinion of Italian oncologists regarding the management of patients with genitourinary malignancies. Similar considerations would probably apply to other solid tumors. In our opinion, the main message is that in spite of huge sudden changes in a geographic area representing an epicenter of the COVID-19 pandemic, oncologists are still determined to achieving treatment delivery as close as possible to clinical guidelines or routine clinical practice, at least for treatments supported by evidence of a clinically relevant gain in life expectancy. In the setting of advanced disease without curative intent, a non-negligible number of oncologists would delay treatment initiation (or consider interruption) in the second or further lines of treatment associated with a lower clinical benefit. For patients who deserve a systemic treatment with curative intent, we should still rely on the multidisciplinary approach among several other specialists. This continuing collaboration will require profound organizational changes, primarily related to the obvious delays in biopsies or radical surgical interventions that were promptly outlined by Italian urologists [5]. Conflicts of interest: Massimo Di Maio has received advisory board or consultant fees from Merck Sharp & Dohme, Bristol Myers Squibb, Eisai, Janssen, Astellas, AstraZeneca, Pfizer, and Takeda and an institutional research grant from Tesaro. Giuseppe Procopio has received advisory board or consultant fees from AstraZeneca, Bayer, Bristol Myers Squibb, Janssen, Ipsen, Merck Sharp & Dohme, Novartis, and Pfizer. The remaining authors have nothing to disclose. References 1. Grasselli G, Pesenti A, Cecconi M. Critical care utilization for the COVID-19 outbreak in Lombardy, Italy: early experience and forecast during an emergency response. JAMA. In press. https://doi.org/10.1001/jama.2020.4031 2. Liang W, Guan W, Chen R, et al. Cancer patients in SARS-CoV-2 infection: a nationwide analysis in China. Lancet Oncol 2020;21:335–7. 3. Zhang L, Zhu F, Xie L, et al. Clinical characteristics of COVID-19-infected cancer patients: a retrospective case study in three hospitals within Wuhan, China. Ann Oncol. In press. https://doi.org/10.1016/j.annonc.2020.03.296 4. Gillessen Sommer S, Powles T. Advice regarding systemic therapy in patients with urological cancers during the COVID-19 pandemic. Eur Urol. In press. 5. Naspro R, Da Pozzo LF. Urology in the time of corona. Nat Rev Urol. In press. https://doi.org/10.1038/s41585-020-0312-1 Fig. 1 – Questions and corresponding answers collected during the survey.
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    a Department of MedicalOncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy b Department of Oncology, University of Turin, Azienda Ospedaliera Ordine Mauriziano, Turin, Italy c Medical Oncology & Breast Unit, Antonio Perrino Hospital, Brindisi, Italy d Medical Oncology Department, Humanitas Gavazzeni Clinic, Bergamo, Italy * Corresponding author. Department of Medical Oncology; Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian 1, 20133 Milan, Italy. Tel. +39 02 23902402; Fax: +39 02 23903150. E-mail address: laura.marandino@istitutotumori.mi.it (L. Marandino).
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    RENAL CELL CARCINOMA •Do you consider it appropriate to evaluate a delay in treatment initiation in these clinical settings? 56 26 9 35 16 44 62 36 0% 20% 40% 60% 80% 100% Metastatic renal cell carcinoma – Third and further lines Metastatic renal cell carcinoma - Second Line Metastatic renal cell carcinoma – First Line; Intermediate/Poor risk Metastatic renal cell carcinoma – First Line; Favorable risk Yes No Figure 1A figure one
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    RENAL CELL CARCINOMA •Do you consider it appropriate to evaluate interruption of treatment in these clinical settings? 44 55 22 33 3 27 16 49 37 68 0% 20% 40% 60% 80% 100% Metastatic renal cell carcinoma – Long responders to Antiangiogenic Drugs Metastatic renal cell carcinoma – Long responders to Immunotherapy Metastatic renal cell carcinoma – Second and further Lines, Antiangiogenic Drugs Metastatic renal cell carcinoma - Second and further Lines, Immunotherapy Metastatic renal cell carcinoma – First Line Yes No Figure 1B
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    UROTHELIAL CANCER • Doyou consider it appropriate to evaluate NOT starting a systemic treatment in these clinical settings? 38 15 10 38 33 56 61 33 0% 20% 40% 60% 80% 100% Muscle-invasive bladder cancer– Adjuvant therapy Muscle-invasive bladder cancer– Neoadjuvant therapy, in case of long waiting list for radical surgery Muscle-invasive bladder cancer cT3-4N0 – Neoadjuvant therapy Muscle-invasive bladder cancer cT2N0 – Neoadjuvant therapy Yes No Figure 1C
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    UROTHELIAL CANCER • Doyou consider it appropriate to evaluate a delay in treatment initiation in these clinical settings? 58 38 8 15 13 33 63 56 0% 20% 40% 60% 80% 100% Metastatic Urothelial Cancer - Second and further lines Metastatic Urothelial Cancer- First Line, in patients without visceral disease or rapid progression Metastatic Urothelial Cancer- First Line, all cases Locally advanced disease N+ Yes No Figure 1D
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    UROTHELIAL CANCER • Doyou consider it appropriate to evaluate interruption of treatment in these clinical settings? 58 37 51 61 4 11 35 20 10 66 0% 20% 40% 60% 80% 100% Metastatic Urothelial Cancer - Second and further lines, long responders to immunotherapy Metastatic Urothelial Cancer - Second and further lines, immunotherapy regardless of the number of cycles administered Metastatic Urothelial Cancer - Second and further lines, chemotherapy Metastatic Urothelial Cancer - First Line, after 4 cycles of platinum-based chemotherapy Metastatic Urothelial Cancer - First Line, regardless of the number of cycles administered Yes No Figure 1E
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    GERM CELL TUMOURS •Do you consider it appropriate to evaluate NOT starting a systemic treatment in these clinical settings? 34 16 25 38 31 53 43 30 0% 20% 40% 60% 80% 100% In all these cases, I would request an opinion from a referral center Stage I non seminoma - adjuvant therapy; in case of vascular invasion Stage I non seminoma - adjuvant therapy; all cases Stage I seminoma - adjuvant therapy Yes No Figure 1F
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    GERM CELL TUMOURS •Do you consider it appropriate to evaluate a delay in treatment initiation in these clinical settings? 35 22 5 9 25 28 49 66 60 46 0% 20% 40% 60% 80% 100% In all these cases I would request an opinion from a referral center Advanced disease - Second Line Advanced disease - Poor prognosis risk group Advanced disease - Intermediate prognosis risk group Advanced disease - Good prognosis risk group Yes No Figure 1G
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    PROSTATE CANCER • Doyou consider it appropriate to evaluate a delay in treatment initiation in these clinical settings? 50 56 15 25 21 15 56 47 0% 20% 40% 60% 80% 100% Metastatic castration-resistant prostate cancer – Second and further lines Metastatic castration-resistant prostate cancer – First Line, absence of visceral disease and asymptomatic patient Metastatic castration-resistant prostate cancer – First Line, regardless of disease characteristics Newly diagnosed hormone-sensitive metastatic prostate cancer – high volume Yes No Figure 1H
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    CLINICAL TRIALS • Doyou consider it appropriate to enrol patients in clinical trials during the emergency period? 28, 39% 5, 7% 39, 54% No, due to concerns about logistics and human resources Yes, in all cases where clinical trials are available Yes, for selected patients and in case of favourable logistics Figure 1I
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    ORAL ANTICANCER THERAPY •How are you managing patients receiving oral anticancer drugs during this emergency period? 20 27 30 52 14 Drug interruption for patients who report toxicity at telephone interview/mail conversation and update through telephone interview/mail Physical examination for patients who report toxicity at telephone interview/mail conversation Drug dispensation for more than one cycle of treatment Telephone interview/Mail conversation + blood tests in a lab near patient’s residence and drug dispensation directly in the hospital pharmacy/home delivery My clinical practice has not changed 0 10 20 30 40 50 60 Figure 1L (20%) (73%) (42%) (38%) (28%) Respondents
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    IMMUNOTHERAPY • Do youconsider it appropriate to evaluate treatment interruption for patients receiving immunotherapy during the emergency period? 7, 10% 2, 3% 6, 8% 33, 46% 20, 28% 4, 5% Yes, in case of prolonged complete response Yes, in case of prolonged partial response Yes, in case of prolonged complete or partial response Yes, but only evaluating case by case in case of prolonged complete or partial response No, but I consider to «skip» some cycle to reduce hospital visits No, due to the lack of solid evidence Figure 1M
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    CHOICE OF TREATMENT •What are the main factors that you consider in the choice of treatment during this emergency period? (max 2 choices) 22 16 13 18 11 53 Number of required visits in the hospital Route of administration (ev/os) Toxicity Quality of life benefit Progression free survival benefit Proven overall survival benefit 0 20 40 60 (31%) (22%) (18%) (25%) (15%) (74%) Figure 1N Respondents
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    FOLLOW-UP • How areyou managing follow-up of off-treatment patients during this emergency period? 2, 3% 6, 8% 62, 86% 2, 3% Follow-up visits are continuing Follow-up visits have been reduced Follow-up visits have been cancelled and they are carried out through telephone/mail Follow-up visits have been cancelled and we are still unable to carry follow-up in an alternative way Figure 1O
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    CHANGE IN CLINICALPRACTICE • To what extent has the public health emergency changed your clinical practice? (0 = minimum; 10 = maximum) 0 0 0 1 4 7 12 17 21 10 1 2 3 4 5 6 7 8 9 10 0 5 10 15 20 25 Figure 1P
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    For TS. Figures. Please usesentence case throughout (no change to acronyms). Ensure all data are legible/visible. Change ‘max 2 choices’ to ‘max. two choices’. Ensure one space between digits and opening bracket. INSTRUCTION TO TYPE SETTER
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    Supplementary Table 1 Clickhere to access/download Supplementary file RLE-D-20-00508_Suppl Table 1_compuscript_mk_edited.docx