Prosecution Insights
Last updated: July 26, 2026
Application No. 17/257,206

METHOD FOR PREDICTING RESPONSE TO ANTICANCER IMMUNOTHERAPY USING DNA METHYLATION ABERRATION

Non-Final OA §101§103§112
Filed
Mar 07, 2022
Priority
Sep 18, 2019 — RE 10-2019-0114977 +1 more
Examiner
SALMON, KATHERINE D
Art Unit
1682
Tech Center
1600 — Biotechnology & Organic Chemistry
Assignee
Pentamedix Co. Ltd.
OA Round
3 (Non-Final)
42%
Grant Probability
Moderate
3-4
OA Rounds
0m
Est. Remaining
81%
With Interview

Examiner Intelligence

Grants 42% of resolved cases
42%
Career Allowance Rate
335 granted / 790 resolved
-17.6% vs TC avg
Strong +38% interview lift
Without
With
+38.2%
Interview Lift
resolved cases with interview
Typical timeline
4y 0m
Avg Prosecution
68 currently pending
Career history
896
Total Applications
across all art units

Statute-Specific Performance

§101
12.0%
-28.0% vs TC avg
§103
51.8%
+11.8% vs TC avg
§102
8.8%
-31.2% vs TC avg
§112
15.8%
-24.2% vs TC avg
Black line = Tech Center average estimate • Based on career data from 790 resolved cases

Office Action

§101 §103 §112
DETAILED ACTION Notice of Pre-AIA or AIA Status The present application, filed on or after March 16, 2013, is being examined under the first inventor to file provisions of the AIA . A request for continued examination under 37 CFR 1.114, including the fee set forth in 37 CFR 1.17(e), was filed in this application after final rejection. Since this application is eligible for continued examination under 37 CFR 1.114, and the fee set forth in 37 CFR 1.17(e) has been timely paid, the finality of the previous Office action has been withdrawn pursuant to 37 CFR 1.114. Applicant's submission filed on 2/02/2026 has been entered. Applicant’s election without traverse of Group I in the reply filed on 3/17/2025 is acknowledged. Claims 1, 4, 6-7 are pending. Claims 2-3, 5, 8-16 have been cancelled. The following rejections is modified necessitated by amendment. Response to arguments following. This action is NONFINAL. Newly Applied Claim Rejections - 35 USC § 112 The following is a quotation of 35 U.S.C. 112(b): (b) CONCLUSION.—The specification shall conclude with one or more claims particularly pointing out and distinctly claiming the subject matter which the inventor or a joint inventor regards as the invention. The following is a quotation of 35 U.S.C. 112 (pre-AIA ), second paragraph: The specification shall conclude with one or more claims particularly pointing out and distinctly claiming the subject matter which the applicant regards as his invention. Claims 1, 4, 6-7 are rejected under 35 U.S.C. 112(b) or 35 U.S.C. 112 (pre-AIA ), second paragraph, as being indefinite for failing to particularly point out and distinctly claim the subject matter which the inventor or a joint inventor (or for applications subject to pre-AIA 35 U.S.C. 112, the applicant), regards as the invention. Claims 1, 4, 6-7 are indefinite over the calculating step of claim 1. In particular the calculating step requires a global DNA methylation level by averaging methylation values of probe mapping, however, the step of measuring does not require probes used in the measurement. Claim Rejections - 35 USC § 101 35 U.S.C. 101 reads as follows: Whoever invents or discovers any new and useful process, machine, manufacture, or composition of matter, or any new and useful improvement thereof, may obtain a patent therefor, subject to the conditions and requirements of this title. Claims 1, 4, 6-7 are rejected under 35 U.S.C. 101 because the claimed invention is directed to a judicial exception of a natural correlation and abstract idea without significantly more. The claim(s) recite(s) the judicial exception of the correlation of predicting response to cancer treatment and global DNA methylation level (law of nature) and abstract steps of “evaluating a response”. This judicial exception is not integrated into a practical application because the steps of the claims are considered abstract ideas. The claim(s) does/do not include additional elements that are sufficient to amount to significantly more than the judicial exception because these steps are considered routine as discussed below. The claims are drawn to steps of “evaluating a response”. As the phrases are not defined in the application, the terms are interpreted broadly. In particular, the terms can be interpreted as reading printouts and making mental analysis of the treatments. The dependent claims are limited to performing known biotechnical techniques for determination of methylation level of LINE-1 transposons. The unpatentability of laws of nature was confirmed by the U.S. Supreme Court in Mayo Collaborative Services v. Prometheus Laboratories, Inc., No. 10-1150 (March 20, 2012). The unpatentability of abstract ideas was confirmed by the U.S. Supreme court in Bilski v. Kappos, No. 08-964, 2010 WL 2555192 (June 28, 2010) and in Alice Corp. v. CLS Bank Int'l, 134 S. Ct. 2347, 2354 (2014). The following three inquiries are used to determine whether a claim is drawn to patent-eligible subject matter: Step 1. Is the claim to a process, machine, manufacture, or composition of matter? Yes- the claims are clearly directed to a process. Step 2A. Is the claim directed to a law of nature, a natural phenomenon, or an abstract idea (judicially recognized exceptions)? Yes- The claims are directed to a judicial exception. The judicial exception is the correlation of methylation level and predicting a response to cancer treatment and the abstract steps of “obtaining” and “evaluating”. These correlations are naturally occurring and exist apart from any human action. Step 2B. Does the claim recite additional elements that amount to significantly more than the judicial exception? No-there are no elements or combination of elements in the claim that are sufficient to ensure that the claim as a whole amounts to significantly more than the judicial exception: The claims are directed to judicial exceptions without significantly more. The claim(s) does/do not include additional elements that are sufficient to amount to significantly more than the judicial exception because the claims require general and routine steps that do not provide an "inventive step" as indicated above or abstract steps. The abstract steps are considered mental steps as it could encompass reading printouts and mental analysis. Therefore the present claims do not require performing any steps that are not routine and conventional. For example, the claims do not require using a novel reagent to amplify. The claims also do not require the use of a particular machine, wherein the particular machine implements one or more of the judicial exceptions or integrates the judicial exception(s) into a particular practical application. Note that the Supreme Court in Mayo v. Prometheus has made clear that to transform an unpatentable law of nature into a patent-eligible application of such a law, one must do more than simply state the law of nature while adding the words "apply it." Essentially, appending conventional steps, specified at a high level of generality, to laws of nature, natural phenomena, and abstract ideas cannot make those laws, phenomena, and ideas patent-eligible. In Prometheus, the Court found that "[i]f a law of nature is not patentable, then neither is a process reciting a law of nature, unless that process has additional features that provide practical assurance that the process is more than a drafting effort designed to monopolize the law of nature itself." Additionally, "conventional or obvious" "[pre]solution activity" is normally not sufficient to transform an unpatentable law of nature into a patent-eligible application of such a law". Flook, 437 U. S., at 590; see also Bilski, 561 U. S., at __ (slip op., at 14) ("[T]he prohibition against patenting abstract ideas 'cannot be circumvented by'.., adding 'insignificant post-solution activity'" (quoting Diehr, supra, at 191-192)). The Court also summarized their holding by stating "[t]o put the matter more succinctly, the claims inform a relevant audience about certain laws of nature; any additional steps consist of well understood, routine, conventional activity already engaged in by the scientific community; and those steps, when viewed as a whole, add nothing significant beyond the sum of their parts taken separately." With regard to the dependent claims and the steps of extracting DNA and measuring methylation, the detection of levels for methylation uses known assays in the art. Lizardi et al. (US Patent Application 2012/0157324 June 21, 2012) teaches a method of measuring global DNA methylation level in a sample from a cancer patient (para 316). Although Lizardi et al. does not teach evaluating a response to immunotherapy, Lizardi et al. teaches that a calculation of an average value of methylation levels of LINE-1 provides global methylation levels between a sample with cancer and a sample that is normal (para 316). Lizardi et al. teaches that one can determine changes in a repetitive element family accuracy (para 316). For these reasons the claims are rejected under section 101 as being directed to non-statutory subject matter. Response to Arguments The reply traverses the rejection. A summary of the arguments is provided below with response to arguments following. The reply asserts that the claims as amended require specific laboratory method that includes extracting DNA, measuring methylation using defined biochemical assays, calculating and evaluating. The reply asserts that the claims are not amended to simply observe methylation levels or invite mental inference (p. 5). The reply asserts that Lizardi and Sigalotti does not teach the calculation step or using a global LINE 1 derived metric to evaluate response to immunotherapy. These arguments have been considered but are not found persuasive. The reply asserts that the claims have been amended to include steps that are more than the judicial exception. However, the steps of obtaining a sample and measuring methylation are general and routine methods of isolating samples and measuring methylation levels. These steps use known and conventual assays such as PCR. As such the steps do not appear to encompass something more than the judicial exception. With regard to the calculating step, this step does not require any particular steps more than obtaining data from the methylation measurement. As such this “calculating” step can include data collection. Finally the evaluation of response is considered the judicial exception itself. Claim Rejections - 35 USC § 103 In the event the determination of the status of the application as subject to AIA 35 U.S.C. 102 and 103 (or as subject to pre-AIA 35 U.S.C. 102 and 103) is incorrect, any correction of the statutory basis (i.e., changing from AIA to pre-AIA ) for the rejection will not be considered a new ground of rejection if the prior art relied upon, and the rationale supporting the rejection, would be the same under either status. The following is a quotation of 35 U.S.C. 103 which forms the basis for all obviousness rejections set forth in this Office action: A patent for a claimed invention may not be obtained, notwithstanding that the claimed invention is not identically disclosed as set forth in section 102, if the differences between the claimed invention and the prior art are such that the claimed invention as a whole would have been obvious before the effective filing date of the claimed invention to a person having ordinary skill in the art to which the claimed invention pertains. Patentability shall not be negated by the manner in which the invention was made. This application currently names joint inventors. In considering patentability of the claims the examiner presumes that the subject matter of the various claims was commonly owned as of the effective filing date of the claimed invention(s) absent any evidence to the contrary. Applicant is advised of the obligation under 37 CFR 1.56 to point out the inventor and effective filing dates of each claim that was not commonly owned as of the effective filing date of the later invention in order for the examiner to consider the applicability of 35 U.S.C. 102(b)(2)(C) for any potential 35 U.S.C. 102(a)(2) prior art against the later invention. Claim(s) 1,4,6-7 is/are rejected under 35 U.S.C. 103 as being unpatentable over Lizardi et al. (US Patent Application 2012/0157324 June 21, 2012) in view of Sigalotti et al. (US Patent Application Publication 2013/0316931 November 28, 2013 previously cited). With regard to Claim 1, Lizardi et al. teaches obtaining a cancer sample (para 44 and 54). Lizardi et al. teaches a method of measuring global DNA methylation level in a sample from a cancer patient using PCR (para 39 and 316). Although Lizardi et al. does not teach evaluating a response to immunotherapy, Lizardi et al. teaches that a calculation of an average value of methylation levels of LINE-1 provides global methylation levels between a sample with cancer and a sample that is normal (para 316). Lizardi et al. teaches that one can determine changes in a repetitive element family accuracy (para 316). Lizardi et al. teaches using probes of the transposons to determine average methylation levels of the subsets (para 48). However, Lizardi et al. does not teach evaluating response to immunotherapy or the use of LIHS. With regard to claim 1, Sigalotti et al. teaches obtaining DNA methylation level from a sample of a cancer subject (para 10). Sigalotti et al. calculating an average methylation level of the genes (para 139). Sigalotti et al. evaluating response to cancer treatment based upon global DNA methylation level (para 10-15). Sigalotti et al. teaches immunotherapy (para 28). Sigalotti et al. teaches that LINE-1 transposons is L1HS (table 4). With regard to claim 4, Sigalotti et al. suggests a method of evaluating response to treatment with the global level of LINE 1 methylation is increased compared to a reference (para 27-28). With regard to Claim 6, Sigalotti et al. teaches a sample can include blood, serum, cerebrospinal fluid, sputum and urine (para 25). With regard to Claim 7, Sigalotti et al. teaches that the cancer is melanoma (para 93). Therefore it would be prima facie obvious to modify the method of Lizardi et al. to determine the average as taught by Lizardi in global DNA methylation from the LiHS of Sigalotti (e.g. LINE 1 transposon type) to evaluate immunotherapy. The ordinary artisan would be motivated to evaluate immunotherapy as Sigalotti et al. suggests that methylation of LIHS differs based on rather the patient is responding. Response to Arguments The reply traverses the rejection. A summary of the arguments is provided below with response to arguments following. The reply asserts that Lizardi does not teach evaluating immunotherapy, LINE1 methylation, and the calculating step (p. 6). The reply asserts that Sigalotti does not discoes the use of median based decision rule, use of global methylation or predicting immunotherapy response (p. 7). These arguments have been reviewed but have not been found persuasive. In response to applicant's arguments against the references individually, one cannot show nonobviousness by attacking references individually where the rejections are based on combinations of references. See In re Keller, 642 F.2d 413, 208 USPQ 871 (CCPA 1981); In re Merck & Co., 800 F.2d 1091, 231 USPQ 375 (Fed. Cir. 1986). It is noted that the combination of the two references suggests the steps of the claims. It is further noted for the wherein clause, as noted int eh 35 USC 112b, the claims have not provided a clear recitation of the steps required. Lizardi et al. teaches the calculation of an average value of methylation levels using probes. Furthermore Sigalotti et al. suggests a method of evaluating response to treatment with the global level of LINE 1 methylation is increased compared to a reference (para 27-28). Conclusion No claims are allowed. Any inquiry concerning this communication or earlier communications from the examiner should be directed to KATHERINE D SALMON whose telephone number is (571)272-3316. The examiner can normally be reached 9-530. Examiner interviews are available via telephone, in-person, and video conferencing using a USPTO supplied web-based collaboration tool. To schedule an interview, applicant is encouraged to use the USPTO Automated Interview Request (AIR) at http://www.uspto.gov/interviewpractice. If attempts to reach the examiner by telephone are unsuccessful, the examiner’s supervisor, Wu Cheng (Winston) Shen can be reached on 5712723157. The fax phone number for the organization where this application or proceeding is assigned is 571-273-8300. Information regarding the status of published or unpublished applications may be obtained from Patent Center. Unpublished application information in Patent Center is available to registered users. To file and manage patent submissions in Patent Center, visit: https://patentcenter.uspto.gov. Visit https://www.uspto.gov/patents/apply/patent-center for more information about Patent Center and https://www.uspto.gov/patents/docx for information about filing in DOCX format. For additional questions, contact the Electronic Business Center (EBC) at 866-217-9197 (toll-free). If you would like assistance from a USPTO Customer Service Representative, call 800-786-9199 (IN USA OR CANADA) or 571-272-1000. /KATHERINE D SALMON/Primary Examiner, Art Unit 1682
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Prosecution Timeline

Show 1 earlier event
May 09, 2025
Non-Final Rejection mailed — §101, §103, §112
Aug 11, 2025
Response Filed
Oct 02, 2025
Final Rejection mailed — §101, §103, §112
Feb 02, 2026
Request for Continued Examination
Feb 04, 2026
Response after Non-Final Action
Feb 11, 2026
Examiner Interview Summary
Feb 11, 2026
Applicant Interview (Telephonic)
Apr 16, 2026
Non-Final Rejection mailed — §101, §103, §112 (current)

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Prosecution Projections

3-4
Expected OA Rounds
42%
Grant Probability
81%
With Interview (+38.2%)
4y 0m (~0m remaining)
Median Time to Grant
High
PTA Risk
Based on 790 resolved cases by this examiner. Grant probability derived from career allowance rate.

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