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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1310201 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type2 L. r6 K; q& F
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 * {# `! o$ g! w% A9 v8 |' X
+ Author Affiliations3 g- H& H6 n; j
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ! n! B- }! t' H; ^
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
" ]3 @4 E% r2 k3 M" p7 E3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
! \% U, t4 P: W5 Q- a5 {7 z4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 9 ?# r% W1 q$ t  I
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
7 s  v# F+ S. x5 n, z' u& P% y6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
+ k1 C$ x" T1 h7Kinki University School of Medicine, Osaka 589-8511, Japan 5 e2 P5 |8 h; `1 \/ F7 s) c
8Izumi Municipal Hospital, Osaka 594-0071, Japan & m+ `1 \) f: w8 y  q
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
7 E; g& O( d, T- s  \' a" L. TCorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
4 V. }8 p( V/ {( V4 BAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
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' u( `9 y- @6 c7 D& ^Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato : N1 a0 h% T& n3 B7 q7 ?  o
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Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  " L: `0 S2 s' i5 q, O

, E* S/ g( A* `1 v& V" ^1 OPublished online on: Thursday, December 1, 2011 8 h" o& v# z  W, e& C- r! ]6 w
' a  E" O  {8 E% X' _
Doi: 10.3892/ol.2011.507 . A/ U! F+ v3 }# W- g. b4 k' y
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Pages: 405-410 " P. P3 W  j' G# k$ Z

' D3 O$ [! p% {0 zAbstract:8 z) {6 X  q0 I+ M9 ]
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population; Q$ w# k! l4 u
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
3 u( B" p/ ?/ G' h5 e+ Author Affiliations
( w" Z, t* q% x1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ' W# ]5 y# G; R. s- o  K; k8 y
2Department of Thoracic Surgery, Kyoto University, Kyoto ' w! a. d+ P6 t; T+ V
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan ) i% m  f; u) D5 _/ i$ g% m
&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp # Q* I! p6 e% c- ?- t, ?* K6 U
Received September 3, 2010. - W0 g! u, v$ N  b+ K& A# f+ c. F$ V
Revision received November 11, 2010.
8 m$ c" F9 p; D  w1 ^' TAccepted November 17, 2010. ! T# Z. X8 C3 w
Abstract! ^2 y: ]8 l" t7 R
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. % c8 w3 F3 ]* m1 A( ~
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes.
1 n# R8 l! {+ w9 Q3 NResults: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
  q5 I1 R. C3 [) d7 FConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。/ \9 t3 f; r/ P2 F* B- m
今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?8 d# m1 |4 B8 f; N0 U. n) D$ m' |
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy; @/ d: B. r: i6 X" z8 S% Z
http://clinicaltrials.gov/ct2/show/NCT01523587* c4 A! T2 \( g

/ p( a6 G- h0 t. WBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
# e0 w1 X- P# j8 Q# F3 ^http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 : V6 u1 T4 g# L% I$ I+ I

8 a6 Q8 f% A. e/ d0 Y; H! h8 v1 ]0 i从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
4 R5 N! p5 ^. s, L5 C0 X* z至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53 ) z. e  ^7 u2 ~: g. ]" S0 s
从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。& I- @( y. K9 n) \
至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。
2 J$ t! [9 N1 h1 G4 U9 u6 f不错。

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