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Article
Peer-Review Record

In Vivo Preclinical Assessment of the VEGF Targeting Potential of the Newly Synthesized [52Mn]Mn-DOTAGA-Bevacizumab Using Experimental Cervix Carcinoma Mouse Model

Diagnostics 2023, 13(2), 236; https://doi.org/10.3390/diagnostics13020236
by Csaba Csikos 1,2, Adrienn Vágner 3, Gábor Nagy 3, Ibolya Kálmán-Szabó 1, Judit P. Szabó 1, Minh Toan Ngo 1,2, Zoltán Szoboszlai 3, Dezső Szikra 1, Zoárd Tibor Krasznai 4, György Trencsényi 1,2,*,† and Ildikó Garai 1,2,3,†
Reviewer 1:
Reviewer 2:
Diagnostics 2023, 13(2), 236; https://doi.org/10.3390/diagnostics13020236
Submission received: 24 November 2022 / Revised: 19 December 2022 / Accepted: 5 January 2023 / Published: 8 January 2023
(This article belongs to the Special Issue Imaging of Cervical Cancer)

Round 1

Reviewer 1 Report

The paper of Trencsényi and collaborators reports the preparation and in vivo preclinical assessment of [52Mn]Mn-DOTAGA-bevacizumab on subcutaneously injected KB-3-1 tumor-bearing mice. Bevacizumab targets VEGF-A and it is used in the antiangiogenesis therapy, therefore the authors propone the use of this PET ligand for patient selection to bevacizumab therapy or to monitor the effectiveness of bevacizumab therapy (or other therapies targeting angiogenesis).

Since the monoclonal antibodies have a long circulating time, the authors suggest that the use of manganese-52 positron-emitting isotope could be ideal because of its long half-life (t1/2= 5.59 days). 52Mn is an interesting emerging radiometal for immuno-PET, and there are only few studies reporting on the in vivo evaluation of a 52Mn-labeled mAb, and for tis reason this paper is an interesting contribution to this field.

The results are good in terms of tumor accumulation and tumor-to-organ ratios and well-described. For these reasons I suggest the publication in Diagnostics.

 Only a point should be clarified. The authors describe the synthesis of DOTAGA-Bevacizumab, and at line 270, the say that “the new [52Mn]Mn-DOTAGA-bevacizumab PET probe was synthesized with high chemical purity”. How did they check the chemical purity? Did they perform a mass analysis? How many DOTAGA units were bound per antibody? These data should be interesting for a reader.

Other minor points:

At Line 94 the authors write they used Trastuzumab (Ontruzant®), and so at line 97 DOTAGA-trastuzumab. Please correct.

Some typos:

Line 128   Immunodefficient  

Line 247    that he ratio

Line 296   the administration if  

Author Response

Please see the attachment.

Author Response File: Author Response.pdf

Reviewer 2 Report

Very nice research and the manuscript. 

It would be nice if you could cite some clinical experience or clinical trials with MaB and radiopharmaceuticals in oncology.

Author Response

Please see the attachment.

Author Response File: Author Response.pdf

Reviewer 3 Report

Dear Author, 

Please find the minor comments.

Rewrite second sentence in introduction.

41st line - pdgf is correct not PIGE

Rewrite 45th sentence.

comma is missing in 299 prepositional phrase.

 

 

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Author Response

Please see the attachment.

Author Response File: Author Response.pdf

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