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Paper Citation Record · LEDGER

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology

As of 22 August 2026, this Paper Citation Record lists 38 of 38 outbound references and 0 inbound Pith citation observations for arXiv:2411.08698.

A citation records a reference. It does not transfer a finding from one paper to another.

pith.paper-citation-record.v1
2411.08698 v1

Coverage vector

measured 38 of 38 reference resolution

Typed states for the displayed outbound observations.

Source: paper_references, paper_reference_links, observed 2026-08-12T21:30:32.654756Z

measured 38 of 38 standing notices

One-hop event checks from named stored sources.

Source: scholarly_work_events, retraction_status_cache, observed 2026-08-22T06:32:14.747728+00:00

measured 0 of 0 inbound itemization

Pith citing papers itemized under the disclosed page cap.

Source: paper_references, paper_reference_links

measured 0 of 1 external citation measurements

A source-named dated measurement, never combined with another source.

Source: cited_works

Reference resolution

38 of 38 outbound references displayed

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External citation measurements

No source-named external measurement is stored.

Outbound references

Observation 71cfbb4b-9651-451d-8445-5a08dff9a9a0 · outbound

This paper cites Contemporary dose-escalation methods for early phase studies in the im- munotherapeutics era.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Contemporary dose-escalation methods for early phase studies in the im- munotherapeutics era

Reference 1

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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 791a3f9f-51dc-44ef-ab1b-4b5915cb5f62 · outbound

This paper cites Cancer phase I clinical trials: efficient dose escalation with overdose control.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Cancer phase I clinical trials: efficient dose escalation with overdose control

Reference 2

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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 9fc6985f-f384-4f91-98be-c1c41c4fa405 · outbound

This paper cites A Bayesian dose-finding design for oncology clinical trials of combinational biological agents.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology A Bayesian dose-finding design for oncology clinical trials of combinational biological agents

Reference 3

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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 588a694d-45b6-4a57-8fe9-807d38483321 · outbound

This paper cites Project optimus: Reforming the dose optimization and dose selection paradigm in oncology, 2022.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Project optimus: Reforming the dose optimization and dose selection paradigm in oncology, 2022

Reference 4

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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation aa465e08-3f77-4715-80e4-c65ea2fafa5a · outbound

This paper cites an unresolved cited work.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Unresolved cited work

Reference 5

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unresolved
raw_fallback, observed 2026-08-12T21:30:38.414754Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 8bd3f98a-7828-4a1d-9c90-2219cb099cbb · outbound

This paper cites A Bayesian interval dose-finding design addressingockham’s razor: mTPI-2.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology A Bayesian interval dose-finding design addressingockham’s razor: mTPI-2

Reference 6

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verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:31.464751Z digest=sha256:114f882270e69277d0a6e50fa2c8c045ca38d4ae035e4e00b10f477b7bbb9f98

Observation be1e6e83-f054-4e38-85e6-292286deb63a · outbound

This paper cites Continual reassessment and related designs in dose-finding studies.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Continual reassessment and related designs in dose-finding studies

Reference 7

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raw_fallback, observed 2026-08-12T21:30:38.105466Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation b0355a2c-c837-46f6-89cd-f3bf6a35e090 · outbound

This paper cites A modified toxicity probability interval method for dose-finding trials.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology A modified toxicity probability interval method for dose-finding trials

Reference 8

Resolution
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raw_fallback, observed 2026-08-12T21:30:37.945189Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:31.594913Z digest=sha256:e3b0e2b60b95cb0c284a50102c2c5f15efe318a0f197cfda5808ed5fb9e2ea5b

Observation 2e35055e-e220-4651-a9c6-839c68f7a991 · outbound

This paper cites Toxicity and efficacy probability interval design for phase I adoptive cell therapy dose-finding clinical trials.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Toxicity and efficacy probability interval design for phase I adoptive cell therapy dose-finding clinical trials

Reference 9

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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:31.644847Z digest=sha256:2ac27387cf98611c241ba24b001ca9b469e0fdf3f9e734ee07bbc9a294c0a372

Observation 2bb52219-670e-4453-b72a-2e4335316e52 · outbound

This paper cites TEPI-2 and UBI: designs for optimal immuno-oncology and cell therapy dose finding with toxicity and efficacy.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology TEPI-2 and UBI: designs for optimal immuno-oncology and cell therapy dose finding with toxicity and efficacy

Reference 10

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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:31.694798Z digest=sha256:28f1f03e2c94e551d1f59ebbc2ac3df6d341c7b1fa42a1957f0bd7332bd948d7

Observation c5d2991e-98d9-4368-91ff-6d28d3de30f2 · outbound

This paper cites Comparison between simultaneous and se- quential utilization of safety and efficacy for optimal dose determination in Bayesian model-assisted designs.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Comparison between simultaneous and se- quential utilization of safety and efficacy for optimal dose determination in Bayesian model-assisted designs

Reference 11

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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 6e1cf004-557e-4b1c-bdc4-ab81dc8c6ee2 · outbound

This paper cites STEIN: A simple toxicity and efficacy interval design for seamless phase I/II clinical trials.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology STEIN: A simple toxicity and efficacy interval design for seamless phase I/II clinical trials

Reference 12

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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 0313e8cd-c3aa-4fd7-9fdd-3dadfbdba54e · outbound

This paper cites BOIN12: Bayesian optimal interval phase i/ii trial design for utility-based dose finding in im- munotherapy and targeted therapies.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology BOIN12: Bayesian optimal interval phase i/ii trial design for utility-based dose finding in im- munotherapy and targeted therapies

Reference 13

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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 06894c9f-5ca4-4816-abde-275f6ba5263f · outbound

This paper cites Probability intervals of toxicity and efficacy design for dose- finding clinical trials in oncology.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Probability intervals of toxicity and efficacy design for dose- finding clinical trials in oncology

Reference 14

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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:31.874755Z digest=sha256:c0874d3d7d0b90af6c5669d6fde1c3d66cad6f94e9e65859f7cdff3368e7d6d8

Observation 6d285e25-842a-4eb5-bafa-e4620d83690a · outbound

This paper cites A robust Bayesian dose-finding design for phase I/II clinical trials.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology A robust Bayesian dose-finding design for phase I/II clinical trials

Reference 15

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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:31.914754Z digest=sha256:a2fc56de33e08f548712b875f06dc4a2371ef3124ff0baab8aa5b85bf1bba978

Observation 424faf72-4ccd-4951-a322-0291bcbc1293 · outbound

This paper cites Bayesian optimal interval designs for phase I clinical trials.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Bayesian optimal interval designs for phase I clinical trials

Reference 16

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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 28d6d696-3108-440f-807b-2b0200b400f7 · outbound

This paper cites Serious ethical dilemma of single-agent pegylated liposomal dox- orubicin employed as a control arm in ovarian cancer chemotherapy trials.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Serious ethical dilemma of single-agent pegylated liposomal dox- orubicin employed as a control arm in ovarian cancer chemotherapy trials

Reference 17

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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation fcc16289-5f35-439a-9d66-f4e43d54d814 · outbound

This paper cites Optimizing dosing of oncology drugs.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Optimizing dosing of oncology drugs

Reference 18

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raw_fallback, observed 2026-08-12T21:30:36.303033Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.009987Z digest=sha256:f8d28c33c81a119dd3f93518ff67fe7876d90b800e02bef045dabad185a4d012

Observation a2b2ea55-f621-43ee-9c3b-339a42d02012 · outbound

This paper cites Critical aspects of the Bayesian approach to phase I cancer trials.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Critical aspects of the Bayesian approach to phase I cancer trials

Reference 19

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raw_fallback, observed 2026-08-12T21:30:36.139892Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.022219Z digest=sha256:e1d671fa916a72ce8c2e972d6bbd9581ba634ee0267a48a4ac3786e808f2658f

Observation 80598ab8-56ac-4e20-b530-c034bf39179f · outbound

This paper cites Keyboard design for phase I drug-combination trials.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Keyboard design for phase I drug-combination trials

Reference 20

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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.040257Z digest=sha256:2b1d49137d0bf90d4784e42254b261243a1286bda044ab21950e97708f31bd7a

Observation 5bdbd738-7a50-4eac-84e3-62dc7b320029 · outbound

This paper cites Phase I trials of molecularly targeted agents: should we pay more attention to late toxicities.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Phase I trials of molecularly targeted agents: should we pay more attention to late toxicities

Reference 21

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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.052376Z digest=sha256:c6e82c63a95837bf98136c579e6adb10c4faf4bfd5cfc8037d4163dec4a47518

Observation 63157d38-b2b3-4005-8273-5d365fdb3a9c · outbound

This paper cites Anti-bcma car t-cell therapy bb2121 in relapsed or refractory multiple myeloma.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Anti-bcma car t-cell therapy bb2121 in relapsed or refractory multiple myeloma

Reference 22

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verified fuzzy
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Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.092063Z digest=sha256:9e3d1cf993ae11a896dd62bd116d82376ecc8b87f69485df5062091f79226725

Observation 62754dc1-154e-444e-9ee2-2b9dca15e7af · outbound

This paper cites An adaptive dose-finding method using a change-point model for molecularly targeted agents in phase I trials.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology An adaptive dose-finding method using a change-point model for molecularly targeted agents in phase I trials

Reference 23

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verified fuzzy
raw_fallback, observed 2026-08-12T21:30:35.484756Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.100147Z digest=sha256:8aa996933d9e4a6d555046268ac0bb4ee60c28d5b1263569593e543977d11d96

Observation 6b9e140d-6ac0-4436-ac80-9ac10060978f · outbound

This paper cites uTPI: A utility-based toxicity probability interval design for phase I/II dose-finding trials.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology uTPI: A utility-based toxicity probability interval design for phase I/II dose-finding trials

Reference 24

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verified fuzzy
raw_fallback, observed 2026-08-12T21:30:35.304755Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.113800Z digest=sha256:e3b4c9991eeede139266b43ad01ad0a30d06d6613186542a5292884df6ee5287

Observation 07269774-4e72-40a8-9e82-f5c054572906 · outbound

This paper cites Comparative review of novel model-assisted designs for phase I/II clinical trials.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Comparative review of novel model-assisted designs for phase I/II clinical trials

Reference 25

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verified fuzzy
raw_fallback, observed 2026-08-12T21:30:35.134756Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.138407Z digest=sha256:d85a4aa4601aea5ab7dfd0313f638a5f6bfdd05506f234a5682f3b5eb5af6ee5

Observation 6feee087-89fb-4d94-a8ec-c3467fc91b39 · outbound

This paper cites Pkboin-12: A bayesian optimal interval phase i/ii design incor- porating pharmacokinetics outcomes to find the optimal biological dose.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Pkboin-12: A bayesian optimal interval phase i/ii design incor- porating pharmacokinetics outcomes to find the optimal biological dose

Reference 26

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verified fuzzy
raw_fallback, observed 2026-08-12T21:30:34.974754Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.153873Z digest=sha256:b5489a52a3227e1129a44ec7ae932495aa6f601fd1748f2bf442138f5f5e18af

Observation f08c73a0-62d1-4a53-b61c-2aa10002a5c5 · outbound

This paper cites BOIN-ET: Bayesian optimal interval design for dose finding based on both efficacy and toxicity outcomes.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology BOIN-ET: Bayesian optimal interval design for dose finding based on both efficacy and toxicity outcomes

Reference 27

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verified fuzzy
raw_fallback, observed 2026-08-12T21:30:34.794759Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.193261Z digest=sha256:6d23c3bf3fa35638e407e3dad4673b8faecc048ffd1b565cca3995a4cec7ffe9

Observation 991eac41-3982-4c5d-a8ed-d9a0fd88639c · outbound

This paper cites TITE-BOIN-ET: time-to-event Bayesian optimal interval design to accelerate dose-finding based on both efficacy and toxicity outcomes.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology TITE-BOIN-ET: time-to-event Bayesian optimal interval design to accelerate dose-finding based on both efficacy and toxicity outcomes

Reference 28

Resolution
verified fuzzy
raw_fallback, observed 2026-08-12T21:30:34.634840Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.225719Z digest=sha256:3c3145b3c76977f7b247f7d89ef5bee99f127e70d4daf9b0345d3eb134c38721

Observation 3bcec4a4-3063-4f50-865f-70f8b63631ae · outbound

This paper cites gBOIN-ET: The generalized Bayesian optimal interval design for optimal dose-finding accounting for ordinal graded efficacy and toxicity in early clinical trials.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology gBOIN-ET: The generalized Bayesian optimal interval design for optimal dose-finding accounting for ordinal graded efficacy and toxicity in early clinical trials

Reference 29

Resolution
verified fuzzy
raw_fallback, observed 2026-08-12T21:30:34.454828Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.265266Z digest=sha256:abb38deaa6cf946672d816ed813fd4dd69c14b32ea60e5e69bd8ec58d006bd11

Observation f1ddd41f-3848-4483-be4a-4bb673cc35bf · outbound

This paper cites TITE- gBOIN-ET: Time-to-event generalized Bayesian optimal interval design to accelerate dose-finding accounting for ordinal graded efficacy and toxicity outcomes.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology TITE- gBOIN-ET: Time-to-event generalized Bayesian optimal interval design to accelerate dose-finding accounting for ordinal graded efficacy and toxicity outcomes

Reference 30

Resolution
verified fuzzy
raw_fallback, observed 2026-08-12T21:30:34.264835Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.312833Z digest=sha256:b914e9bee8670ea1cfa2cd704c52c75dd4996898cdeae33c0576e63c5f7cc3e3

Observation 1882351b-9fc4-46da-803b-08f386dd7f2b · outbound

This paper cites Dose-finding based on efficacy–toxicity trade-offs.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Dose-finding based on efficacy–toxicity trade-offs

Reference 31

Resolution
verified fuzzy
raw_fallback, observed 2026-08-12T21:30:34.094833Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.355109Z digest=sha256:a6b1c418bc05387faf2cf1582859eb0db94fe5ac5271e35ccc6df0839efade83

Observation e92ce4da-4f3c-4f2d-8318-1805fd63a6f2 · outbound

This paper cites Toxicities of immunotherapy for the practitioner.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Toxicities of immunotherapy for the practitioner

Reference 32

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verified fuzzy
raw_fallback, observed 2026-08-12T21:30:33.935141Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

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Observation 6d6b669e-ff75-41dc-8b76-ff3dc8dec4ea · outbound

This paper cites Optimal biological dose selection in dose-finding trials with model-assisted designs based on ef- ficacy and toxicity: a simulation study.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Optimal biological dose selection in dose-finding trials with model-assisted designs based on ef- ficacy and toxicity: a simulation study

Reference 33

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verified fuzzy
raw_fallback, observed 2026-08-12T21:30:33.754751Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.414754Z digest=sha256:67b55f1dfb66e7b4f9784e17a5a1ef2a209eed68216856e3e20450c026bdb142

Observation 6625a000-a4b7-4f78-bce0-20b5992273fe · outbound

This paper cites Keyboard: A novel Bayesian toxicity probability interval design for phase I clinical trials.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Keyboard: A novel Bayesian toxicity probability interval design for phase I clinical trials

Reference 34

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verified fuzzy
raw_fallback, observed 2026-08-12T21:30:33.574869Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.464846Z digest=sha256:f2361c3edfddb187f2c51fb6a37e55cd4d987a42a56ccfa38f7ca7d51e117921

Observation ae1de6ff-6dc2-4821-851b-2482967fa092 · outbound

This paper cites Bayesian optimal interval design: A simple and well-performing design for phase I oncology trials.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Bayesian optimal interval design: A simple and well-performing design for phase I oncology trials

Reference 35

Resolution
verified fuzzy
raw_fallback, observed 2026-08-12T21:30:33.390403Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.505437Z digest=sha256:5ede1e7fec149d51cb6433adce7b8b9bba22734dd57c19c4453da5b8e3de8b3b

Observation ccf4b27c-9f4e-4ed1-9e01-0ee0f619ef9d · outbound

This paper cites Model-assisted designs for early-phase clinical trials: simplicity meets superiority.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Model-assisted designs for early-phase clinical trials: simplicity meets superiority

Reference 36

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verified fuzzy
raw_fallback, observed 2026-08-12T21:30:33.214834Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.555270Z digest=sha256:2e3bcd913264375276db31ffd3c0313f66c92a4baf4cde5c5f01c1b943fa8089

Observation cc75c906-9e76-44e4-ac48-43b4fbd68cf4 · outbound

This paper cites Adaptive designs for identifying optimal biological dose for molecularly targeted agents.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology Adaptive designs for identifying optimal biological dose for molecularly targeted agents

Reference 37

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verified fuzzy
raw_fallback, observed 2026-08-12T21:30:33.055040Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.595234Z digest=sha256:38405d53ab5c92b29443e2a7f347298a6c76f2c2319475b6b0da89c30ddbc63a

Observation c891c67c-b2f3-4655-a791-6a1ee7547ad8 · outbound

This paper cites 33 Characteristics of Early Phase Dose Finding Designs 34 TITE-BOIN12: A Bayesian phase I/II trial design to find the optimal biological dose with late-onset toxicity and efficacy.

Statistical Operating Characteristics of Current Early Phase Dose Finding Designs with Toxicity and Efficacy in Oncology 33 Characteristics of Early Phase Dose Finding Designs 34 TITE-BOIN12: A Bayesian phase I/II trial design to find the optimal biological dose with late-onset toxicity and efficacy

Reference 38

Resolution
malformed identifier
raw_fallback, observed 2026-08-12T21:30:32.874756Z

Source-reported events for the cited work

No event found in the named queried sources as of 2026-08-22T06:32:14.747728+00:00.

source=pdf_text observed=2026-08-12T21:30:32.654756Z digest=sha256:6ee49abf00e99c6fd4fe48f70d0108bd5dc443ae3115a847345d6b36d59e5bb1

Pith citing papers

No inbound Pith citation observations are available.