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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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1290887 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 Type3 n& Z! c% C0 R0 v" h+ s' ]
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 3 P# M1 r. f1 y2 U$ u, @
+ Author Affiliations
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) v; x1 n" Q( W4 y3 ?& q+ F  e1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 6 Y, C- d8 g% Y) U% W3 c. T
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
, j( `( P3 m/ j! G' |+ J5 e3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
/ y  [) Q- E/ S" V, K4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
  b" K+ P3 {! x) i* E5 [; @' N5 D5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
( u. ?9 l5 ]' ~  `7 Z  p6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 7 \- Y6 V8 B( h
7Kinki University School of Medicine, Osaka 589-8511, Japan 7 {1 j6 z7 c& v$ K  N
8Izumi Municipal Hospital, Osaka 594-0071, Japan
# I  d* m! b" V; [4 j9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
9 z, x* k6 |- n) _% n. e0 pCorrespondence 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 8 A! g; v9 d/ a1 V+ D+ B. i
AbstractBackground: 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. 9 n" o9 E0 Z) t1 k* g$ M1 L: ^
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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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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
% }& a  Z2 v* z; q% p0 G) i! Z' ?# P& n: A
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  % X8 r, }& F$ V: F! j0 ~
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Published online on: Thursday, December 1, 2011   o( H; S7 P$ L" m
, J, g: ^/ _- I3 R9 K8 @6 N& O
Doi: 10.3892/ol.2011.507
  ]0 T& M' ^- J9 n* R9 q8 e3 v( F: M
Pages: 405-410 2 a1 J/ n. W  O% w

$ n' M; n' u( E+ O' aAbstract:
: Y6 w& U/ I0 m9 g! l- X+ KS-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.+ }, Y9 v# \' e' B9 N$ B2 M

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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  a/ }/ D! M* u
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
/ _3 J. ^( k' W$ W6 r( D4 G+ Author Affiliations' Z% A; y* E. n0 n; i
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
0 k9 r" ~3 v5 d1 q/ a- Q  y3 Z2Department of Thoracic Surgery, Kyoto University, Kyoto
: v) p' e) a9 J1 @6 E7 a3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan % `; }# I. u. h  `! ~' n
&#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
, ]5 G* |! H% r; aReceived September 3, 2010.
6 Y! l- T: _1 h- Y% W- s7 xRevision received November 11, 2010.
7 p6 N# c; Y' l: qAccepted November 17, 2010.
+ q4 T7 R5 A: AAbstract
! u3 K" ~$ S8 c: h0 P6 {) G  rBackground: 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. # K; i+ S/ M0 k3 ?8 {: k% {
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.
$ @  d( }8 o4 PResults: 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. / x" E: k$ s' P  i
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. # _2 [8 ]' M, ^$ V" Y
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。
3 I* S+ o$ N! {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?
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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
: C9 L, a( K: S$ E/ z6 Whttp://clinicaltrials.gov/ct2/show/NCT01523587
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! r" H/ s: w; T) d  j4 R* nBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
1 K% d2 J6 b* N  \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 1 h. u) a* Y% f
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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。: D7 y" Y1 N$ r0 A; k+ Z* Q
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 9 _5 [* m6 W" }* Z7 z2 E; W0 v
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。
. L$ e( e2 n$ V2 d* ~6 v; E至今为止,未出 ...

: h' t9 N# \0 @$ v+ Q没有副作用是第一追求,效果显著是第二追求。
# F% m/ V7 s& @& G  n不错。

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